Cargando…
High prevalence of ACE DD genotype among north Indian end stage renal disease patients
BACKGROUND: The Renin-Angiotensin system (RAS) is a key regulator of both blood pressure and kidney functions and their interaction. In such a situation, genetic variability in the genes of different components of RAS is likely to contribute for its heterogeneous association in the renal disease pat...
Autores principales: | , , , , , |
---|---|
Formato: | Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2006
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC1626448/ https://www.ncbi.nlm.nih.gov/pubmed/17042963 http://dx.doi.org/10.1186/1471-2369-7-15 |
_version_ | 1782130599910178816 |
---|---|
author | Tripathi, Gaurav Dharmani, Poonam Khan, Faisal Sharma, RK Pandirikkal Baburajan, Vinod Agrawal, Suraksha |
author_facet | Tripathi, Gaurav Dharmani, Poonam Khan, Faisal Sharma, RK Pandirikkal Baburajan, Vinod Agrawal, Suraksha |
author_sort | Tripathi, Gaurav |
collection | PubMed |
description | BACKGROUND: The Renin-Angiotensin system (RAS) is a key regulator of both blood pressure and kidney functions and their interaction. In such a situation, genetic variability in the genes of different components of RAS is likely to contribute for its heterogeneous association in the renal disease patients. Angiotensin converting enzyme-1 (ACE-1) is an important component of RAS which determines the vasoactive peptide Angiotensin-II. METHODS: In the present study, we have investigated 127 ESRD patients and 150 normal healthy controls from north India to deduce the association between ACE gene polymorphism and ESRD. The inclusion criteria for patients included a constantly elevated serum creatinine level above normal range (ranging from 3.4 to 15.8) and further the patients were recommended for renal transplantation. A total of 150 normal healthy controls were also genotyped for ACE I/D polymorphism. The criterion of defining control sample as normal was totally based on the absence of any kidney disease determined from the serum creatinin level. Genotyping of ACE I/D were assayed by polymerase chain reaction (PCR) based DNA amplification using specific flanking primers Based on the method described elsewhere. RESULTS: The difference of DD and II genotypes was found highly significant among the two groups (p = 0.025; OR = 3.524; 95%CI = 1.54-8.07). The combined genotype DD v/s ID+II comparison validated that DD genotype is a high risk genotype for ESRD (p = 0.001; OR = 5.74; 95%CI limit = 3.4-8.5). However, no correlation was obtained for different biochemical parameters of lipid profile and renal function among DD and non DD genotype. Interestingly, ~87% of the DD ESRD patients were found hypertensive in comparison to the 65% patients of non DD genotype CONCLUSION: Based on these observations we conclude that ACE DD genotype implicate a strong possible role in the hypertensive state and in renal damage among north Indians. The study will help in predetermining the timing, type and doses of anti-hypertensive therapy for ESRD patients. |
format | Text |
id | pubmed-1626448 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2006 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-16264482006-10-28 High prevalence of ACE DD genotype among north Indian end stage renal disease patients Tripathi, Gaurav Dharmani, Poonam Khan, Faisal Sharma, RK Pandirikkal Baburajan, Vinod Agrawal, Suraksha BMC Nephrol Research Article BACKGROUND: The Renin-Angiotensin system (RAS) is a key regulator of both blood pressure and kidney functions and their interaction. In such a situation, genetic variability in the genes of different components of RAS is likely to contribute for its heterogeneous association in the renal disease patients. Angiotensin converting enzyme-1 (ACE-1) is an important component of RAS which determines the vasoactive peptide Angiotensin-II. METHODS: In the present study, we have investigated 127 ESRD patients and 150 normal healthy controls from north India to deduce the association between ACE gene polymorphism and ESRD. The inclusion criteria for patients included a constantly elevated serum creatinine level above normal range (ranging from 3.4 to 15.8) and further the patients were recommended for renal transplantation. A total of 150 normal healthy controls were also genotyped for ACE I/D polymorphism. The criterion of defining control sample as normal was totally based on the absence of any kidney disease determined from the serum creatinin level. Genotyping of ACE I/D were assayed by polymerase chain reaction (PCR) based DNA amplification using specific flanking primers Based on the method described elsewhere. RESULTS: The difference of DD and II genotypes was found highly significant among the two groups (p = 0.025; OR = 3.524; 95%CI = 1.54-8.07). The combined genotype DD v/s ID+II comparison validated that DD genotype is a high risk genotype for ESRD (p = 0.001; OR = 5.74; 95%CI limit = 3.4-8.5). However, no correlation was obtained for different biochemical parameters of lipid profile and renal function among DD and non DD genotype. Interestingly, ~87% of the DD ESRD patients were found hypertensive in comparison to the 65% patients of non DD genotype CONCLUSION: Based on these observations we conclude that ACE DD genotype implicate a strong possible role in the hypertensive state and in renal damage among north Indians. The study will help in predetermining the timing, type and doses of anti-hypertensive therapy for ESRD patients. BioMed Central 2006-10-17 /pmc/articles/PMC1626448/ /pubmed/17042963 http://dx.doi.org/10.1186/1471-2369-7-15 Text en Copyright © 2006 Tripathi et al; licensee BioMed Central Ltd. http://creativecommons.org/licenses/by/2.0 This is an Open Access article distributed under the terms of the Creative Commons Attribution License ( (http://creativecommons.org/licenses/by/2.0) ), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Research Article Tripathi, Gaurav Dharmani, Poonam Khan, Faisal Sharma, RK Pandirikkal Baburajan, Vinod Agrawal, Suraksha High prevalence of ACE DD genotype among north Indian end stage renal disease patients |
title | High prevalence of ACE DD genotype among north Indian end stage renal disease patients |
title_full | High prevalence of ACE DD genotype among north Indian end stage renal disease patients |
title_fullStr | High prevalence of ACE DD genotype among north Indian end stage renal disease patients |
title_full_unstemmed | High prevalence of ACE DD genotype among north Indian end stage renal disease patients |
title_short | High prevalence of ACE DD genotype among north Indian end stage renal disease patients |
title_sort | high prevalence of ace dd genotype among north indian end stage renal disease patients |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC1626448/ https://www.ncbi.nlm.nih.gov/pubmed/17042963 http://dx.doi.org/10.1186/1471-2369-7-15 |
work_keys_str_mv | AT tripathigaurav highprevalenceofaceddgenotypeamongnorthindianendstagerenaldiseasepatients AT dharmanipoonam highprevalenceofaceddgenotypeamongnorthindianendstagerenaldiseasepatients AT khanfaisal highprevalenceofaceddgenotypeamongnorthindianendstagerenaldiseasepatients AT sharmark highprevalenceofaceddgenotypeamongnorthindianendstagerenaldiseasepatients AT pandirikkalbaburajanvinod highprevalenceofaceddgenotypeamongnorthindianendstagerenaldiseasepatients AT agrawalsuraksha highprevalenceofaceddgenotypeamongnorthindianendstagerenaldiseasepatients |