Distributional changes in gene-specific methylation associated with temperature

被引:13
|
作者
Bind, Marie-Abele C. [1 ]
Coull, Brent A. [2 ]
Baccarelli, Andrea [3 ]
Tarantini, Letizia [4 ,5 ]
Cantone, Laura [4 ,5 ]
Vokonas, Pantel [6 ,7 ]
Schwartz, Joel [3 ]
机构
[1] Harvard Univ, Dept Stat, Fac Arts & Sci, Cambridge, MA 02138 USA
[2] Harvard Sch Publ Hlth, Dept Biostat, Boston, MA 02115 USA
[3] Harvard Sch Publ Hlth, Dept Environm Hlth, Boston, MA 02115 USA
[4] Univ Milan, Dept Clin Sci & Community Hlth, Ctr Mol & Genet Epidemiol, Milan, Italy
[5] Fdn Ca Granda, IRCCS Osped Maggiore Policlin, Milan, Italy
[6] Boston Univ, Sch Med, VA Boston Healthcare Syst, VA Normat Aging Study, Boston, MA 02118 USA
[7] Boston Univ, Sch Med, Dept Med, Boston, MA 02118 USA
关键词
Quantile regression; Temperature; DNA methylation; Susceptibility; C-REACTIVE PROTEIN; AIR-TEMPERATURE; TISSUE FACTOR; INFLAMMATION; DISEASE; COAGULATION; RESPONSES; CORONARY; MARKERS; STRESS;
D O I
10.1016/j.envres.2016.05.034
中图分类号
X [环境科学、安全科学];
学科分类号
08 ; 0830 ;
摘要
Temperature has been related to mean differences in DNA methylation. However, heterogeneity in these associations may exist across the distribution of methylation outcomes. This study examined whether the association between three-week averaged of temperature and methylation differs across quantiles of the methylation distributions in nine candidate genes. We measured gene-specific blood methylation repeatedly in 777 elderly men participating in the Normative Aging Study (1999-2010). We fit quantile regressions for longitudinal data to investigate whether the associations of temperature on methylation (expressed as %5mC) varied across the distribution of the methylation outcomes. We observed heterogeneity in the associations of temperature across percentiles of methylation in F3, TLR-2, CRAT, iNOS, and ICAM-1 genes. For instance, an increase in three-week temperature exposure was associated with a longer left-tail of the F3 methylation distribution. A 5 degrees C increase in temperature was associated with a 0.15%5mC (95% confidence interval (CI): -0.27, -0.04) decrease on the 20th quantile of F3 methylation, but was not significantly related to the 80th quantile of this distribution (Estimate:0.06%5mC, 95%Cl: -0.22, 0.35). Individuals with low values of F3, TLR-2, CRAT, and iNOS methylation, as well as a high value of IGAM-1 methylation, may be more susceptible to temperature effects on systemic inflammation. (C) 2016 Elsevier Inc. All rights reserved.
引用
收藏
页码:38 / 46
页数:9
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