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Muscle weakness

Muscle weakness is a medical symptom characterized by a reduction in the force-generating capacity of one or more muscles, leading to difficulty in performing normal physical activities such as lifting objects, climbing stairs, or maintaining posture.^[1] It can be localized to specific muscle groups or generalized across the body, and it often results from disruptions in the neuromuscular system rather than a standalone disease.^[2] This condition affects individuals of all ages but becomes more prevalent with advancing age due to natural muscle mass decline.^[3] The causes of muscle weakness are multifaceted, encompassing neurological disorders that impair nerve signals to muscles, such as stroke or multiple sclerosis; neuromuscular disorders like myasthenia gravis or primary muscle diseases like muscular dystrophy (the latter directly damaging muscle fibers); and systemic factors including infections, electrolyte imbalances, or chronic conditions like diabetes and thyroid disorders.^[1] Certain medications, such as corticosteroids or statins, can also induce weakness as a side effect, while temporary triggers like viral illnesses (e.g., flu or COVID-19) or muscle injuries may cause short-term episodes.^[3] In older adults, sarcopenia—a progressive loss of muscle mass and function—represents a common physiologic cause, often exacerbated by inactivity.^[3] Symptoms typically include not only diminished strength but also associated fatigue, muscle pain, cramps, or tremors, with severity varying based on the underlying etiology—proximal muscles (e.g., hips and shoulders) are often affected first in myopathies, while distal weakness may signal neuropathy.^[2] Diagnosis involves a thorough history, physical examination using standardized strength scales (e.g., Medical Research Council scale from 0 to 5), and targeted tests like blood work, electromyography, or imaging to identify the root cause.^[1] Management focuses on addressing the primary condition through approaches such as physical therapy to rebuild strength, medications to control inflammation or autoimmune responses, nutritional support, or, in severe cases, surgical interventions; early intervention is crucial to prevent complications like falls or dependency.^[2] Individuals experiencing sudden, one-sided, or progressive weakness should seek immediate medical evaluation to rule out emergencies like stroke.^[1]

Overview

Definition

Muscle weakness is defined as a reduction in the force-generating capacity of skeletal muscles during voluntary contraction, resulting in diminished muscle strength compared to expected norms for an individual's age, sex, and activity level.^[4]^[2] This condition is clinically assessed using standardized scales, such as the Medical Research Council (MRC) scale, which grades muscle power from 0 (no contraction) to 5 (normal strength against full resistance), allowing for objective quantification relative to typical performance in healthy individuals.^[5]^[6] It is important to distinguish muscle weakness from related but distinct conditions, such as hypotonia and atrophy. Hypotonia refers to decreased muscle tone at rest, characterized by reduced resistance to passive movement and a "floppy" quality, whereas muscle weakness specifically impairs active force production during contraction, though the two may coexist.^[7] Atrophy, on the other hand, involves the physical wasting or loss of muscle mass and tissue, often leading to secondary weakness but representing a structural change rather than a functional deficit alone.^[8]^[9] The term muscle weakness gained prominence in neurology during the early 20th century as a way to describe and quantify deficits in muscle power, particularly with the development of standardized assessment tools. A key milestone was the introduction of the MRC scale in 1943, which provided a systematic method to evaluate and document muscle strength in clinical and research settings, facilitating the separation of primary muscle disorders from neurological conditions.^[6]^[10]

Epidemiology

Muscle weakness, often manifesting as a key component of sarcopenia in aging populations, affects approximately 10-16% of adults over 60 years worldwide, with prevalence escalating to 30-50% among those over 80 due to progressive muscle mass decline.^[11]^[12] This age-related pattern underscores the condition's role in geriatric health, where sarcopenia contributes to frailty and reduced mobility. Incidence rates are notably elevated in chronic neurological conditions; for instance, up to 80% of individuals with multiple sclerosis experience muscle weakness as a primary symptom, impacting daily function from early disease stages.^[13] Similarly, post-stroke hemiparesis or weakness affects 65-70% of survivors, often persisting and complicating rehabilitation efforts.^[14]^[15] Demographic factors significantly influence the distribution of muscle weakness. Age is a primary driver, with individuals over 50 experiencing an annual muscle mass loss of 1-2%, accelerating vulnerability to weakness and associated disabilities.^[16]^[17] Gender disparities are evident in specific etiologies, such as autoimmune myopathies, where the condition is twice as prevalent in females compared to males, potentially linked to hormonal and immunological differences.^[18]^[19] The global burden of muscle weakness is reflected in its contribution to disability-adjusted life years (DALYs), particularly through weakness-related mobility impairments. According to the 2021 Global Burden of Disease Study (IHME)—with trends continuing into 2023—musculoskeletal disorders, encompassing sarcopenia and weakness-induced limitations, account for about 17% of total global DALYs, a major contributor among disease categories and highlighting the need for targeted interventions.^[20]

Etiology

Neurological Causes

Neurological causes of muscle weakness primarily involve disruptions in the central nervous system (CNS), peripheral nervous system (PNS), or neuromuscular junction due to diseases or injuries affecting neural pathways that control muscle function. These conditions lead to impaired signal transmission from the brain to muscles, resulting in true weakness rather than perceived fatigue. Central causes often produce upper motor neuron signs like spasticity, while peripheral causes typically manifest as lower motor neuron features such as flaccid paralysis and atrophy. Central nervous system disorders are a major contributor to muscle weakness. In stroke, ischemic or hemorrhagic events damage motor cortex or pathways, leading to hemiparesis in approximately 80% of hospitalized patients. Multiple sclerosis, particularly the relapsing-remitting form, involves demyelinating plaques that disrupt descending motor pathways in the CNS, causing weakness, spasticity, and slowed movements. Parkinson's disease, characterized by dopaminergic neuron loss in the substantia nigra, presents with rigidity and bradykinesia that can mimic muscle weakness, often leading to misdiagnosis as a cerebrovascular event. Peripheral nervous system involvement results in acute or progressive weakness through demyelination or axonal damage. Guillain-Barré syndrome is an acute immune-mediated polyneuropathy causing demyelination of peripheral nerves, leading to ascending symmetrical weakness starting in the lower limbs and potentially progressing to respiratory failure. Amyotrophic lateral sclerosis (ALS) features progressive degeneration of upper and lower motor neurons, resulting in muscle weakness, atrophy, and fasciculations, with an annual incidence of approximately 2 per 100,000 individuals. Spinal cord pathology, including trauma or degenerative compression, can cause weakness by interrupting corticospinal tracts. For instance, cervical spondylosis leads to spinal cord compression and myelopathy, often resulting in quadriparesis with gait instability and upper extremity involvement. This is the most common cause of nontraumatic paraparesis or quadriparesis in older adults. Botulism exemplifies neurotoxin-mediated weakness at the neuromuscular junction, where Clostridium botulinum toxin inhibits acetylcholine release from presynaptic terminals, producing descending flaccid paralysis. In foodborne cases, symptoms typically onset 12 to 36 hours after toxin ingestion, beginning with cranial nerve involvement and progressing to limb weakness.

