کد مقاله کد نشریه سال انتشار مقاله انگلیسی نسخه تمام متن
1971595 1538910 2008 6 صفحه PDF دانلود رایگان
عنوان انگلیسی مقاله ISI
Association between lipoprotein(a) levels, apo(a) isoforms and family history of premature CAD in young Asian Indians
موضوعات مرتبط
علوم زیستی و بیوفناوری بیوشیمی، ژنتیک و زیست شناسی مولکولی زیست شیمی
پیش نمایش صفحه اول مقاله
Association between lipoprotein(a) levels, apo(a) isoforms and family history of premature CAD in young Asian Indians
چکیده انگلیسی

ObjectivesThe purpose of this study was to explore the association between lipoprotein (a) [Lp(a)] levels, apo(a) isoforms and family history of premature coronary artery disease (CAD) in young Asian Indians.Design and methods220 patients (age < 40 years) with angiographic evidence of CAD and 160 age matched healthy controls were enrolled for the study. Thirty one percent of the patients and 17% of the controls had positive family history (PFH) of premature CAD. Plasma Lp(a) levels were determined by ELISA and apo(a) isoform size was determined using high-resolution immunoblotting method.ResultsMedian plasma Lp(a) levels were 2.5 times higher in patients as compared to controls (30 mg/dL vs 12.7 mg/dL; p < 0.05). The patient group having a heterozygous apo(a) isoform pattern showed higher Lp(a) levels as compared to the homozygous group (44.0 ± 38.7 vs 28.0 ± 26.4 mg/dL; p < 0.001). Further low molecular weight apo(a) isoforms (LMW; < 22 KIV repeats) were prevalent among CAD patients with PFH as compared to negative family history (62% vs 14%, p < 0.05) and this group had the highest Lp(a) levels. Stepwise regression analysis showed that Lp(a) levels and not the apo(a) isoform size, entered the model as significant independent predictors of CAD in young Asian Indians.ConclusionsThis study suggests that elevated Lp(a) levels confer genetic predisposition to CAD in young Asian Indians. Thus determination of Lp(a) levels along with other risk factors should be used to assess overall risk for CAD in this ethnic group.

ناشر
Database: Elsevier - ScienceDirect (ساینس دایرکت)
Journal: Clinical Biochemistry - Volume 41, Issues 7–8, May 2008, Pages 453–458
نویسندگان
, , , , ,