Garagnani Paolo, Giuliani Cristina, Pirazzini Chiara, Olivieri Fabiola, Bacalini Maria Giulia, Ostan Rita, Mari Daniela, Passarino Giuseppe, Monti Daniela, Bonfigli Anna Rita, Boemi Massimo, Ceriello Antonio, Genovese Stefano, Sevini Federica, Luiselli Donata, Tieri Paolo, Capri Miriam, Salvioli Stefano, Vijg Jan, Suh Yousin, Delledonne Massimo, Testa Roberto, Franceschi Claudio
DIMES - Department of Experimental, Diagnostic and Specialty Medicine, University of Bologna, Bologna, 40126 Italy.
Aging (Albany NY). 2013 May;5(5):373-85. doi: 10.18632/aging.100562.
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 /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.
针对与年龄相关的慢性人类疾病的基因关联研究常常缺乏检测适度效应的能力。在此,我们提出一种替代方法,即将健康的百岁老人纳入作为更同质且极端的对照组。作为原理验证,我们聚焦于2型糖尿病(T2D),并评估了与T2D、糖尿病并发症和代谢疾病相关的31个单核苷酸多态性(SNP)以及与端粒稳定性和年龄相关疾病相关基因的SNP的基因型关联。我们假设风险变异的频率与健康和寿命的降低呈负相关。我们先进行了比较糖尿病患者和非糖尿病对照的关联分析,随后进行了与极端表型组(有并发症的T2D患者和百岁老人)的关联分析。结果凸显了rs7903146(TCF7L2基因),其风险基因型(TT)的频率从百岁老人到出现大血管并发症的糖尿病患者持续增加,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值 = 9.066×10⁻⁷)。我们得出结论,当比较极端表型时,即使样本量较小,也能获得稳健且具有生物学相关性的关联。