Muscular and Metabolic Causes

Primary myopathies encompass a range of inherited and acquired disorders directly affecting skeletal muscle structure and function, leading to progressive weakness. Duchenne muscular dystrophy (DMD), the most common severe form of childhood muscular dystrophy, is an X-linked recessive disorder caused by mutations in the DMD gene on the X chromosome, which encodes the dystrophin protein essential for muscle cell stability.^[21] Symptoms typically onset between ages 3 and 5, manifesting as delayed motor milestones, frequent falls, and proximal muscle weakness, with affected boys often becoming wheelchair-dependent by their early teens due to rapid progression.^[22] Polymyositis, an acquired inflammatory myopathy, arises from autoimmune-mediated inflammation targeting muscle fibers, resulting in symmetric proximal weakness, fatigue, and dysphagia.^[23] Laboratory findings include markedly elevated serum creatine kinase (CK) levels, often exceeding 10 times the upper limit of normal (typically >1,000-2,000 U/L), reflecting ongoing muscle damage.^[24] Metabolic disturbances can precipitate muscle weakness through electrolyte imbalances or endocrine dysregulation, disrupting normal muscle contraction and energy metabolism. Hypokalemia, defined as serum potassium levels below 3.5 mEq/L, impairs muscle excitability and can cause acute flaccid paralysis, particularly affecting proximal muscles and respiratory function in severe cases (<2.5 mEq/L).^[25] Thyroid disorders also contribute: hyperthyroidism accelerates muscle protein catabolism via excess thyroid hormone, leading to proximal weakness, tremors, and atrophy, while hypothyroidism slows metabolism and induces myoedema—a localized muscle contraction elicited by percussion due to delayed relaxation.^[26]^[27] Toxic and drug-induced myopathies arise from environmental exposures or medications that damage muscle fibers or interfere with mitochondrial function. Statin-associated myopathy, a common adverse effect of cholesterol-lowering therapy, ranges from mild myalgias to severe rhabdomyolysis, with the latter carrying a risk of 0.01-0.1% in users, often linked to higher doses or drug interactions.^[28] Chronic alcohol consumption induces alcoholic myopathy through direct ethanol toxicity and nutritional deficiencies, preferentially causing necrosis and atrophy of type II (fast-twitch) muscle fibers, resulting in proximal weakness and reduced endurance.^[29]^[30] Infectious causes, particularly viral myositis, can lead to acute muscle inflammation and weakness as a post-infectious complication. Influenza virus, for instance, is associated with benign acute childhood myositis, where 5-10% of pediatric cases following infection present with sudden calf pain and gait disturbance due to elevated CK and transient inflammation, typically resolving within days to weeks.^[31]

Classification

True Versus Perceived Weakness

True weakness refers to an objective reduction in muscle force generation, typically assessed using standardized scales such as the Medical Research Council (MRC) manual muscle testing scale, where a score below 5/5 indicates impaired strength against resistance.^[32] This deficit arises from structural or physiological disruptions, such as denervation in motor neuron diseases or myopathic processes in inflammatory conditions like dermatomyositis.^[32] In contrast, perceived weakness involves a subjective sensation of reduced capacity or effort intolerance despite normal objective muscle power on formal testing.^[4] It often stems from non-neuromuscular factors, including early fatigue in chronic conditions, deconditioning, or psychogenic influences like anxiety and depression.^[33] Differentiating the two requires careful clinical evaluation, as true weakness persists or worsens with repetitive testing, reflecting underlying pathology, whereas perceived weakness may improve with encouragement, distraction, or rest, revealing intact motor function.^[2] For instance, in true weakness due to neurological causes like stroke, patients exhibit consistent force deficits and associated signs such as atrophy or reflex changes.^[4] Perceived weakness, however, lacks these objective markers and may fluctuate based on psychological state or perceived exertion.^[32] A classic example of perceived weakness occurs in functional neurological disorder (FND), where patients may present with unilateral limb paresis mimicking hemiparesis from a cerebrovascular event, but without muscle atrophy, pyramidal signs, or electrophysiological evidence of organic damage.^[34] Diagnosis in such cases relies on positive clinical signs, like Hoover's sign (involuntary leg extension during contralateral effort), which demonstrate inconsistent weakness and preserved subconscious motor control.^[34] This distinction is crucial, as misattributing perceived weakness to structural disease can delay appropriate psychological or rehabilitative interventions.^[2]

Proximal Versus Distal Weakness

Muscle weakness can be classified based on its anatomical distribution as proximal or distal, which provides key insights into the underlying pathology. Proximal weakness primarily affects the muscles of the shoulder and hip girdles, leading to difficulties in tasks such as rising from a seated position, climbing stairs, or lifting objects overhead.^[32] This pattern is characteristic of many myopathies, including polymyositis, an inflammatory condition that causes symmetrical proximal muscle involvement due to endomysial inflammation.^[23] In contrast, distal weakness targets the more peripheral muscles, such as those in the hands and feet, manifesting as challenges with fine motor skills, dropping objects, or foot drop.^[32] Diabetic polyneuropathy exemplifies this, typically presenting with progressive distal sensory and motor deficits starting in the lower extremities.^[35] Specific patterns of weakness further refine diagnostic considerations. Symmetric proximal weakness is frequently observed in endocrine disorders, such as hypothyroidism or hyperthyroidism, where hormonal imbalances lead to proximal myopathy affecting limb girdles bilaterally.^[36] Conversely, asymmetric distal weakness is a hallmark of certain motor neuron diseases, like amyotrophic lateral sclerosis, involving selective lower motor neuron degeneration that spares sensory functions and progresses unevenly.^[37] The distribution of weakness holds significant clinical relevance for localizing the lesion. Proximal-predominant weakness often implicates primary muscle disorders or anterior horn cell pathology, as these structures directly innervate girdle musculature.^[38] Distal weakness, however, more commonly indicates peripheral nerve involvement, where length-dependent axonal degeneration affects distant nerve terminals first.^[39] This distinction guides targeted investigations, such as electromyography or nerve conduction studies, to differentiate between myopathic and neuropathic etiologies.^[32]

