共 1 条
Apolipoprotein(a) gene polymorphisms (TTTTA)n and G/A-914 affect Lp(a) levels in ischemic heart disease patients from SerbiaApolipoprotein(a)-Gen-Polymorphismen (TTTTA)n and G/A-914 beeinflussen Lp(a) Konzentrationen in serbischen Patienten mit ischämischer Herzerkrankung
被引:0
|作者:
Dragan Dinčić
Maja Živković
Aleksandra Stanković
Tamara Djurić
Svetlana Vujanić
Branko Gligić
Dragan Alavantić
机构:
[1] Military Medical Academy,Clinic for Urgent Internal Medicine
[2] Laboratory for Radiobiology and Molecular Genetics,VINČA Institute of Nuclear Sciences
[3] Military Medical Academy,Institute for Medical Biochemistry
来源:
关键词:
Apolipoprotein(a);
G/A-914;
Gene polymorphism;
Ischemic heart disease;
Lipoprotein(a);
(TTTTA);
D O I:
暂无
中图分类号:
学科分类号:
摘要:
OBJECTIVES: Lipoprotein(a) (Lp(a)) concentration is determined primarily by the apolipoprotein(a) (apo(a)) gene. The pentanucleotide (TTTTA)n repeat and G/A-914 polymorphisms are in the 5′ promoter region of the apo(a) gene. To elucidate whether these polymorphisms affect Lp(a) levels, a total of 211 Serbian adults were investigated. DESIGN: One hundred and eleven patients with ischemic heart disease and 100 healthy controls were genotyped and Lp(a) levels determined. RESULTS: Lp(a) concentrations differed according to the (TTTTA)n genotypes: among those having at least one allele 8, patients had significantly higher Lp(a) values than controls. A decreasing trend of Lp(a) values was associated with the –914A allele in controls but the opposite was true in patients. Patients with genotype TTTTA allele 8/AA-914 had significantly higher Lp(a) values than those without allele 8/AA (p < 0.05). The >8>8/GG genotype was not detected. Significant linkage disequilibrium between (TTTTA)n and G/A-914 polymorphism (p < 0.001) was found. In multivariate regression analysis, the G/A-914 polymorphism significantly (p < 0.05) affected Lp(a) levels in patients, after taking into account the (TTTTA)n polymorphism. CONCLUSION: These results indicate that (TTTTA)n and G/A-914 polymorphisms affect Lp(a) levels in ischemic heart disease as a consequence of the linkage disequlibrium.
引用
收藏
页码:406 / 411
页数:5
相关论文