Park Hae-Yeon, Oh Hyun-Mi, Kim Tae-Woo, Kim Youngkook, Park Geun-Young, Hwang Hyemi, Im Sun
Department of Rehabilitation Medicine, Seoul St. Mary's Hospital, College of Medicine, The Catholic University of Korea, Seoul 06591, Korea.
Department of Rehabilitation Medicine, National Traffic Injury Rehabilitation Hospital, Yangpyeong 12564, Korea.
Curr Issues Mol Biol. 2022 Aug 19;44(8):3735-3745. doi: 10.3390/cimb44080255.
This study aimed to evaluate whether genetic polymorphism is associated with an increased risk of infection, specifically post-stroke aspiration pneumonia. Blood samples were obtained from a total of 206 post-stroke participants (males, n = 136; mean age, 63.8 years). Genotyping was performed for catechol-O-methyltransferase (rs4680, rs165599), dopamine receptors (DRD1; rs4532, DRD2; rs1800497, DRD3; rs6280), brain-derived neurotrophic factor (rs6265), apolipoprotein E (rs429358, rs7412), and the interleukin-1 receptor antagonist gene (rs4251961). The subjects were stratified into two groups, aged < 65 (young) and ≥ 65 (elderly). Functional parameters and swallowing outcomes were measured at enrollment and at 3 months post-onset. The primary outcome was the incidence of aspiration pneumonia. Analysis of the association between genetic polymorphisms and aspiration pneumonia history showed that a minor C rs429358 allele was associated with the occurrence of aspiration pneumonia in the young group, both in the additive and the dominant models (odds ratio: 4.53; 95% CI: 1.60−12.84, p = 0.004). In the multivariable analysis, the minor C rs429358 allele increased the risk of post-stroke aspiration pneumonia in young stroke patients by 5.35 (95% CI: 1.64−20.88). In contrast, no such association was observed in the elderly group. Apolipoprotein E polymorphism may affect the risk of post-stroke aspiration pneumonia.
本研究旨在评估基因多态性是否与感染风险增加相关,特别是与中风后吸入性肺炎相关。共从206名中风后参与者(男性,n = 136;平均年龄63.8岁)获取血样。对儿茶酚-O-甲基转移酶(rs4680、rs165599)、多巴胺受体(DRD1;rs4532、DRD2;rs1800497、DRD3;rs6280)、脑源性神经营养因子(rs6265)、载脂蛋白E(rs429358、rs7412)以及白细胞介素-1受体拮抗剂基因(rs4251961)进行基因分型。将受试者分为两组,年龄<65岁(年轻组)和≥65岁(老年组)。在入组时和发病后3个月测量功能参数和吞咽结果。主要结局是吸入性肺炎的发生率。基因多态性与吸入性肺炎病史之间的关联分析显示,rs429358基因的次要C等位基因在年轻组中与吸入性肺炎的发生相关,在加性模型和显性模型中均如此(比值比:4.53;95%置信区间:1.60−12.84,p = 0.004)。在多变量分析中,rs429358基因的次要C等位基因使年轻中风患者中风后吸入性肺炎的风险增加5.35倍(95%置信区间:1.64−20.88)。相比之下,在老年组中未观察到此类关联。载脂蛋白E多态性可能影响中风后吸入性肺炎的风险。