The effect of polychlorinated biphenyls on type 2 diabetes risk is mediated via DNA methylation

Polychlorinated biphenyls (PCBs) have been identified as diabetogens and potential epigenetic regulators. Epigenetic variation is implicated in the pathogenesis of type 2 diabetes (T2D) and is therefore a potential mechanism linking PCB exposure and T2D. We here investigate the effect of PCB exposure on T2D risk and the extent to which this is mediated via DNA methylation (DNAm) using two epigenome-wide association studies and mediation analysis. Exposure to PCBs, especially congeners 74, 99, 118, 138 and 183, increased the risk of T2D (range of ORs 1.38-1.54). Five CpG sites were identified as potential mediators. Together, methylation at these sites was estimated to mediate 40 % (95 % CI: 20, 60 %) of the effect of PCBs on T2D. The strongest evidence was obtained for cg00574958, located in the first intron of the CPT1A gene. This study is among the largest to date assessing the link between PCBs and T2D, and the first to investigate the mediation by DNAm. The evidence for methylation at cg00574958 as a mediator of the PCB-T2D relationship supports the widely-replicated link of CPT1A DNA methylation to a range of metabolic phenotypes including obesity, dyslipidemia and T2D and indicates a possible future target for epigenetic intervention.

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Publication Details

Journal
Environment International
Published
2025-09-01
DOI
https://doi.org/10.1016/j.envint.2025.109779
Citations
1
Primary Topic
Epigenetics and DNA Methylation
Type
article
Field-Weighted Citation Impact
0.81
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article

The effect of polychlorinated biphenyls on type 2 diabetes risk is mediated via DNA methylation

Boris Novakovic, Markus Juonala, Kari Auranen, Juha Mykkänen et al.
1 citations
Environment International
Epigenetics and DNA Methylation
0.81
article

The effect of polychlorinated biphenyls on type 2 diabetes risk is mediated via DNA methylation

Boris Novakovic, Markus Juonala, Kari Auranen, Juha Mykkänen, Mika A. P. Kähönen, Jaakko Nevalainen, Suvi Rovio, Emma Raitoharju, Hannu Kiviranta, Noora Kartiosuo, Toby Mansell, Panu Rantakokko, Pashupati P. Mishra, Olli Tuomas Raitakari, Jorma S.A. Viikari, David Burgner, Anne‐Louise Ponsonby, Katja Pahkala, Terho J. Lehtimäki, Richard Saffery, Jari Kaikkonen, Sam Tanner
article en
1 citations

Abstract

Polychlorinated biphenyls (PCBs) have been identified as diabetogens and potential epigenetic regulators. Epigenetic variation is implicated in the pathogenesis of type 2 diabetes (T2D) and is therefore a potential mechanism linking PCB exposure and T2D. We here investigate the effect of PCB exposure on T2D risk and the extent to which this is mediated via DNA methylation (DNAm) using two epigenome-wide association studies and mediation analysis. Exposure to PCBs, especially congeners 74, 99, 118, 138 and 183, increased the risk of T2D (range of ORs 1.38-1.54). Five CpG sites were identified as potential mediators. Together, methylation at these sites was estimated to mediate 40 % (95 % CI: 20, 60 %) of the effect of PCBs on T2D. The strongest evidence was obtained for cg00574958, located in the first intron of the CPT1A gene. This study is among the largest to date assessing the link between PCBs and T2D, and the first to investigate the mediation by DNAm. The evidence for methylation at cg00574958 as a mediator of the PCB-T2D relationship supports the widely-replicated link of CPT1A DNA methylation to a range of metabolic phenotypes including obesity, dyslipidemia and T2D and indicates a possible future target for epigenetic intervention.

Environment InternationalVol. 203
Tampere University of Applied Sciences (FI), University of Turku (FI), Turku University of Applied Sciences (FI), Tampere University (FI), Florey Institute of Neuroscience and Mental Health (AU), Turku University Hospital (FI), Finnish Institute for Health and Welfare (FI), Tampere University Hospital (FI), Tampere University (FI), Fimlab (Finland) (FI), Murdoch Children's Research Institute (AU)
Openalex Percentile: Top 24%
Epigenetics and DNA Methylation
0.81
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