TY - JOUR
T1 - Gut microbiota and plasma metabolites associated with bone mineral density in women with or at risk of HIV infection
AU - Mei, Zhendong
AU - Yin, Michael T.
AU - Sharma, Anjali
AU - Wang, Zheng
AU - Peters, Brandilyn A.
AU - Chandran, Aruna
AU - Weber, Kathleen M.
AU - Ross, Ryan D.
AU - Gustafson, Deborah
AU - Zheng, Yan
AU - Kaplan, Robert C.
AU - Burk, Robert D.
AU - Qi, Qibin
N1 - Funding Information:
U01-AI-103401; Atlanta WIHS (Ighovwerha Ofotokun and Gina Wingood), U01-AI-103408; Bronx WIHS (Kathryn Anastos and Anjali Sharma), U01-AI-035004; Brooklyn WIHS (Howard Minkoff and Deborah Gustafson), U01-AI-031834; Chicago WIHS (Mardge Cohen and Audrey French), U01-AI-034993; Metropolitan Washington WIHS (Seble Kassaye), U01-AI-034994; Miami WIHS (Margaret Fischl and Lisa Metsch), U01-AI-103397; UNC WIHS (Adaora Adimora), U01-AI-103390; ConnieWofsy Women's HIV Study, Northern California (Ruth Greenblatt, Bradley Aouizerat, and Phyllis Tien), U01-AI-034989; WIHS Data Management and Analysis Center (Stephen Gange and Elizabeth Golub), U01-AI-042590; Southern California WIHS (Joel Milam), U01-HD-032632 (WIHS I – WIHS IV). The WIHS is funded primarily by the National Institute of Allergy and Infectious Diseases (NIAID), with additional co-funding from the Eunice Kennedy Shriver National Institute of Child Health and Human Development (NICHD), the National Cancer Institute (NCI), the National Institute on Drug Abuse (NIDA), and the National Institute on Mental Health (NIMH). Targeted supplemental funding for specific projects is also provided by the National Institute of Dental and Craniofacial Research (NIDCR), the National Institute on Alcohol Abuse and Alcoholism (NIAAA), the National Institute on Deafness and other Communication Disorders (NIDCD), and the NIH Office of Research on Women's Health. WIHS data collection is also supported by UL1-TR000004 (UCSF CTSA), UL1-TR000454 (Atlanta CTSA), and P30-AI-050410 (UNC CFAR).
Funding Information:
This study was supported by the National Heart, Lung, and Blood Institute (NHLBI) K01HL129892 and R01HL140976, and Feldstein Medical Foundation Research Grant to Q.Q. R.C.K. was supported by NHLBI 5R01HL126543, R01 HL132794 and the National Institute on Mental Health (NIMH) 5R01MD011389-03, and J.R.K. was supported by NHLBI R01 HL132794 and K24 HL135413. Other funding sources include NHLBI R01HL083760, and R01HL095140, the National Institute of Allergy and Infectious Diseases (NIAID) U01 AI035004, and the Einstein Cancer Research Center (P30CA013330), the Einstein Liver Research Center (P30DK041296), the Einstein-Rockefeller-CUNY Center for AIDS Research funded by the NIAID (P30AI124414), and the Stable Isotope and Metabolomics Core Facility of the Einstein-Mount Sinai Diabetes Research Center (ES-DRC) of the Albert Einstein College of Medicine funded by National Cancer Institute (P60DK020541). M.T.Y. was supported by R01 AI-095089.
Publisher Copyright:
© 2023 Lippincott Williams and Wilkins. All rights reserved.
PY - 2023/1/1
Y1 - 2023/1/1
N2 - Objective:To evaluate gut microbiota (GMB) alterations and metabolite profile perturbations associated with bone mineral density (BMD) in the context of HIV infection.Design:Cross-sectional studies of 58 women with chronic HIV infection receiving antiretroviral therapy and 33 women without HIV infection.Methods:We examined associations of GMB and metabolites with BMD among 91 women. BMD was measured by dual-energy X-ray absorptiometry (DXA), and T-scores of lumbar spine or total hip less than -1 defined low BMD. GMB was measured by 16S rRNA V4 region sequencing on fecal samples, and plasma metabolites were measured by liquid chromatography-tandem mass spectrometry. Associations of GMB with plasma metabolites were assessed in a larger sample (418 women; 280 HIV+ and 138 HIV-).Results:Relative abundances of five predominant bacterial genera (Dorea, Megasphaera, unclassified Lachnospiraceae, Ruminococcus, and Mitsuokella) were higher in women with low BMD compared with those with normal BMD (all linear discriminant analysis (LDA) scores >2.0). A distinct plasma metabolite profile was identified in women with low BMD, featuring lower levels of several metabolites belonging to amino acids, carnitines, caffeine, fatty acids, pyridines, and retinoids, compared with those with normal BMD. BMD-associated bacterial genera, especially Megasphaera, were inversely associated with several BMD-related metabolites (e.g. 4-pyridoxic acid, C4 carnitine, creatinine, and dimethylglycine). The inverse association of Megasphaera with dimethylglycine was more pronounced in women with HIV infection compared with those without HIV infection (P for interaction = 0.016).Conclusion:Among women with and at risk of HIV infection, we identified altered GMB and plasma metabolite profiles associated with low BMD.
AB - Objective:To evaluate gut microbiota (GMB) alterations and metabolite profile perturbations associated with bone mineral density (BMD) in the context of HIV infection.Design:Cross-sectional studies of 58 women with chronic HIV infection receiving antiretroviral therapy and 33 women without HIV infection.Methods:We examined associations of GMB and metabolites with BMD among 91 women. BMD was measured by dual-energy X-ray absorptiometry (DXA), and T-scores of lumbar spine or total hip less than -1 defined low BMD. GMB was measured by 16S rRNA V4 region sequencing on fecal samples, and plasma metabolites were measured by liquid chromatography-tandem mass spectrometry. Associations of GMB with plasma metabolites were assessed in a larger sample (418 women; 280 HIV+ and 138 HIV-).Results:Relative abundances of five predominant bacterial genera (Dorea, Megasphaera, unclassified Lachnospiraceae, Ruminococcus, and Mitsuokella) were higher in women with low BMD compared with those with normal BMD (all linear discriminant analysis (LDA) scores >2.0). A distinct plasma metabolite profile was identified in women with low BMD, featuring lower levels of several metabolites belonging to amino acids, carnitines, caffeine, fatty acids, pyridines, and retinoids, compared with those with normal BMD. BMD-associated bacterial genera, especially Megasphaera, were inversely associated with several BMD-related metabolites (e.g. 4-pyridoxic acid, C4 carnitine, creatinine, and dimethylglycine). The inverse association of Megasphaera with dimethylglycine was more pronounced in women with HIV infection compared with those without HIV infection (P for interaction = 0.016).Conclusion:Among women with and at risk of HIV infection, we identified altered GMB and plasma metabolite profiles associated with low BMD.
KW - HIV infection
KW - bone mineral density
KW - gut microbiota
KW - metabolomics
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U2 - 10.1097/QAD.0000000000003400
DO - 10.1097/QAD.0000000000003400
M3 - Article
C2 - 36205320
AN - SCOPUS:85143645024
VL - 37
SP - 149
EP - 159
JO - AIDS
JF - AIDS
SN - 0269-9370
IS - 1
ER -