MMP-2基因rs243866多态性与未控制高血压患者靶器官损伤的关系

Q2 Medicine
Huynh Thi Ngoc Giau, Tran Viet An, Trinh Thi Hong Cua, Bui The Dung
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引用次数: 0

摘要

背景:未控制的高血压(UHT)与靶器官损伤(TOD)的风险增加有关。基质金属蛋白酶-2 (Matrix metalloproteinase-2, MMP-2)在血管重构中发挥作用,rs243866 (-1575G/ a)多态性与心血管疾病有关。目的:本研究旨在评估UHT患者rs243866与TOD的相关性。方法:对越南两家医院的134例UHT患者进行横断面研究。采用PCR对rs243866进行基因分型,并通过超声心动图(左心室肥厚- LVH)、肾功能检查(eGFR、蛋白尿)和颈动脉超声(颈动脉粥样硬化)评估TOD。结果:基因型分布为GG(79.9%)、GA(18.6%)和AA(1.5%),等位基因频率分别为89.2% (G)和10.8% (A)。A等位基因与LVH (OR=2.553, 95% CI: 1.052 ~ 6.196, p=0.035)、CKD (OR=2.639, 95% CI: 0.986 ~ 7.066, p=0.048)和颈动脉粥样硬化(OR=6.806, 95% CI: 2.201 ~ 21.024, p)的高风险相关。结论:MMP-2 rs243866多态性与UHT中TOD独立相关,尤其是LVH、CKD和颈动脉粥样硬化。rs243866基因筛查可能为风险分层和个体化高血压管理提供见解。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Association Between rs243866 Polymorphism of the MMP-2 Gene and Target Organ Damage in Patients with Uncontrolled Hypertension.

Background: Uncontrolled hypertension (UHT) is associated with an increased risk of target organ damage (TOD). Matrix metalloproteinase-2 (MMP-2) plays a role in vascular remodeling, and the rs243866 (-1575G/A) polymorphism has been implicated in cardiovascular diseases.

Objective: This study aimed to evaluate the association between rs243866 and TOD in UHT patients.

Methods: A cross-sectional study was conducted on 134 UHT patients at two hospitals in Vietnam. Genotyping of rs243866 was performed using PCR, and TOD was assessed via echocardiography (left ventricular hypertrophy - LVH), renal function tests (eGFR, albuminuria), and carotid ultrasound (carotid atherosclerosis).

Results: The genotypic distribution was GG (79.9%), GA (18.6%), and AA (1.5%), with allele frequencies of 89.2% (G) and 10.8% (A). The A allele was associated with higher risks of LVH (OR=2.553, 95% CI: 1.052-6.196, p=0.035), CKD (OR=2.639, 95% CI: 0.986-7.066, p=0.048), and carotid atherosclerosis (OR=6.806, 95% CI: 2.203-21.024, p<0.001). These associations remained significant after adjusting for confounders.

Conclusion: The rs243866 polymorphism of MMP-2 is independently associated with TOD in UHT, particularly LVH, CKD, and carotid atherosclerosis. Genetic screening for rs243866 may provide insights into risk stratification and personalized hypertension management.

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来源期刊
Acta Informatica Medica
Acta Informatica Medica Medicine-Medicine (all)
CiteScore
2.90
自引率
0.00%
发文量
37
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