Publication:
Primary glomerulonephritis: A single-center retrospective experience

dc.contributor.buuauthorAyar, Yavuz
dc.contributor.buuauthorErsoy, Alparslan
dc.contributor.buuauthorCan, Fatma Ezgi
dc.contributor.buuauthorGüllülü, Mustafa
dc.contributor.buuauthorBayrakcı, İsmail
dc.contributor.buuauthorDemirayak, Dilay
dc.contributor.buuauthorDüger, Hakan
dc.contributor.buuauthorOcak, Tuğba
dc.contributor.buuauthorOruç, Ayşegül
dc.contributor.buuauthorYıldız, Abdülmecit
dc.contributor.buuauthorKorkut, Bayram
dc.contributor.buuauthorŞahin, Ahmet Bilgehan
dc.contributor.buuauthorCamcı, Nihal Yücel
dc.contributor.buuauthorVuruşkan, Berna Aytaç
dc.contributor.departmentTıp Fakültesi
dc.contributor.departmentTıp Fakültesi
dc.contributor.departmentTıp Fakültesi
dc.contributor.departmentTıp Fakültesi
dc.contributor.departmentPatoloji Ana Bilim Dalı
dc.contributor.departmentİç Hastalıkları Nefroloji Ana Bilim Dalı
dc.contributor.departmentBiyoistatistik Ana Bilim Dalı
dc.contributor.departmentİç Hastalıkları Ana Bilim Dalı
dc.contributor.orcid0000-0002-0342-9692
dc.contributor.orcid0000-0002-7846-0870
dc.contributor.orcid0000-0001-5478-3192
dc.contributor.orcid0000-0003-4607-9220
dc.contributor.orcid0000-0002-0710-0923
dc.contributor.orcid0000-0003-4607-9220
dc.contributor.orcid0000-0003-4607-9220
dc.contributor.researcheridAAH-4002-2021
dc.contributor.researcheridAAM-4927-2020
dc.contributor.researcheridGPK-6118-2022
dc.contributor.researcheridO-9948-2015
dc.contributor.researcheridAAH-9746-2021
dc.contributor.researcheridAAH-5054-2021
dc.contributor.researcheridGSE-0029-2022
dc.contributor.researcheridGDL-7686-2022
dc.contributor.researcheridCTG-8811-2022
dc.contributor.researcheridELN-3407-2022
dc.contributor.researcheridEQO-1344-2022
dc.contributor.researcheridFPM-3131-2022
dc.contributor.researcheridHIG-9032-2022
dc.contributor.researcheridFFH-4157-2022
dc.contributor.researcheridCHG-6819-2022
dc.contributor.scopusid55860143300
dc.contributor.scopusid35612977100
dc.contributor.scopusid56689608500
dc.contributor.scopusid6602684544
dc.contributor.scopusid57191504355
dc.contributor.scopusid57191498699
dc.contributor.scopusid58423722100
dc.contributor.scopusid57191501503
dc.contributor.scopusid55133912100
dc.contributor.scopusid56256977500
dc.contributor.scopusid57191504817
dc.contributor.scopusid57188809248
dc.contributor.scopusid57191628115
dc.contributor.scopusid56527372000
dc.date.accessioned2023-10-12T06:26:05Z
dc.date.available2023-10-12T06:26:05Z
dc.date.issued2016-09-02
dc.description.abstractAim: Primary glomerular diseases (PGD) are seen frequently. Age, gender, geographical characteristics and genetic affect the distribution of the disease. Despite the treatment, a part of the disease may progress to end-stage renal disease. We evaluated the PGD patients and retrospectively regarding to their clinical and histopathological characteristics.Materials and methods: In this study PGD patients, who have had renal biopsy between 1st January 2009 and 31st December 2014 were evaluated. Clinical and laboratory characteristics, response of the treatment, biopsy evidences, and the risk factors associated with mortality were analyzed. We also compared the cases of primary glomerulonephritis retrospectively. The mean value of the follow-up periods was 22 months (range: 8 - 76 months).Results: The median age was 42 years (18 - 80) in 264 patients. When five groups were compared, there was statistically important difference between the groups (p < 0.001). The distributions of PGD subgroups were 40.5% for membranous glomerulonephritis (MGN), 20.4% for IgA nephropathy (IgAN), 25.7% for focal segmental glomerulosclerosis (FSGS), 7.9% for minimal change disease (MCD) and 5.3% for membranoproliferative glomerulonephritis (MPGN). The distrubition of gender was not significantly in the five PGD groups (p=0.269). Nephrotic syndrome was the most biopsy indication in MGN patients (76.6%). Nephritic syndrome was more seen in immunoglobulin A nephropathy (IgAN) patients (63%). Chronic kidney disease was more detected in focal segmental glomerulosclerosis (FSGS) patients as biopsy indication (p<0.001). Minimal change disease (MCD) and IgAN patients were more received with steroid treatment (85.7% and 55.5% respectively). Cyclophosphamide was more received in MGN patients. Serum IgG levels were more higher in FSGS and IgAN patients (p<0.001). Partial remission was more seen in MCD patients. Complete remission was more detected in MGN and FSGS patients. 