muscular dystrophies in childhood

Muscular Dystrophies In Childhood

Dr Alpana SKDept of Pediatrics

Dr Alpana SK, www.peditips.com


What is muscular dystrophy?

Increasing weakness and loss of muscle mass and function until the patient is confined to a wheelchair

A problem with the synthesis of proteins in the muscle fibers causes deterioration

Four forms of the disease are recognized, based on: Pattern of inheritance Age when symptoms are first noted Distribution of the muscles first involved

Dystrophinopathy: disorders involving dystrophin

Duchenne MD and Becker MD are the muscular disorders – the two most common and severe dystrophies

Dystrophin is a very large gene on the X-chromosome, ubiquitous in the human body

Dystrophin-Associated Protein (DAP) Complex – composed of the extracellular, transmembrane, and intracellular components


Classification of types of MD

Heritable MDs include the following:

Sex-linked MDs Duchenne Becker Emery-Dreifuss

Autosomal dominant MDs Facioscapulohumeral Distal Ocular Oculopharyngeal

Autosomal recessive MD – limb-girdle form


What is Duchenne’s Muscular Dystrophy?

The disease is characterized Early onset often before school years By progressive muscular deterioration

and death by 14 to 18 years of age A defect of a large gene on the X


Prevalence of DMD

Affects one in 3500 to 5000 newborn males

1/3 of these with previous family history.

2/3 sporadic


What is the pattern of inheritance?

X-linked recessive inheritance


Duchenne Muscular Dystrophy Inheritance.

Mother carries the recessive gene and passes it to her child

Trait is usually expressed in males only


The gene for dystrophin production sits on the X chromosome.

Dystrophin is a cytosolic protein associated with the external membrane of skeletal, cardiac and smooth muscle cells and of some neurons

If a normal gene for dystrophin is present, then the protein will be made.

If the gene is missing or altered, dystrophin may not be produced at all or only in abnormal forms, resulting in Duchenne muscular dystrophy

Xp21 band is responsible for dystrophin production


In Duchenne muscular dystrophy (DMD) patients with a deletion of exons 45–54, an out-of-frame transcript is generated in which exon 44 is spliced to exon 55. Owing to the frame shift, a stop codon occurs in exon 55, which prematurely aborts dystrophin synthesis. b | Using an exon-internal antisense oligonucleotide (AON) in exon 44, the skipping of this exon can be induced in cultured muscle cells. Accordingly, the transcript is back in-frame and a Becker muscular dystrophy (BMD)-like dystrophin can be synthesized


http://genetics.kaiser.org/images/xlinkedrecessive.gif


In the Duchenne muscular dystrophy, the attachment of muscle fibers to their surrounding endomysium (extracellular matrix) becomes weakened due to mutations in the dystrophin gene.

(Image courtesy of the National Cancer Institute)

http://training.seer.cancer.gov/module_anatomy/images/illu_muscle_structure.jpg


What are the symptoms?

difficulty in walking at about the

age of four years increased size in calf muscles Loss of the ability to walk at about

the age of 11 Death at about the age of 18 or

later, usually because of respiratory failure.


Symptoms of DMD

Awkward gait (patients tend to walk on their forefeet, because of an increased calve tonus)

Frequent falls Progressive difficulty walking , Eventual loss of ability to walk (usually

by the age of 12) Difficulty with motor skills (running, hopping, jumping) Fatigue Higher risk of behaviour and learning difficulties. Skeletal deformities (including scoliosis in some cases) Muscle deformities of tongue and calf muscles. The enlarged muscle

tissue is eventually replaced by fat and connective tissue, hence the term pseudohypertrophy.

of heels and legs, rendering them unusable because the muscle fibers shorten and fibrosis occurs in connective tissue

http://en.wikipedia.org/wiki/Motor_skill

http://en.wikipedia.org/wiki/Scoliosis

http://en.wikipedia.org/wiki/Fibrosis

http://en.wikipedia.org/wiki/Connective_tissue


Posture changes during progression of Duchenne muscular dystrophy.


