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STK33 连锁 SNP rs4929949 与瑞典和希腊儿童的两个独立队列中的肥胖和 BMI 相关。

The STK33-linked SNP rs4929949 is associated with obesity and BMI in two independent cohorts of Swedish and Greek children.

机构信息

Department of Neuroscience, Functional Pharmacology, Uppsala University BMC, Uppsala, Sweden.

出版信息

PLoS One. 2013 Aug 15;8(8):e71353. doi: 10.1371/journal.pone.0071353. eCollection 2013.

Abstract

Recent genome wide association studies (GWAS) have identified a locus on chromosome 11p15.5, closely associated with serine/threonine kinase 33 (STK33), to be associated with body mass. STK33, a relatively understudied protein, has been linked to KRAS mutation-driven cancers and explored as a potential antineoplastic drug target. The strongest association with body mass observed at this loci in GWAS was rs4929949, a single nucleotide polymorphism located within intron 1 of the gene encoding STK33. The functional implications of rs4929949 or related variants have not been explored as of yet. We have genotyped rs4929949 in two cohorts, an obesity case-control cohort of 991 Swedish children, and a cross-sectional cohort of 2308 Greek school children. We found that the minor allele of rs4929949 was associated with obesity in the cohort of Swedish children and adolescents (OR = 1.199 (95%CI: 1.002-1.434), p = 0.047), and with body mass in the cross-sectional cohort of Greek children (β = 0.08147 (95% CI: 0.1345-0.1618), p = 0.021). We observe the effects of rs4929949 on body mass to be detectable already at adolescence. Subsequent analysis did not detect any association of rs4929949 to phenotypic measurements describing body adiposity or to metabolic factors such as insulin levels, triglycerides and insulin resistance (HOMA).

摘要

最近的全基因组关联研究(GWAS)已经确定了 11p15.5 染色体上的一个位点,该位点与丝氨酸/苏氨酸激酶 33(STK33)密切相关,与体重有关。STK33 是一种相对研究较少的蛋白质,与 KRAS 突变驱动的癌症有关,并被探索作为一种潜在的抗肿瘤药物靶点。在 GWAS 中,该基因座与体重相关性最强的是 rs4929949,这是一个单核苷酸多态性,位于编码 STK33 的基因的内含子 1 内。rs4929949 或相关变体的功能意义尚未得到探索。我们在两个队列中对 rs4929949 进行了基因分型,一个是 991 名瑞典儿童的肥胖病例对照队列,另一个是 2308 名希腊学龄儿童的横断面队列。我们发现,rs4929949 的次要等位基因与瑞典儿童和青少年肥胖(OR=1.199(95%CI:1.002-1.434),p=0.047)以及希腊儿童横断面队列的体重(β=0.08147(95%CI:0.1345-0.1618),p=0.021)有关。我们观察到 rs4929949 对体重的影响在青春期就已经可以检测到。随后的分析没有发现 rs4929949 与描述身体肥胖的表型测量值或代谢因素(如胰岛素水平、甘油三酯和胰岛素抵抗(HOMA))之间存在任何关联。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/712a/3744548/9f07955e0420/pone.0071353.g001.jpg

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