Spinal Muscular Atrophy (SMA)

Original Editor - Evelin Milev Top Contributors - Evelin Milev, Jeremy Bryan, Nikhil Benhur Abburi, Lucinda hampton, Kim Jackson, Rucha Gadgil, Momina Khalid, Aminat Abolade, Rachael Lowe and Meaghan Rieke

Introduction

Spinal Muscular Atrophy (SMA) is a genetic disorder also considered to be a neurodegenerative disorder, specifically a motor neurone disease. SMA is characterised by the degeneration of alpha motor neurons in the spinal cord, affecting the control of voluntary muscle movement. It occurs in roughly one in 6,000–10,000 births. There are several classifications of SMA, which are assigned based on the age at which symptoms first occur along with the highest level of muscle activation attained or expected to be attained.

Pathological Process

SMA is considered to be an autosomal recessive condition resulting from the homozygous deletion of the gene SMN1 (survival of motor neuron 1). In some cases, it is possible for the neighboring SMN2 gene to compensate for a lack of the SMN1 gene. Therefore, if there is one or more additional copies of the SMN2 gene, later-onset and less severe SMA symptoms can occur.

Clinical Presentation and Classification

SMA is classified based on the age at which symptoms first occur as well as the level of muscle activation attained or expected to be attained. SMA symptoms range in severity but often include hypotonia, muscle weakness (proximal muscles greater than distal muscles and lower extremity than upper extremity), bone or joint issues, difficulty swallowing, and/or difficulty breathing.

Types of SMA

	TYPE 1 (MOST SEVERE)(Werdnig-Hoffmann disease of acute infantile SMA)	TYPE 2	TYPE 3 (Kugelberg-Welander syndrome or juvenile SMA)	TYPE 4
AGE OF ONSET	First 6 months	6-18 months	18 months or older	Adulthood (after 21 years)
SYMPTOMS	Reduce muscle tone Contractures Reflexes absent Swallowing,feeding difficulty	Can sit Unable to stand/walk without support Respiratory difficulties	Walk independently Difficulty in running, stair climbing Scoliosis	Mild to moderate leg weakness.
LIFE EXPENTANCY	Die before 2 years	Adolescence or young adulthood	Normal lifespan (with regular physical rehabilitations)	Normal lifespan(with little physical training)

Diagnostic Procedures

Diagnosis generally starts with genetic testing to determine whether or not the SMN1 gene is absent. Genetic testing has been found to have a 95% sensitivity (test shows the absence of SMN1 the gene when it is truly absent) and an almost 100% specificity (test shows the presence of SMN the gene when it is truly present). If genetic testing does return a result consistent with clinical signs and symptoms, additional testing in the form of electrocardiography, a muscle biopsy, a nerve conduction velocity study, or blood tests can be performed.

Differential Diagnosis

DD of spinal Muscular Atrophy

Outcome Measures

There are several outcome measures which can be used to detect changes in the course of treatment for patients with SMA. These tools should be appropriately selected according to the age and severity of the disease.

• Six-Minute Walking Test (6MWT) - The Six-Minute-Walking-Test can be safely performed in ambulant patients with SMA. It has been proven to detect fatigue-related changes in this population of patients and also correlates with other established outcome measures for patients with spinal muscular atrophy.

• Revised Hammersmith Scale for SMA (RHS) - The RHS is predominantly used in patients with SMA types 2 and 3. In combination with the World Health Organisation (WHO) motor milestones, the scale can be more sensitive toward the description of the SMA phenotype. The RHS has been designed to capture a wide range of abilities across a broad spectrum of SMA, from very young children to adolescents and adults.

• WHO Developmental Milestones - The WHO scales aim to link the growth of the child and motor development in one single reference. The final version of the protocol includes six items: "Sitting without support," "hands-and-knees crawling," "standing with assistance," "walking with assistance," "standing alone," and "walking alone.". The WHO provides important information about a child's gross motor development in different cultural settings.

• Revised Upper Limb Module (RULM) for SMA - The RULM is a specifically designed outcome measure for upper limb function in patients with Spinal muscular atrophy. The scale has shown good reliability and validity, which makes it a good choice for assessing arm function in children and adults with SMA.