Pathophysiology

Central Mechanisms

Central mechanisms of muscle weakness primarily involve impairments in the supraspinal and spinal neural drive that initiate and sustain voluntary muscle contractions, distinct from peripheral muscle dysfunction. These processes reduce the efficiency of motor unit recruitment and firing rates without altering the intrinsic contractile properties of muscles. Central fatigue represents a core central mechanism, characterized by a progressive decline in motor cortex output and failure to adequately drive spinal motoneurons during prolonged or intense activity. This reduction in central drive is linked to alterations in neurotransmitter systems, particularly the accumulation of serotonin (5-hydroxytryptamine, 5-HT) in the brain, which elevates the serotonin-to-dopamine ratio and suppresses dopaminergic signaling, thereby diminishing arousal, motivation, and the perceived capacity for effort.^[40] The "central fatigue hypothesis" posits that this imbalance, often exacerbated during endurance exercise, inhibits motor cortical excitability and contributes to an unwillingness to maintain muscle activation, independent of peripheral factors.^[41] Lesions affecting upper motor neurons (UMNs), such as damage to the pyramidal (corticospinal) tract from stroke, trauma, or demyelinating diseases like multiple sclerosis, disrupt descending inhibitory pathways from the cortex to spinal interneurons. This leads to disinhibition of spinal reflexes, resulting in spasticity—a velocity-dependent increase in muscle tone—and concomitant weakness, particularly in antigravity muscles like leg extensors.^[42] Weakness manifests as reduced voluntary force generation, often with hyperreflexia, clonus, and a positive Babinski sign, reflecting the loss of precise corticospinal control over fractionated movements.^[43] Cortical and supraspinal factors further impair descending volitional control, limiting the recruitment and rate coding of motor units. In conditions such as depression or chronic pain, neuroplastic changes in the motor cortex lead to disinhibition and reduced output, where dysfunctional descending antinociceptive pathways exacerbate inhibitory influences on motoneuron pools, contributing to perceived and actual weakness.^[44] Functional MRI (fMRI) studies of sustained motor tasks reveal central fatigue through changes in blood-oxygen-level-dependent (BOLD) signal in the primary motor cortex, indicating diminished neural activation and supraspinal contribution to fatigability.^[45]

Peripheral Mechanisms

Peripheral mechanisms of muscle weakness involve disruptions at the neuromuscular junction, within muscle fibers themselves, and in metabolic pathways that impair force generation and sustainment, independent of central neural drive. These processes lead to localized failures in excitation-contraction coupling, structural integrity, or energy supply, resulting in reduced muscle performance during activity. Unlike central mechanisms, which affect supraspinal and spinal control, peripheral issues manifest as task-specific or progressive declines in strength due to bioenergetic or biophysical impairments. At the neuromuscular junction, failure often arises from autoimmune blockade of acetylcholine receptors, as seen in myasthenia gravis, where circulating autoantibodies bind to postsynaptic nicotinic acetylcholine receptors, preventing efficient neurotransmitter binding and signal transmission. This blockade reduces the endplate potential amplitude, leading to incomplete muscle fiber activation and characteristic fatigable weakness that worsens with repeated contractions. Complement-mediated damage and accelerated receptor internalization further exacerbate the junctional dysfunction, contributing to fluctuating weakness predominantly in ocular, bulbar, and proximal limb muscles.^[46]^[47] Muscle fiber damage represents another key peripheral mechanism, particularly in muscular dystrophies where genetic defects disrupt sarcolemmal stability, leading to calcium dysregulation and contraction-induced injury. In conditions like Duchenne muscular dystrophy, absence of dystrophin allows excessive calcium influx through membrane tears during forceful contractions, elevating intracellular calcium levels and activating proteolytic enzymes such as calpains. This dysregulation promotes myofiber necrosis, fibrosis, and progressive weakness, as repeated eccentric contractions amplify damage and impair regenerative capacity. Studies in animal models confirm that blocking calcium channels can mitigate fiber degeneration, underscoring the role of dysregulated calcium homeostasis in chronic muscle wasting.^[48]^[49] Metabolic depletion contributes to peripheral weakness through impaired energy substrate availability, exemplified by glycogen exhaustion in McArdle's disease, a myophosphorylase deficiency that prevents glycogen breakdown during exercise. Without phosphorylase activity, muscles rely solely on aerobic glycolysis and free glucose, leading to rapid ATP depletion and exercise intolerance characterized by early fatigue, cramps, and myoglobinuria after brief intense efforts. Patients often exhibit a "second wind" phenomenon as alternative fuels mobilize, but sustained activity remains limited due to blocked glycogenolysis.^[50]^[51] Additionally, lactic acid accumulation during anaerobic metabolism induces acute peripheral weakness by causing intracellular pH drops that hinder cross-bridge cycling in actin-myosin interactions. High-intensity efforts shift to glycolysis, producing lactate and hydrogen ions that lower muscle pH below 7.0, reducing actomyosin ATPase activity and calcium sensitivity of troponin, thereby slowing contraction velocity and force output. This acidosis-related impairment is particularly evident in short bursts of maximal effort, where proton buildup directly interferes with excitation-contraction coupling without involving central fatigue.^[52]^[53]

Clinical Presentation

Symptoms

Patients commonly describe muscle weakness as a sensation of heaviness or fatigue in the limbs, which can make routine movements feel disproportionately effortful.^[4] This subjective experience often manifests as difficulty with everyday tasks, such as rising from a chair, combing hair, or climbing stairs, especially when proximal muscles in the shoulders, hips, and thighs are affected.^[54]^[55] Associated symptoms frequently include generalized fatigue that worsens with activity, muscle cramps or tenderness, and occasional tremors, particularly in neurological etiologies.^[1]^[56] In chronic cases, prolonged disuse can lead to muscle atrophy and subsequent weight loss, further compounding the sense of debility.^[57] The temporal pattern of symptoms varies widely: acute onset may occur rapidly following viral infections, presenting as sudden limb heaviness and inability to perform basic actions, whereas insidious progression is typical in neurodegenerative conditions like amyotrophic lateral sclerosis (ALS), where weakness develops gradually over months to years.^[58]^[59]^[60] These patient-reported experiences profoundly affect quality of life, with in older adults approximately 60% of individuals with weakness reporting limitations in instrumental activities of daily living, such as shopping or managing finances, resulting in diminished independence.^[61]

Physical Signs

Physical signs of muscle weakness are identified through systematic clinical examination, revealing objective deficits in muscle function, tone, and structure. Reduced grip strength is a key observable finding, often assessed by dynamometry or manual testing, where patients exhibit diminished force during hand closure, indicating involvement of forearm and intrinsic hand muscles. This sign is particularly prominent in conditions affecting upper limb motor pathways or peripheral nerves.^[2] In proximal myopathies, a positive Gowers' sign is a characteristic manifestation, observed when patients use their hands and arms to "climb" up their legs from a supine or squatting position to stand, compensating for weakness in the pelvic girdle and hip extensors. This compensatory maneuver highlights the selective impairment of proximal lower limb muscles while sparing distal ones.^[62] Reflex changes provide insight into the underlying neural pathway affected. Hyperreflexia, with exaggerated deep tendon reflexes such as brisk knee jerks, is typical of upper motor neuron lesions causing weakness, due to loss of inhibitory control from higher centers. Conversely, hyporeflexia or areflexia accompanies peripheral or lower motor neuron weakness, reflecting disrupted reflex arcs at the spinal or neuromuscular junction level.^[42] Muscle atrophy and fasciculations are visible signs of chronic denervation. Atrophy presents as symmetric or asymmetric wasting of affected muscle groups, most evident in chronic processes like disuse or nerve injury, leading to a reduction in muscle bulk and contour. Fasciculations, manifested as fine, irregular twitching beneath the skin, are hallmark features of motor neuron diseases, arising from spontaneous firing of denervated muscle fibers.^[63] Functional tests further quantify physical signs of weakness. The timed up-and-go test, which measures the time taken to rise from a chair, walk 3 meters, turn, return, and sit, taking ≥12 seconds indicates risk for falling and suggests significant lower limb weakness and mobility impairment, correlating with overall functional decline.^[64]

