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Mitochondrial DNA copy number augments performance of A₁C and oral glucose tolerance testing in the prediction of type 2 diabetes

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dc.contributor.authorCho, Seong Beom-
dc.contributor.authorKoh, InSong-
dc.contributor.authorNam, Hye-Young-
dc.contributor.authorJeon, Jae-Pil-
dc.contributor.authorLee, Hong Kyu-
dc.contributor.authorHan, Bok-Ghee-
dc.date.accessioned2022-07-14T12:36:18Z-
dc.date.available2022-07-14T12:36:18Z-
dc.date.created2021-05-12-
dc.date.issued2017-03-
dc.identifier.issn2045-2322-
dc.identifier.urihttps://scholarworks.bwise.kr/hanyang/handle/2021.sw.hanyang/152783-
dc.description.abstractHere, we tested the performance of the mitochondrial DNA copy number (mtDNA-CN) in predicting future type 2 diabetes (n = 1108). We used the baseline clinical data (age, sex, body mass index, waist-to-hip ratio, systolic and diastolic blood pressure) and the mtDNA-CN, hemoglobin A(1c) (A(1)C) levels and results of oral glucose tolerance test (OGTT) including fasting plasma glucose, 1-hour glucose, and 2-hour glucose levels, to predict future diabetes. We built a prediction model using the baseline data and the diabetes status at biannual follow-up of 8 years. The mean area under curve (AUC) for all followups of the full model including all variables was 0.92 +/- 0.04 (mean +/- standard deviation), while that of the model excluding the mtDNA-CN was 0.90 +/- 0.03. The sensitivity of the f4ull model was much greater than that of the model not including mtDNA-CN: the mean sensitivities of the model with and without mtDNA-CN were 0.60 +/- 0.06 and 0.53 +/- 0.04, respectively. We found that the mtDNA-CN of peripheral leukocytes is a biomarker that augments the predictive power for future diabetes of A1C and OGTT. We believe that these results could provide invaluable information for developing strategies for the management of diabetes.-
dc.language영어-
dc.language.isoen-
dc.publisherNATURE PUBLISHING GROUP-
dc.titleMitochondrial DNA copy number augments performance of A₁C and oral glucose tolerance testing in the prediction of type 2 diabetes-
dc.typeArticle-
dc.contributor.affiliatedAuthorKoh, InSong-
dc.identifier.doi10.1038/srep43203-
dc.identifier.scopusid2-s2.0-85014422708-
dc.identifier.wosid000395370000001-
dc.identifier.bibliographicCitationSCIENTIFIC REPORTS, v.7, pp.1 - 8-
dc.relation.isPartOfSCIENTIFIC REPORTS-
dc.citation.titleSCIENTIFIC REPORTS-
dc.citation.volume7-
dc.citation.startPage1-
dc.citation.endPage8-
dc.type.rimsART-
dc.type.docTypeArticle-
dc.description.journalClass1-
dc.description.isOpenAccessY-
dc.description.journalRegisteredClassscie-
dc.description.journalRegisteredClassscopus-
dc.relation.journalResearchAreaScience & Technology - Other Topics-
dc.relation.journalWebOfScienceCategoryMultidisciplinary Sciences-
dc.subject.keywordPlusFASTING PLASMA-GLUCOSE-
dc.subject.keywordPlusPREVALENCE-
dc.subject.keywordPlusHBA1C-
dc.subject.keywordPlusRISK-
dc.identifier.urlhttps://www.nature.com/articles/srep43203-
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