Possible Complications

Deformities Permanent, progressive disability

Decreased mobility Decreased ability for self-care

Mental impairment (varies, usually minimal) Pneumonia or other respiratory infections Respiratory failure Cardiomyopathy Congestive heart failure (rare) Heart arrhythmias (rare)


Diagnosing Muscular Dystrophy Detailed patient and family history (3 generation pedigree)

Determine the source of the muscle weakness (nerve or muscle

Laboratory tests: Serum CK is very elevated Troponin I is elevated above normal but not to levels in cardiac

ischemia Liver enzymes show high AST & ALT Muscle biopsy - Endomysial fibrosis Variable fiber size: Small

fibers rounded Dystrophic muscle Hypercontracted (opaque) muscle fibers

Myopathic grouping Muscle fiber degeneration & regeneration Muscle fiber internal architecture: Normal or immature Dystrophin: Absent staining Other membrane proteins: Sarcoglycans and Aquaporin 4 are

reduced


Diagnosing Muscular Dystrophy CPK test In DMD patients CPK leaks out of the muscle

cell into the bloodstream, so a high level (nearly 50 to 100 times more) confirms that there is muscle damage. Affected individuals may have a value as high as 15,000 to 35,000iu/l (normal = 60iu/l).

DNA test The dystrophin gene is composed of 79 exons,

and DNA testing and analysis can usually identify the specific type of mutation and the exon or exons that are affected. DNA testing confirms the diagnosis in most cases.[3]

http://en.wikipedia.org/wiki/Exons


a. Hematoxylin and eosin staining of control tissue

b. Hematoxylin and eosin staining of DMD patient, which shows abnormal variation in fiber size, degenerating and regenerating fibers, immune cell infiltration, and increased fibrosis

c. Immunofluorescence analysis of dystrophin in control tissue biopsy

d. Immunofluorescence analysis of dystrophin in a young DMD patient biopsy, illustrating the loss of sarcolemmal staining in DMD


Prenatal tests If one or both parents are 'carriers' of a particular

condition there is a risk that their unborn child will be affected by that condition. 'Prenatal tests' are carried out during pregnancy, to try to find out if the fetus (unborn child) is affected.

The tests are only available for some neuromuscular disorders. Different types of prenatal tests can be carried out after about 10 weeks of pregnancy.

Chorion villus sampling (CVS) - 10-12 weeks amniocentesis - 14-16 weeks, placental biopsy and foetal blood sampling - 18 weeks. Women and/or couples need to consider carefully which

test to have and to discuss this with their genetic counselor.

Earlier testing would allow early termination which would probably be less traumatic for the couple, but it carries a slightly higher risk of miscarriage than later testing (about 2%, as opposed to 0.5%).


Approach to Diagnosis of Childhood Muscular Dystrophy

No DeletionDetected

Diagnosis of Dystrophinopathy (DM D or BM D)

Deletion NotInform ativefor Severity

Deletion Inform ativefor Severity.

Positive Fam ily History

DeletionDetected

DNA Analysisfor Dystrophin

Gene Abnorm ality

M ale

Abnorm alDystrophin

M erosin andAdhalin Analysis

Norm alDystrophin

M uscle Biopsy

Female

Elevated

M uscular DystrophyUnlikely

Norm al

C K

M uscular W eakness


Therapy

Rehabilitation Therapy:

Physical Occupational Respiratory

Promising Therapies:

Pharmacologic Therapy Cell Therapy Gene Transfer Therapy Newer Targets


Treatment

There is no known cure for Duchenne muscular dystrophy

Treatment is generally aimed at control of

symptoms to maximize the quality of life.

Corticosteroids such as prednisone and deflazacort increase energy and strength and defer severity of some symptoms.

Mild, non-jarring physical activity such as swimming is encouraged. Inactivity (such as bed rest) can worsen the muscle disease.

http://en.wikipedia.org/wiki/Corticosteroids

http://en.wikipedia.org/wiki/Prednisone

http://en.wikipedia.org/wiki/Deflazacort

http://en.wikipedia.org/wiki/Bed_rest


Treatment Physical therapy is helpful to maintain muscle strength,

flexibility, and function.

Orthopedic appliances (such as braces and wheelchairs) may improve mobility and the ability for self-care. Form-fitting removable leg braces that hold the ankle in place during sleep can defer the onset of contractures.

