Anthracyclines-Induced Vascular Endothelial Dysfunction in Cancer Patients and Survivors Using Brachial Flow-Mediated Dilation (FMD) Tool: A Systematic Review and Meta-Analysis.

IF 3.4 3区 医学 Q2 CARDIAC & CARDIOVASCULAR SYSTEMS
Lana A Kattan, Sara M Abulola, Mohamed Izham Mohamed Ibrahim, Zaid H Maayah
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引用次数: 0

Abstract

Anthracyclines are effective antineoplastic drugs; however, their use is constrained by dose-dependent cardiotoxicity. Vascular endothelial dysfunction is an early independent event in cardiovascular diseases and may precede anthracycline-induced cardiotoxicity. Brachial flow-mediated dilation (FMD) is a non-invasive technique for evaluating vascular endothelial function. We evaluated the evidence on anthracycline-induced vascular endothelial dysfunction in cancer patients and survivors using FMD. Studies measuring FMD in anthracycline-treated active cancer patients or survivors were retrieved from inception to August 2024 using PubMed, Embase, and Scopus. The primary outcome was the difference in FMD between anthracycline-treated patients and healthy controls or baseline. We performed the meta-analysis using a random-effects model and evaluated the certainty in effect estimates. Overall, 18 studies (n = 841 patients) met the inclusion criteria. Compared to the baseline, a non-significant change toward a decline in FMD was observed. However, a significant reduction in FMD was observed in anthracycline-treated patients compared to healthy controls (standardized mean difference (SMD): - 0.6082; 95% CI: - 0.8963 to - 0.3201; p < 0.0001). Subgroup analyses revealed consistent significant reductions in FMD for childhood cancers (SMD: - 0.7189; 95% CI: - 0.9903 to - 0.4476; p < 0.0001), while adult cancers showed no significant difference. No significant publication bias was detected overall for healthy control comparisons. High heterogeneity was observed in the included studies (I2 = 81.7808% versus healthy controls and I2 = 75.6876% for childhood cancers subgroup analysis). Anthracyclines induce vascular endothelial dysfunction, indicated by lower FMD in cancer patients and survivors, particularly among those with childhood cancers, who might be at risk of long-term cardiovascular complications.

蒽环类药物诱导的血管内皮功能障碍在使用肱血流介导扩张(FMD)工具的癌症患者和幸存者中:一项系统综述和荟萃分析。
蒽环类药物是有效的抗肿瘤药物;然而,它们的使用受到剂量依赖性心脏毒性的限制。血管内皮功能障碍是心血管疾病的早期独立事件,可能先于蒽环类药物引起的心脏毒性。肱血流介导扩张(FMD)是一种评估血管内皮功能的无创技术。我们评估了蒽环类药物诱导的肿瘤患者和使用FMD的幸存者血管内皮功能障碍的证据。通过PubMed、Embase和Scopus检索了从开始到2024年8月,在蒽环类药物治疗的活动性癌症患者或幸存者中测量口蹄疫的研究。主要结局是蒽环类药物治疗患者与健康对照或基线之间口蹄疫的差异。我们使用随机效应模型进行了meta分析,并评估了效应估计的确定性。总的来说,18项研究(n = 841例患者)符合纳入标准。与基线相比,观察到口蹄疫下降的无显著变化。然而,与健康对照组相比,蒽环类药物治疗的患者FMD显著降低(标准化平均差(SMD): - 0.6082;95% CI: - 0.8963 ~ - 0.3201;与健康对照组相比,p 2 = 81.7808%,儿童癌症亚组分析p 2 = 75.6876%)。蒽环类药物可诱导血管内皮功能障碍,这表明癌症患者和幸存者的FMD较低,特别是儿童癌症患者,他们可能有长期心血管并发症的风险。
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
Cardiovascular Toxicology
Cardiovascular Toxicology 医学-毒理学
CiteScore
6.60
自引率
3.10%
发文量
61
审稿时长
>12 weeks
期刊介绍: Cardiovascular Toxicology is the only journal dedicated to publishing contemporary issues, timely reviews, and experimental and clinical data on toxicological aspects of cardiovascular disease. CT publishes papers that will elucidate the effects, molecular mechanisms, and signaling pathways of environmental toxicants on the cardiovascular system. Also covered are the detrimental effects of new cardiovascular drugs, and cardiovascular effects of non-cardiovascular drugs, anti-cancer chemotherapy, and gene therapy. In addition, Cardiovascular Toxicology reports safety and toxicological data on new cardiovascular and non-cardiovascular drugs.
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