Myasthenia Gravis is an auto-immune disorder that impairs the functioning of the skeletal muscles. This happens when the nerve signals to these muscles are not received properly. It affects younger women and older men. The condition can neither be cured nor prevented. The symptoms can be managed well so that the person can live a fairly normal life. In this article, we will learn more about the condition.
Nerves are the carriers of communication signals between the Central Nervous System and muscle-groups located anywhere in the body. This is true of skeletal muscles as well, which are involved in our movement. In Myasthenia Gravis (MG), this communication gets impaired due to reasons explained in the next section. As a result of MG, the person is not able to voluntarily control his/her muscles. The muscles become weak or tired. The person is unable to control movement of muscles in the eyes, face, neck and limbs.
MG is quite common and affects 20 persons in every 1 lakh people. Women are generally diagnosed with MG in the age group of 20-40 years, while men are diagnosed with MG between 60 and 80 years of age. Juvenile MG affects a tiny percentage of youngsters. MG cannot be cured but its symptoms managed through medication, so as to sustain the quality of life.
The communication between nerves and muscles happens over a connection called synapse, at the neuromuscular junction. The nerves release a molecule called acetylcholine. The skeletal muscles have sites called acetylcholine receptors on them. The acetylcholine sent out by the nerves binds to these receptors. In response to that, the muscle fibres contract and movement happens. This is how the normal cycle of nerve-muscle communication. It is seamless in most people and rarely fails.
However, in people with MG, the immune system produces antibodies that attack and destroy the acetylcholine receptors in the muscles. Some or all of the receptors may be destroyed. As a result, the nerve to muscle communication becomes slow or sluggish. Since muscles are not contracting instantly, the movement is impaired. The person can no longer control his movements leading to various symptoms.
Antibodies also can block a protein called muscle-specific receptor tyrosine kinase, referred to as MuSK. This protein is crucial to form the nerve-muscle junction. Antibodies produced by the immune system can destroy this protein, leading to myasthenia gravis.
Another antibody that attacks a protein called lipoprotein-related protein 4 (LRP4), is also known to play a part in causing MG.
Research is uncovering other antibodies and newer ones may emerge with time, all of which have a role to play in causing and sustaining MG.
There is another aspect to MG, which is the connection to the thymus gland. The thymus is a butterfly-shaped gland present in the upper chest region closer to the throat. It is part of the lymphatic system and is responsible for producing antibodies that fight infections and pathogens. It is also known to produce antibodies that block acetylcholine. In two-thirds of people with MG, it is found that the thymus gland is larger than usual and also overactive, the condition being called thymic hyperplasia. In some cases, the thymus gland may have a tumour on it which is benign or not cancerous.
In some infants, there is neonatal MG that was passed on by the mother. However, this is a temporary condition that disappears in 3 months’ time.
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