Giau Huynh Thi Ngoc, An Tran Viet, Cua Trinh Thi Hong, Dung Bui The
Department of Internal Medicine, Can Tho University of Medicine and Pharmacy, Can Tho, Vietnam.
Department of Cardiology, University Medical Center, Ho Chi Minh City, Vietnam.
Acta Inform Med. 2025;33(1):47-49. doi: 10.5455/aim.2024.33.47-49.
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.
This study aimed to evaluate the association between rs243866 and TOD in UHT patients.
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).
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.
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.
未控制的高血压(UHT)与靶器官损害(TOD)风险增加相关。基质金属蛋白酶-2(MMP-2)在血管重塑中起作用,rs243866(-1575G/A)多态性与心血管疾病有关。
本研究旨在评估UHT患者中rs243866与TOD之间的关联。
在越南两家医院对134例UHT患者进行了一项横断面研究。使用聚合酶链反应(PCR)对rs243866进行基因分型,并通过超声心动图(左心室肥厚-LVH)、肾功能测试(估算肾小球滤过率、蛋白尿)和颈动脉超声(颈动脉粥样硬化)评估TOD。
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(比值比[OR]=2.553,95%置信区间[CI]:1.052-6.196,p=0.035)、慢性肾脏病(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:2.203-21.024,p<0.001)的较高风险相关。在调整混杂因素后,这些关联仍然显著。
MMP-2的rs243866多态性与UHT中的TOD独立相关,尤其是LVH、CKD和颈动脉粥样硬化。对rs243866进行基因筛查可能为风险分层和个性化高血压管理提供见解。