Diagnosis

History and Examination

The evaluation of muscle weakness begins with a detailed history to characterize the condition and guide further assessment. Key elements include the onset of symptoms, which may be sudden (over hours to days, often indicating vascular, infectious, or toxic etiologies) or gradual (over weeks to months, suggesting chronic neurologic or metabolic causes).^[32] The distribution of weakness is also critical: proximal involvement, such as difficulty rising from a chair or climbing stairs, commonly points to myopathies, while distal patterns may suggest neuropathies or specific myositides.^[32] Associated symptoms provide additional clues; for instance, sensory loss or pain often accompanies peripheral neuropathies, whereas oropharyngeal issues like dysphagia or dysarthria raise concern for bulbar involvement in conditions such as myasthenia gravis or motor neuron disease.^[32]^[4] The physical examination focuses on confirming and localizing the weakness through systematic testing. Manual muscle testing using the Medical Research Council (MRC) scale is the standard method, grading strength from 0 (no muscle contraction) to 5 (normal power against full resistance).^[5] This involves isolating individual muscle groups, starting with proximal limbs and progressing to distal ones, while observing for patterns such as upper versus lower motor neuron signs (e.g., hyperreflexia or atrophy).^[5] A comprehensive neurologic exam assesses reflexes, sensation, coordination, and gait to differentiate central from peripheral causes. Red flags in the history and examination demand urgent evaluation to rule out life-threatening conditions. These include rapid progression of weakness, which may signal acute inflammatory or compressive neuropathies, and bulbar symptoms like dysphagia, indicating potential respiratory compromise or disorders such as amyotrophic lateral sclerosis.^[4] Asymmetric or focal deficits, along with systemic signs like fever or rash, further heighten suspicion for infectious, inflammatory, or structural etiologies requiring prompt intervention.^[32] If red flags are present, advanced diagnostic tests may be warranted to expedite diagnosis.

Diagnostic Tests

Diagnostic tests for muscle weakness encompass a range of laboratory, electrophysiological, imaging, and histopathological investigations aimed at confirming the presence of weakness, identifying its underlying cause, and localizing the lesion to central or peripheral mechanisms. These tests provide objective evidence beyond clinical history and examination, helping differentiate between myopathic, neuropathic, and neuromuscular junction disorders. Selection of tests depends on the suspected etiology, with initial screening often including blood analyses followed by more invasive procedures if needed. Blood tests are a cornerstone of initial evaluation, particularly for detecting muscle damage or systemic involvement. Serum creatine kinase (CK) levels are routinely measured, with elevations greater than 500 U/L indicating muscle injury, as seen in inflammatory myopathies like polymyositis where levels can range from 5 to 50 times the upper limit of normal (typically 200 U/L).^[65] In necrotizing autoimmune myopathy, CK can exceed 50 times the upper limit, reflecting severe fiber necrosis.^[66] Other blood tests may include electrolytes, thyroid function, and inflammatory markers to rule out metabolic or endocrine contributors to weakness. Electrophysiological studies, including electromyography (EMG) and nerve conduction studies (NCS), are essential for assessing neuromuscular integrity. EMG detects denervation potentials such as fibrillations and positive sharp waves, which signal active muscle fiber damage or reinnervation in neurogenic disorders, often correlating with the degree of weakness and atrophy.^[67] NCS evaluate nerve function, revealing slowed conduction velocities (typically below 80% of normal) characteristic of demyelinating neuropathies, distinguishing them from axonal processes.^[68] For suspected neuromuscular junction disorders like myasthenia gravis, repetitive nerve stimulation at low frequencies (2-5 Hz) demonstrates a decrement in compound muscle action potential amplitude exceeding 10%, confirming impaired transmission.^[69] Imaging modalities aid in visualizing structural abnormalities contributing to weakness. Magnetic resonance imaging (MRI) is particularly sensitive for detecting muscle edema on T2-weighted or STIR sequences in inflammatory myopathies, with abnormalities present in 80-90% of active cases, often involving proximal muscles like the thighs.^[70] Computed tomography (CT) scans are useful for identifying spinal cord compression from tumors or degenerative changes, which can cause bilateral weakness, though MRI is preferred for its superior soft-tissue contrast.^[71] Muscle biopsy remains the gold standard for definitive diagnosis in suspected muscular dystrophies and inflammatory conditions, providing histopathological insights into fiber necrosis, inflammation, or dystrophic changes. In dystrophinopathies like Duchenne muscular dystrophy, biopsy reveals absent dystrophin expression via immunohistochemistry, confirming the diagnosis when genetic testing is inconclusive.^[72] Specimens are typically obtained from moderately affected muscles to avoid sampling errors, with analysis including hematoxylin-eosin staining for inflammation and electron microscopy for ultrastructural details.^[73]

Management

Acute Interventions

Acute interventions for muscle weakness prioritize rapid stabilization to prevent respiratory failure, cardiac complications, or further neurological deterioration in sudden or severe episodes, such as those seen in electrolyte disturbances, myasthenic crisis, or inflammatory neuropathies. Supportive care forms the cornerstone, particularly addressing underlying electrolyte imbalances that can precipitate acute paralysis. For instance, in hypokalemic periodic paralysis, intravenous potassium replacement is essential for severe hypokalemia (serum potassium <2.5 mEq/L), with dosing typically starting at 10-20 mEq/hour under cardiac monitoring to avoid rebound hyperkalemia, alongside IV fluids to maintain hydration and correct associated metabolic acidosis.^[74] This approach rapidly restores muscle function in most cases, with oral potassium preferred for milder episodes once the patient can ingest it. Similarly, for other electrolyte derangements like hyponatremia contributing to weakness, isotonic IV fluids such as 0.9% sodium chloride are administered to normalize sodium levels gradually, preventing osmotic demyelination.^[75] Pharmacologic interventions target specific etiologies in acute settings, with acetylcholinesterase inhibitors like pyridostigmine serving as first-line therapy for myasthenic crisis in myasthenia gravis. Administered orally at 30-60 mg every 4-6 hours or intravenously at 1-2 mg every 3-6 hours (equivalent to 30 mg oral dose), pyridostigmine enhances neuromuscular transmission by inhibiting acetylcholine breakdown, improving muscle strength within hours and reducing the need for intubation in up to 70% of cases when combined with supportive ventilation.^[76] Dosing must be titrated carefully to avoid cholinergic excess, which can exacerbate weakness through muscle cramps or secretions. In parallel, corticosteroids such as methylprednisolone (1 g IV daily for 3-5 days) may be initiated acutely to suppress autoimmune activity, though their benefits peak after 1-2 weeks.^[77] For immune-mediated conditions like Guillain-Barré syndrome (GBS), emergency procedures such as plasmapheresis (plasma exchange) are employed to remove pathogenic antibodies and inflammatory mediators from the circulation. The standard protocol involves 5 sessions over 1-2 weeks, exchanging 200-250 mL/kg of plasma, which accelerates recovery by 1-2 weeks compared to supportive care alone and reduces the risk of mechanical ventilation by approximately 50% in severe cases by hastening nerve conduction improvement.^[78] This intervention is particularly critical in the first 2 weeks of onset, with efficacy comparable to intravenous immunoglobulin but preferred in patients with renal impairment or volume overload.^[79] As of 2025, advancements in monoclonal antibodies have expanded acute options for refractory cases of neuromuscular junction disorders, such as generalized myasthenia gravis with persistent blockade despite standard therapies. Eculizumab, a complement C5 inhibitor, is approved for rapid initiation in refractory AChR-antibody positive myasthenia gravis crises, administered as 900 mg IV weekly for the first 4 weeks, followed by 1200 mg every 2 weeks; clinical trials demonstrate significant improvements in muscle strength and reduced hospitalization rates within 4-12 weeks, with a favorable safety profile in acute settings.^[80] These biologics represent a targeted escalation when plasmapheresis or IVIG fails, bridging to long-term immunosuppression without delaying crisis resolution.^[81]