Appropriate respiratory support as the disease

progresses is important Idebenone is a new drug currently being actively

researched and is expected to be approved in the US and Europe by Santhera Pharmaceuticals. Meanwhile it is sold in the US as a nutritional products mainly by Cognitive Nutrition. www.cognitivenutrition.com/ The effective dose is 450 mg daily.

http://en.wikipedia.org/wiki/Contractures


Advances in Gene Therapy(3)

Researches have developed "minigenes," which carry instructions for a slightly smaller version of dystrophin, that can fit inside a virus. Utrophin.. Is similar to dystrophin and can be engineered.

Researchers have also created the so-called gutted virus, a virus that has had its own genes removed so that it is carrying only the dystrophin gene


Prognosis

Duchenne muscular dystrophy eventually affects all voluntary muscles and involves the heart and respioratory muscles in later stages.

Survival is rare beyond the early 30s,although recent advancements in medicine are extending the lives of those afflicted.

Death in Duchenne muscular dystrophy most commonly results from pulmonary insufficiency, respiratory infections.

In about 10% of cases, death is due to cardiac dysfunction..

Congenital Muscular Dystrophy

Presentation: neonatal onset of severe weakness, delayed motor milestones, contractures

Merosin negative/CMD A1 White matter hypodensities on brain scan but

normal mental capacity Diagnosis by muscle biopsy

immunohistochemistry showing loss of α2-laminin (AR-chromosome 6q22-23)

Neuronal Migration Disorders

With neuronal migration disorders get mental retardation, brain malformations, and clinical eye involvement

Fukuyama’s muscular dystrophy – affects fukutin protein (AR – chromosome 9q31)

Muscle-eye-brain disease – affects POMGnT1, (AR – chromosome 1p32-34)

Walker Warburg – affects POMT1 (AR) Glycosyltransferases are also important in

neuronal development

Myotonic Muscular Dystrophy or Steinert’s disease Presentation – adult with multiple systems affected

Primarily distal and facial weakness Facial features: frontal balding in men, ptosis, low-

set ears, hatchet jaw, dysarthria, swan neck, ^ shaped upper lip

Myotonia: worse in cold weather, after age 20 Heart: conduction block – evaluate syncope Smooth muscle: constipation, care with swallowing,

gallstones, problems with childbirth, BP lability Brain: learning disabilities, increased sleep

requirement Ophthalmology: cataracts Endocrine: insulin resistance, hypothyroidism,

testicular atrophy

FascioScapularHumeral Muscular Dystrophy

Presentation: Facial weakness with trouble blowing up a balloon,

sipping through a straw, whistling, trouble closing the eyes at night, scapular winging that may be asymmetric, pain

May have absence of pectoralis, biceps, or brachioradialis

Also affected: mild high pitched hearing loss, retinal abnormalities, mental retardation in early onset

Genetics/Testing Southern blot testing available (chromosome 4q35)

for decrease in repeats normally present Muscle biopsy may show lymphocytic infiltrates

Limb Girdle Muscular Dystrophy

Presentation: variable age of onset with weakness and wasting of the limb-girdle

May have calf hypertrophy, involvement of scapular muscle and deltoid in sarcoglycanopathies

Many types involve dysfunctional sarcoglycans – transmembrane proteins of the DAP that interact with cytoplasmic proteins

Table 2 – types of LGMD

Oculopharyngeal Muscular Dystrophy

Presentation: mid-adult with ptosis, facial muscle weakness with difficulty swallowing, proximal muscle weakness, may have extraocular muscle weakness, more common in French-Canadian and Hispanic population

Genetics Muscle biopsy shows filamentous nuclear inclusions

and ubiquitin containing vacuoles Affects poly A binding protein 2 (PABP2) by

expansion of a GCG repeat without anticipation seen – Southern blot (chromosome 14q11-13)

Emery-Dreifuss Muscular DystrophyScapuloperoneal MD

Presentation: stiff joints, shoulder and upper arm weakness, calf weakness, cardiac conduction defects and arrhythmias, contractures

Genetics X-linked type affects emerin

Diagnose by protein analysis of leukocytes or skin fibroblasts

DNA testing available (chromosome Xq28) AD affects lamin A or lamin C (chromosome 1q21) Nuclear membrane proteins

Distal Muscular Dystrophy

Presentation: weakness in forearms, hands, and lower legs clinically similar to a neuropathy but NCV normal

