Hebbar Prashantha, Abu-Farha Mohamed, Mohammad Anwar, Alkayal Fadi, Melhem Motasem, Abubaker Jehad, Al-Mulla Fahd, Thanaraj Thangavel Alphonse
Research Division, Dasman Diabetes Institute, Dasman, Kuwait.
Front Genet. 2020 Jan 31;10:1411. doi: 10.3389/fgene.2019.01411. eCollection 2019.
Association studies have implicated single nucleotide polymorphisms (SNPs), particularly rs1421085, from the fat mass and obesity-associated () gene with body composition phenotypes, obesity, dietary intake, and physical activity in European, East Asian, and African populations. However, the impact of the rs1421085 variant has not been sufficiently tested in ethnic populations (such as Arabs) with high levels of obesity. Further, there is a lack of studies identifying biomarkers that interact with . Therefore, we investigated the association of rs1421085 with obesity and body composition traits and metabolic biomarkers in Arab population. We genotyped rs1421085 SNP in 278 Arab individuals, where multiple biomarkers relating to obesity, inflammation, and other metabolic pathways were quantified. We performed genetic association tests under additive mode of inheritance using linear regression models and found association of rs1421085_C allele with higher levels of body weight, soft lean mass (SLM), and total body water. Examination (using linear regression models under dominant mode of inheritance) of correlation among biomarkers and interaction with genotypes at the variant revealed that measures of these three body composition traits were found mediated by interaction between carrier genotypes (TC+CC) and measures of ghrelin, ApoA1, and ApoB48. Lean body mass (LBM), to which SLM contributes, is an important determinant of physical strength and is a focal point in studies on sarcopenia. Low LBM is known to be associated with higher risk of cardiometabolic disorders. Thus, the finding on the variant as a genetic determinant of SLM interaction with ghrelin, ApoA1, and ApoB48 is important.
关联研究表明,在欧洲、东亚和非洲人群中,来自脂肪量和肥胖相关(FTO)基因的单核苷酸多态性(SNP),尤其是rs1421085,与身体成分表型、肥胖、饮食摄入和身体活动有关。然而,rs1421085变异体在肥胖率较高的种族人群(如阿拉伯人)中的影响尚未得到充分测试。此外,缺乏识别与FTO相互作用的生物标志物的研究。因此,我们调查了rs1421085与阿拉伯人群肥胖、身体成分特征和代谢生物标志物之间的关联。我们对278名阿拉伯个体的rs1421085 SNP进行了基因分型,其中对与肥胖、炎症和其他代谢途径相关的多种生物标志物进行了量化。我们使用线性回归模型在加性遗传模式下进行了基因关联测试,发现rs1421085_C等位基因与更高水平的体重、软瘦体重(SLM)和全身水有关。在显性遗传模式下(使用线性回归模型)对生物标志物之间的相关性以及与该变异体基因型的相互作用进行检查后发现,这三种身体成分特征的测量值是由携带者基因型(TC+CC)与胃饥饿素、载脂蛋白A1和载脂蛋白B48测量值之间的相互作用介导的。SLM所贡献的去脂体重(LBM)是体力的重要决定因素,也是肌肉减少症研究的重点。已知低LBM与心血管代谢疾病的高风险相关。因此,关于rs1421085变异体作为SLM与胃饥饿素、载脂蛋白A1和载脂蛋白B48相互作用的遗传决定因素的发现很重要。