Genetic and environmental influences on IL-6 and TNF-α plasma levels in apparently healthy general population

被引:54
作者
Pantsulaia, I [1 ]
Trofimov, S [1 ]
Kobyliansky, E [1 ]
Livshits, G [1 ]
机构
[1] Tel Aviv Univ, Sackler Fac Med, Dept Anat & Anthropol, IL-69978 Tel Aviv, Israel
基金
美国国家科学基金会;
关键词
heritability; interleukin-6; model-fitting analysis; pedigrees; tumour necrosis factor-alpha;
D O I
10.1006/cyto.2002.1959
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Dysregulation of cytokines; synthesis is thought to play a role in the development of a number of age-related conditions, such as rheumatoid arthritis, osteoporosis, atherosclerosis, and others, but observational studies have led to contradictory results. We investigated potential familial influences on the plasma levels of IL-6 and TNF-alpha in 91 nuclear and more complex pedigrees of Caucasian ethnic origin (N=401 individuals). The maximum likelihood based variance decomposition analysis showed significant positive correlation between circulating IL-6 and age in both genders. The magnitude of these correlations in our sample ranged from 0.22 in females to 0.28 in males (P<0.001). Significant association between TNF-alpha and IL-6 (r=0.28, r=0.43; P<0.001; respectively for men and women) was also observed. Likelihood ratio test clearly revealed that additive genetic effect for TNF-alpha was highly significant (P<0.001), and accounted over 80% of its variation, adjusted for IL-6 levels and age. In contrast, heritability estimate for IL-6 adjusted for age and TNF-alpha, revealed small contribution of genetic factors (24.1 +/- 10.2%). The bivariate variance component analysis demonstrated that significant relationship between IL-6 and TNF-alpha was due to shared environment only (r(E)=0.760 +/- 0.140). As evinced from our complex segregation analysis the nature of the genetic determinant of each of these two cytokines is quite complex and it is probably oligogenic. (C) 2002 Elsevier Science B.V. All rights reserved.
引用
收藏
页码:138 / 146
页数:9
相关论文
共 65 条
[11]  
Falconer DS, 1996, INTRO QUANTITATIVE G, P122
[12]  
Ferrari SL, 2001, ARTHRITIS RHEUM-US, V44, P196, DOI 10.1002/1529-0131(200101)44:1<196::AID-ANR26>3.0.CO
[13]  
2-5
[14]   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
[15]   Inflammatory cytokines regulate proliferation of cultured human osteoblasts [J].
Frost, A ;
Jonsson, KB ;
Nilsson, O ;
Ljunggren, O .
ACTA ORTHOPAEDICA SCANDINAVICA, 1997, 68 (02) :91-96
[16]   Segregation analysis of quantitative traits [J].
Ginsburg, E ;
Livshits, G .
ANNALS OF HUMAN BIOLOGY, 1999, 26 (02) :103-129
[17]  
GINSBURG E, 1997, PROGRAM PACKAGE MEND
[18]   Genetic and environmental correlations between bone formation and bone mineral density: A twin study [J].
Harris, M ;
Nguyen, TV ;
Howard, GM ;
Kelly, PJ ;
Eisman, JA .
BONE, 1998, 22 (02) :141-145
[19]   Quantitative genetic analyses of insulin-like growth factor I (IGF-I), IGF-Binding protein-1 and insulin levels in middle-aged and elderly twins [J].
Hong, YL ;
Pedersen, NL ;
Brismar, K ;
Hall, K ;
deFaire, U .
JOURNAL OF CLINICAL ENDOCRINOLOGY & METABOLISM, 1996, 81 (05) :1791-1797
[20]  
Horowitz Mark C., 1996, P687