Muscle biopsy with autophagocytic vacuoles/ inclusion bodies

Table 3 – Types of DMDWelander distal myopathy AD/2p13 hands first

Anterior tibial/Markesbery-Griggs/Udd

AD/2q31-33

Nonaka/Inclusion body myopathy 2

AR/9p13 Rimmed vacuoles, inclusion bodies, affects GNE

Gowers/Laing distal myopathy AD/14q11

Miyoshi myopathy AR/2p13 Affects dysferlin

Distal myopathy with vocal cord and pharyngeal weakness

AD/5

Myopathies

Central core disease: Ryanodine receptor, Ca channel that mediates

excitation/contraction coupling, (AD – chromosome 19q13) Associated with Malignant Hyperthermia

Myotubular myopathy Myotubularin, important in myogenesis (Xq28)

Nemaline Myopathy Caused by many defects, disorder of thin filaments Rod-like stuctures on muscle biopsy

Inflammatory Juvenile Dermatomyositis Inclusion Body Myositis (usually distal) Adult Polymyositis (associated with malignancy)

Therapy

Contracture prevention Stretching exercises and postural

changing Stretch the most contracture prone

groups (gastrocnemius, hip flexors, iliotibial bands, hamstrings)

AFO at night to supplement

Strengthening/conditioning/endurance Goal is to maintain or improve muscle strength

and maximize functional ability – slight improvement is possible

Additional goal is to avoid muscular damage by overwork or injury

No eccentric contraction or delayed soreness Voluntary active exercise such as

swimming/hydrotherapy or cycling in ambulatory children currently recommended

Mobility aids Walking orthoses – KAFO Standing frames, standing wheelchairs, swivel

walker occasionally used Walkers where arm strength less affected Transfer board Wheelchair – power needed for independence Plan for indoor lift, van with lift, roll in shower

Improving daily activities of daily living Physical and Occupational Therapy – teaching

modified techniques Antigravity orthoses are being developed to assist in

daily living activities Splinting and therapy to prevent hand contractures

comfysplints.com

Surgery note the risk inherent to surgery – malignant

hyperthermia Palliative vs. rehabilitative Tendon releases

Achilles Need KAFO to walk post-op Relieves pain and allow shoe wear

Hamstring and iliotibial band Relieves hip and knee pain or contracture Allows better gait compensation

Scoliosis – spine stabilization Bracing is not effective with progressive

neuromuscular disease Timely correction of scoliosis is important

for patient comfort and respiratory ability Spine and scapular stabilization may aid

function of armsOphthalmology

Deficient eye closure oculomaxillofacial MD and FSH MD may require artificial tears or tarsorrhaphy

Treatment for cataracts in Myotonic MD

Respiratory Patients with morning headache, nightmares,

excessive daytime somnolence, mental dullness, difficulty concentrating, increased colds, coughing, or pneumonia should undergo evaluation

Influenza vaccine and pneumococcal vaccine In-exsufflator for airway clearance, cough assist Pulmonologist, pulmonary function testing

Assisted noninvasive ventilation Oxygen alone does not ventilate! Positive pressure ventilation vs. volume ventilation

with pressure limit Assisted ventilation with tracheostomy

Talk to patient about degree of desired intervention when respiratory status first starts to decline and before an acute event

The goal is home ventilation Cardiology

EKG – pacemaker for conduction defects and arrhythmias

Echocardiogram – afterload reduction, digoxin for cardiomyopathy

Nutrition/GI Overweight and underweight are

common problems Overweight impairs mobility Underweight decreases strength & health

Protein and calorie supplements Assess for dysphagia Intestinal hypomotility in DMD, CMD,

and myotonic dystrophy can require a bowel regimen to prevent constipation

Osteopenia/Osteoporosis Begins before walking stops, fractures may end

walking Worsened by steroids Calcium supplements, Miacalcin may help

Psychology/Neuropsychological Education – aid in planning Special education may not be needed with

accomodation and modifications Progressive loss of function affects patient and

family

muscular dystrophies in childhood

Health & Medicine

dystrophin duchenne

muscular dystrophies

muscular disorders

duchennes muscular dystrophy

dystrophin synthesis

becker muscular dystrophy

recessive gene

severe dystrophies dystrophin