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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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