Omaya Al Salkini , Mohammad Alsultan , Kassem Basha , Qussai Hassan
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Demographic and immunological characteristics were analyzed depending on the 24 h urine protein (Up) excretion that was classified into three groups: Up I (150–500 mg/day), Up II between (0.5–1 g/day), and Up III (>1 g/day).</p></div><div><h3>Results</h3><p>Up was increased subsequently as the transplant progressed, where the greatest excretion of the Up was reported 2 years after KT. At 6 months after KT; the cold ischemic time (CIT), serum creatinine (Cr), using angiotensin-converting enzyme inhibitors (ACEIs)/ angiotensin II receptor blockers (ARBs), and GFR showed strong significant differences between Up groups (<em>P</em> = 0.00003, 0.0001, 0.00001, and 0.026; respectively). The CIT and Cr were higher in the Up III group compared to Up I and UP II groups. At 12 months after KT; Cr, using ACEIs/ARBs, and GFR showed strong significant differences between Up groups (<em>P</em> = 0.00009, <0.0001, and <0.0001; respectively). The mean Cr was higher in Up II and Up III groups (1.7 mg/dL; for each) compared to the Up I group (1.0 mg/dL). At 24 months after KT; CIT, using ACEIs/ARBs, Cr, and GFR showed strong significant differences between Up groups (<em>P</em> = 0.02, <0.0001, 0.00008, and <0.0001; respectively).</p></div><div><h3>Conclusion</h3><p>This is the first study from Syria that conducted in KT patients. The prevalence and amount of proteinuria showed subsequently increased as the transplant progressed. Serum Cr, GFR, CIT, and using ACEIs/ARBs showed differences between Up groups at 6 months, 1 year, and 2 years after KT. Our data suggest that the use of ACEIs/ARBs is not a contraindication in early posttransplant period. Due to several known cardiovascular and renal benefits of ACEIs/ARBs future studied in KT population should investigated to determine if these drugs could give beneficial effects on grafts and patients survival.</p></div>","PeriodicalId":37786,"journal":{"name":"Transplantation Reports","volume":"9 3","pages":"Article 100159"},"PeriodicalIF":0.0000,"publicationDate":"2024-06-26","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.sciencedirect.com/science/article/pii/S2451959624000106/pdfft?md5=62db12851e39bc8664786b007e90254f&pid=1-s2.0-S2451959624000106-main.pdf","citationCount":"0","resultStr":"{\"title\":\"Prevalence of proteinuria after living donor kidney transplantation and related risk factors: A retrospective cohort study from Syria\",\"authors\":\"Omaya Al Salkini , Mohammad Alsultan , Kassem Basha , Qussai Hassan\",\"doi\":\"10.1016/j.tpr.2024.100159\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<div><h3>Introduction</h3><p>proteinuria is associated with poor allograft and patient survival in kidney transplant recipients (KTRs). This study aims to investigate the prevalence and risk factors of proteinuria in KTRs and its impact on kidney function during the first two years after kidney transplantation (KT).</p></div><div><h3>Materials and methods</h3><p>200 KTRs were included in this retrospective cohort study from living donors, performed in two University hospitals in Syria, from January 2018 to March 2021. Demographic and immunological characteristics were analyzed depending on the 24 h urine protein (Up) excretion that was classified into three groups: Up I (150–500 mg/day), Up II between (0.5–1 g/day), and Up III (>1 g/day).</p></div><div><h3>Results</h3><p>Up was increased subsequently as the transplant progressed, where the greatest excretion of the Up was reported 2 years after KT. At 6 months after KT; the cold ischemic time (CIT), serum creatinine (Cr), using angiotensin-converting enzyme inhibitors (ACEIs)/ angiotensin II receptor blockers (ARBs), and GFR showed strong significant differences between Up groups (<em>P</em> = 0.00003, 0.0001, 0.00001, and 0.026; respectively). The CIT and Cr were higher in the Up III group compared to Up I and UP II groups. At 12 months after KT; Cr, using ACEIs/ARBs, and GFR showed strong significant differences between Up groups (<em>P</em> = 0.00009, <0.0001, and <0.0001; respectively). The mean Cr was higher in Up II and Up III groups (1.7 mg/dL; for each) compared to the Up I group (1.0 mg/dL). At 24 months after KT; CIT, using ACEIs/ARBs, Cr, and GFR showed strong significant differences between Up groups (<em>P</em> = 0.02, <0.0001, 0.00008, and <0.0001; respectively).</p></div><div><h3>Conclusion</h3><p>This is the first study from Syria that conducted in KT patients. 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引用次数: 0
