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dc.contributor.authorUnsal, Oktay
dc.contributor.authorSipahioglu, Murat
dc.contributor.authorDERVİŞOĞLU, ERKAN
dc.contributor.authorAydemir, Nihal
dc.contributor.authorUzun, Sami
dc.contributor.authorIstemihan, Zulal
dc.contributor.authorTatar, Erhan
dc.contributor.authorBerktas, Haci Bayram
dc.contributor.authorOzdemir, Arzu
dc.contributor.authorSumnu, Abdullah
dc.contributor.authorKUMRU ŞAHİN, GİZEM
dc.contributor.authorCetinkaya, Hakki
dc.contributor.authorKazan, Sinan
dc.contributor.authorKOÇYİĞİT, İSMAİL
dc.contributor.authorGokalp, Cenk
dc.contributor.authorHasbal, Baris
dc.contributor.authorArtan, Ayse Serra
dc.contributor.authorOzelsancak, Ruya
dc.contributor.authorTaymez, Dilek
dc.contributor.authorYadigar, Serap
dc.contributor.authorAlagoz, Selma
dc.contributor.authorAslan, Bilal Burcak
dc.contributor.authorYAYLACI, SELÇUK
dc.contributor.authorJabrayilov, Jabrayil
dc.contributor.authorTURGUTALP, KENAN
dc.contributor.authorDURSUN, BELDA
dc.contributor.authorŞAHİN, GARİP
dc.contributor.authorAydin, Zeki
dc.contributor.authorYilmaz, Murvet
dc.date.accessioned2023-02-21T08:06:01Z
dc.date.available2023-02-21T08:06:01Z
dc.identifier.citationAydin Z., Yilmaz M., Sipahioglu M., DERVİŞOĞLU E., Aydemir N., Uzun S., Istemihan Z., Unsal O., Tatar E., Berktas H. B., et al., "Demographic, clinical and laboratory characteristics of adult-onset minimal change disease in Turkey: Turkish Society of Nephrology-Glomerular Diseases (TSN-GOLD) Working Group", INTERNATIONAL UROLOGY AND NEPHROLOGY, 2022
dc.identifier.issn0301-1623
dc.identifier.othervv_1032021
dc.identifier.otherav_1411c572-b3e1-406b-b722-f45a12dd3526
dc.identifier.urihttp://hdl.handle.net/20.500.12627/186370
dc.identifier.urihttps://doi.org/10.1007/s11255-022-03382-3
dc.description.abstractPurpose In our study, diagnostic and demographic characteristics of patients diagnosed with minimal change disease (MCD) by biopsy, clinical and laboratory findings in our country were investigated. Methods Data were obtained from the Turkish Society of Nephrology Glomerular Diseases (TSN-GOLD) Working Group database. Demographic characteristics, indications for biopsy, diagnosis of the glomerular diseases, comorbidities, laboratory and biopsy findings of all patients were recorded. The data presented are cross-sectional and includes application data for the biopsy period. Results Of 3875 patients, 233 patients with MCD (median age 35.0 years) were included in the study, which constitutes 6.0% of the total glomerulonephritis database. Renal biopsy was performed in 196 (84.1%) patients due to nephrotic syndrome. Median serum creatinine was 0.7 (0.6-1.0) mg/dl, mean eGFR was 104 +/- 33 ml/min/1.73 m(2) and median proteinuria 6000 mg/day. The number of patients under the age of 40 years was 139 (59.7%) (Group A), and the number of patients aged 40 years and over was 94 (40.3%) (Group B). Compared to Group A, global sclerotic glomeruli (24 vs. 43, p < 0.001) interstitial inflammation (15 vs. 34, p < 0.001), interstitial fibrosis (20 vs. 31, p = 0.001, vascular changes (10 vs. 25, p < 0.001) and tubular atrophy (18 vs. 30, p < 0.001) were found to be significantly higher in Group B. There was no difference in immunofluorescent staining properties between the two groups. Conclusion Our data are generally compatible with the literature. Chronic histopathological changes were more common in patients aged 40 years and older than younger patients. Studies investigating the effects of these different features on renal survival are needed.
dc.language.isoeng
dc.subjectKlinik Tıp
dc.subjectÜROLOJİ VE NEFROLOJİ
dc.subjectKlinik Tıp (MED)
dc.subjectTıp
dc.subjectDahili Tıp Bilimleri
dc.subjectİç Hastalıkları
dc.subjectNefroloji
dc.subjectSağlık Bilimleri
dc.subjectÜroloji
dc.titleDemographic, clinical and laboratory characteristics of adult-onset minimal change disease in Turkey: Turkish Society of Nephrology-Glomerular Diseases (TSN-GOLD) Working Group
dc.typeMakale
dc.relation.journalINTERNATIONAL UROLOGY AND NEPHROLOGY
dc.contributor.departmentUniv Hlth Sci , ,
dc.contributor.firstauthorID4063701


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