Rossi Niccolo', Aliyev Elbay, Visconti Alessia, Akil Ammira S A, Syed Najeeb, Aamer Waleed, Padmajeya Sujitha S, Falchi Mario, Fakhro Khalid A
Department of Twin Research and Genetics Epidemiology, King's College London, London, UK.
Department of Human Genetics, Sidra Medicine, Doha, Qatar.
NPJ Genom Med. 2021 Feb 9;6(1):8. doi: 10.1038/s41525-021-00170-3.
Studies assessing the impact of amylase genes copy number (CN) on adiposity report conflicting findings in different global populations, likely reflecting the impact of ancestral and ethnic-specific environment and lifestyle on selection at the amylase loci. Here, we leverage population size and detailed adiposity measures from a large population biobank to resolve confounding effects and determine the relationship between salivary (AMY1) and pancreatic (AMY2A) amylase genes CN and adiposity in 2935 Qatari individuals who underwent whole-genome sequencing (WGS) as part of the Qatar Genome Programme. We observe a negative association between AMY1 CNs and trunk fat percentage in the Qatari population (P = 7.50 × 10) and show that Qataris of Arab descent have significantly lower CN at AMY1 (P = 1.32 × 10) as well as less favorable adiposity and metabolic profiles (P < 1.34 × 10) than Qataris with Persian ancestry. Indeed, lower AMY1 CN was associated with increased total and trunk fat percentages in Arabs (P < 4.60 × 10) but not in Persians. Notably, overweight and obese Persians reported a significant trend towards dietary restraint following weight gain compared to Arabs (P = 4.29 × 10), with AMY1 CN showing negative association with dietary self-restraint (P = 3.22 × 10). This study reports an association between amylase gene CN and adiposity traits in a large Middle Eastern population. Importantly, we leverage rich biobank data to demonstrate that the strength of this association varies with ethnicity, and may be influenced by population-specific behaviors that also contribute to adiposity traits.
评估淀粉酶基因拷贝数(CN)对肥胖影响的研究在不同全球人群中报告了相互矛盾的结果,这可能反映了祖先和特定种族的环境与生活方式对淀粉酶基因座选择的影响。在此,我们利用来自大型人群生物样本库的人口规模和详细的肥胖测量数据来解决混杂效应,并确定2935名卡塔尔个体中唾液淀粉酶基因(AMY1)和胰腺淀粉酶基因(AMY2A)的CN与肥胖之间的关系,这些个体作为卡塔尔基因组计划的一部分接受了全基因组测序(WGS)。我们观察到卡塔尔人群中AMY1的CN与躯干脂肪百分比呈负相关(P = 7.50×10),并表明阿拉伯血统的卡塔尔人在AMY1处的CN显著更低(P = 1.32×10),且与波斯血统的卡塔尔人相比,其肥胖和代谢特征更不理想(P < 1.34×10)。事实上,较低的AMY1 CN与阿拉伯人总脂肪和躯干脂肪百分比增加相关(P < 4.60×10),但与波斯人无关。值得注意的是,与阿拉伯人相比,超重和肥胖的波斯人在体重增加后报告了显著的饮食限制趋势(P = 4.29×10)——AMY1 CN与饮食自我限制呈负相关(P = 3.22×10)。本研究报告了中东一大群人中淀粉酶基因CN与肥胖特征之间的关联。重要的是,我们利用丰富的生物样本库数据证明这种关联的强度因种族而异,并且可能受到也导致肥胖特征的特定人群行为的影响。