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DNA methylation and smoking in Korean adults: epigenome-wide association study

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dc.contributor.authorLee, Mi Kyeong-
dc.contributor.authorHong, Yoonki-
dc.contributor.authorKim, Sun-Young-
dc.contributor.authorLondon, Stephanie J.-
dc.contributor.authorKim, Woo Jin-
dc.date.accessioned2017-02-06T01:51:59Z-
dc.date.available2017-02-06T01:51:59Z-
dc.date.issued2016-09-22-
dc.identifier.citationClinical Epigenetics, 8(1):103ko_KR
dc.identifier.urihttps://hdl.handle.net/10371/100428-
dc.descriptionThis article is distributed under the terms of the Creative Commons Attribution 4.0
International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and
reproduction in any medium, provided you give appropriate credit to the original author(s) and the source, provide a link to
the Creative Commons license, and indicate if changes were made.
ko_KR
dc.description.abstractAbstract

Background
Exposure to cigarette smoking can increase the risk of cancers and cardiovascular and pulmonary diseases. However, the underlying mechanisms of how smoking contributes to disease risks are not completely understood. Epigenome-wide association studies (EWASs), mostly in non-Asian populations, have been conducted to identify smoking-associated methylation alterations at individual probes. There are few data on regional methylation changes in relation to smoking. Few data link differential methylation in blood to differential gene expression in lung tissue.


Results
We identified 108 significant (false discovery rate (FDR) < 0.05) differentially methylated probes (DMPs) and 87 significant differentially methylated regions (DMRs) (multiple-testing corrected p < 0.01) in current compared to never smokers from our EWAS of cotinine-validated smoking in blood DNA from a Korean chronic obstructive pulmonary disease cohort (n = 100 including 31 current, 30 former, and 39 never smokers) using Illumina HumanMethylation450 BeadChip. Of the 108 DMPs (FDR < 0.05), nine CpGs were statistically significant based on Bonferroni correction and 93 were novel including five that mapped to loci previously associated with smoking. Of the 87 DMRs, 66 were mapped to novel loci. Methylation correlated with urine cotinine levels in current smokers at six DMPs, with pack-years in current smokers at six DMPs, and with duration of smoking cessation in former smokers at eight DMPs. Of the 143 genes to which our significant DMPs or DMRs annotated, gene expression levels at 20 genes were associated with pack-years in lung tissue transcriptome data of smokers (Asan Biobank, n = 188).


Conclusions
Our study of differential methylation in Koreans confirmed previous findings from non-Asian populations and revealed novel loci in relation to smoking. Smoking-related differential methylation in blood is associated with gene expression in lung tissue, an important target of adverse health effects of smoking, supporting the potential functional importance of methylation in smoking-related disease.
ko_KR
dc.language.isoenko_KR
dc.publisherBioMed Centralko_KR
dc.subjectDNA methylationko_KR
dc.subjectSmokingko_KR
dc.subjectEpigenome-wide association studyko_KR
dc.subjectCotinineko_KR
dc.subjectDuration of smoking cessationko_KR
dc.subjectGene expressionko_KR
dc.titleDNA methylation and smoking in Korean adults: epigenome-wide association studyko_KR
dc.typeArticleko_KR
dc.contributor.AlternativeAuthor이미경-
dc.contributor.AlternativeAuthor홍윤기-
dc.contributor.AlternativeAuthor김선영-
dc.contributor.AlternativeAuthor김우진-
dc.identifier.doi10.1186/s13148-016-0266-6-
dc.language.rfc3066en-
dc.rights.holderThe Author(s).-
dc.date.updated2017-01-06T09:58:32Z-
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