Panicker Vijay, Cluett Christie, Shields Beverley, Murray Anna, Parnell Kirstie S, Perry John R B, Weedon Michael N, Singleton Andrew, Hernandez Dena, Evans Jonathan, Durant Claire, Ferrucci Luigi, Melzer David, Saravanan Ponnusamy, Visser Theo J, Ceresini Graziano, Hattersley Andrew T, Vaidya Bijay, Dayan Colin M, Frayling Timothy M
Henry Wellcome Laboratories for Integrative Neurosciences and Endocrinology, University of Bristol, Dorothy Hodgkin Building, Whitson Street, Bristol BS1 3NY, United Kingdom.
J Clin Endocrinol Metab. 2008 Aug;93(8):3075-81. doi: 10.1210/jc.2008-0397. Epub 2008 May 20.
Genetic factors influence circulating thyroid hormone levels, but the common gene variants involved have not been conclusively identified. The genes encoding the iodothyronine deiodinases are good candidates because they alter the balance of thyroid hormones. We aimed to thoroughly examine the role of common variation across the three deiodinase genes in relation to thyroid hormones.
We used HapMap data to select single-nucleotide polymorphisms (SNPs) that captured a large proportion of the common genetic variation across the three deiodinase genes. We analyzed these initially in a cohort of 552 people on T(4) replacement. Suggestive findings were taken forward into three additional studies in people not on T(4) (total n = 2513) and metaanalyzed for confirmation.
A SNP in the DIO1 gene, rs2235544, was associated with the free T(3) to free T(4) ratio with genome-wide levels of significance (P = 3.6 x 10(-13)). The C-allele of this SNP was associated with increased deiodinase 1 (D1) function with resulting increase in free T(3)/T(4) ratio and free T(3) and decrease in free T(4) and rT(3). There was no effect on serum TSH levels. None of the SNPs in the genes coding for D2 or D3 had any influence on hormone levels.
This study provides convincing evidence that common genetic variation in DIO1 alters deiodinase function, resulting in an alteration in the balance of circulating free T(3) to free T(4). This should prove a valuable tool to assess the relative effects of circulating free T(3) vs. free T(4) on a wide range of biological parameters.
遗传因素会影响循环甲状腺激素水平,但其中涉及的常见基因变异尚未得到最终确认。编码碘甲状腺原氨酸脱碘酶的基因是很好的候选基因,因为它们会改变甲状腺激素的平衡。我们旨在全面研究三个脱碘酶基因的常见变异与甲状腺激素的关系。
我们使用HapMap数据选择单核苷酸多态性(SNP),这些SNP捕获了三个脱碘酶基因中大部分常见遗传变异。我们首先在一组接受T(4)替代治疗的552人中对这些SNP进行分析。有提示性的发现被纳入另外三项针对未接受T(4)治疗人群的研究(总计n = 2513),并进行荟萃分析以确认结果。
DIO1基因中的一个SNP,rs2235544,与游离T(3)与游离T(4)的比值相关,具有全基因组水平的显著性(P = 3.6 x 10(-13))。该SNP的C等位基因与脱碘酶1(D1)功能增强相关,导致游离T(3)/T(4)比值和游离T(3)升高,游离T(4)和反T(3)降低。对血清促甲状腺激素(TSH)水平没有影响。编码D2或D3的基因中的SNP均对激素水平没有任何影响。
本研究提供了令人信服的证据,表明DIO1中的常见遗传变异会改变脱碘酶功能,导致循环游离T(3)与游离T(4)的平衡发生改变。这将成为评估循环游离T(3)与游离T(4)对广泛生物学参数的相对影响的有价值工具。