The causal relationship between gut microbiota and bone mineral density: a Mendelian randomization study

被引:15
作者
Wang, Ying [1 ,2 ]
Zhang, Xuejian [2 ]
Tang, Guangjun [1 ,2 ]
Deng, Pin [3 ]
Qin, Yuyan [1 ,2 ]
Han, Jinglu [1 ,2 ]
Wang, Shulong [1 ,2 ]
Sun, Xiaojie [1 ,2 ]
Li, Dongxiao [1 ,2 ]
Chen, Zhaojun [2 ]
机构
[1] Beijing Univ Chinese Med, Dongzhimen Hosp, Beijing, Peoples R China
[2] Beijing Univ Chinese Med, Affiliated Hosp 3, Beijing, Peoples R China
[3] China Acad Chinese Med Sci, Inst Basic Theory Tradit Chinese Med, Beijing, Peoples R China
关键词
gut microbiota; bone mineral density; Mendelian randomization; age; causal relationship; CHAIN FATTY-ACIDS; COLONIZATION; INFLAMMATION; METABOLISM;
D O I
10.3389/fmicb.2023.1268935
中图分类号
Q93 [微生物学];
学科分类号
071005 ; 100705 ;
摘要
BackgroundThe gut microbiota has emerged as an intriguing and potentially influential factor in regulating bone health. However, the causal effect of the gut microbiota on bone mineral density (BMD) appears to differ throughout various life stages.MethodsWe conducted a Mendelian randomization (MR) analysis to investigate the potential causal relationship between gut microbiota and BMD in five distinct age groups: 0-15, 15-30, 30-45, 45-60, and 60 years and older. The analysis employed three different methods, namely MR-Egger, weighted median, and Inverse-variance weighting, to ensure the robustness of our findings, a series of sensitivity analyses were also conducted, such as horizontal pleiotropy tests, heterogeneity tests, and leave-one-out sensitivity tests.ResultsIn the age group of 0-15 years, Eubacterium_fissicatena_group and Eubacterium_hallii_group were identified as risk factors for BMD. During the 15-30 age group, Phascolarctobacterium, Roseburia, and Ruminococcaceae_UCG_003 were found to be protective factors for BMD. In the 30-45 age group, Lachnospira genus demonstrated a protective effect on BMD, while Barnesiella and Lactococcus were identified as risk factors for BMD. Moving on to the 45-60 age group, Eubacterium_ventriosum_group, Lachnospiraceae_UCG_004, and Subdoligranulum were observed to be protective factors for BMD, while Eubacterium_coprostanoligenes_group, Fusicatenibacter, and Lactococcus were associated with an increased risk of BMD. In individuals aged 60 years and older, Fusicatenibacter and Ruminococcaceae_UCG_002 were also noted as risk factors for BMD. Conversely, Eubacterium_ruminantium_group, Ruminococcus_gauvreauii_group, Alistipes, and Coprococcus_3 were found to be protective factors for BMD, whereas Barnesiella and Sellimonas were identified as risk factors for BMD.ConclusionA robust causal relationship between gut microbiota and bone mineral density (BMD) exists throughout all stages of life, with Firmicutes phylum being the primary group associated with BMD across age groups. Gut microbiota linked with BMD primarily belong to the Firmicutes phylum across age groups. The diversity of gut microbiota phyla associated with BMD depicts relatively stable patterns during the ages of 0-45 years. However, for individuals aged 45 years and above, there is an observed increase in the number of gut microbiota species linked with BMD, and by the age of 60 years, a trend toward an increase in the Bacteroidetes phylum categories is proposed.
引用
收藏
页数:11
相关论文
共 68 条
[1]   Through Ageing, and Beyond: Gut Microbiota and Inflammatory Status in Seniors and Centenarians [J].
Biagi, Elena ;
Nylund, Lotta ;
Candela, Marco ;
Ostan, Rita ;
Bucci, Laura ;
Pini, Elisa ;
Nikkila, Janne ;
Monti, Daniela ;
Satokari, Reetta ;
Franceschi, Claudio ;
Brigidi, Patrizia ;
De Vos, Willem .
PLOS ONE, 2010, 5 (05)
[2]   Probiotics-induced changes in gut microbial composition and its effects on cognitive performance after stress: exploratory analyses [J].
Bloemendaal, Mirjam ;
Szopinska-Tokov, Joanna ;
Belzer, Clara ;
Boverhoff, David ;
Papalini, Silvia ;
Michels, Franziska ;
van Hemert, Saskia ;
Arias Vasquez, Alejandro ;
Aarts, Esther .
TRANSLATIONAL PSYCHIATRY, 2021, 11 (01)
[3]   The Gut Microbiome and Bone Strength [J].
Castaneda, Macy ;
Strong, Jasmin M. ;
Alabi, Denise A. ;
Hernandez, Christopher J. .
CURRENT OSTEOPOROSIS REPORTS, 2020, 18 (06) :677-683
[4]   Role of Gut Microbiota-Generated Short-Chain Fatty Acids in Metabolic and Cardiovascular Health [J].
Chambers E.S. ;
Preston T. ;
Frost G. ;
Morrison D.J. .
Current Nutrition Reports, 2018, 7 (4) :198-206
[5]   Effect of blockade of TNF-α and interleukin-1 action on bone resorption in early postmenopausal women [J].
Charatcharoenwitthaya, Natthinee ;
Khosla, Sundeep ;
Atkinson, Elizabeth J. ;
McCready, Louise K. ;
Riggs, B. Lawrence .
JOURNAL OF BONE AND MINERAL RESEARCH, 2007, 22 (05) :724-729
[6]   Gut Microbiota and Bone Diseases: A Growing Partnership [J].
Chen, Yu ;
Wang, Xin ;
Zhang, Chunlei ;
Liu, Zhiyong ;
Li, Chao ;
Ren, Zhigang .
FRONTIERS IN MICROBIOLOGY, 2022, 13
[7]   Association Between Gut Microbiota and Bone Health: Potential Mechanisms and Prospective [J].
Chen, Yuan-Cheng ;
Greenbaum, Jonathan ;
Shen, Hui ;
Deng, Hong-Wen .
JOURNAL OF CLINICAL ENDOCRINOLOGY & METABOLISM, 2017, 102 (10) :3635-3646
[8]   Gut Microbiota, Immune System, and Bone [J].
D'Amelio, P. ;
Sassi, F. .
CALCIFIED TISSUE INTERNATIONAL, 2018, 102 (04) :415-425
[9]   The role of short-chain fatty acids in the interplay between diet, gut microbiota, and host energy metabolism [J].
den Besten, Gijs ;
van Eunen, Karen ;
Groen, Albert K. ;
Venema, Koen ;
Reijngoud, Dirk-Jan ;
Bakker, Barbara M. .
JOURNAL OF LIPID RESEARCH, 2013, 54 (09) :2325-2340
[10]   Association between Body Composition and Bone Mineral Density in Children and Adolescents: A Systematic Review and Meta-Analysis [J].
Deng, Kai-Li ;
Yang, Wan-Yu ;
Hou, Jin-Li ;
Li, Hui ;
Feng, Hao ;
Xiao, Su-Mei .
INTERNATIONAL JOURNAL OF ENVIRONMENTAL RESEARCH AND PUBLIC HEALTH, 2021, 18 (22)