Management / Interventions

The management of SMA warrants a multi-disciplinary approach coordinated by the patient's primary clinician.

Orthopedic Management

• Spinal deformities
  • Scoliosis
    • Bracing
      • Limit scoliosis progression during growth years, not corrective
    • Surgical intervention (hardware implantation)
      • The goal is to ultimately promote better breathing mechanics and sitting alignment
• Contractures
  • Management through Physical Therapy
  • Surgical intervention if significant impairment or pain is present
• Fractures
  • Cast immobilization if non-ambulatory
  • Surgical fixation, if ambulatory

Nutrition Management

• Maintenance of adequate nutritional intake
  • Adequate calcium and vitamin D
• Maintenance of appropriate body mass index
• Screening and monitoring for complications such as...
  • Glucose abnormalities
  • Hyperlipidemia
  • Abnormal fatty acid metabolism
  • Metabolic acidosis

Speech and Language Pathology

• Screening and intervention for dysphagia

Medical Management:

• Neuroprotective drugs like riluzole
• Drugs to improve energy metabolism
• Drugs affecting the gene expression of SMN.

Gene Therapy:

• Along with advances in medical management, gene therapy approaches have been evaluated for SMA, using viral vectors to replace the SMN1 gene.

Physiotherapy

• Merconi et al. provide a comprehensive outline of physiotherapy management for SMA broken down by functional level.

Table derived from Merconi et al.

Functional Level	Goals	Possible Deficits	Possible Interventions/Adaptations
Patients not able to sit unsupported	Facilitate optimal function	Deficiencies in postural control Decreased sitting tolerance Contractures Muscular weakness	Thoracic and cervical bracing to promote appropriate positioning and posture Orthoses, splints, serial casting, AAROM, PROM, stretching, and or standing frame use to facilitate contracture prevention and management Adaptive equipment Sitting brace or sitting system Postural support equipment Positioning equipment Hoist or lift system Recline/tilt wheelchair Eye tracking equipment for communication and computer use
Patients able to sit unsupported	Contracture management/prevention Scoliosis management/prevention Facilitate independence with function and mobility	Deficiencies in postural control Contractures Muscle weakness	Thoracic and cervical bracing to promote appropriate posture Orthoses, splints, serial casting, AAROM, PROM, stretching, and or standing frame use to facilitate contracture prevention and management Adaptive equipment If needed, any equipment suggested for patients not able to sit unsupported Gait training devices UE support devices Power or lightweight wheelchair with appropriate postural support
Patients able to ambulate	Facilitate highest level of function Improve or maintain joint ROM/contracture management and or prevention Improve of maintain endurance Improve or maintain balance	Deficiencies in postural control Contractures Muscle weakness Decreased endurance Decreased balance	Thoracic and cervical bracing to promote appropriate posture (while in sitting) Orthoses, splints, serial casting, AAROM, PROM, stretching, and or standing frame use to facilitate contracture prevention and management Adaptive equipment If needed, any equipment suggested for patients not able to sit unsupported Power wheelchair, lightweight wheelchair, or scooter for longer distances Gait training for improvement of endurance, efficiency, and safety Balance training

Respiratory Care

Many children and adults with Spinal muscular atrophy will be dependent on pulmonary management due to a loss of muscle function. A respiratory therapist should be included in the multidisciplinary treatment team from an early stage to ensure proper respiratory management.

• Chest physiotherapy - assists with respiratory management and should be one of the primary airway clearance therapies.
• Mechanical insufflation–exsufflation - devices such as Cough Assist or Vit alCough can be used and this should be one of the primary airway clearance therapies.
• Suctioning is a critical part of the treatment and should be used in all patients with excessive secretions or in those with an ineffective cough.
• The high-frequency chest wall oscillation (Vest) is another option for managing secretions. However, there is no evidence that the Vest improves airway clearance or secretions.
• Non-invasive positive pressure ventilation (NIV) should be used for respiratory failure or to prevent chest wall distortion.
• Continuous positive airway pressure (CPAP) should be used only when NIV is not tolerated or in the treatment of chronic respiratory failure.