STUDY CITES GENETIC VARIATION AS HIGH RISK FOR PARKINSON'S DISEASE IN AFRICA

STUDY CITES  GENETIC VARIANT AS HIGH RISK FOR PARKINSON'S DISEASE IN AFRICA


By Alfonso Kasongo

The first genome-wide association study on Parkinson’s disease in African populations has revealed a genetic variant that increases the risk of developing the disease.

Parkinson's disease,a disorder of the central nervous system that affects movement, often including tremors.

Published in The Lancet Neurology, the study found a new genetic risk factor in GBA1 in people of African ancestry, which has not been seen studies on European populations. The authors say it could be a significant factor underlying Parkinson's disease in African populations. 
The variant (Rs3115534-G) was found to be present in 39% of the cases assessed.

In June 2022, Zambia recorded a mysterious movement disorder affecting about 27 pupils at Lunte Technical School in Lunte district of Northern.

The condition appeared to be affecting the nervous system causing the patients to lose the firmness.
Out of the affected pupils, 15 were sent home.

Geneticist Ellen Sidransky at the National Human Genome Research Institute (NHGRI) was the recipient of one of this year’s US$3-million Breakthrough prizes — the most lucrative awards in science - for her discovery of GBA1.

Although Parkinson’s disease has been extensively investigated with respect to its environmental and genetic etiology in various populations, studies on people of African ancestry are rare.

The study showed that people of African ancestry who carry one copy of the Rs3115534-G variant, located on human chromosome 1, are about 1.5 times more likely to develop Parkinson’s disease compared to those without it. Those who are carriers of two copies of the gene have a 3.5-fold risk.

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