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The prevalence, metabolic risk and effects of lifestyle intervention for metabolically healthy obesity: a systematic review and meta-analysis: A PRISMA-compliant article.代谢健康型肥胖的患病率、代谢风险及生活方式干预的效果:一项系统评价和荟萃分析:一篇遵循PRISMA规范的文章
Medicine (Baltimore). 2017 Nov;96(47):e8838. doi: 10.1097/MD.0000000000008838.
2
[The investigation the combined effect of SNP rs9939609 (gene FTO) and rs4994 (gene ADRB3) polymorphisms on risk of obesity].[关于单核苷酸多态性rs9939609(FTO基因)和rs4994(ADRB3基因)多态性对肥胖风险的联合影响的研究]
Vopr Pitan. 2016;85(4):29-34.
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Updates on obesity pharmacotherapy.肥胖症药物治疗的最新进展。
Ann N Y Acad Sci. 2018 Jan;1411(1):106-119. doi: 10.1111/nyas.13542.
4
Obesity, body weight regulation and the brain: insights from fMRI.肥胖、体重调节与大脑:功能磁共振成像的见解
Br J Radiol. 2018 Sep;91(1089):20170910. doi: 10.1259/bjr.20170910. Epub 2018 Feb 16.
5
Incretin hormones: Their role in health and disease.肠降血糖素:它们在健康和疾病中的作用。
Diabetes Obes Metab. 2018 Feb;20 Suppl 1:5-21. doi: 10.1111/dom.13129.
6
Utility values for childhood obesity interventions: a systematic review and meta-analysis of the evidence for use in economic evaluation.儿童肥胖干预措施的效用值:用于经济评价的证据的系统评价和荟萃分析。
Obes Rev. 2018 Jul;19(7):905-916. doi: 10.1111/obr.12672. Epub 2018 Jan 21.
7
Establishing a genetic link between FTO and VDR gene polymorphisms and obesity in the Emirati population.在阿联酋人群中建立FTO基因与维生素D受体(VDR)基因多态性和肥胖之间的遗传联系。
BMC Med Genet. 2018 Jan 17;19(1):11. doi: 10.1186/s12881-018-0522-z.
8
Genetic variation in the obesity gene FTO is not associated with decreased fat oxidation: the NEO study.肥胖基因 FTO 的遗传变异与脂肪氧化减少无关:NEO 研究。
Int J Obes (Lond). 2017 Oct;41(10):1594-1600. doi: 10.1038/ijo.2017.146. Epub 2017 Jun 19.
9
Evaluation of a multiprofessional, nonsurgical obesity treatment program: which parameters indicated life style changes and weight loss?一项多专业非手术肥胖治疗项目的评估:哪些参数表明生活方式改变和体重减轻?
J Eat Disord. 2017 May 15;5:14. doi: 10.1186/s40337-017-0144-4. eCollection 2017.
10
The role of macronutrient intake in reducing the risk of obesity and overweight among carriers of different polymorphisms of FTO gene. A review.宏量营养素摄入在降低FTO基因不同多态性携带者肥胖和超重风险中的作用。综述。
Rocz Panstw Zakl Hig. 2017;68(1):5-13.

蒙古族人群脂肪质量和肥胖相关基因(FTO)多态性与肥胖及代谢综合征的关系。

Relationship Between Fat Mass and Obesity-Associated (FTO) Gene Polymorphisms with Obesity and Metabolic Syndrome in Ethnic Mongolians.

机构信息

Physical Examination Center of The Affiliated Hospital of Inner Mongolia Medical University, Hohhot, Inner Mongolia, China (mainland).

出版信息

Med Sci Monit. 2018 Nov 16;24:8232-8238. doi: 10.12659/MSM.910928.

DOI:10.12659/MSM.910928
PMID:30442880
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC6251077/
Abstract

BACKGROUND The distribution of fat mass and obesity-associated gene (FTO) genes rs9939609 and rs1421085 in obese and normal ethnic Mongolians was analyzed to investigate the association of FTO gene polymorphisms with obesity and metabolic syndrome in ethnic Mongolians. MATERIAL AND METHODS The genotypes of FTO genes rs9939609 and rs1421085 in 500 subjects were detected by allele-specific PCR (AS-PCR). General characteristics and clinical biochemical indicators were compared between the obesity group and the control group. The correlation between different genotypes and obesity metabolic index was also analyzed. RESULTS Body mass, body mass index (BMI), waist circumference (WC), hip circumference (HC), waist-hip ratio (WHR), SBP, DBP, FPG, triglyceride (TG), total cholesterol (TC), and low-density lipoprotein cholesterol (LDL-C) were higher, while HDL-C was lower in the obesity group compared with controls. The frequencies of TT genotype and T allele in the obesity group were higher than those in the control group. The frequencies of these 3 genotypes and allele frequencies of Rs1421085 were comparable between the 2 groups (P>0.05). The risk of obesity in Mongolian individuals carrying rs9939609 AT genotype was 1.312 times higher and the risk in those carrying AA genotype was 1.896 times higher than in individuals with TT genotype. The body weight, BMI, WC, HC, and WHR in individuals with rs9939609 AA and AT genotypes were significantly higher than in those with TT genotype. CONCLUSIONS The AT/AA genotype and allele A of rs9939609 are associated with an increased risk of obesity.

摘要

背景

分析肥胖相关基因(FTO)基因 rs9939609 和 rs1421085 在肥胖和正常蒙古族人群中的分布,探讨 FTO 基因多态性与蒙古族肥胖和代谢综合征的关系。

材料与方法

采用等位基因特异性 PCR(AS-PCR)检测 500 例研究对象 FTO 基因 rs9939609 和 rs1421085 的基因型。比较肥胖组和对照组的一般特征和临床生化指标,分析不同基因型与肥胖代谢指标的相关性。

结果

肥胖组体重、体重指数(BMI)、腰围(WC)、臀围(HC)、腰臀比(WHR)、收缩压(SBP)、舒张压(DBP)、空腹血糖(FPG)、甘油三酯(TG)、总胆固醇(TC)、低密度脂蛋白胆固醇(LDL-C)均高于对照组,高密度脂蛋白胆固醇(HDL-C)低于对照组。肥胖组 TT 基因型和 T 等位基因频率高于对照组。2 组 rs1421085 3 种基因型及等位基因频率差异无统计学意义(P>0.05)。携带 rs9939609 AT 基因型的蒙古族个体肥胖风险是 TT 基因型的 1.312 倍,携带 AA 基因型的肥胖风险是 TT 基因型的 1.896 倍。携带 rs9939609 AA 和 AT 基因型的个体体重、BMI、WC、HC 和 WHR 明显高于 TT 基因型。

结论

rs9939609 的 AT/AA 基因型和 A 等位基因与肥胖风险增加相关。