4.7 Article

Gut microbiota and plasma metabolites associated with diabetes in women with, or at high risk for, HIV infection

Journal

EBIOMEDICINE
Volume 37, Issue -, Pages 392-400

Publisher

ELSEVIER
DOI: 10.1016/j.ebiom.2018.10.037

Keywords

Gut microbiota; Metabolite; Diabetes; HIV

Funding

  1. National Heart, Lung, and Blood Institute (NHLBI) [K01HL129892, R01HL140976]
  2. Feldstein Medical Foundation Research Grant
  3. NHLBI [R01HL083760, R01HL095140, R01 HL132794, K24 HL135413]
  4. National Institute on Mental Health (NIMH) [5R01MD011389-03]
  5. National Institute of Allergy and Infectious Diseases (NIAID) [U01 AI035004]
  6. Einstein Cancer Research Center [P30CA013330]
  7. Einstein Liver Research Center [P30DK041296]
  8. Einstein-Rockefeller-CUNY Center for AIDS Research - NIAID [P30AI124414]
  9. Stable Isotope and Metabolomics Core Facility of the Einstein-Mount Sinai Diabetes Research Center (ES-DRC) of the Albert Einstein College of Medicine - National Cancer Institute [P60DK020541]
  10. National Institute of Allergy and Infectious Diseases (NIAID)
  11. Eunice Kennedy Shriver National Institute of Child Health and Human Development (NICHD)
  12. National Cancer Institute (NCI)
  13. National Institute on Drug Abuse (NIDA)
  14. National Institute on Mental Health (NIMH)
  15. National Institute of Dental and Craniofacial Research (NIDCR)
  16. National Institute on Alcohol Abuse and Alcoholism (NIAAA)
  17. National Institute on Deafness and other Communication Disorders (NIDCD)
  18. NIH Office of Research on Women's Health
  19. [UL1-TR000004]
  20. [UL1-TR000454]
  21. [P30-AI-050410]
  22. NATIONAL HEART, LUNG, AND BLOOD INSTITUTE [R01HL140976, K01HL129892] Funding Source: NIH RePORTER
  23. NATIONAL INSTITUTE OF GENERAL MEDICAL SCIENCES [K12GM102779] Funding Source: NIH RePORTER

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Background: Gut microbiota alteration has been implicated in HIV infection and metabolic disorders. The relationship between gut microbiota and diabetes has rarely been studied in HIV-infected individuals, who have excess risk of metabolic disorders. Methods: Our study during 2015-2016 enrolled predominantly African Americans and Hispanics in the Women's Interagency HIV Study. We studied 28 women with long-standing HIV infection under antiretroviral therapy and 20 HIV-uninfected, but at high risk of infection, women (16 HIV+ and 6 HIV- with diabetes). Fecal samples were analyzed by sequencing prokaryotic 16S rRNA gene. Plasma metabolomics profiling was performed by liquid chromatography-tandem mass spectrometry. Findings: No significant differences in bacterial alpha- or beta-diversity were observed by diabetes or HIV serostatus (all P> .1). Relative abundances of four genera (Finegoldia, Anaerococcus, Sneathia, and Adlercreutzia) were lower in women with diabetes compared to those without diabetes (all P< .01). In women with diabetes, plasma levels of several metabolites in tryptophan catabolism (e,g., kynurenine/tryptophan ratio), branched-chain amino acid and proline metabolism pathways were higher, while glycerophospholipids were lower (all P < .05). Results were generally consistent between HIV-infected and HIV-uninfected women, and no significant modification effects by HIV serostatus were observed (all P-interaction> 0.05). Anaerococcus, known to produce butyrate which is involved in anti-inflammation and glucose metabolism, showed an inverse correlation with kynurenine/tryptophan ratio (r = -0.38, P < .01). Interpretation: Among women with or at high risk for HIV infection, diabetes is associated with gut microbiota and plasma metabolite alteration, including depletion of butyrate-producing bacterial population along with higher tryptophan catabolism. (C) 2018 The Authors. Published by Elsevier B.V.

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