Department of Medicine, Mackay Medical College, New Taipei City 25245, Taiwan.
Division of Cardiology, Departments of Internal Medicine, MacKay Memorial Hospital, Taipei 10449, Taiwan.
Biomolecules. 2021 Oct 21;11(11):1559. doi: 10.3390/biom11111559.
Aldehyde dehydrogenase 2 (ALDH2) rs671 polymorphism is a common genetic variant in Asians that is responsible for defective toxic aldehyde and lipid peroxidation metabolism after alcohol consumption. The extent to which low alcohol consumption may cause atrial substrates to trigger atrial fibrillation (AF) development in users with ALDH2 variants remains to be determined. We prospectively enrolled 249 ethnic Asians, including 56 non-drinkers and 193 habitual drinkers (135 (70%) as ALDH2 wild-type: GG, rs671; 58 (30%) as ALDH2 variants: G/A or A/A, rs671). Novel left atrial (LA) mechanical substrates with dynamic characteristics were assessed using a speckle-tracking algorithm and correlated to daily alcohol consumption and ALDH2 genotypes. Despite modest and comparable alcohol consumption by the habitual alcohol users (14.3 [8.328.6] and 12.3 [6.330.7] g/day for those without and with ALDH2 polymorphism, = 0.31), there was a substantial and graded increase in the 4-HNE adduct and prolonged PR, and a reduction in novel LA mechanical parameters (including peak atrial longitudinal strain (PALS) and phasic strain rates (reservoir, conduit, and booster pump functions), < 0.05), rather than an LA emptying fraction (LAEF) or LA volume index across non-drinkers, and in habitual drinkers without and with ALDH2 polymorphism (all < 0.05). The presence of ALDH2 polymorphism worsened the association between increasing daily alcohol dose and LAEF, PALS, and phasic reservoir and booster functions (all P: <0.05). Binge drinking superimposed on regular alcohol use exclusively further worsened LA booster pump function compared to regular drinking without binge use (1.66 ± 0.57 vs. 1.97 ± 0.56 1/s, = 0.001). Impaired LA booster function further independently helped to predict AF after consideration of the CHARGE-AF score (adjusted 1.68 (95% CI: 1.06-2.67), = 0.028, per 1 z-score increment). Habitual modest alcohol consumption led to mechanical LA substrate formation in an ethnic Asian population, which was more pronounced in subjects harboring ALDH2 variants. Impaired LA booster functions may serve as a useful predictor of AF in such populations.
乙醛脱氢酶 2 (ALDH2) rs671 多态性是亚洲人群中常见的遗传变异,可导致饮酒后有毒醛和脂质过氧化代谢缺陷。低酒精摄入是否会导致携带 ALDH2 变异的个体的心房底物引发心房颤动 (AF) 发展,目前仍有待确定。我们前瞻性地招募了 249 名亚洲人,包括 56 名不饮酒者和 193 名习惯性饮酒者(135 名(70%)为 ALDH2 野生型:GG,rs671;58 名(30%)为 ALDH2 变异型:G/A 或 A/A,rs671)。使用斑点跟踪算法评估了具有动态特征的新型左心房(LA)机械底物,并与每日饮酒量和 ALDH2 基因型相关联。尽管习惯性饮酒者的饮酒量适中且相当(无 ALDH2 多态性者为 14.3 [8.328.6] 和 12.3 [6.330.7] g/天, = 0.31),但与不饮酒者相比,4-HNE 加合物和 PR 延长,以及新型 LA 机械参数(包括峰值心房纵向应变(PALS)和时相应变率(储存、传导和助力泵功能)均有明显且逐渐增加, < 0.05),而 LA 排空分数(LAEF)或 LA 体积指数则无变化;在无 ALDH2 多态性的习惯性饮酒者中也是如此(均 < 0.05)。ALDH2 多态性的存在使每日饮酒量增加与 LAEF、PALS 和时相储存和助力泵功能之间的关联恶化(均 P:<0.05)。与不饮酒相比,在定期饮酒的基础上叠加狂饮会使 LA 助力泵功能进一步恶化(1.66 ± 0.57 比 1.97 ± 0.56 1/s, = 0.001)。在考虑 CHARGE-AF 评分后,受损的 LA 助力功能进一步独立有助于预测 AF(校正后 1.68(95%CI:1.06-2.67), = 0.028,每增加 1 个 z 分数)。在亚洲人群中,习惯性适度饮酒导致 LA 机械底物形成,在携带 ALDH2 变异的个体中更为明显。受损的 LA 助力功能可能是此类人群中 AF 的有用预测指标。