APOA1/C3/A5 haplotype and risk of hypertriglyceridemia in Taiwanese

被引:32
作者
Chien, Kuo-Liong [2 ]
Fang, Woei-Horng [1 ]
Wen, Hui-Chin [1 ]
Lin, Hsing-Pei [1 ]
Lin, Yen-Lin [1 ]
Lin, Shu-Wha [1 ]
Wu, June-Hsieh
Kao, Jau-Tsuen [1 ,3 ]
机构
[1] Natl Taiwan Univ, Coll Med, Dept Clin Lab Sci & Med Biotechnol, Taipei, Taiwan
[2] Natl Taiwan Univ, Coll Publ Sch, Inst Prevent Med, Taipei, Taiwan
[3] Natl Taiwan Univ Hosp, Dept Lab Med, Taipei 100, Taiwan
关键词
apolipoprotein A1/C3/A5; triglyceride; HDL cholesterol; haplotype;
D O I
10.1016/j.cca.2007.12.014
中图分类号
R446 [实验室诊断]; R-33 [实验医学、医学实验];
学科分类号
1001 ;
摘要
Background: Apolipoprotein A5 gene (APOA5) has been shown to modulate plasma triglyceride concentrations. We investigated 2 distinct APOA1/C3/A5 haplotypes roles for hypertriglyceridemia. Methods: We recruited 308 cases of hypertriglyceridemia and 281 normal controls from a hospital. Twelve single nucleotide polymorphisms (SNPs) across the APOA1/C3/A5 gene region were genotyped. Results: One haplotype containing the minor alleles of the APOA5 (-1131T>C, c.553G>T) and APOA1 (-3013C>T,-75G>A) was more prevalent in cases than in controls (11.3% vs. 1.1%, respectively) and was statistically significantly associated with high triglycerides (adjusted odds ratio: 12.83, 95% confidence interval [CI]: 5.1-32.4, P<0.001). Another haplotype that was associated with hypertriglyceridemia (adjusted odds ratio 2.13, 95% CI, 1.37-3.29, P=0.001). Participants carrying both minor alleles of APOA5-1131CC and c.553TT had a 116% higher triglyceride concentration compared with those carrying common allele. Conclusions: The APOA1/C3/A5 haplotype represents an important locus for predicting risk of hypertriglyceridemia among Taiwanese. (C) 2007 Elsevier B.V. All rights reserved.
引用
收藏
页码:56 / 62
页数:7
相关论文
共 31 条
[1]   HYPERTRIGLYCERIDEMIA ASSOCIATED WITH DEFICIENCY OF APOLIPOPROTEIN-C-II [J].
BRECKENRIDGE, WC ;
LITTLE, JA ;
STEINER, G ;
CHOW, A ;
POAPST, M .
NEW ENGLAND JOURNAL OF MEDICINE, 1978, 298 (23) :1265-1273
[2]  
CARLSON LA, 1986, ACTA MED SCAND, V219, P435
[3]   Standardizing mutation nomenclature: Why bother.? [J].
den Dunnen, JT ;
Paalman, MH .
HUMAN MUTATION, 2003, 22 (03) :181-182
[4]   Mechanism of triglyceride lowering in mice expressing human apolipoprotein A5 [J].
Fruchart-Najib, J ;
Baugé, E ;
Niculescu, LS ;
Pham, T ;
Thomas, B ;
Rommens, C ;
Majd, Z ;
Brewer, B ;
Pennacchio, LA ;
Fruchart, JC .
BIOCHEMICAL AND BIOPHYSICAL RESEARCH COMMUNICATIONS, 2004, 319 (02) :397-404
[5]  
HARTL D, 1989, DARWINIAN EVOLUTION, P1
[6]  
HAYDEN MR, 1987, AM J HUM GENET, V40, P421
[7]  
Hokanson J E, 1996, J Cardiovasc Risk, V3, P213, DOI 10.1097/00043798-199604000-00014
[8]   A novel genetic variant in the apolipoprotein A5 gene is associated with hypertriglyceridemia [J].
Kao, JT ;
Wen, HC ;
Chien, KL ;
Hsu, HC ;
Lin, SW .
HUMAN MOLECULAR GENETICS, 2003, 12 (19) :2533-2539
[9]   Accounting for haplotype uncertainty in matched association studies: A comparison of simple and flexible techniques [J].
Kraft, P ;
Cox, DG ;
Paynter, RA ;
Hunter, D ;
De Vivo, I .
GENETIC EPIDEMIOLOGY, 2005, 28 (03) :261-272
[10]  
MCCONATHY WJ, 1992, J LIPID RES, V33, P995