Pharmacological Interventions in the Management of Alport Syndrome: A Systematic Review

Mohamed Sami, Uchechukwu Christiana Nwankwo, Ome Valentina Akpughe, M. Goshe, Riyotta T. Cutliff, Saanchia Andria Madtha, Nadiya Grynchak, N. L. Ho-Sang, Farzana Rahman, Khudija Nayab, Saeed Razaq, Henry Onyemarim, Kibrom Hailemariam Mesfin, Thitna Surafeal Berhe, Mark Majid Haddad
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Abstract

Background: Alport syndrome is a genetic disorder primarily affecting the kidney, with significant renal and extrarenal complications. Despite progress in the management of Alport syndrome, effective treatment options are limited. This systematic review aimed to synthesize current evidence regarding potential therapeutic interventions for Alport syndrome. Methods: A comprehensive literature search was conducted across databases including PubMed, Embase, and Cochrane Library. The eligibility criteria included studies involving patients with Alport syndrome undergoing interventions such as bardoxolone methyl, ramipril, or losartan. Both randomized control trials and non-randomized clinical trials were considered. Key outcomes were changes in renal function parameters and disease progression. Study selection, data extraction, and synthesis were conducted according to standard systematic review guidelines. Results: A total of 137 studies were identified initially, with four studies meeting the eligibility criteria. These studies collectively included 313 patients with a mean age range of 8.8 to 39.2 years. Three pharmacological interventions were evaluated - bardoxolone methyl, ramipril, and losartan. All demonstrated beneficial impacts on kidney function parameters. Bardoxolone methyl and ramipril showed potential in slowing disease progression, while losartan significantly lowered proteinuria. An additional finding was that the severity of the genetic variant of the disease might impact disease progression and treatment outcomes. Conclusion: The findings of this systematic review suggest that bardoxolone methyl, ramipril, and losartan may offer promising interventions for managing Alport syndrome, potentially slowing disease progression and improving kidney function. However, the need for larger, more rigorous trials is evident to substantiate these findings and to explore the impact of genetic variant severity on disease progression and treatment response. This review underscores the importance of continued research efforts in improving therapeutic strategies and personalizing treatment for patients with Alport syndrome.
治疗阿尔波特综合征的药物干预:系统回顾
背景:阿尔波特综合征是一种主要影响肾脏的遗传性疾病,具有严重的肾脏和肾外并发症。尽管在治疗阿尔波特综合征方面取得了进展,但有效的治疗方案仍然有限。本系统综述旨在综合目前有关阿尔波特综合征潜在治疗干预措施的证据。方法:在 PubMed、Embase 和 Cochrane Library 等数据库中进行了全面的文献检索。资格标准包括涉及阿尔波特综合征患者接受甲基巴多虑龙、雷米普利或洛沙坦等干预措施的研究。随机对照试验和非随机临床试验均在考虑之列。主要结果为肾功能参数变化和疾病进展。研究的选择、数据提取和综合均按照标准的系统综述指南进行。结果:最初共确定了 137 项研究,其中 4 项研究符合资格标准。这些研究共纳入了 313 名患者,平均年龄为 8.8 岁至 39.2 岁。研究评估了三种药物干预措施--甲基巴度唑酮、雷米普利和洛沙坦。所有药物都对肾功能参数产生了有益的影响。甲基巴度唑酮和雷米普利显示出延缓疾病进展的潜力,而洛沙坦则显著降低了蛋白尿。另一项发现是,该疾病遗传变异的严重程度可能会影响疾病的进展和治疗效果。结论本系统综述的研究结果表明,甲基巴多隆、雷米普利和洛沙坦可为阿尔波特综合征的治疗提供有前景的干预措施,有可能减缓疾病进展并改善肾功能。然而,显然需要更大规模、更严格的试验来证实这些发现,并探索基因变异严重程度对疾病进展和治疗反应的影响。本综述强调了继续开展研究以改进阿尔波特综合征患者的治疗策略和个性化治疗的重要性。
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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