Muscle mitochondrial bioenergetic capacities are associated with multimorbidity burden in older adults: the Study of Muscle, Mobility and Aging (SOMMA)

Theresa Mau, Terri L Blackwell, Peggy M Cawthon, Anthony J A Molina, Paul M Coen, Giovanna Distefano, Philip A Kramer, Sofhia V Ramos, Daniel E Forman, Bret H Goodpaster, Frederico G S Toledo, Kate A Duchowny, Lauren M Sparks, Anne B Newman, Stephen B Kritchevsky, Steven R Cummings
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Abstract

Background The geroscience hypothesis posits that aging biological processes contribute to many age-related deficits, including the accumulation of multiple chronic diseases. Though only one facet of mitochondrial function, declines in muscle mitochondrial bioenergetic capacities may contribute to this increased susceptibility to multimorbidity. Methods The Study of Muscle, Mobility and Aging (SOMMA) assessed ex vivo muscle mitochondrial energetics in 764 older adults (mean age =76.4, 56.5% women, 85.9% non-Hispanic white) by high-resolution respirometry of permeabilized muscle fibers. We estimated the proportional odds ratio (POR [95%CI]) for the likelihood of greater multimorbidity (four levels: 0 conditions, N=332; 1 condition, N=299; 2 conditions, N=98; or 3+ conditions, N=35) from an index of 11 conditions, per SD decrement in muscle mitochondrial energetic parameters. Distribution of conditions allowed for testing the associations of maximal muscle energetics with some individual conditions. Results Lower oxidative phosphorylation supported by fatty acids and/or complex-I and -II linked carbohydrates (e.g., Max OXPHOSCI+CII) was associated with a greater multimorbidity index score (POR=1.32[1.13,1.54]) and separately with diabetes mellitus (OR=1.62[1.26,2.09]), depressive symptoms (OR=1.45[1.04,2.00]) and possibly chronic kidney disease (OR=1.57[0.98,2.52]) but not significantly with other conditions (e.g., cardiac arrhythmia, chronic obstructive pulmonary disease). Conclusions Lower muscle mitochondrial bioenergetic capacities was associated with a worse composite multimorbidity index score. Our results suggest that decrements in muscle mitochondrial energetics may contribute to a greater global burden of disease and is more strongly related to some conditions than others.
肌肉线粒体生物能与老年人多病负担的关系:肌肉、活动能力和老龄化研究(SOMMA)
背景 地球科学假说认为,衰老的生物过程会导致许多与年龄有关的缺陷,包括多种慢性疾病的累积。肌肉线粒体生物能量能力的下降虽然只是线粒体功能的一个方面,但也可能是导致多种疾病易感性增加的原因之一。方法 肌肉、运动和老化研究(SOMMA)通过对透化肌肉纤维进行高分辨率呼吸测定法,评估了 764 名老年人(平均年龄 =76.4,56.5% 为女性,85.9% 为非西班牙裔白人)的体外肌肉线粒体能量。我们根据肌肉线粒体能量参数每标准差的下降,从 11 种情况的指数中估算出多发病(四种情况:0 种情况,332 人;1 种情况,299 人;2 种情况,98 人;或 3+ 种情况,35 人)可能性的比例几率比(POR [95%CI])。通过条件分布可以测试最大肌肉能量与某些个别条件的关联。结果 脂肪酸和/或与复合物 I 和 II 相连的碳水化合物支持的氧化磷酸化较低(例如:最大 OXPHOSCI+CO2Max OXPHOSCI+CII)与更高的多病症指数评分(POR=1.32[1.13,1.54])相关,并分别与糖尿病(OR=1.62[1.26,2.09])、抑郁症状(OR=1.45[1.04,2.00])和可能的慢性肾病(OR=1.57[0.98,2.52])相关,但与其他病症(如心律失常、慢性阻塞性肺病)无明显关系。结论 肌肉线粒体生物能较低与较差的多病综合指数评分有关。我们的研究结果表明,肌肉线粒体能量的降低可能会加重全球疾病负担,而且与某些疾病的关系比与其他疾病的关系更为密切。
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