Association Between Angiotensin I-Converting Enzyme Gene Insertion/Deletion Polymorphism and Risk of Rheumatic Heart Disease
スポンサーリンク
概要
- 論文の詳細を見る
Scarring and collagen deposition in the valves and destruction of myocytes may result from the combined effects of a smoldering rheumatic process and a constant trauma to the mitral valve or aortic valve by the turbulent flow in rheumatic heart disease (RHD). It has been suggested that angiotensin I-converting enzyme (ACE) may be responsible for the increased valvular fibrosis and calcification in the pathogenesis of RHD. However, the role of ACE genetic variant in RHD has not been studied among the Chinese population in Taiwan. Hence, a case-controlled study was carried out to investigate the possible relationship between the ACE gene insertion/deletion (I/D) and G2350A polymorphisms and RHD. A group of 115 patients with RHD documented by echocardiography and 100 age- and sex-matched normal control subjects were studied. ACE gene I/D and G2350A polymorphisms were identified by polymerase chain reaction-based restriction analysis. There was a significant difference in the distribution of ACE I/D genotypes (P = 0.02) and allelic frequencies (P = 0.04) between RHD cases and normal controls. An odds ratio for the risk of RHD associated with the ACE I/D II genotype was 2.12 (95% CI, 1.21-3.71). An odds ratio for the risk of RHD associated with the ACE I allele was 1.50 (95% CI, 1.02-2.21). The ACE G2350A polymorphism showed no association with RHD (P = 0.90). Further categorization of RHD patients into mitral valve disease and combined valve disease subgroups revealed no statistical difference in these gene polymorphisms when compared between the two subgroups. This study shows that patients with RHD have a higher frequency of ACE II genotype and I allele, which supports a role for ACE I/D gene polymorphisms in determining the risk of RHD in Taiwan Chinese.
著者
-
Chou Hsiang-tai
Division Of Cardiology Department Of Medicine
-
Tsai Fuu-jen
Department Of Medical Research China Medical College Hospital
-
Tsai Chang-hai
Taichung Healthcare And Management University
-
Tsai Fuu-Jen
Department of Pediatrics, Medical Research and Medical Genetics, China Medical University Hospital, and College of Chinese Medicine, China Medical University
-
Chou Hsiang-Tai
Division of Cardiology, Department of Medicine, China Medical University Hospital
関連論文
- Molecular analysis of syndromic congenital heart disease using short tandem repeat markers and semiquantitative polymerase chain reaction method
- Angiotensin II Type 1 Receptor Gene Adenine/Cytosine^ Polymorphism is not Associated With Mitral Valve Prolapse Syndrome in Taiwan Chinese
- Molecular analysis of Wilson disease in Taiwan: identification of one novel mutation and evidence of haplotype-mutation association
- Mutation analysis of Crouzon syndrome and identification of one novel mutation in Taiwanese patients
- Association of the Neuronal Nicotinic Acetylcholine Receptor Subunit α4 Polymorphisms with Febrile Convulsions
- Electrophysiological Characteristics and Radiofrequency Ablation of Focal Atrial Tachycardia Originating From the Superior Vena Cava
- Lack of Association of Genetic Polymorphisms in the Interleukin-1 β, Interleukin-1 Receptor Antagonist, Interleukin-4, and Interleukin-10 Genes With Risk of Rheumatic Heart Disease in Taiwan Chinese
- Association Between Angiotensin I-Converting Enzyme Gene Insertion/Deletion Polymorphism and Risk of Rheumatic Heart Disease
- The Polymorphisms of Codon 727 and 52 of Thyroid-Stimulating Hormone Receptor Gene are not Associated with Mitral Valve Prolapse Syndrome in Taiwan Chinese
- Response : Febrile Convulsions and Genetic Susceptibility : Role of the Neuronal Nicotinic Acetylcholine Receptor α4 Subunit
- 台湾人 Wilson 病患者のATP7B遺伝子異常とハプロタイプ
- Safety and Outcomes of Short-Term Multiple Femoral Venous Sheath Placement in Cardiac Electrophysiological Study and Radiofrequency Catheter Ablation