Gut microbiota signatures and fecal metabolites in postmenopausal women with osteoporosis

被引:17
|
作者
Wang, Han [1 ,2 ]
Liu, Jing [3 ]
Wu, Zuoxing [1 ,2 ]
Zhao, Yangyang [3 ]
Cao, Man [4 ]
Shi, Baohong [1 ,2 ]
Chen, Baolong [4 ]
Chen, Ning [5 ]
Guo, Hao [6 ]
Li, Na [1 ,2 ]
Chen, Jian [3 ]
Xu, Ren [1 ,2 ]
机构
[1] Fac Med & Life Sci, Sch Med, State Key Lab Cellular Stress Biol, 4221 Xiangan South Rd, Xiamen 361102, Fujian, Peoples R China
[2] Xiamen Univ, Affiliated Hosp 1, ICMRS Collaborating Ctr Skeletal Stem Cells, Xiamen Key Lab Regenerat Med,Fujian Prov Key Lab O, Xiamen 361005, Peoples R China
[3] Xiamen Univ, Zhongshan Hosp, Dept Rehabil, 201-209 Hubinnan Rd, Xiamen 361000, Fujian, Peoples R China
[4] Xiamen Treatgut Biotechnol Co Ltd, Xiamen 361001, Fujian, Peoples R China
[5] Fudan Univ, Zhongshan Hosp Xiamen, Dept Endocrinol, Xiamen 361000, Peoples R China
[6] Xiamen Univ, Fac Med & Life Sci, Sch Life Sci, State Key Lab Cellular Stress Biol, Xiamen 361102, Peoples R China
基金
中国国家自然科学基金;
关键词
Postmenopausal women; Gut microbiota; Fecal metabolites; Osteoporosis; ALPHA-LINOLENIC ACID; BONE LOSS; MENOPAUSE;
D O I
10.1186/s13099-023-00553-0
中图分类号
R57 [消化系及腹部疾病];
学科分类号
摘要
BackgroundWomen 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).ResultsWe found that bacterial & alpha;-diversity and & beta;-diversity were significantly altered in PMO compared to non-PMO patients. Interestingly, fungi composition showed larger changes, and the differences in & beta;-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.ConclusionsOur 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.
引用
收藏
页数:13
相关论文
共 50 条
  • [1] Gut microbiota signatures and fecal metabolites in postmenopausal women with osteoporosis
    Han Wang
    Jing Liu
    Zuoxing Wu
    Yangyang Zhao
    Man Cao
    Baohong Shi
    Baolong Chen
    Ning Chen
    Hao Guo
    Na Li
    Jian Chen
    Ren Xu
    Gut Pathogens, 15
  • [2] Gut microbiota and fecal metabolic signatures in rat models of disuse-induced osteoporosis
    Qiao, Xiaochen
    Zhang, Kun
    Li, Xiaoyan
    Lv, Zhi
    Wei, Wenhao
    Zhou, Ruhao
    Yan, Lei
    Pan, Yongchun
    Yang, Sen
    Sun, Xiaojuan
    Li, Pengcui
    Xu, Chaojian
    Feng, Yi
    Tian, Zhi
    FRONTIERS IN CELLULAR AND INFECTION MICROBIOLOGY, 2022, 12
  • [3] Gut microbiota and microbial metabolites for osteoporosis
    Zheng, Xuan-Qi
    Wang, Ding-Ben
    Jiang, Yi-Rong
    Song, Chun-Li
    GUT MICROBES, 2025, 17 (01)
  • [4] Impact of Dietary Isoflavone Supplementation on the Fecal Microbiota and Its Metabolites in Postmenopausal Women
    Guadamuro, Lucia
    Azcarate-Peril, M. Andrea
    Tojo, Rafael
    Mayo, Baltasar
    Delgado, Susana
    INTERNATIONAL JOURNAL OF ENVIRONMENTAL RESEARCH AND PUBLIC HEALTH, 2021, 18 (15)
  • [5] Gut microbiota alterations in postmenopausal women with osteoporosis and osteopenia from Shanghai, China
    Ji, Jiaqing
    Gu, Zhengrong
    Li, Na
    Dong, Xin
    Wang, Xiong
    Yao, Qiang
    Zhang, Zhongxiao
    Zhang, Li
    Cao, Liehu
    PEERJ, 2024, 12
  • [6] Osteoporosis in postmenopausal women is associated with disturbances in gut microbiota and migration of peripheral immune cells
    Ma, Zongjun
    Liu, Yuanyuan
    Shen, Wenke
    Yang, Jiaxiao
    Wang, Ting
    Li, Yiwei
    Ma, Junbai
    Zhang, Xiaoxia
    Wang, Hao
    BMC MUSCULOSKELETAL DISORDERS, 2024, 25 (01)
  • [7] Identifying microbial signatures for patients with postmenopausal osteoporosis using gut microbiota analyses and feature selection approaches
    Huang, Dageng
    Wang, Jihan
    Zeng, Yuhong
    Li, Qingmei
    Wang, Yangyang
    FRONTIERS IN MICROBIOLOGY, 2023, 14
  • [8] GUT MICROBIOTA AND SHORT-CHAIN FATTY ACID SIGNATURES IN POSTMENOPAUSAL OSTEOPOROSIS PATIENTS: A RETROSPECTIVE STUDY
    Li, S.
    Zhang, Y.
    Ma, C.
    Dong, Q.
    Sun, P.
    AGING CLINICAL AND EXPERIMENTAL RESEARCH, 2024, 36 : S33 - S33
  • [9] Gut microbiota and short-chain fatty acids signatures in postmenopausal osteoporosis patients: A retrospective study
    Li, Shimei
    Wang, Jinzhi
    Zhang, Yingtong
    Wang, Jiangyan
    Zhou, Tianyu
    Xie, Youhong
    Zhou, Yilin
    Tang, Lin
    Hu, Li
    Dong, Qunwei
    Sun, Ping
    MEDICINE, 2024, 103 (47)
  • [10] GUT MICROBIOTA AND SHORT-CHAIN FATTY ACID SIGNATURES IN POSTMENOPAUSAL OSTEOPOROSIS PATIENTS: A RETROSPECTIVE STUDY
    Li, S.
    Zhang, Y.
    Ma, C.
    Dong, Q.
    Sun, P.
    AGING CLINICAL AND EXPERIMENTAL RESEARCH, 2024, 36 : S504 - S505