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在南方汉族人群中,川崎病患者的多态性(rs7251246 T > C)、冠状动脉瘤和血栓形成。

polymorphism (rs7251246 T > C), coronary artery aneurysms, and thrombosis in patients with Kawasaki disease in a Southern Han Chinese population.

机构信息

Department of Pediatrics, First Affiliated Hospital, Guangxi Medical University, Nanning, China.

出版信息

Front Immunol. 2023 Jun 19;14:1184162. doi: 10.3389/fimmu.2023.1184162. eCollection 2023.

DOI:10.3389/fimmu.2023.1184162
PMID:37404818
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC10315485/
Abstract

OBJECTIVES

Kawasaki disease (KD) is a commonly acquired pediatric systemic vasculitis disease resulting in coronary artery aneurysm (CAA). The relationship between the polymorphism (rs7251246) and the severity and susceptibility to KD in the Han Chinese population in Southern China remains unclear.

METHODS

We enrolled 262 children as controls and 221 children with KD (46 [20.8%] with intravenous immunoglobulin resistance and 82 [37.1%] with CAA). The relationship between the rs7251246 polymorphism, KD susceptibility, and CAA formation was investigated.

RESULTS

While the rs7251246 T>C polymorphism was not significantly associated with KD susceptibility, it was significantly related to the CAA risk in children with KD [CC/CT vs. TT: adjusted odds ratio [OR] 2.089, 95% confidence interval [CI] 1.085-4.020]. Male children with the rs7251246 CT/TT genotype had a significantly lower risk of thrombosis [CT/TT vs. CC: adjusted OR 0.251, 95% CI 0.068-0.923]. Children with KD, especially those with CAA, had significantly downregulated mRNA compared to healthy children. mRNA levels were lower in children with CAA who developed thrombosis (=0.039). In children with KD, the CC genotype showed lower mRNA levels of (=0.035).

CONCLUSION

The rs7251246 T>C polymorphism may be a risk factor for CAA and thrombosis in children with KD in the Han Chinese population, likely due to differences in mature mRNA levels caused by interference of RNA splicing. Dual antiplatelet therapy for thrombosis is recommended for male children with the rs7251246 CC genotype.

摘要

目的

川崎病(KD)是一种常见的获得性儿科全身血管炎疾病,可导致冠状动脉瘤(CAA)。在中国南方汉族人群中,该基因多态性(rs7251246)与 KD 的严重程度和易感性之间的关系尚不清楚。

方法

我们纳入了 262 名对照儿童和 221 名 KD 患儿(46 名[20.8%]存在静脉免疫球蛋白抵抗,82 名[37.1%]存在 CAA)。研究了 rs7251246 多态性与 KD 易感性和 CAA 形成之间的关系。

结果

虽然 rs7251246 T>C 多态性与 KD 易感性无显著相关性,但与 KD 患儿的 CAA 风险显著相关[CC/CT 与 TT:校正优势比(OR)2.089,95%置信区间(CI)1.085-4.020]。携带 rs7251246 CT/TT 基因型的男性患儿发生血栓的风险显著降低[CT/TT 与 CC:校正 OR 0.251,95%CI 0.068-0.923]。KD 患儿,尤其是 CAA 患儿,其 mRNA 表达水平明显低于健康儿童。发生血栓的 CAA 患儿的 mRNA 水平较低(=0.039)。KD 患儿中,CC 基因型的 mRNA 水平较低(=0.035)。

结论

rs7251246 T>C 多态性可能是汉族 KD 患儿 CAA 和血栓形成的危险因素,这可能是由于 RNA 剪接干扰导致成熟 mRNA 水平不同所致。建议携带 rs7251246 CC 基因型的男性 KD 患儿进行双联抗血小板治疗。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2058/10315485/97f4bf5ea5aa/fimmu-14-1184162-g005.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2058/10315485/6097838fce0a/fimmu-14-1184162-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2058/10315485/9f715507fd47/fimmu-14-1184162-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2058/10315485/5182bc9428f5/fimmu-14-1184162-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2058/10315485/cbb2398291ab/fimmu-14-1184162-g004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2058/10315485/97f4bf5ea5aa/fimmu-14-1184162-g005.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2058/10315485/6097838fce0a/fimmu-14-1184162-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2058/10315485/9f715507fd47/fimmu-14-1184162-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2058/10315485/5182bc9428f5/fimmu-14-1184162-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2058/10315485/cbb2398291ab/fimmu-14-1184162-g004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2058/10315485/97f4bf5ea5aa/fimmu-14-1184162-g005.jpg

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