Efficacy and safety of pyruvate kinase activator in treating hemolytic anemias: a systematic review.

IF 2.3 4区 医学 Q2 HEMATOLOGY
Syed Hassan Ahmed, Laila Tul Qadar, Jawad Ahmed, Zohaib Yousaf, Afsana Ansari Shaik, Muhammad Sohaib Asghar
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引用次数: 0

Abstract

Introduction: Pyruvate kinase (PK) is an important glycolytic enzyme responsible for erythrocytic ATP production. PK allosteric activators have been shown to increase ATP and reduce 2,3-disphosphoglycerate among red blood cells leading to improved oxygen affinity, sickling, and hemolysis. In this systematic review, we aim to evaluate the efficacy and safety of PK activators in hemolytic anemias.

Methods: This study was conducted following the PRISMA guidelines. A literature search was conducted using relevant keywords over PubMed/Medline, Google Scholar, Cochrane Library, and clinicaltrial.gov, till 29 September 2024. Relevant data was extracted into a spreadsheet and synthesized qualitatively.

Results: The literature search yielded 7,153 results, with seven studies ultimately included in the review. These studies involved 206 patients, 166 of whom received mitapivat and the rest received placebo. Hemoglobin response was achieved by 38.0% to 80.0% of participants receiving mitapivat, with an average increase of 0.4 to 1.7 g/dL. Most studies reported improvements in bilirubin, lactate dehydrogenase, haptoglobin, and reticulocyte levels. Adverse events (AEs) were experienced by 93.2% of participants, with rates of 93.97% and 89.7% in the intervention and control groups, respectively. However, most AEs were mild and transient, and 23.4% were graded as 3 or higher.

Conclusions: In this study, PK activators, particularly mitapivat, demonstrated promising efficacy and safety profiles in managing hemolytic anemias. These agents significantly improved hemoglobin levels, markers of hemolysis, and hematopoietic response, offering a beneficial therapeutic option for various hemolytic conditions, including pyruvate kinase deficiency, sickle cell disease, and thalassemia.

Registration: A protocol was registered at the International Prospective Register of Systematic Reviews (PROSPERO) before study initiation, CRD42024598980.

丙酮酸激酶激活剂治疗溶血性贫血的疗效和安全性:系统综述。
丙酮酸激酶(Pyruvate kinase, PK)是一种重要的糖酵解酶,负责红细胞ATP的产生。PK变抗激活剂已被证明可以增加红细胞中的ATP并减少2,3-二磷酸甘油,从而改善氧亲和力,镰状细胞和溶血。在这篇系统综述中,我们旨在评估PK激活剂在溶血性贫血中的有效性和安全性。方法:本研究遵循PRISMA指南进行。使用相关关键词检索PubMed/Medline、谷歌Scholar、Cochrane Library和clinicaltrial.gov,检索时间截止到2024年9月29日。将相关数据提取到电子表格中进行定性合成。结果:文献检索共获得7153项结果,其中7项研究最终纳入综述。这些研究涉及206名患者,其中166名患者接受米他伐,其余患者接受安慰剂。接受米他维特治疗的参与者血红蛋白反应达到38.0%至80.0%,平均增加0.4至1.7 g/dL。大多数研究报告了胆红素、乳酸脱氢酶、触珠蛋白和网织红细胞水平的改善。不良事件(ae)发生率为93.2%,其中干预组为93.97%,对照组为89.7%。然而,大多数ae是轻微和短暂的,23.4%的ae评分为3级或更高。结论:在这项研究中,PK激活剂,特别是米他伐特,在治疗溶血性贫血方面显示出有希望的有效性和安全性。这些药物显著改善了血红蛋白水平、溶血标志物和造血反应,为各种溶血疾病提供了有益的治疗选择,包括丙酮酸激酶缺乏、镰状细胞病和地中海贫血。注册:一项方案在研究开始前在国际前瞻性系统评价登记册(PROSPERO)注册,编号为CRD42024598980。
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
CiteScore
4.70
自引率
3.60%
发文量
98
审稿时长
6-12 weeks
期刊介绍: Advanced molecular research techniques have transformed hematology in recent years. With improved understanding of hematologic diseases, we now have the opportunity to research and evaluate new biological therapies, new drugs and drug combinations, new treatment schedules and novel approaches including stem cell transplantation. We can also expect proteomics, molecular genetics and biomarker research to facilitate new diagnostic approaches and the identification of appropriate therapies. Further advances in our knowledge regarding the formation and function of blood cells and blood-forming tissues should ensue, and it will be a major challenge for hematologists to adopt these new paradigms and develop integrated strategies to define the best possible patient care. Expert Review of Hematology (1747-4086) puts these advances in context and explores how they will translate directly into clinical practice.
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