German Cancer Research Center (DKFZ), Division of Cancer Epidemiology, Im Neuenheimer Feld 581, 69120 Heidelberg, Germany.
Biobank of the National Center for Tumor Diseases (NCT) Heidelberg, Im Neuenheimer Feld 460, 69120 Heidelberg, Germany.
Nutrients. 2019 Mar 16;11(3):639. doi: 10.3390/nu11030639.
Smaller cross-sectional studies and bariatric surgery trials suggest that weight loss may change the expression of genes in adipose tissue that have been implicated in the development of metabolic diseases, but well-powered intervention trials are lacking. In post hoc analyses of data from a 12-week dietary intervention trial initially designed to compare metabolic effects of intermittent vs. continuous calorie restriction, we analyzed the effects of overall weight loss on the subcutaneous adipose tissue (SAT) transcriptome. Changes in the transcriptome were measured by microarray using SAT samples of 138 overweight or obese individuals (age range: 35⁻65 years, BMI range: 25⁻40, non-smokers, non-diabetics). Participants were grouped post hoc according to the degree of their weight loss by quartiles (average weight loss in quartiles 1 to 4: 0%, -3.2%, -5.9%, and -10.7%). Candidate genes showing differential expression with weight loss according to microarray analyses were validated by reverse transcription quantitative polymerase chain reaction (RT-qPCR), and fold changes (FCs) were calculated to quantify differences in gene expression. A comparison of individuals in the highest vs. the lowest weight loss quartile revealed 681 genes to be differentially expressed (corrected < 0.05), with 40 showing FCs of at least 0.4. Out of these, expression changes in secreted frizzled-related protein 2 (SFRP2, FC = 0.65, = 0.006), stearoyl-CoA desaturase (SCD, FC = -1.00, < 0.001), and hypoxia inducible lipid droplet-associated (HILPDA, FC = -0.45, = 0.001) with weight loss were confirmed by RT-qPCR. Dietary weight loss induces significant changes in the expression of genes implicated in lipid metabolism (SCD and HILPDA) and WNT-signaling (SFRP2) in SAT.
较小的横断面研究和减重手术试验表明,体重减轻可能会改变脂肪组织中与代谢性疾病发展有关的基因表达,但缺乏有力的干预试验。在最初设计用于比较间歇性与连续热量限制对代谢影响的 12 周饮食干预试验的数据的事后分析中,我们分析了整体体重减轻对皮下脂肪组织 (SAT) 转录组的影响。使用 138 名超重或肥胖个体 (年龄范围:35⁻65 岁,BMI 范围:25⁻40,不吸烟,非糖尿病患者) 的 SAT 样本通过微阵列测量转录组的变化。根据体重减轻程度将参与者事后分为四组 (第 1 至 4 组的平均体重减轻量分别为 0%、-3.2%、-5.9%和-10.7%)。根据微阵列分析,用体重减轻显示差异表达的候选基因通过逆转录定量聚合酶链反应 (RT-qPCR) 进行验证,并计算折叠变化 (FC) 以量化基因表达的差异。比较体重减轻最高和最低四分位的个体,发现 681 个基因差异表达 (校正后 < 0.05),其中 40 个基因的 FC 至少为 0.4。在这些基因中,分泌卷曲相关蛋白 2 (SFRP2,FC = 0.65, = 0.006)、硬脂酰辅酶 A 去饱和酶 (SCD,FC = -1.00, < 0.001) 和缺氧诱导的脂质滴相关蛋白 (HILPDA,FC = -0.45, = 0.001) 的表达变化通过 RT-qPCR 得到证实。饮食引起的体重减轻会导致 SAT 中与脂质代谢 (SCD 和 HILPDA) 和 WNT 信号 (SFRP2) 相关的基因表达发生显著变化。