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Characteristics of the gut microbiota and serum metabolites in postmenopausal women with reduced bone mineral density.
Yan, Litao; Wang, Xianfeng; Yu, Tiantian; Qi, Zhiming; Li, Huan; Nan, Hao; Wang, Kun; Luo, Di; Hua, Fei; Wang, Wendong.
Afiliación
  • Yan L; Department of Articular Orthopaedics, The First People's Hospital of Changzhou, The Third Affiliated Hospital of Soochow University, Changzhou, China.
  • Wang X; Department of Orthopedic Surgery, Beijing Jishuitan Hospital Guizhou Hospital, Guiyang, China.
  • Yu T; Department of Gynaecology and Obstetrics, Dalian Municipal Woman and Children's Medical Center, Dalian, China.
  • Qi Z; Department of Articular Orthopaedics, The Second People's Hospital of Dalian, Dalian, China.
  • Li H; Changzhou Medical Center, Nanjing Medical University, Nanjing, China.
  • Nan H; Department of Articular Orthopaedics, The First People's Hospital of Changzhou, The Third Affiliated Hospital of Soochow University, Changzhou, China.
  • Wang K; Department of Articular Orthopaedics, The First People's Hospital of Changzhou, The Third Affiliated Hospital of Soochow University, Changzhou, China.
  • Luo D; Department of Clinical Laboratory, The Second People's Hospital of Dalian, Dalian, China.
  • Hua F; Department of Endocrinology and Metabolism, The First People's Hospital of Changzhou, The Third Affiliated Hospital of Soochow University, Changzhou, China.
  • Wang W; Department of Articular Orthopaedics, The Second People's Hospital of Dalian, Dalian, China.
Front Cell Infect Microbiol ; 14: 1367325, 2024.
Article en En | MEDLINE | ID: mdl-38912210
ABSTRACT

Introduction:

Emerging evidence suggests that the gut microbiota is closely associated with bone homeostasis. However, little is known about the relationships among the bone mineral density (BMD) index, bone turnover markers, and the gut microbiota and its metabolites in postmenopausal women.

Methods:

In this study, to understand gut microbiota signatures and serum metabolite changes in postmenopausal women with reduced BMD, postmenopausal individuals with normal or reduced BMD were recruited and divided into normal and OS groups. Feces and serum samples were collected for 16S rRNA gene sequencing, liquid chromatography coupled with mass spectrometry (LC-MS)-based metabolomics and integrated analysis.

Results:

The results demonstrated that bacterial richness and diversity were greater in the OS group than in the normal group. Additionally, distinguishing bacteria were found among the two groups and were closely associated with the BMD index and bone turnover markers. Metabolomic analysis revealed that the expression of serum metabolites, such as etiocholanolone, testosterone sulfate, and indole-3-pyruvic acid, and the corresponding signaling pathways, especially those involved in tryptophan metabolism, fatty acid degradation and steroid hormone biosynthesis, also changed significantly. Correlation analysis revealed positive associations between normal group-enriched Bacteroides abundance and normal group-enriched etiocholanolone and testosterone sulfate abundances; in particular, Bacteroides correlated positively with BMD. Importantly, the tryptophan-indole metabolism pathway was uniquely metabolized by the gut bacteria-derived tnaA gene, the predicted abundance of which was significantly greater in the normal group than in the control group, and the abundance of Bacteroides was strongly correlated with the tnaA gene.

Discussion:

Our results indicated a clear difference in the gut microbiota and serum metabolites of postmenopausal women. Specifically altered bacteria and derived metabolites were closely associated with the BMD index and bone turnover markers, indicating the potential of the gut microbiota and serum metabolites as modifiable factors and therapeutic targets for preventing osteoporosis.
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Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Asunto principal: Bacterias / ARN Ribosómico 16S / Densidad Ósea / Posmenopausia / Metabolómica / Heces / Microbioma Gastrointestinal Límite: Aged / Female / Humans / Middle aged Idioma: En Revista: Front Cell Infect Microbiol Año: 2024 Tipo del documento: Article País de afiliación: China Pais de publicación: Suiza

Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Asunto principal: Bacterias / ARN Ribosómico 16S / Densidad Ósea / Posmenopausia / Metabolómica / Heces / Microbioma Gastrointestinal Límite: Aged / Female / Humans / Middle aged Idioma: En Revista: Front Cell Infect Microbiol Año: 2024 Tipo del documento: Article País de afiliación: China Pais de publicación: Suiza