PMID- 33831052 OWN - NLM STAT- MEDLINE DCOM- 20210920 LR - 20240331 IS - 1932-6203 (Electronic) IS - 1932-6203 (Linking) VI - 16 IP - 4 DP - 2021 TI - Long term outcome of immunoglobulin A (IgA) nephropathy: A single center experience. PG - e0249592 LID - 10.1371/journal.pone.0249592 [doi] LID - e0249592 AB - INTRODUCTION: IgA nephropathy (IgAN) has a heterogeneous presentation and the progression to end stage renal disease (ESRD) is often influenced by demographics, ethnicity, as well as choice of treatment regimen. In this study, we investigated the long term survival of IgAN patients in our center and the factors affecting it. METHODS: This study included all biopsy-proven IgAN patients with >/= 1year follow-up. Patients with diabetes mellitus at diagnosis and secondary IgAN were excluded. Medical records were reviewed for demographics, clinical presentation, blood pressure, 24-hour urine protein, serum creatinine, renal biopsy and treatment received. The primary outcome was defined as combined event of 50% estimated glomerular filtration rate (eGFR) reduction or ESRD. RESULTS: We included 130 (74 females; 56 males) patients of mean age 38.0 +/- 14.0 years and median eGFR of 75.2 (interquartile range (IQR) 49.3-101.4) ml/min/1.73m2. Eighty-four (64.6%) were hypertensive at presentation, 35 (26.9%) had nephrotic syndrome and 57 (43.8%) had nephrotic range proteinuria (NRP). Median follow-up duration was 7.5 (IQR 4.0-13.0) years. It was noted that 18 (13.8%) developed ESRD and 34 (26.2%) reached the primary outcome. Annual eGFR decline was -2.1 (IQR -5.3 to -0.1) ml/min/1.73m2/year, with median survival of 20 years. Survival rates from the combined event (50% decrease in eGFR or ESRD) at 10, 20 and 30 years were 80%, 53% and 25%, while survival from ESRD were 87%, 73% and 65%, respectively. In the univariate analysis, time-average proteinuria (hazard ratio (HR) = 2.41, 95% CI 1.77-3.30), eGFR <45ml/min/1.73m2 at biopsy (HR = 2.35, 95% CI 1.03-5.32), hypertension (HR = 2.81, 95% CI 1.16-6.80), mean arterial pressure (HR = 1.02, 95% CI 1.01-1.04), tubular atrophy/interstitial fibrosis score (HR = 3.77, 95% CI 1.84-7.73), and cellular/fibrocellular crescent score (HR = 2.44, 95% CI 1.19-5.00) were found to be significant. Whereas only time-average proteinuria (TA-proteinuria) remained as a significant predictor in the multivariate analysis (HR = 2.23, 95% CI 1.57-3.16). CONCLUSION: In our cohort, TA-proteinuria was the most important predictor in the progression of IgAN, irrespective of degree of proteinuria at presentation. FAU - Mohd, Rozita AU - Mohd R AD - Department of Medicine, Universiti Kebangsaan Malaysia Medical Centre, Kuala Lumpur, Malaysia. FAU - Mohammad Kazmin, Nur Ezzaty AU - Mohammad Kazmin NE AUID- ORCID: 0000-0002-9797-3735 AD - Faculty of Medicine and Health Sciences, Universiti Sains Islam Malaysia, Nilai, Negeri Sembilan, Malaysia. FAU - Abdul Cader, Rizna AU - Abdul Cader R AD - Park City Medical Centre, Kuala Lumpur, Malaysia. FAU - Abd Shukor, Nordashima AU - Abd Shukor N AD - Department of Pathology, Faculty of Medicine, Universiti Kebangsaan Malaysia, Kuala Lumpur, Malaysia. FAU - Wong, Yin Ping AU - Wong YP AUID- ORCID: 0000-0003-4897-9927 AD - Department of Pathology, Faculty of Medicine, Universiti Kebangsaan Malaysia, Kuala Lumpur, Malaysia. FAU - Shah, Shamsul Azhar AU - Shah SA AD - Department of Community Health, Faculty of Medicine, Universiti Kebangsaan Malaysia, Kuala Lumpur, Malaysia. FAU - Alfian, Nurwardah AU - Alfian N AD - Department of Pathology, Faculty of Medicine, Universiti Kebangsaan Malaysia, Kuala Lumpur, Malaysia. LA - eng PT - Clinical Trial PT - Journal Article DEP - 20210408 PL - United States TA - PLoS One JT - PloS one JID - 101285081 RN - AYI8EX34EU (Creatinine) SB - IM MH - Adult MH - Creatinine/*blood MH - Disease Progression MH - Female MH - Follow-Up Studies MH - *Glomerular Filtration Rate MH - Glomerulonephritis, IGA/blood/drug therapy/*pathology MH - Humans MH - Male MH - Prognosis MH - Retrospective Studies MH - Risk Factors MH - Survival Rate PMC - PMC8031432 COIS- The authors have declared that no competing interests exists. EDAT- 2021/04/09 06:00 MHDA- 2021/09/21 06:00 PMCR- 2021/04/08 CRDT- 2021/04/08 17:27 PHST- 2020/11/24 00:00 [received] PHST- 2021/03/22 00:00 [accepted] PHST- 2021/04/08 17:27 [entrez] PHST- 2021/04/09 06:00 [pubmed] PHST- 2021/09/21 06:00 [medline] PHST- 2021/04/08 00:00 [pmc-release] AID - PONE-D-20-36829 [pii] AID - 10.1371/journal.pone.0249592 [doi] PST - epublish SO - PLoS One. 2021 Apr 8;16(4):e0249592. doi: 10.1371/journal.pone.0249592. eCollection 2021.