研究脂肪组织在运动和衰老中的作用:肌肉、运动和衰老研究(SOMMA-AT)辅助脂肪组织的设计和方法。

Reichelle X Yeo, Theresa Mau, Zana M Ross, Nicholas P Edenhoffer, Jingfang Liu, Haley N Barnes, Li-Yung Lui, Joshua N Adkins, James A Sanford, Marcus M Seldin, Carlos H Viesi, Mingqi Zhou, Heather L Gregory, Frederico G S Toledo, Maja Stefanovic-Racic, Mary Lyles, Ashlee N Wood, Polly E Mattila, Elizabeth A Blakley, Iva Miljkovic, Peggy M Cawthon, Anne B Newman, Stephen B Kritchevsky, Steven R Cummings, Bret H Goodpaster, Jamie N Justice, Erin E Kershaw, Lauren M Sparks
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引用次数: 0

摘要

背景:年龄相关的脂肪组织变化影响慢性医学疾病和行动障碍,但机制尚不清楚。本研究的目的是确定老年人脂肪组织的独特表型特征的方法。方法:选择参加肌肉、运动和衰老研究的老年人进行脂肪组织辅助(SOMMA-AT;N=210, 52.38%的女性(76.12±4.37岁)通过全身磁共振(AMRA)评估局部肥胖,并进行腹部皮下脂肪组织针吸活检(ASAT)。ASAT活组织切片被快速冷冻、固定或处理以供下游应用,并存放在生物库中。在ASAT外植体条件培养基中测量活检产量、定性特征、脂肪细胞大小和脂肪因子浓度。测定测量间Spearman相关性。结果:局部而非全部肥胖在性别上存在差异:女性的ASAT质量更大(8.20±2.73kg)。结论:除了本报告中详细的ASAT活检处理外,我们发现脂肪细胞面积与ASAT质量相关,并且这两项指标都与外植体条件培养基中的一些关键脂肪因子有关。这些结果、方法和生物学知识库强调了这一独特队列的潜力,以影响对衰老脂肪生物学对疾病、残疾和其他衰老组织的理解。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Investigating the role of adipose tissue in mobility and aging: design and methods of the Adipose Tissue ancillary to the Study of Muscle, Mobility, and Aging (SOMMA-AT).

Background: Age-related changes in adipose tissue affect chronic medical diseases and mobility disability but mechanism remains poorly understood. The goal of this study is to define methods for phenotyping unique characteristics of adipose tissue from older adults.

Methods: Older adults enrolled in study of muscle, mobility, and aging selected for the adipose tissue ancillary (SOMMA-AT; N = 210, 52.38% women, 76.12 ± 4.37 years) were assessed for regional adiposity by whole-body magnetic resonance (AMRA) and underwent a needle-aspiration biopsy of abdominal subcutaneous adipose tissue (ASAT). ASAT biopsies were flash frozen, fixed, or processed for downstream applications and deposited at the biorepository. Biopsy yields, qualitative features, adipocyte sizes, and concentration of adipokines secreted in ASAT explant conditioned media were measured. Inter-measure Spearman correlations were determined.

Results: Regional, but not total, adiposity differed by sex: women had greater ASAT mass (8.20 ± 2.73 kg, p < .001) and biopsy yield (3.44 ± 1.81 g, p < .001) than men (ASAT = 5.95 ± 2.30 kg, biopsy = 2.30 ± 1.40 g). ASAT mass correlated with leptin (r = 0.54, p < .001) and not resistin (p = .248) and adiponectin (p = .353). Adipocyte area correlated with ASAT mass (r = 0.34, p < .001), BMI (r = 0.33, p < .001), adiponectin (r = -0.22, p = .005) and leptin (r = 0.18, p = .024) but not with resistin (p = .490).

Conclusion: In addition to the detailed ASAT biopsy processing in this report, we found that adipocyte area correlated with ASAT mass, and both measures related to some key adipokines in the explant conditioned media. These results, methods, and biological repositories underscore the potential of this unique cohort to impact the understanding of aging adipose biology on disease, disability, and other aging tissues.

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