Unit of Molecular Biology and Genomic Medicine, Instituto Nacional de Ciencias Médicas y Nutrición Salvador Zubirán, Vasco de Quiroga #15, Tlalpan, Belisario Domínguez Sección XVI, 14080, Mexico City, Mexico.
Universidad Autónoma Metropolitana, Mexico City, Mexico.
J Endocrinol Invest. 2020 Aug;43(8):1061-1071. doi: 10.1007/s40618-020-01187-8. Epub 2020 Feb 3.
Type 2 diabetes (T2D) and low serum concentration of high-density lipoprotein cholesterol (HDL-c) are common coexisting metabolic disorders. ABCA1 variants have been shown to be associated to these conditions. We sought to test the combined effect of two ABCA1 gene common variants, rs2422493 (- 565C > T) and rs9282541 (R230C) on HDL-c levels and T2D risk.
Path analysis was conducted in 3,303 Mexican-mestizos to assess the specific contributions of rs2422493 and rs9282541 ABCA1 variants, insulin resistance, waist-to-height ratio (WHtR), and age on HDL-c levels and T2D risk. Participants were classified into four groups according to their ABCA1 variants carrier status: (i) the reference group carried wild type alleles for both ABCA1 variants (-/-), (ii) +/- were carriers of rs2422493 but non-carriers of rs9282541, (iii) -/+ for carriers of rs9282541 but not carriers of rs2422493 and (iv) carriers of minor alleles for both SNPs (+/+). Principal components from two previous genome-wide association studies were used to control for ethnicity.
We identified significant indirect effects on T2D risk mediated by HDL-c in groups -/+ and +/+ (β = 0.04; p = 0.03 and β = 0.06; p < 0.01, respectively) in comparison to the -/- reference group. Low concentrations of HDL-c were directly and significantly associated with increased T2D risk (β = -0.70; p < 0.01). WHtR, male gender, age, and insulin resistance were also associated with T2D risk (p < 0.05). There was no significant direct effect for any of the ABCA1 groups on T2D risk: p = 0.99, p = 0.58, and p = 0.91 for groups +/-, -/+, and +/+ respectively.
The ABCA1 rs9282541 (R230C) allele is associated with T2D in Mexicans through its effect on lowering HDL-c levels. This is the first report demonstrating that HDL-c levels act as an intermediate factor between an ABCA1 variant and T2D.
2 型糖尿病(T2D)和低血清高密度脂蛋白胆固醇(HDL-c)浓度是常见的并存代谢紊乱。已经证明 ABCA1 变体与这些情况有关。我们试图检测两种常见的 ABCA1 基因变体 rs2422493(-565C>T)和 rs9282541(R230C)对 HDL-c 水平和 T2D 风险的联合影响。
对 3303 名墨西哥裔混合人群进行路径分析,以评估 rs2422493 和 rs9282541 ABCA1 变体、胰岛素抵抗、腰高比(WHtR)和年龄对 HDL-c 水平和 T2D 风险的具体贡献。根据他们的 ABCA1 变体携带状态,参与者被分为四组:(i)参考组携带两种 ABCA1 变体的野生型等位基因(-/-),(ii)+/- 是 rs2422493 的携带者但不是 rs9282541 的携带者,(iii)-/+是 rs9282541 的携带者但不是 rs2422493 的携带者,(iv)两种 SNP 的次要等位基因携带者(+/+)。使用来自两项先前全基因组关联研究的主成分来控制种族。
我们发现,与-/-参考组相比,-/+和+/+组中 HDL-c 介导的 T2D 风险存在显著的间接影响(β=0.04;p=0.03 和 β=0.06;p<0.01)。低浓度的 HDL-c 与 T2D 风险增加直接相关(β=-0.70;p<0.01)。WHtR、男性、年龄和胰岛素抵抗也与 T2D 风险相关(p<0.05)。对于任何 ABCA1 组,都没有对 T2D 风险有显著的直接影响:p=0.99、p=0.58 和 p=0.91 分别对应+/-、-/+和+/+组。
在墨西哥人中,ABCA1 rs9282541(R230C)等位基因通过降低 HDL-c 水平与 T2D 相关。这是第一个证明 HDL-c 水平作为 ABCA1 变体和 T2D 之间中间因子的报告。