スギヤマ　ヒトシ   杉山　斉    所属   川崎医療短期大学  教育部 医療介護福祉学科    職種   教授
論文種別	原著
言語種別	英語
査読の有無	査読あり
表題	Urine 5MedC, a Marker of DNA Methylation, in the Progression of Chronic Kidney Disease.
掲載誌名	正式名：Disease markers 略　 称：Dis Markers ISSNコード：18758630/02780240
掲載区分	国外
巻・号・頁	2019,pp.5432453
著者・共著者	Onishi Akifumi, Sugiyama Hitoshi, Kitagawa Masashi, Yamanari Toshio, Tanaka Keiko, Ogawa-Akiyama Ayu, Kano Yuzuki, Mise Koki, Tanabe Katsuyuki, Morinaga Hiroshi, Kinomura Masaru, Uchida Haruhito A, Wada Jun
発行年月	2019
概要	BACKGROUND:Alterations in DNA methylation may be involved in disease progression in patients with chronic kidney disease (CKD). Recent studies have suggested that 5-methyl-2'-deoxycytidine (5MedC) may be a marker of hypermethylation of DNA. Currently, there is no information available regarding the urine levels of 5MedC and its association with the progression of CKD.METHOD:We examined the urine levels of 5MedC in spot urine samples from 308 patients with CKD (median age: 56 years, male: 53.2%, and glomerulonephritis: 51.0%) using a competitive enzyme-linked immunosorbent assay and investigated the relationships among urine 5MedC, urine albumin, urine α1-microglobulin (α1MG), and the laboratory parameters associated with CKD. The patients were followed for three years to evaluate renal endpoints in a prospective manner.RESULTS:The urine 5MedC level was significantly increased in the later stages of CKD compared to the early to middle stages of CKD. In multiple logistic regression models, urine 5MedC was significantly associated with the prediction of later CKD stages. Urine 5MedC (median value, 65.9 μmol/gCr) was significantly able to predict a 30% decline in the estimated GFR or a development of end-stage renal disease when combined with macroalbuminuria or an increased level of urine α1MG (median value, 5.7 mg/gCr).CONCLUSION:The present data demonstrate that the urine 5MedC level is associated with a reduced renal function and can serve as a novel and potent biomarker for predicting the renal outcome in CKD patients. Further studies will be necessary to elucidate the role of urine DNA methylation in the progression of CKD.
DOI	10.1155/2019/5432453
PMID	31354889