4.6 Article

Gut Microbiota Dysbiosis Is Associated with Elevated Bile Acids in Parkinson's Disease

期刊

METABOLITES
卷 11, 期 1, 页码 -

出版社

MDPI
DOI: 10.3390/metabo11010029

关键词

Parkinson’ s disease; microbiome; bile acids; appendix; gut

资金

  1. Farmer Family Foundation
  2. Department of Defense [W81XWH1810512]
  3. National Institute of Neurological Disorders and Stroke [1R21NS112614-01, 1R01NS113894-01A1, 1R01NS114409-01A1, 1R01NS11083801A1]
  4. Gibby & Friends vs. Parky Award
  5. National Institutes on Aging [1R21AG067083-01]
  6. Alzheimer's Association [AARG-17530020]
  7. Michael J. Fox Foundation [MJFF16201]

向作者/读者索取更多资源

The gut microbiome can impact brain health and is altered in Parkinson's disease. The vermiform appendix, a lymphoid tissue in the cecum, is implicated in the storage and regulation of the gut microbiota. Changes in the appendix microbiome in PD patients include dysbiosis affecting lipid metabolism and an increase in toxic bile acids.
The gut microbiome can impact brain health and is altered in Parkinson's disease (PD). The vermiform appendix is a lymphoid tissue in the cecum implicated in the storage and regulation of the gut microbiota. We sought to determine whether the appendix microbiome is altered in PD and to analyze the biological consequences of the microbial alterations. We investigated the changes in the functional microbiota in the appendix of PD patients relative to controls (n = 12 PD, 16 C) by metatranscriptomic analysis. We found microbial dysbiosis affecting lipid metabolism, including an upregulation of bacteria responsible for secondary bile acid synthesis. We then quantitatively measure changes in bile acid abundance in PD relative to the controls in the appendix (n = 15 PD, 12 C) and ileum (n = 20 PD, 20 C). Bile acid analysis in the PD appendix reveals an increase in hydrophobic and secondary bile acids, deoxycholic acid (DCA) and lithocholic acid (LCA). Further proteomic and transcriptomic analysis in the appendix and ileum corroborated these findings, highlighting changes in the PD gut that are consistent with a disruption in bile acid control, including alterations in mediators of cholesterol homeostasis and lipid metabolism. Microbially derived toxic bile acids are heightened in PD, which suggests biliary abnormalities may play a role in PD pathogenesis.

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