RT Journal Article
T1 Gut microbiota steroid sexual dimorphism and its impact on gonadal steroids: influences of obesity and menopausal status
A1 Mayneris-Perxachs, Jordi
A1 Arnoriaga-Rodríguez, María
A1 Luque-Córdoba, Diego
A1 Priego-Capote, Feliciano
A1 Pérez-Brocal, Vicente
A1 Moya, Andrés
A1 Burokas, Aurelijus
A1 Maldonado, Rafael
A1 Fernández-Real, José-Manuel
K1 Sex
K1 Gender
K1 Gonadal steroids
K1 Testosterone
K1 Progesterone
K1 Microbiome
K1 Sexual dimorphism
K1 Sexo
K1 Identidad de género
K1 Testosterona
K1 Progesterona
K1 Microbiota
K1 Caracteres sexuales
AB Background: Gonadal steroid hormones have been suggested as the underlying mechanism responsible for the sexual dimorphism observed in metabolic diseases. Animal studies have also evidenced a causal role of the gut microbiome and metabolic health. However, the role of sexual dimorphism in the gut microbiota and the potential role of the microbiome in influencing sex steroid hormones and shaping sexually dimorphic susceptibility to disease have been largely overlooked. Although there is some evidence of sex-specific differences in the gut microbiota diversity, composition, and functionality, the results are inconsistent. Importantly, most of these studies have not taken into account the gonadal steroid status. Therefore, we investigated the gut microbiome composition and functionality in relation to sex, menopausal status, and circulating sex steroids. Results: No significant differences were found in alpha diversity indices among pre- and post-menopausal women and men, but beta diversity differed among groups. The gut microbiota from post-menopausal women was more similar to men than to pre-menopausal women. Metagenome functional analyses revealed no significant differences between post-menopausal women and men. Gonadal steroids were specifically associated with these differences. Hence, the gut microbiota of pre-menopausal women was more enriched in genes from the steroid biosynthesis and degradation pathways, with the former having the strongest fold change among all associated pathways. Microbial steroid pathways also had significant associations with the plasma levels of testosterone and progesterone. In addition, a specific microbiome signature was able to predict the circulating testosterone levels at baseline and after 1-year follow-up. In addition, this microbiome signature could be transmitted from humans to antibiotic-induced microbiome-depleted male mice, being able to predict donor’s testosterone levels 4 weeks later, implying that the microbiota profile of the recipient mouse was influenced by the donor’s gender. Finally, obesity eliminated most of the differences observed among non-obese pre-menopausal women, post-menopausal women, and men in the gut microbiota composition (Bray-Curtis and weighted unifrac beta diversity), functionality, and the gonadal steroid status. Conclusions: The present findings evidence clear differences in the gut microbial composition and functionality between men and women, which is eliminated by both menopausal and obesity status. We also reveal a tight link between the gut microbiota composition and the circulating levels of gonadal steroids, particularly testosterone.
PB BioMed Central, Springer Nature
YR 2020
FD 2020-09-20
LK http://hdl.handle.net/10668/3844
UL http://hdl.handle.net/10668/3844
LA en
NO Mayneris-Perxachs J, Arnoriaga-Rodríguez M, Luque-Córdoba D, Priego-Capote F, Pérez-Brocal V, Moya A, et al. Gut microbiota steroid sexual dimorphism and its impact on gonadal steroids: influences of obesity and menopausal status. Microbiome. 2020 Sep 20;8(1):136
DS RISalud
RD Apr 5, 2025