Please use this identifier to cite or link to this item: http://hdl.handle.net/11452/34300
Title: Primary glomerulonephritis: A single-center retrospective experience
Authors: Uludağ Üniversitesi/Tıp Fakültesi/İç Hastalıkları Nefroloji Anabilim Dalı.
Uludağ Üniversitesi/Tıp Fakültesi/Biyoistatistik Anabilim Dalı.
Uludağ Üniversitesi/Tıp Fakültesi/İç Hastalıkları Anabilim Dalı.
Uludağ Üniversitesi/Tıp Fakültesi/Patoloji Anabilim Dalı.
0000-0002-0342-9692
0000-0002-7846-0870
0000-0001-5478-3192
0000-0003-4607-9220
0000-0002-0710-0923
0000-0003-4607-9220
0000-0003-4607-9220
Ayar, Yavuz
Ersoy, Alparslan
Can, Fatma Ezgi
Güllülü, Mustafa
Bayrakcı, İsmail
Demirayak, Dilay
Düger, Hakan
Ocak, Tuğba
Oruç, Ayşegül
Yıldız, Abdülmecit
Korkut, Bayram
Şahin, Ahmet Bilgehan
Camcı, Nihal Yücel
Vuruşkan, Berna Aytaç
AAH-4002-2021
AAM-4927-2020
GPK-6118-2022
O-9948-2015
AAH-9746-2021
AAH-5054-2021
GSE-0029-2022
GDL-7686-2022
CTG-8811-2022
ELN-3407-2022
EQO-1344-2022
FPM-3131-2022
HIG-9032-2022
FFH-4157-2022
CHG-6819-2022
55860143300
35612977100
56689608500
6602684544
57191504355
57191498699
58423722100
57191501503
55133912100
56256977500
57191504817
57188809248
57191628115
56527372000
Keywords: General & internal medicine
Primary glomerular disease
Proteinuria
Renal biopsy
Prognosis
Issue Date: 2-Sep-2016
Publisher: Carbone Editore
Citation: Ayar, Y. vd. (2016). "Primary glomerulonephritis: A single-center retrospective experience". Acta Medica Mediterranea, 32(5), 1723-1727.
Abstract: Aim: 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.
URI: http://hdl.handle.net/11452/34300
ISSN: 0393-6384
2283-9720
Appears in Collections:Scopus
Web of Science

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