摘要
导言蛋白尿与肾移植受者(KTR)的异体移植和患者存活率低下有关。本研究旨在调查肾移植(KT)后头两年中蛋白尿在肾移植受者中的发生率、风险因素及其对肾功能的影响。材料与方法 2018年1月至2021年3月,叙利亚两所大学医院对200名活体供体肾移植受者进行了回顾性队列研究。根据 24 小时尿蛋白(Up)排泄量分析了人口统计学和免疫学特征,并将其分为三组:结果随着移植的进展,尿蛋白随之增加,KT 2 年后尿蛋白排泄量最大。KT 6 个月后,Up 组之间的冷缺血时间(CIT)、血清肌酐(Cr)、血管紧张素转换酶抑制剂(ACEIs)/血管紧张素 II 受体阻滞剂(ARBs)和肾小球滤过率显示出显著差异(P = 0.00003、0.0001、0.00001 和 0.026;分别为 0.00003、0.0001、0.00001 和 0.026)。与 Up I 组和 Up II 组相比,Up III 组的 CIT 和 Cr 更高。KT 12 个月后,Up 组之间在 Cr、使用 ACEIs/ARBs 和 GFR 方面存在显著差异(分别为 P = 0.00009、<0.0001 和 <0.0001)。与 Up I 组(1.0 mg/dL)相比,Up II 组和 Up III 组的平均 Cr 值更高(均为 1.7 mg/dL)。KT 24 个月后,使用 ACEIs/ARBs 的 CIT、Cr 和 GFR 在 Up 组之间显示出显著差异(分别为 P = 0.02、<0.0001、0.00008 和 <0.0001)。随着移植的进展,蛋白尿的发生率和数量随之增加。在 KT 术后 6 个月、1 年和 2 年,血清 Cr、GFR、CIT 和使用 ACEIs/ARBs 的情况在 Up 组之间存在差异。我们的数据表明,在移植后早期使用 ACEIs/ARBs 并非禁忌。由于已知 ACEIs/ARBs 对心血管和肾脏有多种益处,因此今后应对 KT 患者进行研究,以确定这些药物是否会对移植物和患者存活产生有益影响。
Prevalence of proteinuria after living donor kidney transplantation and related risk factors: A retrospective cohort study from Syria
Introduction
proteinuria is associated with poor allograft and patient survival in kidney transplant recipients (KTRs). This study aims to investigate the prevalence and risk factors of proteinuria in KTRs and its impact on kidney function during the first two years after kidney transplantation (KT).
Materials and methods
200 KTRs were included in this retrospective cohort study from living donors, performed in two University hospitals in Syria, from January 2018 to March 2021. Demographic and immunological characteristics were analyzed depending on the 24 h urine protein (Up) excretion that was classified into three groups: Up I (150–500 mg/day), Up II between (0.5–1 g/day), and Up III (>1 g/day).
Results
Up was increased subsequently as the transplant progressed, where the greatest excretion of the Up was reported 2 years after KT. At 6 months after KT; the cold ischemic time (CIT), serum creatinine (Cr), using angiotensin-converting enzyme inhibitors (ACEIs)/ angiotensin II receptor blockers (ARBs), and GFR showed strong significant differences between Up groups (P = 0.00003, 0.0001, 0.00001, and 0.026; respectively). The CIT and Cr were higher in the Up III group compared to Up I and UP II groups. At 12 months after KT; Cr, using ACEIs/ARBs, and GFR showed strong significant differences between Up groups (P = 0.00009, <0.0001, and <0.0001; respectively). The mean Cr was higher in Up II and Up III groups (1.7 mg/dL; for each) compared to the Up I group (1.0 mg/dL). At 24 months after KT; CIT, using ACEIs/ARBs, Cr, and GFR showed strong significant differences between Up groups (P = 0.02, <0.0001, 0.00008, and <0.0001; respectively).
Conclusion
This is the first study from Syria that conducted in KT patients. The prevalence and amount of proteinuria showed subsequently increased as the transplant progressed. Serum Cr, GFR, CIT, and using ACEIs/ARBs showed differences between Up groups at 6 months, 1 year, and 2 years after KT. Our data suggest that the use of ACEIs/ARBs is not a contraindication in early posttransplant period. Due to several known cardiovascular and renal benefits of ACEIs/ARBs future studied in KT population should investigated to determine if these drugs could give beneficial effects on grafts and patients survival.
期刊介绍:
To provide to national and regional audiences experiences unique to them or confirming of broader concepts originating in large controlled trials. All aspects of organ, tissue and cell transplantation clinically and experimentally. Transplantation Reports will provide in-depth representation of emerging preclinical, impactful and clinical experiences. -Original basic or clinical science articles that represent initial limited experiences as preliminary reports. -Clinical trials of therapies previously well documented in large trials but now tested in limited, special, ethnic or clinically unique patient populations. -Case studies that confirm prior reports but have occurred in patients displaying unique clinical characteristics such as ethnicities or rarely associated co-morbidities. Transplantation Reports offers these benefits: -Fast and fair peer review -Rapid, article-based publication -Unrivalled visibility and exposure for your research -Immediate, free and permanent access to your paper on Science Direct -Immediately citable using the article DOI