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Predictive value of mesangial C3 and C4d deposition in IgA nephropathy

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dc.contributor.author윤해룡-
dc.contributor.author유태현-
dc.contributor.author박정탁-
dc.contributor.author남기헌-
dc.contributor.author강신욱-
dc.contributor.author한승혁-
dc.contributor.author임범진-
dc.contributor.author정현주-
dc.contributor.author주영수-
dc.date.accessioned2020-09-28T01:28:50Z-
dc.date.available2020-09-28T01:28:50Z-
dc.date.issued2020-02-
dc.identifier.issn1521-6616-
dc.identifier.urihttps://ir.ymlib.yonsei.ac.kr/handle/22282913/179017-
dc.description.abstractWe aimed to determine the relative contribution of each complement (C3 and C4d) deposition to the progression of IgA nephropathy (IgAN). We enrolled a total of 380 patients with biopsy-confirmed IgAN. Mesangial deposition of C3(<2+ vs. ≥2+) and C4d(positive vs. negative) was evaluated by immunofluorescence staining and immunohistochemistry, respectively. Study endpoint was the composite of a 30% decline in eGFR or ESRD. The risk of reaching the primary outcome was significantly higher in patients having C3 ≥ 2+ and C4d(+) than in corresponding counterparts. Adding C3 deposition to clinical data acquired at kidney biopsy modestly increased the area under the receiver-operating characteristic curve, net reclassification improvement, and integrated discrimination improvement (IDI); adding C4d increased IDI only. In conclusion, mesangial C3 and C4d deposition was an independent risk factor for progression of IgAN. C3 showed better predictability than C4d, suggesting that lectin pathway alone has limited clinical prognostic value.-
dc.description.statementOfResponsibilityrestriction-
dc.languageEnglish-
dc.publisherAcademic Press-
dc.relation.isPartOfCLINICAL IMMUNOLOGY-
dc.rightsCC BY-NC-ND 2.0 KR-
dc.titlePredictive value of mesangial C3 and C4d deposition in IgA nephropathy-
dc.typeArticle-
dc.contributor.collegeCollege of Medicine (의과대학)-
dc.contributor.departmentDept. of Internal Medicine (내과학교실)-
dc.contributor.googleauthorKi Heon Nam-
dc.contributor.googleauthorYoung Su Joo-
dc.contributor.googleauthorChanghyun Lee-
dc.contributor.googleauthorSangmi Lee-
dc.contributor.googleauthorJoohwan Kim-
dc.contributor.googleauthorHae-Ryong Yun-
dc.contributor.googleauthorJung Tak Park-
dc.contributor.googleauthorTae Ik Chang-
dc.contributor.googleauthorDong-Ryeol Ryu-
dc.contributor.googleauthorTae-Hyun Yoo-
dc.contributor.googleauthorHo Jun Chin-
dc.contributor.googleauthorShin-Wook Kang-
dc.contributor.googleauthorHyeon Joo Jeong-
dc.contributor.googleauthorBeom Jin Lim-
dc.contributor.googleauthorSeung Hyeok Han-
dc.contributor.googleauthorKorean GlomeruloNEphritis sTudy (KoGNET) Group-
dc.identifier.doi10.1016/j.clim.2019.108331-
dc.contributor.localIdA04617-
dc.contributor.localIdA02526-
dc.contributor.localIdA01654-
dc.contributor.localIdA01244-
dc.contributor.localIdA00053-
dc.contributor.localIdA04304-
dc.contributor.localIdA03363-
dc.contributor.localIdA03771-
dc.relation.journalcodeJ00578-
dc.identifier.eissn1521-7035-
dc.identifier.pmid31899330-
dc.identifier.urlhttps://www.sciencedirect.com/science/article/pii/S1521661619305777-
dc.subject.keywordC3-
dc.subject.keywordC4d-
dc.subject.keywordComplement-
dc.subject.keywordIgA nephropathy-
dc.contributor.alternativeNameYun, Hae Ryong-
dc.contributor.affiliatedAuthor윤해룡-
dc.contributor.affiliatedAuthor유태현-
dc.contributor.affiliatedAuthor박정탁-
dc.contributor.affiliatedAuthor남기헌-
dc.contributor.affiliatedAuthor강신욱-
dc.contributor.affiliatedAuthor한승혁-
dc.contributor.affiliatedAuthor임범진-
dc.contributor.affiliatedAuthor정현주-
dc.citation.volume211-
dc.citation.startPage108331-
dc.identifier.bibliographicCitationCLINICAL IMMUNOLOGY, Vol.211 : 108331, 2020-02-
Appears in Collections:
1. College of Medicine (의과대학) > Dept. of Internal Medicine (내과학교실) > 1. Journal Papers
1. College of Medicine (의과대학) > Dept. of Pathology (병리학교실) > 1. Journal Papers

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