Articles / Journals
Nalini, Atchayaram, Narayanappa Gayathri, Ischizo Nishino, and Yukiko K. Hayashi. “GNE myopathy in India.” Neurology India 61, no. 4 (2013): 371.
What is GNE myopathy?
Shubraa Sinha: GNE Myopathy – Moving the ‘awareness’ needle: Blue Ribbon Symposium 2018
What is GNE Myopathy?
GNE myopathy is a rare, autosomal recessive disorder which causes progressive skeletal muscle weakness and atrophy.
- GNE myopathy was also known as:
hereditary inclusion body myopathy (HIBM)
- inclusion body myopathy type 2 (IBM2)
- Nonaka myopathy
GNE myopathy has a high prevalence in the Jewish population where almost 1 in 500 people present with the condition. The general prevalence is thought to be 1 in a million people. The National Human Genome Research Institute estimates at least 40,000 cases worldwide with almost 13,000 in Asia. GNE myopathy can go undiagnosed for several years and this may be the reason for the muted numbers of those affected.
Currently there is no approved therapy for GNE myopathy. Mouse models for gene therapy are in progress. The National Institute of Health is also researching the possibility of using N-acetyl-D-mannosamine (ManNAc). ManNAc is an intermediate molecule involved in the production of sialic acid within cells. Patients with GNE myopathy usually have insufficient sialic acid produced in the muscle cells which leads to muscle wasting. Mouse models using ManNAc have showed increased production of sialic acid thereby improving muscle function.
GNE myopathy is an autosomal recessive disorder which means both parents have the carrier gene with 25% chance of each child having the disease. GNE Myopathy is caused by various mutations in the GNE gene (which produces an enzyme UDP-N-acetylglucosamine-2-epimerase/N-acetylmannosamine kinase). A child with GNE Myopathy inherits two copies of the mutated GNE gene from each parent and hence expresses the disease.
The enzyme UDP-N-acetylglucosamine-2-epimerase/N-acetylmannosamine kinase is critical for the production of sialic acid in the cell. Incorrect coding of the enzyme results in insufficient levels of sialic acid leading to the degeneration of muscle cells.
GNE myopathy presents itself between 20 to 30 years of age. Symptoms begin with foot drop and difficulty in walking. Tripping is a common symptom of this condition. People with GNE find it hard to climb stairs and experience difficulties in getting up when sitting. The disease also leads to weakness in the arm muscles. GNE may lead to varying degrees of disability and loss of movement. Usually the heart, respiratory system, speech and swallowing are not affected.
- Some of the early signs of GNE myopathy include:
- Change in gait
- Difficulty in w
alking fast, running and climbing stairs
Muscle weakness and fatigue is a common symptom of GNE myopathy and individuals may experience strain with light physical activity.
GNE myopathy is often hard to diagnose because of generalized symptoms. A good orthopedist or neurologist take a detailed medical history and look for key signs like foot drop and frequent falls. Some of the tests that are used to diagnose GNE myopathy include:
biochemical tests – tests like Creatine Kinase (CK) which is a marker of muscle degeneration
molecular test – DNA tests like Next Generation Sequencing (NGS) to confirm the presence of the mutated GNE gene
Currently, no permanent cure is available for GNE myopathy. Treatment is aimed at preventing complications and enabling independent living. An interdisciplinary team of doctors including neurologists, orthopedicians and physiotherapists will be required to take care of the clinical needs of the individual. In the early stages when just diagnosed, it is important to start physiotherapy and exercises to prevent further degeneration of muscles. Diet management is important to avoid gaining weight and over burdening the muscles.
Investigational therapies like gene therapy and gene editing are in the clinical research stage and proving to be exciting.
If there is a known case of GNE myopathy in the family, it is absolutely essential for closest female relatives like siblings, uncles, aunts and cousins to test for carrier status.
If a woman with a carrier status is pregnant, prenatal test is essential to determine if the fetus has the disease mutation.