Long-Term Strategies

Long-term strategies for managing persistent muscle weakness focus on disease-modifying therapies to address underlying causes, supportive interventions to preserve function, nutritional optimization, and multidisciplinary approaches to enhance daily living and safety. These approaches aim to slow progression, improve quality of life, and prevent complications in conditions such as autoimmune myopathies, muscular dystrophies, and sarcopenia. Disease-modifying treatments target the root pathology of muscle weakness. For autoimmune myopathies, immunosuppressants like prednisone are commonly initiated at a dose of 1 mg/kg/day to reduce inflammation and halt muscle damage.^[82] In muscular dystrophies, such as Duchenne muscular dystrophy, gene therapy options like eteplirsen, approved by the FDA in 2016, enable exon-skipping to produce functional dystrophin protein in eligible patients. For example, delandistrogene moxeparvovec (Elevidys), an AAV-based gene therapy delivering a micro-dystrophin transgene, received FDA accelerated approval in June 2023 for ambulatory pediatric patients aged 4-5 years with confirmed DMD gene mutations, with traditional approval expanded in 2024 based on clinical benefits in motor function.^[83]^[84] Ongoing clinical trials continue to explore advanced gene therapies to modify disease course in dystrophies. Supportive therapies emphasize maintaining muscle function and range of motion through structured exercise. Physical therapy, including resistance training performed three times per week, can improve muscle strength by 20-30% in older adults with weakness, helping to counteract atrophy and enhance mobility.^[85] Nutritional interventions play a key role in supporting muscle health, particularly in age-related weakness like sarcopenia. Protein supplementation at 1.2-1.6 g/kg/day is recommended to promote muscle protein synthesis and preserve lean mass in older individuals.^[86] Additionally, vitamin D supplementation provides metabolic support by improving muscle strength and reducing weakness associated with deficiency, especially in those with limited sun exposure or malabsorption.^[87] Multidisciplinary care integrates occupational therapy to adapt the environment and promote independence. Occupational therapists recommend adaptive devices, such as grab bars and mobility aids, which can reduce fall risk by approximately 25% in patients with muscle weakness by addressing environmental hazards and functional limitations.^[88] This holistic approach, often involving coordination with physical therapists and nutritionists, sustains long-term functional gains and minimizes disability.

Prognosis

Influencing Factors

Patient factors play a significant role in modifying the course and severity of muscle weakness. Advanced age, particularly over 65 years, is associated with poorer recovery due to delayed, prolonged, and inefficient muscle repair processes following injury or disuse, as older muscle exhibits anabolic resistance and reduced regenerative capacity.^[89] Comorbidities such as diabetes further exacerbate this by impairing skeletal muscle regeneration, creating an environment of excessive fibrosis and delayed myofiber maturation, which contributes to accelerated muscle atrophy and dysfunction through peripheral neuropathy.^[90]^[91] Disease-specific variables can substantially alter muscle weakness outcomes. For instance, in acute ischemic stroke—a common cause of hemiparesis—early thrombolytic intervention with tissue plasminogen activator (tPA) administered within 4.5 hours of symptom onset improves functional recovery, with clinical trials demonstrating a relative increase of up to 30% in the odds of achieving favorable outcomes such as independence in daily activities.^[92] This time-sensitive approach underscores how prompt disease management can mitigate the extent of persistent weakness. Lifestyle factors influence muscle weakness progression through direct effects on muscle maintenance. Smoking accelerates skeletal muscle atrophy by impairing protein synthesis and increasing expression of atrophy-related factors like MAFbx, leading to reduced muscle mass and function that heightens vulnerability to weakness.^[93] Conversely, regular exercise mitigates sarcopenia—the age-related loss of muscle mass and strength—by promoting muscle protein synthesis, enhancing mitochondrial function, and delaying progression, with resistance and aerobic training showing consistent benefits in preserving muscle health.^[94] Socioeconomic determinants, particularly access to rehabilitation services, significantly shape long-term trajectories of muscle weakness. Disparities in rehabilitation access contribute to variability in recovery, with health services research indicating that systemic barriers influence disability outcomes by limiting opportunities for structured physical therapy and support, thereby perpetuating weakness in underserved populations.^[95]

Outcomes by Cause

Muscle weakness outcomes vary significantly depending on the underlying cause, with neurological etiologies often leading to partial recovery but persistent deficits, while metabolic causes tend toward high reversibility with prompt intervention. In neurological conditions, post-stroke muscle weakness, such as hemiparesis, shows variable recovery; approximately 64% of patients achieve functional independence by 6 months post-event, though full motor restoration is less common and depends on lesion size and rehabilitation intensity.^[96] For amyotrophic lateral sclerosis (ALS), muscle weakness progresses relentlessly, with a median survival of 2-5 years from symptom onset, during which patients experience escalating limb and respiratory involvement leading to dependency.^[97] Muscular disorders present diverse prognoses. In myasthenia gravis, symptoms including fluctuating weakness can be controlled or achieve remission in 70-80% of cases with immunosuppressive therapies like corticosteroids, enabling many patients to maintain daily function.^[98] Conversely, progressive muscular dystrophies, such as Duchenne type, result in severe weakness and high mortality without advanced supportive care; survival beyond age 30 is around 25-30% in untreated or historically managed cohorts, though with modern multidisciplinary care including corticosteroids, noninvasive ventilation, and targeted therapies, median survival has improved to approximately 28-30 years as of 2025, with over 50% surviving beyond age 30.^[99]^[100] Metabolic causes generally offer favorable outcomes due to their treatability. Electrolyte imbalances, like hypokalemia or hypophosphatemia inducing acute weakness, are reversible in nearly all cases with timely correction, often resolving muscle symptoms within days to prevent complications such as rhabdomyolysis.^[33] For chronic thyroid disorders, such as hypothyroidism causing myopathy, thyroid hormone replacement leads to substantial improvement in muscle strength for most patients, typically within 2-3 weeks, though full recovery may take months.^[26]

