| Literature DB >> 23105390 |
S Chhabra1, D P Agarwal, S Vasisht, K Luthra, R Narang, S C Manchanda, L M Srivastava, N Das.
Abstract
Several studies including a small case-control (hypertriglyceridemic/normotriglyceridemic individuals) study by us revealed close association between rare S2 allele ofAPOC3 Sstl polymorphism and hypertriglyceridemia. With the understanding that Asian Indians are highly vulnerable to the adverse effects of hypertriglyceridemia, we extended the investigation and studied the frequency distribution of this polymorphism in 216 healthy volunteers from Northern plains of India. We found that more than 50% of the study population had one or two S2 allele. This may suggest that a larger fraction of this population is genetically predisposed to hypertriglyceridemia.Entities:
Keywords: APOC3; CAD; Hypertriglyceridemia; India; Sstl polymorphism
Year: 2003 PMID: 23105390 PMCID: PMC3453890 DOI: 10.1007/BF02867365
Source DB: PubMed Journal: Indian J Clin Biochem ISSN: 0970-1915