4.5 Article

A preliminary study of gut microbiome variation and HPA axis reactivity in healthy infants

Journal

PSYCHONEUROENDOCRINOLOGY
Volume 124, Issue -, Pages -

Publisher

PERGAMON-ELSEVIER SCIENCE LTD
DOI: 10.1016/j.psyneuen.2020.105046

Keywords

Gut microbiome; HPA axis; Cortisol reactivity; Infant stress response; Alpha diversity

Funding

  1. NIH [T32 NS007432, T32 GM008719, T32 1T32MH106440-01, P30 DK34987, R21 MH104330, R33 MH104330]
  2. NSF (GRFP Fellowship) [DGE-1650116]

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The study shows that gut microbial composition may influence HPA axis reactivity in early human development, suggesting potential for future clinical interventions targeting gut microbes to promote the development of stress-response systems.
The Hypothalamic Pituitary Adrenal (HPA) axis regulates hormonal responses to stress in both humans and animals and is dysregulated in a wide range of psychiatric disorders. There is strong evidence from rodent studies that gut microbial composition influences HPA axis development. In humans, variation in the gut microbiome has been associated with several psychological domains including depression and cognitive development, but studies focused on HPA axis development are still lacking. We tested whether differences in microbial composition are associated with HPA axis reactivity in a pilot study of 34 healthy human infants. HPA axis reactivity was assessed by measuring salivary cortisol in samples taken both before and after a heel stick, and 16S rRNA amplicon sequencing was used for identification and relative quantification of bacterial taxa. Subjects' alpha diversity levels showed a moderate positive association with their cortisol reactivity at one month of age. Exploratory genus-level analyses suggest that Staphylococcus, Prevotella, and genera in the order Lachnospiraceae may be related to cortisol reactivity at one month as well. The current study gives support for the endocrine pathway as a potential mediator in the microbiome-gut-brain axis during infancy, and as such provides motivation for future clinical work to support the development of stress-response systems through the manipulation of gut microbes.

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