Assessment of fenofibrate-methylation interactions on triglycerides using longitudinal family data
Autor: | Yen-Feng Chiu, Jih-Chang Yu, Fang-Chi Hsu |
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Rok vydání: | 2018 |
Předmět: |
0301 basic medicine
medicine.medical_specialty lcsh:Medicine 030204 cardiovascular system & hematology General Biochemistry Genetics and Molecular Biology 03 medical and health sciences chemistry.chemical_compound 0302 clinical medicine Internal medicine medicine Epigenetics lcsh:Science Fenofibrate Triglyceride Chemistry lcsh:R Confounding General Medicine Methylation 030104 developmental biology Endocrinology CpG site DNA methylation lcsh:Q medicine.drug Lipoprotein |
Zdroj: | BMC Proceedings, Vol 12, Iss S9, Pp 123-128 (2018) |
ISSN: | 1753-6561 1900-3390 |
Popis: | Background Triglyceride (TG) concentrations decrease in response to fenofibrate treatment, and also are associated with DNA methylation. But how interactions between fenofibrate response and DNA methylation affect TGs remains unclear. Methods In the present study, we identified and compared differential methylation sites associated with TG concentrations in individuals before and after fenofibrate treatment. We then estimated interactions between fenofibrate treatment and methylation to identify differential methylation effects associated with fenofibrate treatment on TG concentrations using the entire longitudinal family sample. To account for within-family and within-individual corrections, the generalized estimating equations approach was used to estimate main and interaction effects between methylation sites and fenofibrate treatment, adjusting for potential confounders. Analyses were also performed with and without adjusting for high-density lipoprotein (HDL) concentrations. Results Prior to fenofibrate treatment, 23 cytosine-phosphate-guanine (CpG) sites were significantly associated with TG concentrations, while only 13 CpG sites were identified posttreatment, adjusting for HDL. Without adjusting for HDL, pretreatment, 20 CpG sites were significantly associated with TG concentrations, while only 12 CpG sites were identified posttreatment. Among these sites, only one differential site (cg19003390 in the CPT1A gene) overlapped from pre- and posttreatment measurements regardless of HDL adjustment. Furthermore, 11 methylation sites showed substantial interaction effects (p |
Databáze: | OpenAIRE |
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