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Host variables confound gut microbiota studies of human disease

Author

Listed:
  • Ivan Vujkovic-Cvijin

    (National Institute of Allergy and Infectious Diseases, National Institutes of Health)

  • Jack Sklar

    (National Institute of Allergy and Infectious Diseases, National Institutes of Health
    National Institutes of Health
    National Institute of Standards and Technology)

  • Lingjing Jiang

    (University of California San Diego)

  • Loki Natarajan

    (University of California San Diego)

  • Rob Knight

    (University of California San Diego
    University of California San Diego
    University of California San Diego
    University of California San Diego)

  • Yasmine Belkaid

    (National Institute of Allergy and Infectious Diseases, National Institutes of Health
    National Institutes of Health)

Abstract

Low concordance between studies that examine the role of microbiota in human diseases is a pervasive challenge that limits the capacity to identify causal relationships between host-associated microorganisms and pathology. The risk of obtaining false positives is exacerbated by wide interindividual heterogeneity in microbiota composition1, probably due to population-wide differences in human lifestyle and physiological variables2 that exert differential effects on the microbiota. Here we infer the greatest, generalized sources of heterogeneity in human gut microbiota profiles and also identify human lifestyle and physiological characteristics that, if not evenly matched between cases and controls, confound microbiota analyses to produce spurious microbial associations with human diseases. We identify alcohol consumption frequency and bowel movement quality as unexpectedly strong sources of gut microbiota variance that differ in distribution between healthy participants and participants with a disease and that can confound study designs. We demonstrate that for numerous prevalent, high-burden human diseases, matching cases and controls for confounding variables reduces observed differences in the microbiota and the incidence of spurious associations. On this basis, we present a list of host variables that we recommend should be captured in human microbiota studies for the purpose of matching comparison groups, which we anticipate will increase robustness and reproducibility in resolving the members of the gut microbiota that are truly associated with human disease.

Suggested Citation

  • Ivan Vujkovic-Cvijin & Jack Sklar & Lingjing Jiang & Loki Natarajan & Rob Knight & Yasmine Belkaid, 2020. "Host variables confound gut microbiota studies of human disease," Nature, Nature, vol. 587(7834), pages 448-454, November.
  • Handle: RePEc:nat:nature:v:587:y:2020:i:7834:d:10.1038_s41586-020-2881-9
    DOI: 10.1038/s41586-020-2881-9
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    Cited by:

    1. Lixiang Zhai & Haitao Xiao & Chengyuan Lin & Hoi Leong Xavier Wong & Yan Y. Lam & Mengxue Gong & Guojun Wu & Ziwan Ning & Chunhua Huang & Yijing Zhang & Chao Yang & Jingyuan Luo & Lu Zhang & Ling Zhao, 2023. "Gut microbiota-derived tryptamine and phenethylamine impair insulin sensitivity in metabolic syndrome and irritable bowel syndrome," Nature Communications, Nature, vol. 14(1), pages 1-14, December.
    2. Alexandra M. Cheney & Stephanann M. Costello & Nicholas V. Pinkham & Annie Waldum & Susan C. Broadaway & Maria Cotrina-Vidal & Marc Mergy & Brian Tripet & Douglas J. Kominsky & Heather M. Grifka-Walk , 2023. "Gut microbiome dysbiosis drives metabolic dysfunction in Familial dysautonomia," Nature Communications, Nature, vol. 14(1), pages 1-12, December.
    3. Yue Clare Lou & Benjamin E. Rubin & Marie C. Schoelmerich & Kaden S. DiMarco & Adair L. Borges & Rachel Rovinsky & Leo Song & Jennifer A. Doudna & Jillian F. Banfield, 2023. "Infant microbiome cultivation and metagenomic analysis reveal Bifidobacterium 2’-fucosyllactose utilization can be facilitated by coexisting species," Nature Communications, Nature, vol. 14(1), pages 1-14, December.
    4. Louise Grahnemo & Maria Nethander & Eivind Coward & Maiken Elvestad Gabrielsen & Satya Sree & Jean-Marc Billod & Klara Sjögren & Lars Engstrand & Koen F. Dekkers & Tove Fall & Arnulf Langhammer & Kris, 2023. "Identification of three bacterial species associated with increased appendicular lean mass: the HUNT study," Nature Communications, Nature, vol. 14(1), pages 1-9, December.
    5. Dharti Shantaram & Rebecca Hoyd & Alecia M. Blaszczak & Linda Antwi & Anahita Jalilvand & Valerie P. Wright & Joey Liu & Alan J. Smith & David Bradley & William Lafuse & YunZhou Liu & Nyelia F. Willia, 2024. "Obesity-associated microbiomes instigate visceral adipose tissue inflammation by recruitment of distinct neutrophils," Nature Communications, Nature, vol. 15(1), pages 1-18, December.
    6. Yolanda Y. Huang & Morgan N. Price & Allison Hung & Omree Gal-Oz & Surya Tripathi & Christopher W. Smith & Davian Ho & Héloïse Carion & Adam M. Deutschbauer & Adam P. Arkin, 2024. "Barcoded overexpression screens in gut Bacteroidales identify genes with roles in carbon utilization and stress resistance," Nature Communications, Nature, vol. 15(1), pages 1-17, December.
    7. Cameron Martino & Livia S. Zaramela & Bei Gao & Mallory Embree & Janna Tarasova & Seth J. Parker & Yanhan Wang & Huikuan Chu & Peng Chen & Kuei-Chuan Lee & Daniela Domingos Galzerani & Jivani M. Genga, 2022. "Acetate reprograms gut microbiota during alcohol consumption," Nature Communications, Nature, vol. 13(1), pages 1-11, December.
    8. Braden T Tierney & Yingxuan Tan & Zhen Yang & Bing Shui & Michaela J Walker & Benjamin M Kent & Aleksandar D Kostic & Chirag J Patel, 2022. "Systematically assessing microbiome–disease associations identifies drivers of inconsistency in metagenomic research," PLOS Biology, Public Library of Science, vol. 20(3), pages 1-18, March.

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