Long-term Outcomes in Patients with Membranous Nephropathy: A Retrospective Cohort Study in Iran.

IF 0.8 4区 医学 Q4 UROLOGY & NEPHROLOGY
Iranian journal of kidney diseases Pub Date : 2023-09-01
Seyed Mehdi Hoseini, Neda Najafi, Mitra Mehrazma, Reihane Chegini, Mandana Rahimi, Mohsen Vahedi, Shahrzad Ossareh
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引用次数: 0

Abstract

Introduction: Membranous nephropathy (MN) has variable clinical outcomes, ranging from spontaneous remission to slow progression to kidney failure. Since the clinical outcomes of MN have not been studied in a large sample size in Iran, this study was designed to evaluate the outcome of patients diagnosed with MN at Hasheminejad Kidney Center (HKC), Tehran.

Methods: In this retrospective cohort study, 1086 patients with a diagnosis of MN who were biopsied between 1998 and 2018 in HKC were evaluated through a review of medical records for baseline clinical and laboratory characteristics at the time of biopsy and through a review of follow-up charts and phone calls for the evaluation of clinical outcomes. Of these patients, 551 could be followed for clinical outcomes. The composite outcome included kidney loss (hemodialysis, transplantation, or death). The effect of demographic, clinical, laboratory, and pathological variables on kidney survival was determined by the Cox-regression model using SPSS-16 software at a significance level of .05.

Results: Sex (P < .05), higher weight (P < .05), older age (P < .001), hypertension (P < .001), higher baseline proteinuria and lower glomerular filtration rate (GFR) at the onset of the disease were associated with kidney failure (P < .001). A higher percentage of interstitial fibrosis, tubular atrophy, global sclerosis, and a higher pathological class of membranous nephropathy were significantly associated with disease outcome in the univariate Cox-regression analysis (P < .001). Kidney survival rates at 5, 10, and 15 years were 86%, 74%, and 56%; respectively.

Conclusion: Our study suggests that baseline demographic, clinical and laboratory factors affect kidney outcomes. Patients who are considered high-risk based on the criteria listed above may need to be candidates for more aggressive therapy.  DOI: 10.52547/ijkd.7373.

膜性肾病患者的长期预后:伊朗的回顾性队列研究。
引言:膜性肾病(MN)具有多种临床结果,从自发缓解到缓慢进展再到肾衰竭。由于伊朗尚未对MN的临床结果进行大样本研究,本研究旨在评估德黑兰Hasheminejad肾脏中心(HKC)诊断为MN的患者的结果。方法:在这项回顾性队列研究中,通过审查活检时的基线临床和实验室特征的医疗记录,以及通过审查随访图表和电话评估临床结果,对1998年至2018年间在香港进行活检的1086名诊断为MN的患者进行了评估。在这些患者中,551人可以进行临床结果随访。综合结果包括肾脏损失(血液透析、移植或死亡)。使用SPSS-16软件,通过Cox回归模型确定人口统计学、临床、实验室和病理学变量对肾脏存活率的影响,显著性水平为.05,发病时较高的基线蛋白尿和较低的肾小球滤过率(GFR)与肾衰竭相关(P<0.001),在单变量Cox回归分析中,较高病理级别的膜性肾病与疾病结果显著相关(P<.001)。5年、10年和15年的肾脏存活率分别为86%、74%和56%;分别地结论:我们的研究表明,基线人口统计学、临床和实验室因素会影响肾脏预后。根据上述标准被认为是高风险的患者可能需要接受更积极的治疗。DOI:10.52547/ijkd.7373。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
Iranian journal of kidney diseases
Iranian journal of kidney diseases UROLOGY & NEPHROLOGY-
CiteScore
2.50
自引率
0.00%
发文量
43
审稿时长
6-12 weeks
期刊介绍: The Iranian Journal of Kidney Diseases (IJKD), a peer-reviewed journal in English, is the official publication of the Iranian Society of Nephrology. The aim of the IJKD is the worldwide reflection of the knowledge produced by the scientists and clinicians in nephrology. Published quarterly, the IJKD provides a new platform for advancement of the field. The journal’s objective is to serve as a focal point for debates and exchange of knowledge and experience among researchers in a global context. Original papers, case reports, and invited reviews on all aspects of the kidney diseases, hypertension, dialysis, and transplantation will be covered by the IJKD. Research on the basic science, clinical practice, and socio-economics of renal health are all welcomed by the editors of the journal.
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