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- Publisher Website: 10.1046/j.1523-1755.2003.00933.x
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- PMID: 12675870
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Article: Cardiac hypertrophy and remodeling in relation to ACE and angiotensinogen genes genotypes in Chinese dialysis patients
Title | Cardiac hypertrophy and remodeling in relation to ACE and angiotensinogen genes genotypes in Chinese dialysis patients |
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Authors | |
Keywords | Angiotensinogen Cardiac Dialysis |
Issue Date | 2003 |
Publisher | Nature Publishing Group. The Journal's web site is located at http://www.nature.com/ki/index.html |
Citation | Kidney International, 2003, v. 63 n. 5, p. 1899-1907 How to Cite? |
Abstract | Background. Genetic polymorphisms of the angiotensinogen (AGT) and angiotensin-converting enzyme (ACE) genes are associated with increased risk of hypertension and left ventricular hypertrophy (LVH) in hypertensive subjects. However, the extent to which these polymorphisms are related to LVH and remodeling in dialysis patients remains unknown. Methods. Two hundred and forty-six end-stage renal disease (ESRD) patients on peritoneal dialysis and 183 control subjects, all of Chinese origin, were genotyped for the ACE insertion/deletion (I/D) and the AGT M235T gene polymorphisms. Left ventricular mass index (LVMi) and relative wall thickness were measured using echocardiography. Results. Prevalence of ACE DD and AGT TT genotype was 14% and 83%, respectively, in ESRD patients and did not differ significantly from controls. A total percentage of 95% of our patients had LVH (171 with concentric and 63 with eccentric hypertrophy). Adjusting for age, gender, body mass index, duration of dialysis, diabetes, renal diagnosis, hematocrit, systolic and diastolic blood pressure, dialysis urea clearance, residual glomerular filtration rate, and use of converting enzyme inhibitors or angiotensin receptor blockers, AGT TT genotype remained independently associated with greater LVMi (coefficient = 28.73; 95% CI, 5.72 to 51.75; P = 0.015) and relative wall thickness (coefficient = 0.072; 95% CI, 0.022 to 0.122; P = 0.005) than MT/MM genotypes. LVMi and relative wall thickness did not differ significantly among patients with DD, DI, and II genotypes. No statistical significant interaction was noted between ACE and AGT gene polymorphism in relation to LVMi and relative wall thickness. Conclusion. Polymorphism of the AGT 34235T gene but not ACE I/D gene is associated with greater LVMi and relative wall thickness, indicating more concentric LVH, in Chinese peritoneal dialysis patients. Possible synergistic effects between AGT and ACE gene polymorphism require further evaluation in a larger population. |
Persistent Identifier | http://hdl.handle.net/10722/162680 |
ISSN | 2023 Impact Factor: 14.8 2023 SCImago Journal Rankings: 3.886 |
ISI Accession Number ID | |
References |
DC Field | Value | Language |
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dc.contributor.author | Wang, AYM | en_US |
dc.contributor.author | ChungNgor Chan, J | en_US |
dc.contributor.author | Wang, M | en_US |
dc.contributor.author | Poon, E | en_US |
dc.contributor.author | Lui, SF | en_US |
dc.contributor.author | KamTao Li, P | en_US |
dc.contributor.author | Sanderson, J | en_US |
dc.date.accessioned | 2012-09-05T05:22:16Z | - |
dc.date.available | 2012-09-05T05:22:16Z | - |
dc.date.issued | 2003 | en_US |
dc.identifier.citation | Kidney International, 2003, v. 63 n. 5, p. 1899-1907 | en_US |
dc.identifier.issn | 0085-2538 | en_US |
dc.identifier.uri | http://hdl.handle.net/10722/162680 | - |