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May 27, 2025 · Muscle atrophy is the wasting (thinning) or loss of muscle tissue. Alternative Names. Muscle wasting; Wasting; Atrophy of the muscles. Causes.
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Definition of muscle wasting - NCI Dictionary of Cancer Terms
A weakening, shrinking, and loss of muscle caused by disease or lack of use. Muscle wasting decreases strength and the ability to move.
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MRC Muscle Scale - UKRI
Aug 6, 2025 · The muscle scale grades muscle power on a scale of 0 to 5 in relation to the maximum expected for that muscle.Missing: definition | Show results with:definition
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Epidemiology of sarcopenia: Prevalence, risk factors, and ...
Sarcopenia affects 10 %–16 % of the elderly worldwide. Sarcopenia is associated with a high risk of a wide range of adverse health outcomes.
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Multidisciplinary approach to sarcopenia: a narrative review
Sep 7, 2023 · The prevalence of sarcopenia increases with age, affecting approximately 10% of adults over the age of 65 years and up to 50% of those over 80 ...
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Characteristics and Management of Major Symptoms - NCBI - NIH
Weakness of the limbs is a constant feature of advanced MS and is present in approximately 80 percent of all people with MS (reviewed in Matthews, 1998 ). Both ...
[14]
Incidence, Time Course and Predictors of Impairments Relating to ...
Seventy per cent of people with stroke will experience arm weakness, and 62% of these will not recovery dexterity in the arm at 6 months post‐stroke (Kwakkel ...
[15]
Muscle strengthening for hemiparesis after stroke: A meta-analysis
After a stroke, hemiparesis is a serious motor impairment, affecting 65% of stroke victims [3].
[16]
Sarcopenia: Its assessment, etiology, pathogenesis, consequences ...
For example, after 50 years of age, muscle mass is reported to decline at an annual rate of approximately 1 to 2% (4), but strength declines at 1.5% per year ...
[17]
Strength and muscle mass loss with aging process. Age and ... - NIH
Profound changes with a leg lean body mass loss of 1–2%/year18–20 and a strength loss of 1.5–5%/year11,18–21 are reported for individuals older than 50 years ( ...
[18]
Autoimmune Myopathies - PMC - PubMed Central - NIH
1 These diseases, which affect women about twice as often as men, are rare, with an estimated combined incidence of four cases per 100,000 person-years and ...
[19]
Idiopathic inflammatory myopathies – a guide to subtypes ...
Apart from inclusion body myositis (IBM), all IIM subtypes occur more commonly in women (ratio 2:1); IBM occurs twice as commonly in men as women. Subtypes.
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an ecological study assessing disease burden and research funding
Musculoskeletal diseases were the third leading cause of DALYs, contributing 12.50% of the total, and were the third most prevalent disease, with 40.96% ...
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Comprehensive Analysis of Musculoskeletal Disorders Worldwide
Oct 24, 2024 · We gathered data on the number of prevalent cases, incidences, deaths, and disability-adjusted life years (DALYs) for MSDs from 1990 to 2021.
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Duchenne muscular dystrophy and dystrophin - NIH
Duchenne muscular dystrophy (DMD) is caused by mutations in the gene that encodes the 427-kDa cytoskeletal protein dystrophin.
[23]
Duchenne Muscular Dystrophy - StatPearls - NCBI Bookshelf
Mutations in the dystrophin gene result in diseases known as dystrophinopathies, which encompass Duchenne muscular dystrophy, Becker muscular dystrophy, and an ...Missing: bound | Show results with:bound
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Polymyositis - StatPearls - NCBI Bookshelf
Feb 7, 2023 · Serum creatine kinase (CK) levels can be up to 50 times the normal range (22 to 198 units/liter), indicating myocyte damage due to chronic ...Missing: >10x | Show results with:>10x
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Causes of Creatine Kinase Levels Greater Than 1000 IU/L in ... - NIH
Patients with DM or PM often have high CK concentrations, usually more than 10-fold and sometimes up to 50-fold the upper limit of normal values [10].Missing: >10x | Show results with:>10x
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Hypokalemic periodic paralysis, a rare yet critical condition - NIH
In HPP, flaccid paralysis usually develops when the serum K level is <3. mEq/l. The serum K level in the patient described herein case was 2.66 mEq/l.
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Hypothyroid Myopathy - StatPearls - NCBI Bookshelf
Jun 7, 2024 · Hypothyroid myopathy is a condition that occurs when the thyroid gland does not produce enough thyroid hormones.Missing: catabolism | Show results with:catabolism
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Endocrine myopathies: clinical and histopathological features of the ...
Hyperthyroidism mainly leads to symptoms like muscle wasting and weakness such as proximal muscle weakness, involving both the upper and lower extremities ...Thyroid Disorders · Hypothyroidism · Adrenal Glands Disorders
[29]
Association Between Statin Use and Daptomycin-related ... - NIH
In patients using statins, myopathy is observed in 5%–10% and rhabdomyolysis only in 0.01%–0.1% [8, 9]. Rhabdomyolysis leads to a high mortality rate of ...
[30]
Alcoholic Myopathy: Pathophysiologic Mechanisms and Clinical ...
Skeletal muscle dysfunction (ie, myopathy) is common in patients with AUD, and alcoholic myopathy occurs in 40 to 60 percent of chronic alcoholics.
[31]
Alcohol and Skeletal Muscle in Health and Disease - PMC - NIH
Nov 2, 2023 · Clinical signs associated with CAM are progressive proximal muscle weakness, type II fiber (fast twitch glycolytic fibers) atrophy, pain, and ...
[32]
A crawling case of benign acute childhood myositis - PMC - NIH
Sep 17, 2021 · Benign acute childhood myositis is a relatively uncommon complication of viral illness, particularly influenza A and B infections.
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Muscle Weakness in Adults: Evaluation and Differential Diagnosis
Jan 15, 2020 · True muscle weakness must first be differentiated from subjective fatigue or pain-related motor impairment with normal motor strength.
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Muscle Weakness and Fatigue: Causes and Treatment
Conditions affecting nerves tend to lead to true muscle weakness. This is because if the nerve to a muscle fibre stops working, the muscle fibre can't work ...
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Functional Neurological Disorder: New Phenotypes, Common ... - NIH
Jun 1, 2023 · ... weak gait, antalgic, parkinsonian, hemiparetic, dystonic. Gait ... functional leg weakness and the tremor entrainment test.
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Diabetic neuropathy - Symptoms & causes - Mayo Clinic
This type of neuropathy also may be called distal symmetric peripheral neuropathy. It's the most common type of diabetic neuropathy. It affects the feet and ...
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Diagnostic Approach to Proximal Myopathy - Skills in Rheumatology
Jan 6, 2021 · In symmetrical and diffuse weakness, it is important to know if the weakness is proximal or distal. There are several clues in the history ...Clinical Presentation of... · Differential Diagnosis of... · Diagnostic ApproachMissing: implications | Show results with:implications
[38]
Patterns of Weakness, Classification of Motor Neuron Disease ... - NIH
Nov 1, 2016 · Asymmetric distal weakness without sensory loss (NP5). If a patient comes in with asymmetric onset of distal weakness or muscle wasting and ...
[39]
Progressive Proximal Weakness in a 61-Year-Old Man | Neurology
Oct 21, 2021 · Peripheral nerve localization is possible, but both proximal and distal weaknesses would be expected, and most are hyporeflexic. In symmetric ...Missing: versus implications
[40]
Slowly progressive distal muscle weakness: neuropathy or myopathy?
