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dc.contributor.author강덕희*
dc.contributor.author최규복*
dc.contributor.author김승정*
dc.contributor.author류동열*
dc.date.accessioned2016-08-28T12:08:16Z-
dc.date.available2016-08-28T12:08:16Z-
dc.date.issued2011*
dc.identifier.issn1011-8934*
dc.identifier.otherOAK-7997*
dc.identifier.urihttps://dspace.ewha.ac.kr/handle/2015.oak/221969-
dc.description.abstractWe have hypothesized that non-dipper status and left ventricular hypertrophy (LVH) are associated with the development of chronic kidney disease (CKD) in non-diabetic hypertensive patients. This study included 102 patients with an estimated glomerular filtration rate (eGFR) ≥ 60 mL/min/1.73 m2. Ambulatory blood pressure monitoring and echocardiography were performed at the beginning of the study, and the serum creatinine levels were followed. During the average follow-up period of 51 months, CKD developed in 11 patients. There was a significant difference in the incidence of CKD between dippers and non-dippers (5.0% vs 19.0%, P < 0.05). Compared to patients without CKD, patients with incident CKD had a higher urine albumin/creatinine ratio (52.3 ± 58.6 mg/g vs 17.8 ± 29.3 mg/g, P < 0.01), non-dipper status (72.7% vs 37.4%, P < 0.05), the presence of LVH (27.3% vs 5.5%, P < 0.05), and a lower serum HDL-cholesterol level (41.7 ± 8.3 mg/dL vs 50.4 ± 12.4 mg/dL, P < 0.05). Based on multivariate Cox regression analysis, non-dipper status and the presence of LVH were independent predictors of incident CKD. These findings suggest that non-dipper status and LVH may be the therapeutic targets for preventing the development of CKD in non-diabetic hypertensive patients. © 2011 The Korean Academy of Medical Sciences.*
dc.languageEnglish*
dc.titleNon-dipper status and left ventricular hypertrophy as predictors of incident chronic kidney disease*
dc.typeArticle*
dc.relation.issue9*
dc.relation.volume26*
dc.relation.indexSCI*
dc.relation.indexSCIE*
dc.relation.indexSCOPUS*
dc.relation.indexKCI*
dc.relation.startpage1185*
dc.relation.lastpage1190*
dc.relation.journaltitleJournal of Korean Medical Science*
dc.identifier.doi10.3346/jkms.2011.26.9.1185*
dc.identifier.wosidWOS:000295191500011*
dc.identifier.scopusid2-s2.0-80052807566*
dc.author.googleAn H.R.*
dc.author.googlePark S.*
dc.author.googleYoo T.-H.*
dc.author.googleKang S.-W.*
dc.author.googleRyu J.-H.*
dc.author.googleLee Y.K.*
dc.author.googleYu M.*
dc.author.googleRyu D.-R.*
dc.author.googleKim S.J.*
dc.author.googleKang D.-H.*
dc.author.googleChoi K.B.*
dc.contributor.scopusid강덕희(17233695600)*
dc.contributor.scopusid최규복(36096388100)*
dc.contributor.scopusid김승정(8619054500)*
dc.contributor.scopusid류동열(7103144218;56997547400;56669926200)*
dc.date.modifydate20240419142141*
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