Genotype at a promoter polymorphism of the interleukin-6 gene is associated with baseline levels of plasma C-reactive protein

被引:217
作者
Vickers, MA
Green, FR
Terry, C
Mayosi, BM
Julier, C
Lathrop, M
Ratcliffe, PJ
Watkins, HC
Keavney, B
机构
[1] Univ Newcastle Upon Tyne, Inst Human Genet, Newcastle Upon Tyne NE1 7RU, Tyne & Wear, England
[2] Univ Oxford, Nuffield Dept Med, Oxford, England
[3] Ctr Natl Genotypage, Evry, France
[4] Inst Pasteur, Paris, France
[5] Univ Oxford, Dept Cardiovasc Med, Oxford, England
[6] Univ Aberdeen, Dept Med & Therapeut, Aberdeen, Scotland
基金
英国惠康基金; 英国医学研究理事会;
关键词
atherosclerosis; cytokines; epidemiology; infection/inflammation; sequence (DNA/RNA/prot);
D O I
10.1016/S0008-6363(01)00534-X
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Objective: Baseline concentrations of plasma C-reactive protein (CRP) are associated with coronary heart disease. Interleukin-6 (IL-6) regulates CRP gene expression; a promoter polymorphism (-174G/C) of the JL-6 gene has been shown to influence IL-6 transcription but the relationship between genotype at this polymorphism and circulating levels of inflammatory markers remains unclear. We hypothesised that plasma CRP would be a heritable phenotype that would be influenced by genotype at this polymorphism. Methods: We measured baseline plasma CRP and determined genotypes at the -174G/C polymorphism of the IL-6 gene in 588 members of 98 nuclear families. The heritability of plasma CRP and the association of plasma CRP with genotype were determined using variance components methods. Results: Baseline CRP levels were highly heritable (h(2) =0.39, P<0.0000001). Presence of the -174C allele was associated with higher baseline CRP levels, both in the whole population (P=0.01), and in the founders only (n=128, P=0.001). Family-based analyses confirmed the association (P=0.02) suggesting that it arises from chromosomal proximity or identity of the typed polymorphism with a genetic variant influencing baseline CRP levels. Conclusions: Baseline plasma CRP is a significantly heritable cardiovascular risk factor. Levels are associated with genotype at the -174G/C polymorphism of the IL-6 gene. (C) 2002 Elsevier Science B.V. All rights reserved.
引用
收藏
页码:1029 / 1034
页数:6
相关论文
共 24 条
[1]   A general test of association for quantitative traits in nuclear families [J].
Abecasis, GR ;
Cardon, LR ;
Cookson, WOC .
AMERICAN JOURNAL OF HUMAN GENETICS, 2000, 66 (01) :279-292
[2]   Multipoint quantitative-trait linkage analysis in general pedigrees [J].
Almasy, L ;
Blangero, J .
AMERICAN JOURNAL OF HUMAN GENETICS, 1998, 62 (05) :1198-1211
[3]   Common methylenetetrahydrofolate reductase gene mutation leads to hyperhomocysteinemia but not to vascular disease -: The result of a meta-analysis [J].
Brattström, L ;
Wilcken, DEL ;
Öhrvik, J ;
Brudin, L .
CIRCULATION, 1998, 98 (23) :2520-2526
[4]   Interleukin-6 gene -174G &gt; C and -572G &gt; C promoter polymorphisms are strong predictors of plasma -: Interleukin-6 levels after coronary artery bypass surgery [J].
Brull, DJ ;
Montgomery, HE ;
Sanders, J ;
Dhamrait, S ;
Luong, L ;
Rumley, A ;
Lowe, GDO ;
Humphries, SE .
ARTERIOSCLEROSIS THROMBOSIS AND VASCULAR BIOLOGY, 2001, 21 (09) :1458-1463
[5]   Human C-reactive protein (CRP) 1059G/C polymorphism [J].
Cao, HN ;
Hegele, RA .
JOURNAL OF HUMAN GENETICS, 2000, 45 (02) :100-101
[6]   Low grade inflammation and coronary heart disease: prospective study and updated meta-analyses [J].
Danesh, J ;
Whincup, P ;
Walker, M ;
Lennon, L ;
Thomson, A ;
Appleby, P ;
Gallimore, JR ;
Pepys, MB .
BMJ-BRITISH MEDICAL JOURNAL, 2000, 321 (7255) :199-204
[7]   The effect of novel polymorphisms in the interleukin-6 (IL-6) gene on IL-6 transcription and plasma IL-6 levels, and an association with systemic-onset juvenile chronic arthritis [J].
Fishman, D ;
Faulds, G ;
Jeffery, R ;
Mohamed-Ali, V ;
Yudkin, JS ;
Humphries, S ;
Woo, P .
JOURNAL OF CLINICAL INVESTIGATION, 1998, 102 (07) :1369-1376
[8]  
Jones KG, 2001, CIRCULATION, V103, P2260
[9]   Circadian interrelationships among levels of plasma fibrinogen, blood platelets, and serum interleukin-6 [J].
Kanabrocki, EL ;
Sothern, RB ;
Messmore, HL ;
Roitman-Johnson, B ;
McCormick, JB ;
Dawson, S ;
Bremner, FW ;
Third, JLHC ;
Nemchausky, BA ;
Shirazi, P ;
Scheving, LE .
CLINICAL AND APPLIED THROMBOSIS-HEMOSTASIS, 1999, 5 (01) :37-42
[10]   Five-year intra-individual variability in C-reactive protein levels in a Japanese population-based study - The Jichi Medical School Cohort Study at Yamato, 1993-1998 [J].
Kayaba, K ;
Ishikawa, S ;
Gotoh, T ;
Nago, N ;
Kajii, E ;
Nakamura, Y ;
Kario, K .
JAPANESE CIRCULATION JOURNAL-ENGLISH EDITION, 2000, 64 (04) :303-308