老年男性和女性区域脂肪组织分布与骨骼肌生物能量学之间的关系

Andrea M Brennan, Paul M Coen, Theresa Mau, Megan Hetherington-Rauth, Frederico G.S. Toledo, Erin E Kershaw, Peggy M Cawthon, Philip A Kramer, Sofhia V Ramos, Anne B Newman, Steven R Cummings, Daniel E Forman, Reichelle X Yeo, Giovanna DiStefano, Iva Miljkovic, Jamie N Justice, Anthony J.A. Molina, Michael J Jurczak, Lauren M Sparks, Stephen B Kritchevsky, Bret H Goodpaster
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引用次数: 0

摘要

目的:探讨老年人异位脂肪组织(AT)与骨骼肌(SM)线粒体生物能量学的关系。方法:采用829例≥70岁老年人的横断面数据。腹部、皮下和内脏总AT;MRI量化大腿肌脂肪浸润(MFI)。用体内31P-MRS (ATPmax)和体外高分辨率呼吸测定法(最大氧化磷酸化(OXPHOS))表征SM线粒体能量。使用ActivPal测量PA(步数)。采用调整协变量的线性回归模型,对BMI和PA进行序贯调整。结果:与BMI无关,总腹部(标准化(Std) β=-0.21;R2=0.09)和内脏AT(标准β=-0.16;R2=0.09)与ATPmax相关(p<0.01),但进一步校正PA后无相关性(p≥0.05)。内脏AT (Std. β=-0.16;R2=0.25)和大腿MFI(标准差β=-0.11;R2=0.24)与碳水化合物支持的最大OXPHOS负相关,不依赖于BMI和PA (p<0.05)。腹部总AT (Std. β=-0.19;R2=0.24)和内脏AT(标准β=-0.17;R2=0.24)与脂肪酸支持的最大OXPHOS相关,不依赖于BMI和PA (p<0.05)。结论:在独立于BMI的老年人中,骨骼MFI和腹部内脏(而非皮下)AT与SM线粒体生物能量学呈负相关。异位AT与体内线粒体生物能量学之间的关联被PA减弱。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Associations between regional adipose tissue distribution and skeletal muscle bioenergetics in older men and women
Objective: Examine the association of ectopic adipose tissue (AT) with skeletal muscle (SM) mitochondrial bioenergetics in older adults. Methods: Cross-sectional data from 829 older adults ≥70 years was used. Total abdominal, subcutaneous, and visceral AT; and thigh muscle fat infiltration (MFI) was quantified by MRI. SM mitochondrial energetics were characterized using in vivo 31P-MRS (ATPmax) and ex vivo high-resolution respirometry (maximal oxidative phosphorylation (OXPHOS)). ActivPal was used to measure PA (step count). Linear regression models adjusted for covariates were applied, with sequential adjustment for BMI and PA. Results: Independent of BMI, total abdominal (standardized (Std.) β=-0.21; R2=0.09) and visceral AT (Std. β=-0.16; R2=0.09) were associated with ATPmax (p<0.01), but not after further adjustment for PA (p≥0.05). Visceral AT (Std. β=-0.16; R2=0.25) and thigh MFI (Std. β=-0.11; R2=0.24) were negatively associated with carbohydrate-supported maximal OXPHOS independent of BMI and PA (p<0.05). Total abdominal AT (Std. β=-0.19; R2=0.24) and visceral AT (Std. β=-0.17; R2=0.24) were associated with fatty acid-supported maximal OXPHOS independent of BMI and PA (p<0.05). Conclusions: Skeletal MFI and abdominal visceral, but not subcutaneous AT, are inversely associated with SM mitochondrial bioenergetics in older adults independent of BMI. Associations between ectopic AT and in vivo mitochondrial bioenergetics are attenuated by PA.
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