The association of interleukin-16 gene polymorphisms with susceptibility of coronary artery disease

Clinical Biochemistry

Volumn 46, Issue 3, 2013, Pages 241-244

  Huang, Hao ^a,c   Zeng, Zhi ^a   Zhang, Li ^a   Liu, Rui ^b   Li, Xian ^b   Qiang, Ou ^b   Zhang, Qing ^a   Chen, Yucheng ^a  

^a SICHUAN UNIVERSITY   (China)

^b SICHUAN UNIVERSITY   (China)

^c SICHUAN PROVINCIAL PEOPLE'S HOSPITAL   (China)

Author keywords

Coronary artery disease; Haplotype; IL 16; Polymorphism

Indexed keywords

INTERLEUKIN 16;

ADULT; ARTICLE; CHINESE; COHORT ANALYSIS; CONTROLLED STUDY; CORONARY ARTERY DISEASE; ENZYME LINKED IMMUNOSORBENT ASSAY; FEMALE; GENE FREQUENCY; GENETIC ASSOCIATION; GENETIC SUSCEPTIBILITY; GENETIC VARIABILITY; HAPLOTYPE; HUMAN; MAJOR CLINICAL STUDY; MALE; POLYMERASE CHAIN REACTION; POPULATION BASED CASE CONTROL STUDY; PRIORITY JOURNAL; PROTEIN BLOOD LEVEL; RESTRICTION FRAGMENT LENGTH POLYMORPHISM; SINGLE NUCLEOTIDE POLYMORPHISM;

AGED; ALLELES; ASIAN CONTINENTAL ANCESTRY GROUP; CASE-CONTROL STUDIES; CORONARY ANGIOGRAPHY; CORONARY ARTERY DISEASE; ENZYME-LINKED IMMUNOSORBENT ASSAY; FEMALE; GENE FREQUENCY; GENETIC ASSOCIATION STUDIES; GENETIC MARKERS; GENETIC PREDISPOSITION TO DISEASE; HAPLOTYPES; HUMANS; INTERLEUKIN-16; LOGISTIC MODELS; MALE; MIDDLE AGED; ODDS RATIO; POLYMERASE CHAIN REACTION; POLYMORPHISM, RESTRICTION FRAGMENT LENGTH; POLYMORPHISM, SINGLE NUCLEOTIDE; RISK FACTORS;

EID: 84871961472     PISSN: 00099120     EISSN: 18732933     Source Type: Journal    
DOI: 10.1016/j.clinbiochem.2012.11.009     Document Type: Article

References (28)

