The Association between Use of Renin-Angiotensin-Aldosterone System Inhibitors and the Risk and Mortality of Pancreatic Cancer: A Systematic Review and Meta-Analysis.

IF 1.3 Q4 PHARMACOLOGY & PHARMACY
Rasoul Rahimi, Seyed Mahmoud Reza Hashemi Rafsanjani, S. Heidari-Soureshjani, Catherine Mt Sherwin, Karamali Kasiri
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引用次数: 0

Abstract

BACKGROUND Pancreatic Cancer (PC) is one of the most malignant tumors and highly invasive neoplasms around the world. OBJECTIVE This systematic review and meta-analysis aims to study the relationship between the use of renin-angiotensin-aldosterone system inhibitors and the incidence and mortality of PC. METHODS The electronic search was conducted systematically until October 10, 2023. in databases, including Scopus, Web of Science (WOS), PubMed/MEDLINE, Cochrane Library, and Embase. The required data were extracted from the articles and were analyzed by Stata 15 using statistical tests (Chi-square and I2), Forest plots, and publication bias tests (Begg's and Egger's tests). RESULTS A total of four studies (2011-2019; n=314,856) investigated the relationship between RAS antagonists and PC risk. No significant associations were found between angiotensin receptor blockers (ARBs) (OR=0.94, 95% CI: 0.77-1.14, p=0.513), angiotensin-converting enzyme inhibitors (ACEIs) (OR=0.96, 95% CI: 0.84-1.09, p=0.505), or combination therapy (ARBs + ACEIs) (OR=0.97, 95% CI: 0.87-1.09, p=0.627) and PC risk. Also, nine studies (2010-2023; n=20,483) examined the association between renin-angiotensin-aldosterone system inhibitors and PC mortality. Significant reductions in PC mortality were found for ARBs (OR=0.81, 95% CI: 0.66-0.98, p=0.032), ACEIs (OR=0.89, 95% CI: 0.80-0.99, p=0.038), and combination therapy (OR=0.83, 95% CI: 0.70-0.97, p=0.022). No evidence of publication bias was found in the study results. CONCLUSION In summary, while renin-angiotensin-aldosterone system inhibitors did not appear to impact PC risk, their use was associated with lower PC mortality based on this meta-analysis of the current evidence. More rigorous and well-designed studies are required to validate and support these findings.
使用肾素-血管紧张素-醛固酮系统抑制剂与胰腺癌风险和死亡率之间的关系:系统回顾与元分析》。
背景胰腺癌(PC)是世界上恶性程度最高的肿瘤之一,也是侵袭性很强的肿瘤。方法在 Scopus、Web of Science (WOS)、PubMed/MEDLINE、Cochrane Library 和 Embase 等数据库中系统地进行电子检索,直至 2023 年 10 月 10 日。结果共有四项研究(2011-2019 年;n=314,856)调查了 RAS 拮抗剂与 PC 风险之间的关系。结果显示,血管紧张素受体阻滞剂(ARBs)(OR=0.94,95% CI:0.77-1.14,P=0.513)、血管紧张素转换酶抑制剂(ACEIs)(OR=0.96,95% CI:0.84-1.09,P=0.505)或联合疗法(ARBs + ACEIs)(OR=0.97,95% CI:0.87-1.09,P=0.627)与 PC 风险之间均无明显关联。此外,9 项研究(2010-2023 年;n=20,483)探讨了肾素-血管紧张素-醛固酮系统抑制剂与 PC 死亡率之间的关系。研究发现,ARBs(OR=0.81,95% CI:0.66-0.98,p=0.032)、ACEIs(OR=0.89,95% CI:0.80-0.99,p=0.038)和联合疗法(OR=0.83,95% CI:0.70-0.97,p=0.022)可显著降低 PC 死亡率。结论综上所述,虽然肾素-血管紧张素-醛固酮系统抑制剂似乎不会影响 PC 风险,但根据对现有证据的荟萃分析,使用这些抑制剂与降低 PC 死亡率有关。要验证和支持这些研究结果,还需要进行更严格、设计更合理的研究。
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
4.80
自引率
9.10%
发文量
55
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