29.1% of IgAN patients were not received treatment response. Six year renal survival rates were 84.1% (MGN), 87.1% (IgAN), 95.3% (MCD), 64.3% (MPGN) and 76.5% (FSGS) respectively.Conclusion: Biopsy maintains its diagnostic importance in glomerular diseases. Renal functions at diagnosis are important in response to treatment. Early diagnosis, follow-up and appropriate immunosuppressive medications affect mortality and clinical progress in PGD.
dc.identifier.citationAyar, Y. vd. (2016). "Primary glomerulonephritis: A single-center retrospective experience". Acta Medica Mediterranea, 32(5), 1723-1727.
dc.identifier.endpage1727
dc.identifier.issn0393-6384
dc.identifier.issn2283-9720
dc.identifier.issue5
dc.identifier.scopus2-s2.0-84992193815
dc.identifier.startpage1723
dc.identifier.urihttp://hdl.handle.net/11452/34300
dc.identifier.volume32
dc.identifier.wos000390172000027
dc.indexed.wosSCIE
dc.language.isoen
dc.publisherCarbone Editore
dc.relation.journalActa Medica Mediterranea
dc.relation.publicationcategoryMakale - Uluslararası Hakemli Dergi
dc.rightsinfo:eu-repo/semantics/closedAccess
dc.subjectGeneral & internal medicine
dc.subjectPrimary glomerular disease
dc.subjectProteinuria
dc.subjectRenal biopsy
dc.subjectPrognosis
dc.subject.emtreeAdult
dc.subject.emtreeAged
dc.subject.emtreeAlbumin blood level
dc.subject.emtreeArticle
dc.subject.emtreeCholesterol blood level
dc.subject.emtreeClinical evaluation
dc.subject.emtreeClinical feature
dc.subject.emtreeComparative study
dc.subject.emtreeFemale
dc.subject.emtreeFocal glomerulosclerosis
dc.subject.emtreeFollow up
dc.subject.emtreeGlomerulonephritis
dc.subject.emtreeHemodialysis
dc.subject.emtreeHistopathology
dc.subject.emtreeHuman
dc.subject.emtreeHuman tissue
dc.subject.emtreeImmunoglobulin A nephropathy
dc.subject.emtreeImmunoglobulin blood level
dc.subject.emtreeKidney biopsy
dc.subject.emtreeKidney transplantation
dc.subject.emtreeMajor clinical study
dc.subject.emtreeMale
dc.subject.emtreeMembranoproliferative glomerulonephritis
dc.subject.emtreeMembranous glomerulonephritis
dc.subject.emtreeMinimal change disease
dc.subject.emtreeMortality
dc.subject.emtreeNephrotic syndrome
dc.subject.emtreePrimary glomerulonephritis
dc.subject.emtreePrognosis
dc.subject.emtreeProtein urine level
dc.subject.emtreeProteinuria
dc.subject.emtreeRemission
dc.subject.emtreeRetrospective study
dc.subject.emtreeRisk factor
dc.subject.emtreeSex ratio
dc.subject.emtreeStatistical analysis
dc.subject.emtreeStatistical distribution
dc.subject.emtreeSurvival rate
dc.subject.emtreeTreatment response
dc.subject.emtreeTriacylglycerol blood level
dc.subject.emtreeAlbumin
dc.subject.emtreeAngiotensin receptor antagonist
dc.subject.emtreeAzathioprine
dc.subject.emtreeCholesterol
dc.subject.emtreeCyclophosphamide
dc.subject.emtreeCyclosporin A
dc.subject.emtreeDipeptidyl carboxypeptidase inhibitor
dc.subject.emtreeImmunoglobulin G
dc.subject.emtreeLow density lipoprotein cholesterol
dc.subject.emtreeMycophenolate mofetil
dc.subject.emtreeSteroid
dc.subject.emtreeTriacylglycerol
dc.subject.scopusGlomerulonephritis; Lupus Erythematosus Nephritis; Immunoglobulin A Nephropathy
dc.subject.wosMedicine, general & internal
dc.titlePrimary glomerulonephritis: A single-center retrospective experience
dc.typeArticle
dc.wos.quartileQ4
dspace.entity.typePublication
local.contributor.departmentTıp Fakültesi/İç Hastalıkları Nefroloji Ana Bilim Dalı
local.contributor.departmentTıp Fakültesi/Biyoistatistik Ana Bilim Dalı
local.contributor.departmentTıp Fakültesi/İç Hastalıkları Ana Bilim Dalı
local.contributor.departmentTıp Fakültesi/Patoloji Ana Bilim Dalı
local.indexed.atScopus
local.indexed.atWOS

Files

License bundle

Now showing 1 - 1 of 1
Placeholder
Name:
license.txt
Size:
1.71 KB
Format:
Item-specific license agreed upon to submission
Description: