Related Experiment Video
Updated: Mar 12, 2026

Subcutaneous Angiotensin II Infusion using Osmotic Pumps Induces Aortic Aneurysms in Mice
Published on: September 28, 2015
Matrix metalloproteinase-2 (MMP2) rs243865 polymorphism and target end-organ damage in difficult-to-control
Thuc Tri Nguyen1, An Viet Tran2, An Tuan Huynh2
1Cho Ray Hospital, Ho Chi Minh City, Vietnam.
Background:
The matrix metalloproteinase-2 (MMP2) rs243865 polymorphism has been associated with cardiovascular events; however, its impact on difficult-to-control hypertension remains unclear. This study aims to assess the characteristics of rs243865 polymorphism and its association with target organ damage in adult patients with difficult-to-control hypertension in Vietnam.
Methods:
A cross-sectional study was conducted on 70 difficult-to-control hypertensive patients at two medical centers in Southern Vietnam. All patients underwent Sanger sequencing for analysis of the MMP2 rs243865 polymorphism. Target organ damage (TOD) was assessed across cardiac (left ventricular hypertrophy (LVH), myocardial ischemia), renal (decreased glomerular filtration rate, microalbuminuria), and vascular (carotid stenosis, peripheral vascular disease) systems, with patient-level counts of damaged target-organ systems derived. Data were processed in R 4.5.0 (RStudio, 2025), and associations were analyzed using logistic regression with false discovery rate (FDR) control based on Storey's q-values.
Results:
Analysis of the MMP2 rs243865 polymorphism revealed a predominance of the C allele (87.1%), with the CC genotype being the most common (75.7%). Allele/genotype distributions did not differ across clinical features (p > 0.05) except for higher dyslipidemia in C-allele carriers and the CC genotype (p = 0.035 and p = 0.033). Adjusted models (age, sex, dyslipidemia, duration of hypertension, and duration of diabetes) showed the C allele and CC genotype associated with microalbuminuria (q = 0.041; q = 0.049), echocardiographic LVH (q = 0.039; q = 0.027), and renal TOD (q = 0.019; q = 0.027). CC genotype associations were observed for LVH on echocardiography (q = 0.027), combined LVH (q = 0.028) and cardiac TOD (q = 0.039), and lower odds of carotid artery stenosis (q = 0.039). The C allele was associated with ≥ 2 damaged organ systems (q = 0.026).
Conclusion:
Preliminary findings suggest a possible involvement of the MMP2 rs243865 polymorphism in target organ damage among patients with difficult-to-control hypertension.
Insights
The matrix metalloproteinase-2 (MMP2) rs243865 polymorphism, particularly the C allele and CC genotype, is linked to target organ damage in difficult-to-control hypertension. This genetic factor may influence conditions like microalbuminuria and left ventricular hypertrophy.
Area of Science:
- Genetics and Cardiovascular Disease
- Molecular Biology and Hypertension Research
- Clinical Genetics and Patient Outcomes
Background:
- Difficult-to-control hypertension poses significant risks for cardiovascular events and target organ damage.
- The matrix metalloproteinase-2 (MMP2) rs243865 polymorphism's role in severe hypertension is not well-established.
- Understanding genetic predispositions can aid in managing complex hypertensive cases.
Purpose of the Study:
- To investigate the characteristics of the MMP2 rs243865 polymorphism in Vietnamese patients with difficult-to-control hypertension.
- To assess the association between this polymorphism and target organ damage (TOD) in this patient cohort.
- To explore potential genetic markers for predicting TOD in challenging hypertension cases.
Main Methods:
- Cross-sectional study of 70 patients with difficult-to-control hypertension in Southern Vietnam.
- Sanger sequencing used to analyze MMP2 rs243865 polymorphism.
- Target organ damage assessed across cardiac, renal, and vascular systems; logistic regression with FDR control applied for analysis.
Main Results:
- The C allele (87.1%) and CC genotype (75.7%) predominated for MMP2 rs243865.
- C allele and CC genotype were significantly associated with microalbuminuria, echocardiographic LVH, and renal TOD.
- CC genotype also linked to combined cardiac TOD and lower odds of carotid artery stenosis.
Conclusions:
- The MMP2 rs243865 polymorphism may play a role in the development of target organ damage in difficult-to-control hypertension.
- Genetic variations in MMP2 could be potential biomarkers for assessing TOD risk.
- Further research is warranted to confirm these findings and explore therapeutic implications.
Related Concept Videos
Pharmacogenetics of Drug Targets: β₂-Adrenergic Receptors, Apo E, Thymidylate Synthase
Pharmacogenetic Phenotypes: Alterations in Pharmacokinetics, Drug Targets and Biologic Milieu
Hypertension II: Pathophysiology
Hypertension III: Clinical Manifestations and Diagnostic Studies
Role of Matrix Metalloproteases in Degradation of ECM
