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Receptor Autoradiography Protocol for the Localized Visualization of Angiotensin II Receptors
Published on: June 7, 2016
Gene polymorphism of angiotensin II type 1 and type 2 receptors
Tomohiro Katsuya1, Ryuichi Morishita
1Katsuya Clinic, Department of Clinical Gene Therapy, Osaka University Graduate School of Medicine, 2-17-21 Nanamatsu-cho, Amagasaki, Hyogo 660-0052, Japan. tkatsuya@iris.eonet.ne.jp
Abstract:
Renin-angiotensin system (RAS) plays a key role in pathogenesis of cardiovascular disease and in the responsiveness for various types of medications. A large number of genetic investigations have been carried out to examine the association between gene variants of RAS and predisposition to cardiovascular diseases, such as hypertension, coronary artery disease and stroke. Even though the major results were obtained from genetic association studies of angiotensinogen or angiotensin converting enzyme, unique findings were also elucidated from investigations concerning single nucleotide polymorphisms (SNPs) of 2 types of angioteinsin II receptor genes denoted as AGTR1 and AGTR2. Both genes have many SNPs in the coding and its flanking regions but most of the studies used A1166C polymorphism of AGTR1 and G1675A polymorphism of AGTR2. In the subjects with C1166 allele of AGTR1, several investigations reported increased risk for coronary artery disease, ischemic stroke, heart failure and end-stage renal disease but not for hypertension. Interestingly, a few papers pointed out the possibility that A1166C modulates the efficacy of RAS inhibitors. In the genetic analysis of AGTR2, G1675 allele carriers had increased risk for left ventricular hypertrophy, renal insufficiency and modulated hemodynamic response to RAS inhibitors. In this review, we summarized previous investigations concerning the genetic aspects of AGTR1 and AGTR2 to consider the clinical utility of SNPs of these receptors.
Insights
Genetic variations in the renin-angiotensin system (RAS) receptors, AGTR1 and AGTR2, are linked to cardiovascular disease risks and medication response. Specific single nucleotide polymorphisms (SNPs) offer potential clinical utility.
Area of Science:
- Cardiovascular Genetics
- Pharmacogenomics
- Molecular Medicine
Background:
- The renin-angiotensin system (RAS) is crucial in cardiovascular disease (CVD) pathogenesis and drug response.
- Genetic variations in RAS genes, particularly angiotensinogen and angiotensin-converting enzyme, have been extensively studied.
- Single nucleotide polymorphisms (SNPs) in angiotensin II receptor genes (AGTR1 and AGTR2) also show associations with CVD.
Purpose of the Study:
- To review genetic investigations of AGTR1 and AGTR2.
- To explore the clinical utility of SNPs in these angiotensin II receptor genes.
- To summarize findings on the association between RAS gene variants and cardiovascular diseases.
Main Methods:
- Review of previous genetic association studies.
- Analysis of single nucleotide polymorphisms (SNPs) in AGTR1 and AGTR2 genes.
- Focus on A1166C polymorphism of AGTR1 and G1675A polymorphism of AGTR2.
Main Results:
- The AGTR1 A1166C polymorphism (C1166 allele) is associated with increased risk for coronary artery disease, ischemic stroke, heart failure, and end-stage renal disease, but not hypertension.
- AGTR1 A1166C may modulate the efficacy of RAS inhibitors.
- The AGTR2 G1675A polymorphism (G1675 allele) is linked to increased risk for left ventricular hypertrophy, renal insufficiency, and altered hemodynamic responses to RAS inhibitors.
Conclusions:
- SNPs in AGTR1 and AGTR2 are associated with various cardiovascular conditions and influence response to RAS inhibitors.
- These genetic variants hold potential for clinical utility in personalized medicine.
- Further research is warranted to fully elucidate the clinical significance of these RAS receptor SNPs.
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