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MTHFR and ACE gene polymorphisms and risk of vascular and degenerative dementias in the elderly
Institution:1. Pharmacology Division, Department of Pharmaceutical Sciences and Drug Research, Faculty of Medicine, Punjabi University, Patiala 147002, Punjab, India;2. Department of Pharmacology, School of Pharmacy, Bharat Institute of Technology, Bypass Road, Partapur, Meerut 250103, Uttar Pradesh, India;1. Department of Internal Medicine F-Recanati, Rabin Medical Center, Beilinson Hospital, Petah Tiqva, Israel;2. Sackler Faculty of Medicine, Tel Aviv University, Ramat Aviv, Tel Aviv, Israel;3. Statistical Consulting Unit, Beilinson Hospital, Rabin Medical Center, Petah Tikva, Israel;4. Institute of Hematology, Davidoff Cancer Center, Rabin Medical Center, Petah Tikva, Israel;1. Cardiovascular and Cell Sciences Research Centre, St Georges University of London, London SW17 0RE, UK;2. Sanders-Brown Center on Aging, University of Kentucky, Lexington KY 40536, USA
Abstract:Focal lacunar infarctions due to cerebral small vessel atherosclerosis or single/multiple large cortical infarcts lead to vascular dementia, and different genes and environmental factors have been implicated in causation or aggravation of the disease. Previous reports suggest that some of the risk factors may be common to both vascular as well as degenerative dementia. Among genetic factors, role of angiotensin converting enzyme (ACE) and methylene-tetrahydrofolate reductase (MTHFR) genes as putative risk factors has been examined but the outcome of these studies remain inconclusive. Present study attempted to see the importance of ACE alu insertion/deletion and MTHFR C677T polymorphisms as genetic predisposers to dementia. The study comprised of 80 vascular dementia patients, 90 degenerative dementia patients and 170 age matched controls. All were genotyped for ACE, MTHFR and APOE polymorphisms using PCR-RFLP method. Frequency of ACE D allele was seemingly high in dementia cases (26.7%) when compared to controls (11.2%). However, after adjusting for age and APOE E4*, none of the ACE alleles showed good correlation. MTHFR genotypes or alleles also did not show any correlation. Our study suggests no true correlation of ACE or MTHR genes with dementia in elderly.
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