Department of Clinical Lab, Guangzhou Women and Children's Medical Center, Guangzhou Medical University, Guangzhou, China.
Department of Clinical Biological Resource Bank, Guangzhou Institute of Pediatrics, Guangzhou Women and Children's Medical Center, Guangzhou Medical University, Guangzhou, China.
Angiology. 2023 Oct;74(9):832-839. doi: 10.1177/00033197221118343. Epub 2022 Sep 2.
Kawasaki disease (KD) is an acute systemic vascular disease complicated by coronary artery injury. Although polymorphisms in prostaglandin-endoperoxide synthase 1 () are being increasingly explored in cardiovascular diseases, little is known regarding the connection between polymorphisms and KD risk. We evaluated 834 KD patients and 1474 healthy controls to explore the relationship between polymorphisms (rs1330344 and rs5788) and KD risk. Our results showed that the rs1330344 CC genotype was significantly associated with KD risk and coronary artery injury in children with KD. In combined analysis, individuals with 1-2 unfavorable genotypes had an increased risk of KD, compared with those with no risk genotype. Stratified analysis indicated that the rs1330344 CC genotype is strongly associated with increased risk of KD in children aged ≤60 months and females. Moreover, carrying 1-2 of these SNP genotypes had a higher risk of KD than those who harbored none of them in children ≤60 months of age and females; the risk of coronary artery dilatations/small aneurysms and medium/giant aneurysms was also significantly increased in KD patients. In summary, the rs1330344 CC genotype is associated with increased susceptibility to KD, which may contribute to KD pathogenesis and serve as a genetic biomarker.
川崎病(KD)是一种伴有冠状动脉损伤的急性全身性血管疾病。尽管前列腺素内过氧化物合酶 1()中的多态性在心血管疾病中的研究越来越多,但关于多态性与 KD 风险之间的联系知之甚少。我们评估了 834 名 KD 患者和 1474 名健康对照者,以探讨 多态性(rs1330344 和 rs5788)与 KD 风险之间的关系。我们的结果表明,rs1330344 CC 基因型与 KD 风险和儿童 KD 的冠状动脉损伤显著相关。在联合分析中,与无风险基因型相比,具有 1-2 种不利基因型的个体患 KD 的风险增加。分层分析表明,rs1330344 CC 基因型与≤60 个月儿童和女性患 KD 的风险增加密切相关。此外,在≤60 个月的儿童和女性中,携带 1-2 种这些 SNP 基因型的个体患 KD 的风险高于不携带这些基因型的个体;KD 患者的冠状动脉扩张/小动脉瘤和中/大动脉瘤的风险也显著增加。总之,rs1330344 CC 基因型与 KD 的易感性增加有关,这可能有助于 KD 的发病机制,并可作为遗传生物标志物。