Clinical correlation between intestinal flora profiles and the incidence of postmenopausal osteoporosis

• Published in: Gynecological endocrinology Vol. 41; no. 1; p. 2465587
• Main Authors: Zhu, Cuifeng, Zhang, Yuan, Pan, Yi, Zhang, Zhentian, Liu, Yan, Lin, Xiuping, Cai, Jinchuan, Xiong, Zhuang, Pan, Yong, Nie, Hezhongrong
• Format: Journal Article
• Language: English
• Published: England Taylor & Francis Group 01.12.2025
• Subjects: Aged; Bone Density; bone metabolism; Feces - microbiology; Female; Gastrointestinal Microbiome - genetics; Gastrointestinal Microbiome - physiology; Humans; Incidence; intestinal barrier function; intestinal flora; Middle Aged; Osteoporosis, Postmenopausal - epidemiology; Osteoporosis, Postmenopausal - genetics; Osteoporosis, Postmenopausal - metabolism; Osteoporosis, Postmenopausal - microbiology; Postmenopausal osteoporosis; bone metabolism; Postmenopausal osteoporosis; intestinal barrier function; intestinal flora
• ISSN: 1473-0766; 0951-3590; 1473-0766
• DOI: 10.1080/09513590.2025.2465587

This study aimed to explore the characteristics of intestinal microflora polymorphism in postmenopausal women, and to determine the pathophysiological changes of gene polymorphism of intestinal flora and bone metabolism in postmenopausal osteoporosis (PMOP) patients. A total of 104 postmenopausal women with PMOP or normal bone density were included. Lifestyle, hip T-score, bone metabolism indexes (25(OH)D, PTH, β-CTX, PINP), intestinal mucous membrane barrier function (diamine oxidase, D-lactic acid, LPS), gene polymorphisms, and characteristics of gut microbiota were examined. Women with PMOP had reduced physical activity, less dietary protein and calcium intake, lower levels of 25(OH)D, hip T-score, and BMD, but PMOP group had increased total energy and fat intake, and higher levels of PTH, β-CTX, diamine oxidase, D-lactic acid, and LPS (  < .05 for all), as compared with normal subjects. Analyses of the α- and β-diversity of fecal microbiota indicated remarkably differences in postmenopausal women with or without PMOP. In details, individuals with PMOP had increased abundances of some genera (e.g. and ), but decreased abundances of some genera (e.g. and ). Furthermore, use of a random forest model based on differential abundant taxa and ROC analysis could efficiently identify women with PMOP in the present cohort (AUC = 0.93). The incidence of PMOP was closely associated with fecal microbial compositions and intestinal functional changes. The present findings supported potential applications of gut microbiome analysis for early diagnosis of PMOP, and provided potential therapeutic targets.