Please use this identifier to cite or link to this item: https://hdl.handle.net/11499/46845
Full metadata record
DC FieldValueLanguage
dc.contributor.authorYildiz, Abdulmecit-
dc.contributor.authorUlu, Sena-
dc.contributor.authorOruc, Aysegul-
dc.contributor.authorUcar, Ali Riza-
dc.contributor.authorOzturk, Savas-
dc.contributor.authorAlagoz, Selma-
dc.contributor.authorEren, Necmi-
dc.contributor.authorKocyigit, Ismail-
dc.contributor.authorCevher, Simal Koksal-
dc.contributor.authorHaras, Ali Burak-
dc.contributor.authorSumnu, Abdullah-
dc.contributor.authorArinsoy, Turgay-
dc.contributor.authorSahin, Garip-
dc.contributor.authorSuleymanlar, Gultekin-
dc.contributor.authorCavdar, Caner-
dc.contributor.authorSahin, Gizem Kumru-
dc.contributor.authorKurultak, Ilhan-
dc.contributor.authorUnsal, Abdulkadir-
dc.contributor.authorSahin, Gulizar-
dc.contributor.authorKazan, Sinan-
dc.contributor.authorTatar, Erhan-
dc.contributor.authorDikec, Mehmet-
dc.contributor.authorDursun, Belda-
dc.contributor.authorSayarlioglu, Hayriye-
dc.contributor.authorTurkmen, Kultigin-
dc.contributor.authorArtan, Ayse Serra-
dc.contributor.authorAktas, Nimet-
dc.contributor.authorYilmaz, Zulfikar-
dc.contributor.authorBehlul, Ahmet-
dc.contributor.authorDheir, Hamad-
dc.contributor.authorKutlay, Sim-
dc.contributor.authorSeyahi, Nurhan-
dc.date.accessioned2023-01-09T21:16:27Z-
dc.date.available2023-01-09T21:16:27Z-
dc.date.issued2022-
dc.identifier.issn0886-022X-
dc.identifier.issn1525-6049-
dc.identifier.urihttps://doi.org/10.1080/0886022X.2022.2079526-
dc.identifier.urihttps://hdl.handle.net/11499/46845-
dc.description.abstractBackground We aimed to evaluate the features of primary membranous nephropathy (MNP) in Turkish people. Methods This is a retrospective analysis of patients with biopsy-proven primary MNP. We obtained the data collected between 2009 and 2019 in the primary glomerulonephritis registry of the Turkish Society of Nephrology Glomerular Diseases Study Group (TSN-GOLD). Patients with a secondary cause for MNP were excluded. Clinical, demographic, laboratory, and histopathological findings were analyzed. Results A total of 995 patients with primary MNP were included in the analyses. Males constituted the majority (58.8%). The mean age was 48.4 +/- 13.9 years. The most common presentation was the presence of nephrotic syndrome (81.7%) and sub nephrotic proteinuria (10.3%). Microscopic hematuria was detected in one-third of patients. The median estimated glomerular filtration rate (eGFR) was 100.6 mL/min/1.73 m(2) (IQR, 75.4-116.3), and median proteinuria was 6000 mg/d (IQR, 3656-9457). Serum C3 and C4 complement levels were decreased in 3.7 and 1.7% of patients, respectively. Twenty-four (2.4%) patients had glomerular crescents in their kidney biopsy samples. Basal membrane thickening was detected in 93.8% of cases under light microscopy. Mesangial proliferation and interstitial inflammation were evident in 32.8 and 55.9% of the patients, respectively. The most commonly detected depositions were IgG (93%), C3 complement (68.8%), and kappa and lambda immunoglobulin light chains (70%). Although renal functions were normal at presentation, vascular, interstitial, and glomerular findings were more prominent on biopsy in hypertensive patients. No significant effect of BMI on biopsy findings was observed. Conclusions Despite some atypical findings, the main features of primary MNP in Turkey were similar to the published literature. This is the largest MNP study to date conducted in Turkish people.en_US
dc.language.isoenen_US
dc.publisherTaylor & Francis Ltden_US
dc.relation.ispartofRenal Failureen_US
dc.rightsinfo:eu-repo/semantics/openAccessen_US
dc.subjectHistopathologyen_US
dc.subjectimmunofluorescenceen_US
dc.subjectprimary membranous nephropathyen_US
dc.subjectnephrotic syndromeen_US
dc.subjectTurkeyen_US
dc.subjectkidney biopsyen_US
dc.subjectRenal Pathologyen_US
dc.subjectJourneyen_US
dc.titleClinical and pathologic features of primary membranous nephropathy in Turkey: a multicenter study by the Turkish Society of Nephrology Glomerular Diseases Working Groupen_US
dc.typeArticleen_US
dc.identifier.volume44en_US
dc.identifier.issue1en_US
dc.identifier.startpage1048en_US
dc.identifier.endpage1059en_US
dc.identifier.doi10.1080/0886022X.2022.2079526-
dc.relation.publicationcategoryMakale - Uluslararası Hakemli Dergi - Kurum Öğretim Elemanıen_US
dc.authorscopusid56256977500-
dc.authorscopusid55258968300-
dc.authorscopusid55133912100-
dc.authorscopusid57188847925-
dc.authorscopusid35264796700-
dc.authorscopusid50260925600-
dc.authorscopusid55974394500-
dc.identifier.pmid35786180en_US
dc.identifier.scopus2-s2.0-85133243986en_US
dc.identifier.wosWOS:000820567200001en_US
dc.identifier.scopusqualityQ2-
item.languageiso639-1en-
item.openairetypeArticle-
item.grantfulltextopen-
item.cerifentitytypePublications-
item.fulltextWith Fulltext-
item.openairecristypehttp://purl.org/coar/resource_type/c_18cf-
crisitem.author.dept14.02. Internal Medicine-
Appears in Collections:PubMed İndeksli Yayınlar Koleksiyonu / PubMed Indexed Publications Collection
Scopus İndeksli Yayınlar Koleksiyonu / Scopus Indexed Publications Collection
Tıp Fakültesi Koleksiyonu
WoS İndeksli Yayınlar Koleksiyonu / WoS Indexed Publications Collection
Show simple item record



CORE Recommender

Page view(s)

32
checked on May 27, 2024

Download(s)

20
checked on May 27, 2024

Google ScholarTM

Check




Altmetric


Items in GCRIS Repository are protected by copyright, with all rights reserved, unless otherwise indicated.