Geisler Corinna, Braun Wiebke, Pourhassan Maryam, Schweitzer Lisa, Glüer Claus-Christian, Bosy-Westphal Anja, Müller Manfred J
Institute of Human Nutrition and Food Science, Christian-Albrechts-Universität zu Kiel, Düsternbrooker Weg 17-19, D-24105 Kiel, Germany.
Clinic for Diagnostic Radiology, Section Biomedical Imaging, Molecular Imaging North Competence Center (MOIN CC), Am Botanischen Garten 14, D-24118 Kiel, Germany.
Nutrients. 2016 Jun 1;8(6):322. doi: 10.3390/nu8060322.
Age-related changes in organ and tissue masses may add to changes in the relationship between resting energy expenditure (REE) and fat free mass (FFM) in normal and overweight healthy Caucasians. Secondary analysis using cross-sectional data of 714 healthy normal and overweight Caucasian subjects (age 18-83 years) with comprehensive information on FFM, organ and tissue masses (as assessed by magnetic resonance imaging (MRI)), body density (as assessed by Air Displacement Plethysmography (ADP)) and hydration (as assessed by deuterium dilution (D₂O)) and REE (as assessed by indirect calorimetry). High metabolic rate organs (HMR) summarized brain, heart, liver and kidney masses. Ratios of HMR organs and muscle mass (MM) in relation to FFM were considered. REE was calculated (REEc) using organ and tissue masses times their specific metabolic rates. REE, FFM, specific metabolic rates, the REE-FFM relationship, HOMA, CRP, and thyroid hormone levels change with age. The age-related decrease in FFM explained 59.7% of decreases in REE. Mean residuals of the REE-FFM association were positive in young adults but became negative in older subjects. When compared to young adults, proportions of MM to FFM decreased with age, whereas contributions of liver and heart did not differ between age groups. HOMA, TSH and inflammation (plasma CRP-levels) explained 4.2%, 2.0% and 1.4% of the variance in the REE-FFM residuals, but age and plasma T3-levels had no effects. HMR to FFM and MM to FFM ratios together added 11.8% on to the variance of REE-FFM residuals. Differences between REE and REEc increased with age, suggesting age-related changes in specific metabolic rates of organs and tissues. This bias was partly explained by plasmaT3-levels. Age-related changes in REE are explained by (i) decreases in fat free mass; (ii) a decrease in the contributions of organ and muscle masses to FFM; and (iii) decreases in specific organ and tissue metabolic rates. Age-dependent changes in the REE-FFMassociation are explained by composition of FFM, inflammation and thyroid hormones.
在正常和超重的健康白种人中,器官和组织质量的年龄相关变化可能会加剧静息能量消耗(REE)与去脂体重(FFM)之间关系的变化。对714名健康的正常和超重白种人受试者(年龄18 - 83岁)的横断面数据进行二次分析,这些受试者具备关于FFM、器官和组织质量(通过磁共振成像(MRI)评估)、身体密度(通过空气置换体积描记法(ADP)评估)、水合作用(通过氘稀释法(D₂O)评估)以及REE(通过间接测热法评估)的全面信息。高代谢率器官(HMR)汇总了脑、心脏、肝脏和肾脏的质量。考虑了HMR器官和肌肉质量(MM)与FFM的比率。使用器官和组织质量乘以其特定代谢率来计算REE(REEc)。REE、FFM、特定代谢率、REE - FFM关系、HOMA、CRP和甲状腺激素水平随年龄变化。FFM的年龄相关下降解释了REE下降的59.7%。REE - FFM关联的平均残差在年轻人中为正,但在老年人中变为负。与年轻人相比,MM与FFM的比例随年龄下降,而肝脏和心脏的贡献在不同年龄组之间没有差异。HOMA、促甲状腺激素(TSH)和炎症(血浆CRP水平)分别解释了REE - FFM残差方差的4.2%、2.0%和1.4%,但年龄和血浆三碘甲状腺原氨酸(T3)水平没有影响。HMR与FFM以及MM与FFM的比率共同使REE - FFM残差的方差增加了11.8%。REE与REEc之间的差异随年龄增加,表明器官和组织的特定代谢率存在年龄相关变化。这种偏差部分由血浆T3水平解释。REE的年龄相关变化由以下因素解释:(i)去脂体重下降;(ii)器官和肌肉质量对FFM的贡献减少;(iii)特定器官和组织代谢率下降。REE - FFM关联的年龄依赖性变化由FFM组成、炎症和甲状腺激素解释。