The human intestines are lined with trillions of microorganisms, some helpful and others harmful. Several lines of evidence point to a role for the digestive tract early in PD. For example, clumps of alpha-synuclein – the hallmark of PD in the brain – have been found in nerve cells of the colon in people who later developed PD. In addition, constipation is a common early symptom of PD, as are inflammation of the gut and an overgrowth of certain bacteria in the small intestine.
Researchers led by Samuel M. Goldman, M.D., M.P.H., at the San Francisco Veterans Affairs Medical Center, wanted to understand whether genetics can explain why some people develop PD and others may not. Following up on the gut-PD link, they asked whether variations in the genes encoding key proteins in the intestines may be correlated with increased or decreased risk for PD. These gut proteins are called peptidoglycans and help the body’s immune system recognize and respond to bacteria. But the components of these proteins can vary slightly from person to person.
To test whether variations in the genes for the peptidoglycans proteins were associated with PD risk, the researchers analyzed DNA in blood samples collected from 518 people with PD and 543 healthy individuals. Participants were drawn from two earlier studies.
Results
- Common variants in three of four genes encoding peptidoglycan proteins were associated with an altered risk of PD – both decreased and increased risk.
- The results were similar in two distinct populations of people with PD.
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