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Apolipoprotein E and Presenilin-1 Allelic Variation and Alzheimer's Disease in India

Bibliographic Data

ID7990410
AuthorsGiriraj R Chandak (0000-0002-3095-9453, Centre for Cellular and Molecular Biology), M Uma Sridevi, C J Vas, Dilip M Panikker, L Singh (0000-0001-7534-8528), Lalit P Singh (0000-0002-4600-9137)
Year2002
Volume74
Issue5
Pages683-693
Publication date2002-01-01
Open AccessNo
TypeARTICLE
VenueHuman Biology (JOURNAL)
Journal identifiersISSN: 0018-7143 • E-ISSN: 1534-6617
PublisherProject MUSE (PUBLISHER • US)
DOI10.1353/hub.2002.0051
PMID12495082
OpenAlexW2007309263
LanguageEN
References cited4

As part of a larger epidemiological survey to study the prevalence of dementia in a suburb of Mumbai, Western India, we identified 78 cases with a Clinical Dementia Rating (CDR) > or = 1.0. Of these, 49 Alzheimer's disease (AD) cases were analyzed for risk association with APOE E*4 allele at apolipoprotein E gene (APOE) and presenilin-1 (PS-1) intron-8 polymorphism and were compared with 100 age- and sex-matched nondemented controls. Genotype analysis confirmed the association of APOE E*4 allele with AD as has been reported by various studies. We report a low frequency of APOE E*4 allele, consistent with a low prevalence of AD in this study. Comparisons with other similar studies on APOE from India suggest common risk factors for AD in the Indian population, which is diverse in its ethnic and racial characteristics. The frequency for allele 1 at PS-1 intron-8 polymorphism is the highest among all studies reported. This first report of PS-1 intron-8 polymorphism and AD from India demonstrates no significant association

Allele · Allele frequency · Alzheimer's disease · Apolipoprotein E · Biology · Dementia · Disease · Gene · Genotype · Polymorphism (computer science · Presenilin · Alzheimer's disease research and treatments · Cholinesterase and Neurodegenerative Diseases · Epidemiology · Genetics · Internal Medicine · Medicine · Retinoids in leukemia and cellular processes

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    Open Access•Sarabjit Mastana, S S Mastana et al.•Annals of Human Biology•1998

Highly citedNo

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