1. Lopez A.D., Murray C.C. The global burden of disease, 1990-2020. Nat Med 1998, 4:1241-1243.
2. Castelli W.P. The epidemiology of coronary heart disease: the Framingham study. Am J Med 1984, 76:4-12.
3. Brenn T. Genetic and environmental effects on coronary heart disease risk factors in Northern Norway: the cardiovascular disease study in Finnmark. Ann Hum Genet 1994, 58:369-379.
4. Assmann G., Cullen P., Schulte H. Simple scoring calculating the risk of acute coronary events based on 10year follow-up of the Prospective Cardiovascular Munster (PROCAM) study. Circulation 2002, 105:310-315.
5. Ross R. Atherosclerosis-an inflammatory disease. N Engl J Med 1999, 340:115-126.
6. Kardys I., Klaver C.C., Despriet D.D., et al. A common polymorphism in the complement factor H gene is associated with increased risk of myocardial infarction: the Rotterdam Study. J Am Coll Cardiol 2006, 47(8):1568-1575.
7. Alanne M., Kristiansson K., Auro K., et al. Variation in the selenoprotein S gene locus is associated with coronary heart disease and ischemic stroke in two independent Finnish cohorts. Hum Genet 2007, 122(3-4):355-365.
8. Huang H., Zeng Z., Li J., Zhang L., Chen Y. Variants of arachidonate 5-lipoxygenase-activating protein (ALOX5AP) gene and risk of coronary heart disease: a meta-analysis. Arch Med Res 2010, 41(8):634-641.
9. Hartiala J., Li D., Conti D.V., et al. Genetic contribution of the leukotriene pathway to coronary artery disease. Hum Genet 2011, 129(6):617-627.
10. Cruikshank W., Center D.M. Modulation of lymphocyte migration by human lymphokines. II. Purification of a lymphotactic factor (LCF). J Immunol 1982, 128(6):2569-2574.
11. Kim H.S. Assignment of human interleukin 16 (IL16) to chromosome 15q26.3 by radiation hybrid mapping. Cytogenet Cell Genet 1999, 84(1-2):93.
12. Laberge S., Cruikshank W.W., Kornfeld H., Center D.M. Histamine-induced secretion of lymphocyte chemoattractant factor from CD8+ T cells is independent of transcription and translation. Evidence for constitutive protein synthesis and storage. J Immunol 1995, 155:2902-2910.
13. Rumsaeng V., Cruikshank W.W., Foster B., et al. Human mast cells produce the CD4+ T lymphocyte chemoattractant factor, IL-16. J Immunol 1997, 159(6):2904-2910.
14. Sharma V., Sparks J.L., Vail J.D. Human B-cell lines constitutively express and secrete interleukin-16. Immunology 2000, 99:266-271.
15. Center D.M., Kornfeld H., Cruikshank W.W. Interleukin 16 and its function as a CD4 ligand. Immunol Today 1996, 17:476-481.
16. Mathy N.L., Scheuer W., Lanzendorfer M., et al. Interleukin-16 stimulates the expression and production of pro-inflammatory cytokines by human monocytes. Immunology 2000, 100:63-69.
17. Thomas G., Jacobs K.B., Yeager M., et al. Multiple loci identified in a genome-wide association study of prostate cancer. Nat Genet 2008, 40(3):310-315.
18. Gu X.J., Cui B., Zhao Z.F., et al. Association of the interleukin (IL)-16 gene polymorphisms with Graves' disease. Clin Immunol 2008, 127(3):298-302.
19. Gao L.B., Rao L., Wang Y.Y., et al. The association of interleukin-16 polymorphisms with IL-16 serum levels and risk of colorectal and gastric cancer. Carcinogenesis 2009, 30(2):295-299.
20. Xue H., Gao L., Wu Y., et al. The IL-16 gene polymorphisms and the risk of the systemic lupus erythematosus. Clin Chim Acta 2009, 403(1-2):223-225.
21. Gao L.B., Liang W.B., Xue H., et al. Genetic polymorphism of interleukin-16 and risk of nasopharyngeal carcinoma. Clin Chim Acta 2009, 409(1-2):132-135.
22. Chen Y., Huang H., Liu S., et al. IL-16 rs11556218 gene polymorphism is associated with coronary artery disease in the Chinese Han population. Clin Biochem 2011, 44(13):1041-1044.
23. Huang H., Zeng Z., Zhang L., et al. Implication of genetic variants near TMEM18, BCDIN3D/FAIM2, and MC4R with coronary artery disease and obesity in Chinese: a angiography-based study. Mol Biol Rep 2012, 39(2):1739-1744.
24. Erlich H.A. PCR technology in principles and applications for DNA amplification 1989, Stockton Press, New York. 1st ed.
25. Bannert N., Kurth R., Baier M. The gene encoding mouse interleukin-16 consists of seven exons and maps to chromosome 7 D2-D3. Immunogenetics 1999, 49(7-8):704-706.
26. Reich K., Westphal G., König I.R., et al. Association of allergic contact dermatitis with a promoter polymorphism in the IL16 gene. J Allergy Clin Immunol 2003, 112(6):1191-1194.
27. Zhu J., Qin C., Yan F., et al. IL-16 polymorphism and risk of renal cell carcinoma: association in a Chinese population. Int J Urol 2010, 17(8):700-707.
28. Ying S.Y., Lin S.L. Intron-derived microRNAs-fine tuning of gene functions. Gene 2004, 342(1):25-28.