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Gut microbiota signatures and fecal metabolites in postmenopausal women with osteoporosis.
Wang, Han; Liu, Jing; Wu, Zuoxing; Zhao, Yangyang; Cao, Man; Shi, Baohong; Chen, Baolong; Chen, Ning; Guo, Hao; Li, Na; Chen, Jian; Xu, Ren.
Afiliación
  • Wang H; State Key Laboratory of Cellular Stress Biology, School of Medicine, Faculty of Medicine and Life Sciences, No. 4221 Xiang'an South Road, Xiang'an District, Xiamen, Fujian Province, 361102, China.
  • Liu J; Xiamen Key Laboratory of Regeneration Medicine, Fujian Provincial Key Laboratory of Organ and Tissue Regeneration, School of Medicine, The First Affiliated Hospital of Xiamen University-ICMRS Collaborating Center for Skeletal Stem Cells, Xiamen University, Xiamen, 361005, China.
  • Wu Z; Department of Rehabilitation, Zhongshan Hospital of Xiamen University, No.201-209 Hubinnan Road, Siming District, Xiamen, Fujian Province, 361000, China.
  • Zhao Y; State Key Laboratory of Cellular Stress Biology, School of Medicine, Faculty of Medicine and Life Sciences, No. 4221 Xiang'an South Road, Xiang'an District, Xiamen, Fujian Province, 361102, China.
  • Cao M; Xiamen Key Laboratory of Regeneration Medicine, Fujian Provincial Key Laboratory of Organ and Tissue Regeneration, School of Medicine, The First Affiliated Hospital of Xiamen University-ICMRS Collaborating Center for Skeletal Stem Cells, Xiamen University, Xiamen, 361005, China.
  • Shi B; Department of Rehabilitation, Zhongshan Hospital of Xiamen University, No.201-209 Hubinnan Road, Siming District, Xiamen, Fujian Province, 361000, China.
  • Chen B; Xiamen Treatgut Biotechnology Co., Ltd, Xiamen, Fujian Province, 361001, China.
  • Chen N; State Key Laboratory of Cellular Stress Biology, School of Medicine, Faculty of Medicine and Life Sciences, No. 4221 Xiang'an South Road, Xiang'an District, Xiamen, Fujian Province, 361102, China.
  • Guo H; Xiamen Key Laboratory of Regeneration Medicine, Fujian Provincial Key Laboratory of Organ and Tissue Regeneration, School of Medicine, The First Affiliated Hospital of Xiamen University-ICMRS Collaborating Center for Skeletal Stem Cells, Xiamen University, Xiamen, 361005, China.
  • Li N; Xiamen Treatgut Biotechnology Co., Ltd, Xiamen, Fujian Province, 361001, China.
  • Chen J; Department of Endocrinology, Zhongshan Hospital (Xiamen), Fudan University, Xiamen, 361000, China.
  • Xu R; State Key Laboratory of Cellular Stress Biology, School of Life Sciences, Faculty of Medicine and Life Sciences, Xiamen University, Xiamen, 361102, China.
Gut Pathog ; 15(1): 33, 2023 Jul 06.
Article en En | MEDLINE | ID: mdl-37415173
ABSTRACT

BACKGROUND:

Women suffer from various distress and disturbances after menopause, including osteoporosis, a risk factor associated with multiple diseases. Altered gut microbiota has been implicated in postmenopausal osteoporosis. In this study, to understand gut microbiota signatures and fecal metabolite changes in postmenopausal women with osteoporosis, 108 postmenopausal women were recruited for intestinal microbiota and fecal metabolite detection. Among these participants, 98 patients, who met the inclusion criteria, were divided into postmenopausal osteoporosis (PMO) and non-postmenopausal osteoporosis (non-PMO) groups based on bone mineral density (BMD). The compositions of gut bacteria and fungi were examined by 16 S rRNA gene sequencing and ITS sequencing, respectively. Meanwhile, fecal metabolites were analyzed using liquid chromatography coupled with mass spectrometry (LC-MS).

RESULTS:

We found that bacterial α-diversity and ß-diversity were significantly altered in PMO compared to non-PMO patients. Interestingly, fungi composition showed larger changes, and the differences in ß-diversity were more significant between PMO and non-PMO patients. Metabolomics analysis revealed that fecal metabolites, such as levulinic acid, N-Acetylneuraminic acid, and the corresponding signaling pathways were also changed significantly, especially in the alpha-Linolenic acid metabolism and selenocompound metabolism. The screened differential bacteria, fungi, and metabolites closely correlated with clinical findings between these two groups, for example, the bacterial genus, Fusobacterium, the fungal genus, Devriesia, and the metabolite, L-pipecolic acid, were significantly associated with BMD.

CONCLUSIONS:

Our findings indicated that there were remarkable changes in gut bacteria, fungi, and fecal metabolites in postmenopausal women, and such changes were notably correlated with patients' BMD ​​and clinical findings. These correlations provide novel insights into the mechanism of PMO development, potential early diagnostic indicators, and new therapeutic approaches to improve bone health in postmenopausal women.
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Texto completo: 1 Colección: 01-internacional Banco de datos: MEDLINE Tipo de estudio: Risk_factors_studies Idioma: En Revista: Gut Pathog Año: 2023 Tipo del documento: Article País de afiliación: China

Texto completo: 1 Colección: 01-internacional Banco de datos: MEDLINE Tipo de estudio: Risk_factors_studies Idioma: En Revista: Gut Pathog Año: 2023 Tipo del documento: Article País de afiliación: China