Association of angiotensin-converting enzyme 2 (ACE2) gene polymorphisms with parameters of left ventricular hypertrophy in men
Autor: | Björn Mayer, Anika Götz, Jan Stritzke, Jochen Graf, Stephan R. Holmer, Marcus Fischer, Wolfgang Lieb, Christian Hengstenberg, Angela Döring, Heribert Schunkert, Hannelore Löwel, Jeanette Erdmann, Inke R. König |
---|---|
Rok vydání: | 2005 |
Předmět: |
Adult
Male hypertrophy ACE2 genetics polymorphism medicine.medical_specialty Genotype Heart Ventricles Population Single-nucleotide polymorphism Peptidyl-Dipeptidase A Left ventricular hypertrophy Muscle hypertrophy Risk Factors Internal medicine Drug Discovery medicine Humans Ventricular Function education Genetics (clinical) Aged education.field_of_study Polymorphism Genetic biology Haplotype Angiotensin-converting enzyme Organ Size Odds ratio Middle Aged medicine.disease Endocrinology Echocardiography Angiotensin-converting enzyme 2 biology.protein Molecular Medicine Female Hypertrophy Left Ventricular Angiotensin-Converting Enzyme 2 |
Zdroj: | J. Mol. Med. 84, 88-96 (2006) |
ISSN: | 1432-1440 0946-2716 |
DOI: | 10.1007/s00109-005-0718-5 |
Popis: | Angiotensin-converting enzyme (ACE) activity is considered to be of major importance for the conversion of angiotensin (Ang) I to Ang II. Recently, a second ACE, named ACE2, has been identified. Experimental data provide evidence that ACE2 might be involved in modulating cardiac structure and function. In the present explorative study, we assessed whether polymorphisms in the ACE2 gene are related to echocardiographically determined parameters of left ventricular mass, structure or function in the general population. Five intronic single nucleotide polymorphisms (SNPs) were genotyped using the 5′-exonuclease activity (TaqMan) assay in the echocardiographic substudy of the third MONICA Augsburg survey. As ACE2 is located on the X chromosome, women and men were analysed separately. Four SNPs showed high pairwise linkage disequilibrium (rs4646156, rs879922, rs4240157 and rs233575). The minor alleles of these four SNPs were associated with higher left ventricular mass index (LVMI) and higher septal wall thickness (SWT) in men. Likewise, male carriers of a common haplotype (frequency 29.9%) consisting of the minor alleles of these four SNPs displayed higher values for LVMI and SWT than non-carriers (LVMI: TGGC 98.8±1.52 vs non-TGGC 94.8±0.99 g/m 2, p=0.027; SWT: TGGC 11.5±0.14 vs non-TGGC 11.1±0.09 mm, p=0.019). Furthermore, this haplotype was associated with an increased odds ratio (OR) for left ventricular hypertrophy (OR 3.10, p=0.006). In women, similar but less pronounced and consistent trends were observed. No association was observed between any of these SNPs and parameters of left ventricular systolic or diastolic function nor with blood pressure levels. This study provides evidence that genetic variants in the ACE2 gene may be associated with left ventricular mass, SWT and left ventricular hypertrophy in hemizygous men. © Springer-Verlag 2005. |
Databáze: | OpenAIRE |
Externí odkaz: |