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DOI 10.1007/s12020-024-03699-2

Медицинская библиотека · Endocrine · 2024

Association of serum trimethylamine N-oxide levels and bone mineral density in type 2 diabetes mellitus.

Yuan Yue, Gan Chao, Wang Mengke, Zou Jingyi, Wang Zhen, Li Shuyun, Lv Haihong

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Аннотация

PURPOSE: The relationship between trimethylamine N-oxide (TMAO) and bone mineral density (BMD) in type 2 diabetes mellitus (T2DM) is unclear. We explore the relationship between TMAO levels and BMD in T2DM.

METHODS

This is a cross-sectional study. 254 T2DM patients were enrolled and divided into three groups by TMAO tertiles, and the clinical data were collected. BMD was determined by dual-energy X-ray absorptiometry (DXA) and serum TMAO levels was determined by stable isotope dilution high-performance liquid chromatography tandem mass spectrometry (HPLC-MS/MS).

RESULTS

Patients in the highest tertile of TMAO levels (TMAO > 6.72 μmol/L) showed relatively low BMD and a higher number of fracture history, osteoporosis (OP) than those in the lower tertiles. Spearman correlation analysis showed that serum TMAO was negatively correlated with BMD of whole body (WB), lumbar spine (LS) and femoral neck (FN), while TMAO was positive correlated with osteoporotic fracture (p < 0.05). Logistic regression models showed that TMAO was an independent influencing factor of fracture history after adjusting for confounders in TMAO > 6.72 μmol/L group.

CONCLUSIONS

There is a significant linear correlation between TMAO levels and BMD in T2DM patients. Especially in TMAO > 6.72 μmol/L group, TMAO was negatively correlated with WB, LS, and FN BMD, and was positive correlated with osteoporotic fracture in T2DM patients. The findings suggest that elevated TMAO levels are associated with OP and osteoporotic fracture in T2DM patients.

Для цитирования: Yuan Yue, Gan Chao, Wang Mengke, Zou Jingyi, Wang Zhen, Li Shuyun, Lv Haihong. Association of serum trimethylamine N-oxide levels and bone mineral density in type 2 diabetes mellitus.. Endocrine. 2024. DOI: 10.1007/s12020-024-03699-2.

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