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Exploring human-genome gut-microbiome interaction in Parkinson's disease
被引:21
|作者:
Wallen, Zachary D.
[1
]
Stone, William J.
[1
]
Factor, Stewart A.
[2
]
Molho, Eric
[3
]
Zabetian, Cyrus P.
[4
,5
]
Standaert, David G.
[1
]
Payami, Haydeh
[1
]
机构:
[1] Univ Alabama Birmingham, Dept Neurol, UAB Stn, Birmingham, AL 35294 USA
[2] Emory Univ, Sch Med, Dept Neurol, Atlanta, GA 30322 USA
[3] Albany Med Coll, Dept Neurol, Albany, NY 12208 USA
[4] Univ Washington, VA Puget Sound Hlth Care Syst, Seattle, WA 98195 USA
[5] Univ Washington, Dept Neurol, Seattle, WA 98195 USA
关键词:
ALPHA-SYNUCLEIN EXPRESSION;
WIDE ASSOCIATION;
GENE-REGULATION;
RISK LOCI;
METAANALYSIS;
VISUALIZATION;
VAGOTOMY;
REGION;
CELLS;
MODEL;
D O I:
10.1038/s41531-021-00218-2
中图分类号:
Q189 [神经科学];
学科分类号:
071006 ;
摘要:
The causes of complex diseases remain an enigma despite decades of epidemiologic research on environmental risks and genome-wide studies that have uncovered tens or hundreds of susceptibility loci for each disease. We hypothesize that the microbiome is the missing link. Genetic studies have shown that overexpression of alpha-synuclein, a key pathological protein in Parkinson's disease (PD), can cause familial PD and variants at alpha-synuclein locus confer risk of idiopathic PD. Recently, dysbiosis of gut microbiome in PD was identified: altered abundances of three microbial clusters were found, one of which was composed of opportunistic pathogens. Using two large datasets, we found evidence that the overabundance of opportunistic pathogens in PD gut is influenced by the host genotype at the alpha-synuclein locus, and that the variants responsible modulate alpha-synuclein expression. Results put forth testable hypotheses on the role of gut microbiome in the pathogenesis of PD, the incomplete penetrance of PD susceptibility genes, and potential triggers of pathology in the gut.
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页数:11
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