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Association of angiotensin I-converting enzyme gene insertion/deletion polymorphism with rheumatic heart disease in
Usha Gupta1, Avshesh Mishra, Saurabh S Rathore
1Department of Genetics, Sanjay Gandhi Postgraduate Institute of Medical Sciences, Raebareli Road, Lucknow, 226014, India.
Insights
The angiotensin I-converting enzyme (ACE) ID and DD genotypes are linked to a higher risk of rheumatic heart disease (RHD), especially combined valve lesions. This suggests ACE gene polymorphism plays a role in RHD development.
Area of Science:
- Cardiovascular Genetics
- Molecular Cardiology
- Rheumatic Heart Disease Pathogenesis
Background:
- Rheumatic heart disease (RHD) is a severe sequela of rheumatic fever.
- The angiotensin I-converting enzyme (ACE) is implicated in valvular fibrosis and calcification in RHD pathogenesis.
Purpose of the Study:
- To investigate the association between ACE I/D polymorphism and RHD in the Indian population.
- To evaluate the role of ACE I/D genotypes in the pathogenesis of RHD, including specific valve lesions.
Main Methods:
- A case-control study involving 300 RHD patients and 200 controls.
- ACE I/D polymorphism identified using polymerase chain reaction.
- Meta-analysis of the current study and three published studies (636 RHD cases, 533 controls).
Main Results:
- Significant differences in ACE ID and DD genotype distributions were observed between RHD cases and controls (ORs 1.62-2.08).
- ACE ID and DD genotypes were significantly associated with combined valve lesions (CVL) in RHD patients (FDR Pcorr < 0.014).
- Meta-analysis indicated an association between the ACE D allele and RHD risk (OR 1.22).
Conclusions:
- ACE ID and DD genotypes are associated with an increased risk of RHD.
- The ACE I/D gene polymorphism appears to play a significant role in the pathogenesis of RHD, particularly in cases with combined valve lesions.
Abstract:
Rheumatic heart disease (RHD) is one of the most severe consequences of rheumatic fever. It has been suggested that angiotensin I-converting enzyme (ACE) may be involved in the increased valvular fibrosis and calcification in the pathogenesis of RHD. We conducted a case-control study to look for association of ACE I/D polymorphism with RHD in Indian population. The study incorporated 300 patients (170 males and 130 females) with RHD, and 200 controls (118 males and 82 females). We also subgrouped RHD patients into mitral valve lesion (MVL) and combined valve lesion (CVL). ACE I/D polymorphism was identified using polymerase chain reaction method. We also performed a meta-analysis of three published studies and the present study (636 RHD cases and 533 controls) to evaluate the association between the ACE I/D polymorphisms and RHD risk. A significant difference in ACE ID and DD genotypes distribution between RHD cases (OR = 1.62, 95% CI = 1.11-2.36 and OR = 2.08, 95% CI = 1.02-4.15, respectively) and corresponding controls was observed. On comparing the ACE genotypes of MVL and CVL subgroups with controls, ID and DD genotypes were also significantly associated with CVL (FDR Pcorr = 0.009, OR = 2.19 and FDR Pcorr = 0.014, OR = 3.29, respectively). Meta-analysis also suggested association of the ACE D allele (FDR Pcorr = 0.036, OR-1.22, 95% CI 1.02-1.45) with RHD. In conclusion, ACE ID and DD genotypes are associated with an increased risk of RHD, particularly CVL. This suggests that the ACE I/D gene polymorphism may play an important role in the pathogenesis of RHD.
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