Chathoth Shahanas, Ismail Mona H, Vatte Chittibabu, Cyrus Cyril, Al Ali Zhara, Ahmed Khandaker Ahtesham, Acharya Sadananda, Al Barqi Aisha Mohammed, Al Ali Amein
Department of Genetic Research, Institute for Research and Medical Consultation, Imam Abdulrahman Bin Faisal University, P.O. Box 1982, Dammam, 31441, Saudi Arabia.
Department of Internal Medicine, King Fahd Hospital of the University, Imam Abdulrahman Bin Faisal University, Al-Khobar, Saudi Arabia.
BMC Med Genet. 2018 Nov 20;19(1):203. doi: 10.1186/s12881-018-0715-5.
Obesity is one of the main causes of morbidity and mortality worldwide. More than 120 genes have been shown to be associated with obesity related phenotypes. The aim of this study was to determine the effect of selected genetic polymorphisms in Uncoupling protein 1 (UCP1) and Niemann-Pick C1 (NPC1) genes in an obese population in Saudi Arabia.
The genotypes of rs1800592, rs10011540 and rs3811791 (UCP1 gene) and rs1805081 and rs1805082 (NPC1 gene) were determined in a total of 492 subjects using TaqMan chemistry by Real-time PCR. In addition, capillary sequencing assay was performed to identify two specific polymorphisms viz., rs45539933 (exon 2) and rs2270565 (exon 5) of UCP1 gene.
A significant association of UCP1 polymorphisms rs1800592 [OR, 1.52 (1.10-2.08); p = 0.009] was observed in the obese cohort after adjusting with age, sex and type 2 diabetes. Further BMI based stratification revealed that this association was inconsistent with both moderate and extreme obese cohort. A significant association of UCP1 polymorphisms rs3811791 was observed only in the moderate-obese cohort [OR = 2.89 (1.33-6.25); p = 0.007] but not in the extreme-obese cohort indicating an overlying genetic complexity between moderate-obesity and extreme-obesity. The risk allele frequencies, which were higher in moderate-obese cohort, had abnormal HDL, LDL and triglyceride levels.
The rs1800592 and rs3811791 of UCP1 gene are associated with obesity in general and in the moderate-obese group in particular. The associated UCP1 polymorphisms in the moderate-obese group may regulate the impaired energy metabolism which plays a significant role in the initial stages of obesity.
肥胖是全球发病和死亡的主要原因之一。已证实120多个基因与肥胖相关表型有关。本研究的目的是确定沙特阿拉伯肥胖人群中解偶联蛋白1(UCP1)和尼曼-匹克C1(NPC1)基因中选定基因多态性的影响。
采用实时荧光定量PCR的TaqMan化学方法,对492名受试者的rs1800592、rs10011540和rs3811791(UCP1基因)以及rs1805081和rs1805082(NPC1基因)的基因型进行了测定。此外,还进行了毛细管测序分析以鉴定UCP1基因的两个特定多态性,即rs45539933(外显子2)和rs2270565(外显子5)。
在调整年龄、性别和2型糖尿病后,肥胖队列中观察到UCP1多态性rs1800592有显著关联[比值比(OR),1.52(1.10 - 2.08);p = 0.009]。进一步基于体重指数的分层显示,这种关联在中度肥胖和极度肥胖队列中均不一致。仅在中度肥胖队列中观察到UCP1多态性rs3811791有显著关联[OR = 2.89(1.33 - 6.25);p = 0.007],而在极度肥胖队列中未观察到,这表明中度肥胖和极度肥胖之间存在潜在的遗传复杂性。中度肥胖队列中风险等位基因频率较高,其高密度脂蛋白、低密度脂蛋白和甘油三酯水平异常。
UCP1基因的rs1800592和rs3811791一般与肥胖相关,尤其与中度肥胖组相关。中度肥胖组中相关的UCP1多态性可能调节能量代谢受损,这在肥胖的初始阶段起重要作用。