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| Content Provider | World Health Organization (WHO)-Global Index Medicus |
|---|---|
| Author | Shanmuganathan, R. Kumaresan, R. Giri, P. |
| Description | Author Affiliation: Kumaresan R ( Department of Biotechnology, Periyar Maniammai University, Thanjavur, Tamil Nadu, India.) |
| Abstract | CONTEXT: Chronic Kidney Disease (CKD) is associated with a high risk of developing further severe complications such as, cardiovascular disease and eventually End Stage Renal Disease (ESRD) leading to death. Hypertension plays a key role in the progression of renal failure and is also a chief risk factor for the occurrence of End Stage Renal Disease (ESRD). AIM: This study investigates the possible association of insertion (I) and deletion (D) polymorphism of ACE gene in patients of Chronic Kidney Disease (CKD) with and without hypertension (HT). SETTINGS AND DESIGN: Total 120 participants with 30 members in each group (Control, HT, CKD and CKD-HT) were chosen followed by informed consent. MATERIALS AND METHODS: Blood samples were collected and subjected to biochemical analyses and nested PCR amplification was performed to genotype the DNA, for ACE I/D using specific primers. STATISTICAL ANALYSIS: Statistical analyses were performed using SPSS version 13. Allele and genotypic frequency was calculated by direct gene counting method. Comparison of the different genotypes was done by using Chi square test. Odd's ratios were calculated with a 95% confidence interval limit. RESULTS: The ACE genotype were distributed as II, 27 (90%); DD, 2 (6.67%) and ID, 1 (3.33%) in control, II, 1 (3.33%); DD, 5 (16.67%) and ID, 24 (80%) in HT, II, 4 (13.33%); DD, 24 (80%) and ID, 2 (6.67%) in CKD and II, 0 (0%); DD, 2 (6.67%) and ID, 28 (93.33%) in CKD-HT group. CONCLUSIONS: D allele of ACE gene confers a greater role in genetic variations underlying CKD and hypertension. This result suggest that CKD patients should be offered analysis for defects in ACE I/D polymorphisms, especially if they are hypertensive. |
| File Format | HTM / HTML |
| ISSN | 00223859 |
| e-ISSN | 09722823 |
| DOI | 10.4103/0022-3859.166510 |
| Journal | Journal of Postgraduate Medicine |
| Issue Number | 4 |
| Volume Number | 61 |
| Language | English |
| Publisher | MedKnow Publication |
| Publisher Date | 2015-10-01 |
| Publisher Place | India |
| Access Restriction | Open |
| Subject Keyword | Discipline Medicine Asian Continental Ancestry Group Genetics Hypertension Indel Mutation Peptidyl-dipeptidase A Renal Insufficiency, Chronic Antihypertensive Agents Therapeutic Use Creatinine Blood Disease Progression Genetic Predisposition To Disease Genotype Drug Therapy Ethnology Polymerase Chain Reaction Polymorphism, Genetic Renin-angiotensin System Physiology |
| Content Type | Text |
| Resource Type | Article |
| Subject | Medicine |
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