CYP2C19 Poor Metabolizer Status and High System Inflammation Response Index are Independent Risk Factors for Premature Myocardial Infarction: A Hospital-Based Retrospective Study.

IF 2.1 4区 医学 Q2 MEDICINE, GENERAL & INTERNAL International Journal of General Medicine Pub Date : 2024-10-28 eCollection Date: 2024-01-01 DOI:10.2147/IJGM.S489235
Wendao Han, Nating Xiong, Renkai Zhong, Zhongyi Pan
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Abstract

Objective: Atherosclerosis (AS) is a sustained chronic vascular inflammatory response caused by lipid metabolism disorders and immune response disorders and is the main cause of premature (men ≤ 55 years old, women ≤ 65 years old) myocardial infarction (PMI). Cytochrome P450 2C19 (CYP2C19) (related to vascular function and lipid metabolism) and peripheral immune cell levels and plays an important role in the course of AS. The association CYP2C19 polymorphisms, comprehensive immunoinflammatory indices with PMI susceptibility is unclear.

Methods: This study included 485 PMI patients, and 639 age-matched non-PMI individuals as controls, from January 2019 to March 2024. The relationship between CYP2C19 polymorphisms, peripheral immunoinflammatory indices (pan-immune inflammation value (PIV), systemic immune inflammation index (SII), and system inflammation response index (SIRI)) and PMI risk were analyzed.

Results: The inflammatory indices levels in PMI patients were higher than those in controls (all p<0.05). The frequencies of the CYP2C19 *1/*2 and *2/*2 genotypes were higher, while the frequency of the *1/*1 genotype was lower in the PMI patients than those in controls. The cut-off values of TC, TG, LDL-C, PIV, SII, and SIRI were 5.065, 1.305, 2.805, 410.485, 869.645, and 1.495 for distinguishing PMI, respectively. Logistic regression analysis showed that male (odds ratio (OR): 1.607, 95% confidence interval (CI): 1.134-2.277, p=0.008), history of smoking (OR: 7.108, 95% CI: 4.351-11.614, p<0.001), diabetes mellitus (OR: 4.906, 95% CI: 3.333-7.223, p<0.001), CYP2C19 poor metabolizer (PM) (*2/*2, *2/*3, and *3/*3) (OR: 2.147, 95% CI: 1.279-3.603, p=0.004), and high TG (≥1.305 vs <1.305, OR: 2.598, 95% CI: 1.864-3.623, p<0.001) and SIRI level (≥1.495 vs <1.495, OR: 2.495, 95% CI: 1.432-4.349, p=0.001) were independent risk factors for PMI.

Conclusion: CYP2C19 PM phenotype, high SIRI level (≥1.495) and TG level (≥1.305), male, history of smoking, and diabetes mellitus were independently associated with PMI susceptibility.

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CYP2C19不良代谢状态和高系统炎症反应指数是早发心肌梗死的独立风险因素:一项基于医院的回顾性研究
目的:动脉粥样硬化(AS)是由脂质代谢紊乱和免疫反应失调引起的持续性慢性血管炎症反应,是早发(男性≤55岁,女性≤65岁)心肌梗死(PMI)的主要原因。细胞色素 P450 2C19(CYP2C19)(与血管功能和脂质代谢有关)和外周免疫细胞水平在强直性脊柱炎的病程中起着重要作用。CYP2C19多态性、综合免疫炎症指数与PMI易感性的关系尚不清楚:本研究从2019年1月至2024年3月纳入了485名PMI患者,以及639名年龄匹配的非PMI个体作为对照。分析了CYP2C19多态性、外周免疫炎症指数(泛免疫炎症值(PIV)、系统免疫炎症指数(SII)和系统炎症反应指数(SIRI))与PMI风险之间的关系:PMI患者的炎症指数水平高于对照组(所有pCYP2C19 *1/*2和*2/*2基因型均较高,而PMI患者中*1/*1基因型的频率低于对照组)。区分 PMI 的 TC、TG、LDL-C、PIV、SII 和 SIRI 临界值分别为 5.065、1.305、2.805、410.485、869.645 和 1.495。逻辑回归分析表明,男性(几率比(OR):1.607,95% 置信区间(CI):1.134-2.277,P=0.008)、吸烟史(OR:7.108,95% CI:4.351-11.614,ppp=0.004)和高 TG(≥1.305 vs pp=0.001)是 PMI 的独立危险因素:结论:CYP2C19 PM 表型、高 SIRI 水平(≥1.495)和高 TG 水平(≥1.305)、男性、吸烟史和糖尿病与 PMI 易感性独立相关。
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来源期刊
International Journal of General Medicine
International Journal of General Medicine Medicine-General Medicine
自引率
0.00%
发文量
1113
审稿时长
16 weeks
期刊介绍: The International Journal of General Medicine is an international, peer-reviewed, open access journal that focuses on general and internal medicine, pathogenesis, epidemiology, diagnosis, monitoring and treatment protocols. The journal is characterized by the rapid reporting of reviews, original research and clinical studies across all disease areas. A key focus of the journal is the elucidation of disease processes and management protocols resulting in improved outcomes for the patient. Patient perspectives such as satisfaction, quality of life, health literacy and communication and their role in developing new healthcare programs and optimizing clinical outcomes are major areas of interest for the journal. As of 1st April 2019, the International Journal of General Medicine will no longer consider meta-analyses for publication.
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