Newswise — Bethesda, MD – In a groundbreaking study published May 2, 2024 in Neuron, researchers have identified four new genetic risk factors for multiple system atrophy (MSA), shedding light on this poorly understood disorder. The study, which involved collaboration from over 50 institutions worldwide, including the Uniformed Services University of the Health Sciences (USU), marks a significant step forward in the understanding of MSA.
Led by Sonja W. Scholz, M.D., Ph.D., senior investigator and chief of the Neurodegenerative Diseases Research Section at the National Institute of Neurological Disorders and Stroke (NINDS), the project utilized the expertise of The American Genome Center at USU, among others, to analyze the entire genomes of individuals with MSA.
MSA is an adult-onset sporadic disorder characterized by an abnormal buildup of α-synuclein protein, similar to Parkinson’s disease and Lewy body dementia. However, due to its rarity and variability in symptoms, MSA remains poorly understood.
To address this knowledge gap, the research team assembled the largest whole genome dataset for MSA to date, involving 888 individuals of European ancestry with MSA. By comparing their genomic variation to those of healthy controls, the team identified four new risk loci for MSA and highlighted specific genes associated with increased susceptibility to the disorder.
The American Genome Center at USU directed the high quality genomic data generation and analysis for the study as part of ongoing collaborative efforts led by Dr. Clifton Dalgard, director of USU’s Center for Military Precision Medicine which oversees TAGC, to support neurodegenerative and neurological disease population genetics research with NINDS and NIA.
In addition to genome analysis, the researchers conducted cell-type specific transcript expression analysis to understand the potential impact of genomic changes on specific cell types, such as neurons and oligodendrocytes. This analysis revealed that defects within oligodendrocytes may play a significant role in MSA pathogenesis as a primary oligodendropathy.
Despite the study's limitations, including the need for replication in additional MSA cohorts with genomic data, the team is sharing their data freely with the research community to support further investigations into MSA and facilitate the development of targeted treatments.
"We are proud to have contributed to this effort aimed at unraveling the genetic determinants of MSA," said Dalgard. "By working collaboratively, we hope to accelerate research progress towards effective treatments for this debilitating neurodegenerative disease."
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About the Uniformed Services University: The Uniformed Services University of the Health Sciences, founded by an act of Congress in 1972, is the nation’s federal health sciences university and the academic heart of the Military Health System. USU students are primarily active-duty uniformed officers in the Army, Navy, Air Force and Public Health Service who receive specialized education in tropical and infectious diseases, TBI and PTSD, disaster response and humanitarian assistance, global health, and acute trauma care. USU also has graduate programs in oral biology, biomedical sciences and public health committed to excellence in research. The University's research program covers a wide range of areas important to both the military and public health. For more information about USU and its programs, visit www.usuhs.edu.
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