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本文引用的文献

1
Studies of the peptide YY and neuropeptide Y2 receptor genes in relation to human obesity and obesity-related traits.关于肽YY和神经肽Y2受体基因与人类肥胖及肥胖相关性状的研究。
Diabetes. 2004 Sep;53(9):2461-6. doi: 10.2337/diabetes.53.9.2461.
2
Physiology: does gut hormone PYY3-36 decrease food intake in rodents?生理学:肠道激素PYY3 - 36是否会减少啮齿动物的食物摄入量?
Nature. 2004 Jul 8;430(6996):1 p following 165; discussion 2 p following 165. doi: 10.1038/nature02665.
3
A resistin gene polymorphism is associated with body mass index in women.抵抗素基因多态性与女性体重指数相关。
Hum Genet. 2004 Aug;115(3):208-12. doi: 10.1007/s00439-004-1128-4. Epub 2004 Jun 23.
4
Genetic studies of the etiology of type 2 diabetes in Pima Indians: hunting for pieces to a complicated puzzle.皮马印第安人2型糖尿病病因的遗传学研究:寻找复杂谜题的碎片
Diabetes. 2004 May;53(5):1181-6. doi: 10.2337/diabetes.53.5.1181.
5
Genetic variation in uncoupling protein 3 is associated with dietary intake and body composition in females.解偶联蛋白3的基因变异与女性的饮食摄入及身体组成有关。
Metabolism. 2004 Apr;53(4):458-64. doi: 10.1016/j.metabol.2003.11.019.
6
Neuropeptide Y gene expression in male sheep: influence of photoperiod and testosterone.雄性绵羊中神经肽Y基因的表达:光周期和睾酮的影响
Neuroendocrinology. 2004 Feb;79(2):82-9. doi: 10.1159/000076631.
7
Acute effects of PYY3-36 on food intake and hypothalamic neuropeptide expression in the mouse.PYY3-36对小鼠食物摄入量和下丘脑神经肽表达的急性影响。
Biochem Biophys Res Commun. 2003 Nov 28;311(4):915-9. doi: 10.1016/j.bbrc.2003.10.089.
8
Inhibition of food intake in obese subjects by peptide YY3-36.肽YY3-36对肥胖受试者食物摄入的抑制作用。
N Engl J Med. 2003 Sep 4;349(10):941-8. doi: 10.1056/NEJMoa030204.
9
To eat or not to eat - how the gut talks to the brain.吃还是不吃——肠道如何与大脑对话。
N Engl J Med. 2003 Sep 4;349(10):926-8. doi: 10.1056/NEJMp038114.
10
Characterization of blood-brain barrier permeability to PYY3-36 in the mouse.小鼠血脑屏障对PYY3-36的通透性特征
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肽YY和Y2受体基因的变异与皮马印第安男性的严重肥胖有关。

Variations in peptide YY and Y2 receptor genes are associated with severe obesity in Pima Indian men.

作者信息

Ma Lijun, Tataranni P Antonio, Hanson Robert L, Infante Aniello M, Kobes Sayuko, Bogardus Clifton, Baier Leslie J

机构信息

Diabetes Molecular Genetics Section, National Institute of Diabetes and Digestive and Kidney Diseases, National Institutes of Health, 4212 North 16th St., Phoenix, AZ 85016, USA.

出版信息

Diabetes. 2005 May;54(5):1598-602. doi: 10.2337/diabetes.54.5.1598.

DOI:10.2337/diabetes.54.5.1598
PMID:15855352
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC1350723/
Abstract

Peptide YY (PYY) and Y2 receptor (Y2R) may be important in the central regulation of body weight and food intake. To determine whether genetic variation in PYY and/or Y2R may contribute to morbid obesity in humans, these genes were sequenced in 83 extremely obese Pima Indians (BMI > or = 50 kg/m2). Sequencing of PYY identified three single nucleotide polymorphisms (SNPs) in the untranslated region. Sequencing of the Y2R coding region identified one missense (Ala172Thr) substitution and two silent substitutions. Eight additional SNPs in the 5' untranslated region of Y2R were identified from public databases. These SNPs were genotyped in 489 full-heritage adult Pimas (362 severely obese and 127 nondiabetic, nonobese subjects), who are not first-degree relatives, for association analysis. The PYY variants were not associated with obesity, whereas four variants from two haplotype blocks in Y2R were marginally associated (P = 0.054-0.067) with obesity. However, if the analysis was restricted to men (n = 167, 100 obese and 67 lean), the PYY variants and two SNPs in Y2R that were in complete linkage disequilibrium were significantly associated with severe obesity (P = 0.001 and P = 0.002, respectively). Our data suggest that the PYY-Y2R pathway may influence body weight through a sex-specific mechanism, but this finding requires confirmation in other populations.

摘要

肽YY(PYY)和Y2受体(Y2R)可能在体重和食物摄入的中枢调节中起重要作用。为了确定PYY和/或Y2R的基因变异是否可能导致人类病态肥胖,对83名极度肥胖的皮马印第安人(BMI≥50kg/m²)的这些基因进行了测序。对PYY的测序在非翻译区鉴定出三个单核苷酸多态性(SNP)。对Y2R编码区的测序鉴定出一个错义(Ala172Thr)替换和两个沉默替换。从公共数据库中鉴定出Y2R的5'非翻译区的另外八个SNP。在489名非一级亲属的全血统成年皮马人(362名严重肥胖者和127名非糖尿病、非肥胖受试者)中对这些SNP进行基因分型,以进行关联分析。PYY变体与肥胖无关,而Y2R中两个单倍型块的四个变体与肥胖有边缘关联(P = 0.054 - 0.067)。然而,如果分析仅限于男性(n = 167,100名肥胖者和67名瘦者),PYY变体和Y2R中处于完全连锁不平衡的两个SNP与严重肥胖显著相关(分别为P = 0.001和P = 0.002)。我们的数据表明,PYY - Y2R途径可能通过性别特异性机制影响体重,但这一发现需要在其他人群中得到证实。