dc.description.abstract | Background. Genetic polymorphisms of the angiotensinogen (AGT) and angiotensin-converting enzyme (ACE) genes are associated with increased risk of hypertension and left ventricular hypertrophy (LVH) in hypertensive subjects. However, the extent to which these polymorphisms are related to LVH and remodeling in dialysis patients remains unknown. Methods. Two hundred and forty-six end-stage renal disease (ESRD) patients on peritoneal dialysis and 183 control subjects, all of Chinese origin, were genotyped for the ACE insertion/deletion (I/D) and the AGT M235T gene polymorphisms. Left ventricular mass index (LVMi) and relative wall thickness were measured using echocardiography. Results. Prevalence of ACE DD and AGT TT genotype was 14% and 83%, respectively, in ESRD patients and did not differ significantly from controls. A total percentage of 95% of our patients had LVH (171 with concentric and 63 with eccentric hypertrophy). Adjusting for age, gender, body mass index, duration of dialysis, diabetes, renal diagnosis, hematocrit, systolic and diastolic blood pressure, dialysis urea clearance, residual glomerular filtration rate, and use of converting enzyme inhibitors or angiotensin receptor blockers, AGT TT genotype remained independently associated with greater LVMi (coefficient = 28.73; 95% CI, 5.72 to 51.75; P = 0.015) and relative wall thickness (coefficient = 0.072; 95% CI, 0.022 to 0.122; P = 0.005) than MT/MM genotypes. LVMi and relative wall thickness did not differ significantly among patients with DD, DI, and II genotypes. No statistical significant interaction was noted between ACE and AGT gene polymorphism in relation to LVMi and relative wall thickness. Conclusion. Polymorphism of the AGT 34235T gene but not ACE I/D gene is associated with greater LVMi and relative wall thickness, indicating more concentric LVH, in Chinese peritoneal dialysis patients. Possible synergistic effects between AGT and ACE gene polymorphism require further evaluation in a larger population. | en_US |
dc.language | eng | en_US |
dc.publisher | Nature Publishing Group. The Journal's web site is located at http://www.nature.com/ki/index.html | en_US |
dc.relation.ispartof | Kidney International | en_US |
dc.subject | Angiotensinogen | - |
dc.subject | Cardiac | - |
dc.subject | Dialysis | - |
dc.subject.mesh | Adult | en_US |
dc.subject.mesh | Angiotensinogen - Genetics | en_US |
dc.subject.mesh | Asian Continental Ancestry Group - Genetics | en_US |
dc.subject.mesh | Echocardiography | en_US |
dc.subject.mesh | Female | en_US |
dc.subject.mesh | Genotype | en_US |
dc.subject.mesh | Heart Ventricles - Pathology | en_US |
dc.subject.mesh | Humans | en_US |
dc.subject.mesh | Hypertrophy, Left Ventricular - Ethnology - Genetics - Ultrasonography | en_US |
dc.subject.mesh | Kidney Failure, Chronic - Ethnology - Genetics - Therapy | en_US |
dc.subject.mesh | Male | en_US |
dc.subject.mesh | Middle Aged | en_US |
dc.subject.mesh | Myocardium - Pathology | en_US |
dc.subject.mesh | Peptidyl-Dipeptidase A - Genetics | en_US |
dc.subject.mesh | Peritoneal Dialysis | en_US |
dc.subject.mesh | Polymorphism, Genetic | en_US |
dc.subject.mesh | Prevalence | en_US |
dc.subject.mesh | Ventricular Remodeling - Genetics | en_US |
dc.title | Cardiac hypertrophy and remodeling in relation to ACE and angiotensinogen genes genotypes in Chinese dialysis patients | en_US |
dc.type | Article | en_US |
dc.identifier.email | Wang, M:meiwang@hkucc.hku.hk | en_US |
dc.identifier.authority | Wang, M=rp00281 | en_US |
dc.description.nature | link_to_OA_fulltext | en_US |
dc.identifier.doi | 10.1046/j.1523-1755.2003.00933.x | en_US |
dc.identifier.pmid | 12675870 | - |
dc.identifier.scopus | eid_2-s2.0-0037407289 | en_US |
dc.relation.references | http://www.scopus.com/mlt/select.url?eid=2-s2.0-0037407289&selection=ref&src=s&origin=recordpage | en_US |
dc.identifier.volume | 63 | en_US |
dc.identifier.issue | 5 | en_US |
dc.identifier.spage | 1899 | en_US |
dc.identifier.epage | 1907 | en_US |
dc.identifier.isi | WOS:000182041400035 | - |
dc.publisher.place | United Kingdom | en_US |
dc.identifier.scopusauthorid | Wang, AYM=13606226000 | en_US |
dc.identifier.scopusauthorid | ChungNgor Chan, J=6504370559 | en_US |
dc.identifier.scopusauthorid | Wang, M=7406690398 | en_US |
dc.identifier.scopusauthorid | Poon, E=7003615943 | en_US |
dc.identifier.scopusauthorid | Lui, SF=7102379144 | en_US |
dc.identifier.scopusauthorid | KamTao Li, P=6507664013 | en_US |
dc.identifier.scopusauthorid | Sanderson, J=7202371250 | en_US |
dc.identifier.issnl | 0085-2538 | - |