Gene by smoking interaction: Evidence for effects on low-density lipoprotein size and plasma levels of triglyceride and high-density lipoprotein cholesterol

被引:11
作者
Czerwinski, SA
Mahaney, MC
Rainwater, DL
Vandeberg, JL
Maccluer, JW
Stern, MP
Blangero, J
机构
[1] Wright State Univ, Sch Med, Dept Community Hlth, Lifespan Hlth Res Ctr, Dayton, OH 45420 USA
[2] SW Fdn Biomed Res, Dept Genet, San Antonio, TX USA
[3] Univ Texas, Hlth Sci Ctr, Div Clin Epidemiol, San Antonio, TX USA
关键词
gene X environment interaction; atherosclerosis; gene expression; smoking; cholesterol levels; triglyceride levels; Mexican Americans;
D O I
10.1353/hub.2005.0014
中图分类号
Q98 [人类学];
学科分类号
030303 [人类学];
摘要
We seek to determine whether significant gene X smoking interaction effects exist on plasma triglyceride (TG) levels, HDL cholesterol (HDL-C) level, and median LDL particle diameter (LDL-MPD) in Mexican American families enrolled in the San Antonio Family Heart Study. The sample consisted of 1,392 individuals distributed in 42 extended pedigrees, ranging in age from 16 years to 92 years. Separate quantitative genetic analyses were carried out for TG and HDL-C level and LDL-MPD using a maximum-likelihood-based variance decomposition approach while simultaneously adjusting for age and sex. Initial heritability estimates demonstrated significant (p < 0.001) additive genetic contributions to all three traits (h(2) range 0.50-0.54). To test for a gene X smoking interaction, we included in the model additional smoking-status-specific variance terms and a genetic correlation term between smokers and nonsmokers. Comparisons of nested models revealed significant evidence (p < 0.01) for a gene X smoking interaction effect on TG level and LDL-MPD and possible evidence for an effect on HDL-C level. These results indicate that the gene or suite of genes regulating each of these phenotypes is likely the same in smokers and nonsmokers but that smoking may alter the expression of genes, particularly those influencing TG level and LDL-MPD.
引用
收藏
页码:863 / 876
页数:14
相关论文
共 56 条
[1]
Multipoint quantitative-trait linkage analysis in general pedigrees [J].
Almasy, L ;
Blangero, J .
AMERICAN JOURNAL OF HUMAN GENETICS, 1998, 62 (05) :1198-1211
[2]
[Anonymous], 1993, JAMA, V269, P505
[3]
[Anonymous], 1992, LIKELIHOOD, DOI DOI 10.56021/9780801844454
[4]
PROSPECTIVE-STUDY OF SMALL LDLS AS A RISK FACTOR FOR NON-INSULIN-DEPENDENT DIABETES-MELLITUS IN ELDERLY MEN AND WOMEN [J].
AUSTIN, MA ;
MYKKANEN, L ;
KUUSISTO, J ;
EDWARDS, KL ;
NELSON, C ;
HAFFNER, SM ;
PYORALA, K ;
LAAKSO, M .
CIRCULATION, 1995, 92 (07) :1770-1778
[5]
ATHEROGENIC LIPOPROTEIN PHENOTYPE - A PROPOSED GENETIC-MARKER FOR CORONARY HEART-DISEASE RISK [J].
AUSTIN, MA ;
KING, MC ;
VRANIZAN, KM ;
KRAUSS, RM .
CIRCULATION, 1990, 82 (02) :495-506
[6]
Candidate-gene studies of the atherogenic lipoprotein phenotype: A sib-pair linkage analysis of DZ women twins [J].
Austin, MA ;
Talmud, PJ ;
Luong, LA ;
Haddad, L ;
Day, INM ;
Newman, B ;
Edwards, KL ;
Krauss, RM ;
Humphries, SE .
AMERICAN JOURNAL OF HUMAN GENETICS, 1998, 62 (02) :406-419
[7]
AUSTIN MA, 1997, CIRCULATION S1, V96, P142
[8]
The role of nicotine in smoking-related cardiovascular disease [J].
Benowitz, NL .
PREVENTIVE MEDICINE, 1997, 26 (04) :412-417
[9]
EFFECT OF SMOKING ON SERUM LEVELS OF HDL APOPROTEINS [J].
BERG, K ;
BORRESEN, AL ;
DAHLEN, G .
ATHEROSCLEROSIS, 1979, 34 (03) :339-343
[10]
BLANGERO J, 1993, HUM BIOL, V65, P941