4.5 Article

Sex differences in the relationships between body composition, fat distribution, and mitochondrial energy metabolism: a pilot study

期刊

NUTRITION & METABOLISM
卷 19, 期 1, 页码 -

出版社

BMC
DOI: 10.1186/s12986-022-00670-8

关键词

Adiposity; Body composition; Fat distribution; Mitochondria; MRS; Muscle; Intermuscular fat

资金

  1. National Center for Advancing Translational Sciences of the National Institutes of Health (NIH) [UL1TR002378]
  2. NIH from the National Institute of Diabetes and Digestive and Kidney Diseases [K01 DK102851, R03 DK117246, K24 DK096574, P30 ES019776, T32 CA093423, U54 AG062334, P60DK079626]

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This study found distinct sex-dependent associations between monocyte and skeletal muscle mitochondrial metabolism with body composition. These findings may provide insights for sex-specific interventions to improve mitochondrial function and metabolic health.
Background Adiposity and mitochondrial dysfunction are related factors contributing to metabolic disease development. This pilot study examined whether in vivo and ex vivo indices of mitochondrial metabolism were differentially associated with body composition in males and females. Methods Thirty-four participants including 19 females (mean 27 yr) and 15 males (mean 29 yr) had body composition assessed by dual energy x-ray absorptiometry and magnetic resonance (MR) imaging. Monocyte reserve capacity and maximal oxygen consumption rate (OCR) were determined ex vivo using extracellular flux analysis. In vivo quadriceps mitochondrial function was measured using P-31-MR spectroscopy based on post-exercise recovery kinetics (tau PCr). The homeostatic model assessment of insulin resistance (HOMA-IR) was calculated from fasting glucose and insulin levels. Variables were log-transformed, and Pearson correlations and partial correlations were used for analyses. Results Mitochondrial metabolism was similar between sexes (p > 0.05). In males only, higher fat mass percent (FM%) was correlated with lower reserve capacity (r = - 0.73; p = 0.002) and reduced muscle mitochondrial function (r = 0.58, p = 0.02). Thigh subcutaneous adipose tissue was inversely related to reserve capacity in males (r = - 0.75, p = 0.001), but in females was correlated to higher maximal OCR (r = 0.48, p = 0.046), independent of FM. In females, lean mass was related to greater reserve capacity (r = 0.47, p = 0.04). In all participants, insulin (r = 0.35; p = 0.04) and HOMA-IR (r = 0.34; p = 0.05) were associated with a higher tau PCr. Conclusions These novel findings demonstrate distinct sex-dependent associations between monocyte and skeletal muscle mitochondrial metabolism with body composition. With further study, increased understanding of these relationships may inform sex-specific interventions to improve mitochondrial function and metabolic health.

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