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
[1]   Cytokines and bone loss in a 5-year longitudinal study - Hormone replacement therapy suppresses serum soluble interleukin-6 receptor and increases interleukin-1-receptor antagonist: The Danish Osteoporosis Prevention Study [J].
Abrahamsen, B ;
Bonnevie-Nielsen, V ;
Ebbesen, EN ;
Gram, J ;
Beck-Nielsen, H .
JOURNAL OF BONE AND MINERAL RESEARCH, 2000, 15 (08) :1545-1554
[2]   INTERLEUKIN-6 IN BIOLOGY AND MEDICINE [J].
AKIRA, S ;
TAGA, T ;
KISHIMOTO, T .
ADVANCES IN IMMUNOLOGY, VOL 54, 1993, 54 :1-78
[3]  
ALHUMIDAN A, 1991, J BONE MINER RES, V6, P3
[4]   Evolving methods in genetic epidemiology .1. Analysis of genetic and environmental factors in family studies [J].
Beaty, TH .
EPIDEMIOLOGIC REVIEWS, 1997, 19 (01) :14-23
[5]   PARTITIONING THE VARIABILITY OF FASTING PLASMA-GLUCOSE LEVELS IN PEDIGREES - GENETIC AND ENVIRONMENTAL-FACTORS [J].
BOEHNKE, M ;
MOLL, PP ;
KOTTKE, BA ;
WEIDMAN, WH .
AMERICAN JOURNAL OF EPIDEMIOLOGY, 1987, 125 (04) :679-689
[6]   Secretion of tumour necrosis factor alpha and lymphotoxin alpha in relation to polymorphisms in the TNF genes and HLA-DR alleles. Relevance for inflammatory bowel disease [J].
Bouma, G ;
Crusius, JBA ;
Pool, MO ;
Kolkman, JJ ;
VonBlomberg, BME ;
Kostense, PJ ;
Giphart, MJ ;
Schreuder, GMT ;
Meuwissen, SGM ;
Pena, AS .
SCANDINAVIAN JOURNAL OF IMMUNOLOGY, 1996, 43 (04) :456-463
[7]   Aging and proinflammatory cytokines [J].
Bruunsgaard, H ;
Pedersen, M ;
Pedersen, BK .
CURRENT OPINION IN HEMATOLOGY, 2001, 8 (03) :131-136
[8]   RADIOGRAPHIC ABSORPTIOMETRY - A SIMPLE METHOD FOR DETERMINATION OF BONE MASS [J].
COSMAN, F ;
HERRINGTON, B ;
HIMMELSTEIN, S ;
LINDSAY, R .
OSTEOPOROSIS INTERNATIONAL, 1991, 2 (01) :34-38
[9]   Cytokine polymorphic analyses indicate ethnic differences in the allelic distribution of interleukin-2 and interleukin-6 [J].
Cox, ED ;
Hoffmann, SC ;
DiMercurio, BS ;
Wesley, RA ;
Harlan, DM ;
Kirk, AD ;
Blair, PJ .
TRANSPLANTATION, 2001, 72 (04) :720-726
[10]   GENERAL MODEL FOR GENETIC ANALYSIS OF PEDIGREE DATA [J].
ELSTON, RC ;
STEWART, J .
HUMAN HEREDITY, 1971, 21 (06) :523-&