Apr 3, 2019 · In general, diminished sensory nerve responses would immediately point to a peripheral neuropathy, while diminished motor nerve responses ...
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Central fatigue: the serotonin hypothesis and beyond - PubMed
This revised central fatigue hypothesis suggests that an increase in central ratio of serotonin to dopamine is associated with feelings of tiredness and ...Missing: muscle weakness
[42]
Serotonin and central nervous system fatigue: nutritional ...
THE CENTRAL FATIGUE HYPOTHESIS. Evidence is accumulating in support of a role for the neurotransmitter 5-HT, and perhaps dopamine, in central fatigue during ...
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Neuroanatomy, Upper Motor Neuron Lesion - StatPearls - NCBI - NIH
UMN lesions are designated as any damage to the motor neurons that reside above nuclei of cranial nerves or the anterior horn cells of the spinal cord.
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Neuroanatomy, Pyramidal Tract Lesions - StatPearls - NCBI Bookshelf
Pyramidal tract lesions will present very similarly to upper motor lesions with symptoms such as hyperreflexia, weakness, spasticity, and a Babinski sign.Structure And Function · Clinical Significance · Other IssuesMissing: scholarly | Show results with:scholarly
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Differential Neuroplastic Changes in Fibromyalgia and Depression ...
Thus, the disinhibition of the motor cortex indexed by SICI together with the dysfunction of the descending antinociceptive mechanisms is an essential feature ...Missing: weakness | Show results with:weakness<|separator|>
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Neural Contributions to Muscle Fatigue: From the Brain to the ...
This has been studied by the measurement of changes in short- and long-latency reflexes evoked by weak electrical stimulation of the Ia fibres of the ...
[47]
Myasthenia Gravis - StatPearls - NCBI Bookshelf - NIH
The pathophysiologic mechanisms in MG are dependent on the type of antibodies present. In n-AChR MG, the antibodies are of the IgG1 and IgG3 subtype. They bind ...
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Structural insights into the molecular mechanisms of myasthenia ...
Apr 25, 2017 · The disease occurs when the immune system produces molecules called antibodies that bind to and destroy a receptor protein called nAChR. This ...
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Mechanisms of muscle weakness in muscular dystrophy - PMC
These findings support a model in which calcium dysregulation causes increased myocyte death and gross muscle dysfunction.
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Abnormal Calcium Handling in Duchenne Muscular Dystrophy
An abnormal elevation of the intracellular calcium ( Ca i 2 + ) concentration in the dystrophin-deficient muscle is a major secondary event, which contributes ...
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McArdle Disease (Glycogen Storage Disease Type 5) - NCBI
Jan 22, 2025 · The most frequently reported symptom of McArdle disease is physical activity intolerance. Other symptoms include painful muscle cramps, weakness ...Missing: exhaustion | Show results with:exhaustion
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McArdle Disease and Exercise Physiology - PMC - NIH
Patients with MD have exercise intolerance with symptoms including premature fatigue, myalgia, and/or muscle cramps. Despite this, MD patients are able to ...Missing: exhaustion | Show results with:exhaustion
[53]
Muscle fatigue: general understanding and treatment - PMC
Oct 6, 2017 · Muscle fatigue is defined as a decrease in maximal force or power production in response to contractile activity.
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Biomarkers of peripheral muscle fatigue during exercise - PMC
A key role for muscle fatigue plays intracellular acidosis. Even minimal decrease in muscle pH interferes with cross-bridge binding and ATPase activity due to ...
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Polymyositis - Symptoms and causes - Mayo Clinic
Aug 10, 2022 · Overview. Polymyositis (pol-e-my-o-SY-tis) is an uncommon inflammatory disease that causes muscle weakness affecting both sides of your body.
[56]
Myopathy: Causes, Symptoms, Diagnosis & Treatment
Myopathy refers to diseases that affect skeletal muscles (muscles that connect to your bones). These diseases attack muscle fibers, making your muscles weak.
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Guillain-Barre syndrome: MedlinePlus Medical Encyclopedia
Apr 16, 2025 · Symptoms · Loss of tendon reflexes in the arms and legs · Tingling or numbness (mild loss of sensation) · Muscle tenderness or pain (may be a cramp ...
[58]
Muscle atrophy: Causes, symptoms, and treatments
Muscle atrophy is the loss of muscle mass. Low physical activity, nutritional deficiencies, genetic factors, and some medical conditions may contribute.
[59]
Post-viral syndrome: Symptoms, causes, and treatment
Post-viral syndrome refers to a sense of tiredness and weakness that lingers after a person has recovered from a viral infection, such as the flu.
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Three cases of acute myositis in adults following influenza-like ... - NIH
It is characterized by muscle pain and weakness with an isolated laboratory finding of elevated serum creatine kinase (CK).
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ALS Symptoms and Diagnosis - The ALS Association
A gradual onset of progressive muscle weakness – which is generally painless – is the most common initial symptom of ALS.
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Prevalence of Weakness and its Relationship with Limitations based ...
Overall prevalence of physical limitations, basic and instrumental ADL limitations was 52.9%, 28.1%, and 35.9%. In those with weakness, prevalence of physical ...
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Gower Sign - StatPearls - NCBI Bookshelf - NIH
Feb 13, 2023 · Gowers' sign is a clinical indicator of proximal muscle weakness. There are 3 Gower signs described in the medical literature:Definition/Introduction · Issues of Concern · Clinical Significance
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Motor Neuron Disease - StatPearls - NCBI Bookshelf
Aug 7, 2023 · Motor neuron disease (MND) is said to be a progressive neurological disorder that presents with both lower motor neurons (anterior horn ...
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Is the Timed Up and Go test a useful predictor of risk of falls in ...
Feb 1, 2014 · A TUG score of ≥13.5 seconds was used to identify individuals at higher risk of falling. All included studies were combined using a bivariate ...
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[PDF] EVALUATION, DIAGNOSIS, AND MANAGEMENT OF ...
This is a summary of the American Academy of Neurology (AAN) guideline on the evaluation, diagnosis, and management of facioscapulohumeral muscular dystrophy ( ...
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Polymyositis Workup: Approach Considerations, Imaging Studies ...
Aug 14, 2025 · Muscle enzyme levels Serum creatine kinase (CK) levels are usually elevated in persons with polymyositis, ranging from 5-50 times the reference ...Approach Considerations · Imaging Studies · Electromyography · Biopsy
[68]
Inflammatory Myopathies | Choose the Right Test - ARUP Consult
May 1, 2025 · Myositis-Related Antibody Tests ; DM, Normal or high CK, Affects adults and children ; NAM, Very high CK (can be >50 x ULN); elevations may ...Related Algorithms · Muscle Enzyme Tests · Myositis-Related Antibody...
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Electrodiagnostic Evaluation of Myopathy - StatPearls - NCBI - NIH
Oct 17, 2022 · Fibrillation potentials and positive sharp waves are potentials ... weakness and muscle atrophy in distal myopathies when CMAP can be reduced.
[70]
Nerve Conduction Studies: Demyelination (Chapter 14) - Essential ...
Sep 14, 2023 · Demyelination causes slowed conduction. This may be localised, as typified in entrapment neuropathies, or widespread as in demyelinating peripheral ...
