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Centenarians as super-controls to assess the biological relevance of genetic risk factors for common age-related diseases: A proof of principle on type 2 diabetes

机译:百岁老人作为评估常见年龄相关疾病遗传风险因素生物学相关性的超级对照:2型糖尿病原则的证明

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摘要

Genetic association studies of age-related, chronic human diseases often suffer from a lack of power to detect modest effects. Here we propose an alternative approach of including healthy centenarians as a more homogeneous and extreme control group. As a proof of principle we focused on type 2 diabetes (T2D) and assessed allelic/genotypic associations of 31 SNPs associated with T2D, diabetes complications and metabolic diseases and SNPs of genes relevant for telomere stability and age-related diseases. We hypothesized that the frequencies of risk variants are inversely correlated with decreasing health and longevity. We performed association analyses comparing diabetic patients and non-diabetic controls followed by association analyses with extreme phenotypic groups (T2D patients with complications and centenarians). Results drew attention to rs7903146 (TCF7L2 gene) that showed a constant increase in the frequencies of risk genotype (TT) from centenarians to diabetic patients who developed macro-complications and the strongest genotypic association was detected when diabetic patients were compared to centenarians (p_value = 9.066*10−7). We conclude that robust and biologically relevant associations can be obtained when extreme phenotypes, even with a small sample size, are compared.
机译:与年龄相关的慢性人类疾病的遗传关联研究通常缺乏检测适度影响的能力。在这里,我们提出了另一种方法,将健康的百岁老人作为一个更加统一和极端的控制群体。作为原理的证明,我们集中于2型糖尿病(T2D)并评估了与T2D,糖尿病并发症和代谢性疾病相关的31个SNP的等位基因/基因型关联,以及与端粒稳定性和年龄相关性疾病相关的基因的SNP。我们假设风险变异的频率与健康和寿命的降低呈负相关。我们进行了关联分析,将糖尿病患者和非糖尿病对照进行了比较,然后与极端表型组(患有并发症和百岁老人的T2D患者)进行了关联分析。结果引起人们对rs7903146(TCF7L2基因)的关注,该基因显示从百岁老人到发生宏观并发症的糖尿病患者的风险基因型(TT)的频率不断增加,并且当将糖尿病患者与百岁老人进行比较时,检测到最强的基因型关联(p_value = 9.066 * 10 −7 )。我们得出的结论是,即使将极端表型(即使样本量很小)进行比较,也可以获得牢固且生物学相关的关联。

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