Butler Merlin G, Theodoro Mariana F, Bittel Douglas C, Donnelly Joseph E
Section of Medical Genetics and Molecular Medicine, Children's Mercy Hospitals and Clinics and University of Missouri-Kansas City School of Medicine, Kansas City, Missouri 64108, USA.
Am J Med Genet A. 2007 Mar 1;143A(5):449-59. doi: 10.1002/ajmg.a.31507.
Prader-Willi syndrome (PWS) is a complex neurodevelopmental disorder characterized by hypotonia, suck and feeding difficulties, hypogonadism, small hands and feet, developmental delay, hyperphagia and early childhood obesity and a particular facial appearance. The obesity associated with PWS is the result of a chronic imbalance between energy intake and energy expenditure (EE) due to hyperphagia, decreased physical activity, reduced metabolic rate and an inability to vomit. EE is affected by body composition as well as exercise. Individuals with PWS have a lower lean body mass (LBM) compared with controls which may contribute to reduced basal level EE. To determine the relationship among body composition, activity levels and metabolic rates, dual energy X-ray absorptiometry (DEXA) and a whole-room respiration chamber were used to measure body composition, total EE (TEE), resting EE (REE), physical activity, and mechanical work (MW) during an 8 hr monitoring period. The chamber consisted of a live-in whole-room indirect calorimeter equipped with a force platform floor to allow simultaneous measurement of EE, physical activity, and work efficiency during spontaneous activities and standardized exercise. Participants with PWS (27 with 15q11-q13 deletion and 21 with maternal disomy 15 with an average age of 23 years) had significantly decreased TEE by 20% and reduced LBM compared to 24 obese subjects. Similarly, REE was significantly reduced by 16% in the individuals with PWS relative to the comparison subjects. Total MW performed during the 8 hr monitoring period was significantly reduced by 35% in the PWS group. The energy cost of physical activity is related to the duration, intensity and type of activity and the metabolic efficiency of the individual. After adjusting group differences in LBM by analysis of variance, TEE and REE were no longer different between the two groups. Our data indicate that there is a significant reduction of EE in individuals with PWS resulting from reduced activity but also from lower energy utilization due to reduced LBM which consists primarily of muscle.
普拉德-威利综合征(PWS)是一种复杂的神经发育障碍,其特征为肌张力减退、吸吮和喂养困难、性腺功能减退、手脚小、发育迟缓、食欲亢进、儿童早期肥胖以及特殊面容。与PWS相关的肥胖是由于食欲亢进、体力活动减少、代谢率降低以及无法呕吐导致能量摄入与能量消耗(EE)长期失衡的结果。EE受身体成分以及运动的影响。与对照组相比,PWS患者的瘦体重(LBM)较低,这可能导致基础水平的EE降低。为了确定身体成分、活动水平和代谢率之间的关系,在8小时的监测期内,使用双能X线吸收法(DEXA)和全室呼吸室来测量身体成分、总能量消耗(TEE)、静息能量消耗(REE)、体力活动和机械功(MW)。该呼吸室由一个可居住的全室间接热量计组成,配备有测力平台地板,以便在自发活动和标准化运动期间同时测量EE、体力活动和工作效率。与24名肥胖受试者相比,PWS患者(27名15q11-q13缺失患者和21名母源单亲二倍体15患者,平均年龄23岁)的TEE显著降低20%,LBM减少。同样,与对照受试者相比,PWS患者的REE显著降低16%。在8小时监测期内,PWS组的总MW显著降低35%。体力活动的能量消耗与活动的持续时间、强度和类型以及个体的代谢效率有关。通过方差分析调整LBM的组间差异后,两组之间的TEE和REE不再有差异。我们的数据表明,PWS患者的EE显著降低,这是由于活动减少以及主要由肌肉组成的LBM降低导致能量利用减少所致。