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Repetitive Nerve Stimulation - StatPearls - NCBI Bookshelf - NIH
Jul 15, 2023 · Repetitive nerve stimulation in myasthenia gravis ... Decrement pattern in Lambert-Eaton myasthenic syndrome is different from myasthenia gravis.Continuing Education Activity · Introduction · Anatomy and Physiology · Preparation
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Imaging biomarkers in the idiopathic inflammatory myopathies - NIH
Apr 25, 2023 · MRI is ~80%−90% sensitive in showing muscle edema in active myositis (13, 20). Studies from juvenile DM showed that 76%−97% of patients will ...
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Spinal Cord Compression | Johns Hopkins Medicine
During the exam, they will look for signs of spinal compression, such as loss of sensation, weakness, and abnormal reflexes. Tests that help with your ...
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The Art of Muscle Biopsy in the New Genetic Era: A Narrative Review
Loss of immunohistochemical or immunofluorescent expression of dystrophin antibodies on a frozen muscle sample is still a gold standard for the diagnosis of ...
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Muscle Biopsy and Clinical and Laboratory Features of ...
Aug 17, 2023 · The biopsy of skeletal muscle tissue, typically termed muscle biopsy, plays an integral role in evaluation of the patient with neuromuscular disease.
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Hypokalemic Periodic Paralysis - StatPearls - NCBI Bookshelf - NIH
Mar 19, 2024 · Hypokalemic periodic paralysis (hypoPP) is a rare disorder caused by skeletal muscle ion channel mutations, mainly affecting calcium or sodium channels.Missing: <3.5 | Show results with:<3.5
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Electrolyte Imbalance: Types, Symptoms, Causes & Treatment
Symptoms of an electrolyte imbalance vary depending on the severity and electrolyte type, including weakness and muscle spasms. ... IV fluids like sodium chloride ...Electrolyte Panel · Hyponatremia · Hyperkalemia (High Potassium) · Hypokalemia
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Pyridostigmine Dosage Guide + Max Dose, Adjustments - Drugs.com
Nov 11, 2024 · Usual Adult Dose for Myasthenia Gravis: Immediate-release tablets and syrup: 60 to 1500 mg daily (usually 600 mg/day divided into 5 or 6 doses) spaced to ...
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Treatment of Myasthenia Gravis - PMC - PubMed Central
A typical starting dose is 60 mg every 6 hours during daytime hours (see Table 1). Dosage may be titrated up to 60 to 120 mg every 3 hours aiming to minimize ...
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Diagnosis and management of Guillain–Barré syndrome in ten steps
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Plasma exchange for Guillain‐Barré syndrome - PubMed Central - NIH
Plasma exchange was introduced for the treatment of GBS in the expectation of removing circulating antibodies or other factors responsible for the nerve damage.
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Efficacy and Safety of Eculizumab in Refractory Myasthenia Gravis
Apr 7, 2025 · Eculizumab demonstrates significant efficacy in the treatment of refractory Myasthenia Gravis compared to previous treatments.
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Myasthenia gravis in 2025: five new things and four hopes for the ...
Feb 22, 2025 · Early use of Rituximab in MuSK-antibody-positive patients and Eculizumab for severe or refractory AChR-antibody gMG was also recommended.
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Evaluation and Management of Polymyositis - PMC - NIH
... CK is probably the most reliable enzyme to measure. CK levels may sometimes be normal in late disease, or may remain above normal even after muscle strength ...Missing: >10x | Show results with:>10x<|separator|>
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[PDF] EXONDYS 51 (eteplirsen) injection Label - accessdata.fda.gov
EXONDYS 51 is indicated for the treatment of Duchenne muscular dystrophy (DMD) in patients who have a confirmed mutation of the DMD gene that is amenable to ...
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The time course of changes induced by resistance training and ...
It was found that both arm and leg muscle strength improved significantly (39 ± 27 % and 167 ± 125 %, respectively) over the course of 16 weeks in older ...Missing: percentage | Show results with:percentage
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Dietary protein supplementation in the elderly for limiting muscle ...
Overall, it appears that an intake of approximately 0.4 g protein/kg BW per meal thus representing 1.2-1.6 g protein/kg BW/day may be recommended taking into ...
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Effects of Vitamin D on Muscle Function and Performance - NIH
In seven studies, a beneficial effect of vitamin D treatment was documented on muscle strength of the lower legs, body sway, and/or physical performance.
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Home hazard modification programs for reducing falls in older adults
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Age-Associated Differences in Recovery from Exercise-Induced ...
Jan 30, 2024 · It is evident that aged muscle displays delayed, prolonged, and inefficient recovery. These changes can be attributed to anabolic resistance.Missing: poorer prognosis
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Impaired skeletal muscle regeneration in diabetes - ScienceDirect.com
Jun 4, 2024 · Diabetes creates an unfavorable environment for muscle repair, with excessive fibrosis and delayed myofiber maturation. Muscle regeneration ...
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Declining Skeletal Muscle Function in Diabetic Peripheral Neuropathy
Impairments in lower limb muscles reduce functional capacity and contribute to altered gait, increased fall risk, and impaired balance in patients with DPN.<|separator|>
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Intravenous Thrombolysis for Acute Ischemic Stroke Within 3 Hours ...
Recent clinical trials have provided evidence that IV tPA may be safe and effective in selected patients up to 4.5 hours after symptom onset.
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Smoking impairs muscle protein synthesis and increases the ...
This suggests that smoking has direct adverse effects on muscle protein metabolism, which may lead to loss of independence and disability with advanced age.
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Mitigating Sarcopenia with Diet and Exercise - PMC - NIH
Resistance exercise in healthy older adults, when compared to endurance training, produced larger strength gains with similar improvements in aerobic capacity, ...
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Improving Access to Stroke Rehabilitation and Recovery
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Factors Associated with Changes in Functional Independence after ...
Jul 6, 2020 · Almost all stroke patients recover to a considerable extent, yet only 64.1% of patients achieved functional independence 6 months after stroke ...
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Stages of ALS - The ALS Association
And, while the average survival time is three years, about 20% of people with ALS live five years, 10% survive 10 years and 5% live 20 years or longer.
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The Treatment of Myasthenia Gravis - U.S. Pharmacist
Jan 18, 2024 · In this case, an adult might be able to take the first pyridostigmine dose of the day—60 mg—at lunchtime, followed by 90 mg 4 hours and 8 hours ...
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Life Expectancy Increasing for DMD Patients, 40-year Analysis Finds
Feb 1, 2022 · Survival probabilities decreased with age. It was 99.8% at age 10, 59.5% at age 20, 26.1% at age 30, and 13.3% at age 40. Further analysis ...
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The rate and assessment of muscle wasting during critical illness
Jan 3, 2023 · The overall prevalence of ICU-acquired weakness was 48% (95% CI 39%, 56%). Conclusion. On average, critically ill patients lose nearly 2% of ...