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与非裔美国人皮肤色素沉着相关的遗传位点及其对维生素 D 缺乏症的影响。

Genetic loci associated with skin pigmentation in African Americans and their effects on vitamin D deficiency.

机构信息

Department of Urology, University of Arizona, Tucson, Arizona, United States of America.

Department of Population and Quantitative Health Sciences, Case Western Reserve University, Cleveland, Ohio, United States of America.

出版信息

PLoS Genet. 2021 Feb 18;17(2):e1009319. doi: 10.1371/journal.pgen.1009319. eCollection 2021 Feb.

Abstract

A recent genome-wide association study (GWAS) in African descent populations identified novel loci associated with skin pigmentation. However, how genomic variations affect skin pigmentation and how these skin pigmentation gene variants affect serum 25(OH) vitamin D variation has not been explored in African Americans (AAs). In order to further understand genetic factors that affect human skin pigmentation and serum 25(OH)D variation, we performed a GWAS for skin pigmentation with 395 AAs and a replication study with 681 AAs. Then, we tested if the identified variants are associated with serum 25(OH) D concentrations in a subset of AAs (n = 591). Skin pigmentation, Melanin Index (M-Index), was measured using a narrow-band reflectometer. Multiple regression analysis was performed to identify variants associated with M-Index and to assess their role in serum 25(OH)D variation adjusting for population stratification and relevant confounding variables. A variant near the SLC24A5 gene (rs2675345) showed the strongest signal of association with M-Index (P = 4.0 x 10-30 in the pooled dataset). Variants in SLC24A5, SLC45A2 and OCA2 together account for a large proportion of skin pigmentation variance (11%). The effects of these variants on M-Index was modified by sex (P for interaction = 0.009). However, West African Ancestry (WAA) also accounts for a large proportion of M-Index variance (23%). M-Index also varies among AAs with high WAA and high Genetic Score calculated from top variants associated with M-Index, suggesting that other unknown genomic factors related to WAA are likely contributing to skin pigmentation variation. M-Index was not associated with serum 25(OH)D concentrations, but the Genetic Score was significantly associated with vitamin D deficiency (serum 25(OH)D levels less than 12 ng/mL) (OR, 1.30; 95% CI, 1.04-1.64). The findings support the hypothesis suggesting that skin pigmentation evolved responding to increased demand for subcutaneous vitamin D synthesis in high latitude environments.

摘要

最近在非洲裔人群中进行的全基因组关联研究(GWAS)确定了与皮肤色素沉着相关的新基因座。然而,基因组变异如何影响皮肤色素沉着,以及这些皮肤色素沉着基因变异如何影响血清 25(OH)维生素 D 变异,在非裔美国人(AA)中尚未得到探索。为了进一步了解影响人类皮肤色素沉着和血清 25(OH)D 变异的遗传因素,我们对 395 名 AA 进行了皮肤色素沉着的 GWAS 研究,并对 681 名 AA 进行了复制研究。然后,我们在 AA 的一个亚组(n = 591)中测试了鉴定出的变体是否与血清 25(OH)D 浓度相关。使用窄带反射计测量皮肤色素沉着、黑色素指数(M-Index)。进行多元回归分析以鉴定与 M-Index 相关的变体,并评估它们在调整人群分层和相关混杂变量后对血清 25(OH)D 变异的作用。位于 SLC24A5 基因附近的变体(rs2675345)与 M-Index 的关联信号最强(在合并数据集的 P = 4.0×10-30)。SLC24A5、SLC45A2 和 OCA2 中的变体共同解释了皮肤色素沉着变异的很大一部分(11%)。这些变体对 M-Index 的影响受性别修饰(P 交互=0.009)。然而,西非血统(WAA)也占 M-Index 变异的很大一部分(23%)。M-Index 也在 AA 中有所不同,这些 AA 具有高 WAA 和与 M-Index 相关的顶级变体计算得出的高遗传评分,这表明与 WAA 相关的其他未知基因组因素可能导致皮肤色素沉着的变异。M-Index 与血清 25(OH)D 浓度无关,但遗传评分与维生素 D 缺乏症显著相关(血清 25(OH)D 水平<12ng/mL)(OR,1.30;95%CI,1.04-1.64)。这些发现支持了这样一种假设,即皮肤色素沉着的进化是为了应对高纬度环境中对皮下维生素 D 合成的需求增加。

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