Liu Ying, Chen Xianjun, Xiao Chuan, Yuan Jia, Li Qing, Li Lu, He Juan, Shen Feng
Department of Intensive Care Unit, the Affiliated Hospital of Guizhou Medical University, Guiyang 550004, Guizhou, China. Corresponding author: Shen Feng, Email:
Zhonghua Wei Zhong Bing Ji Jiu Yi Xue. 2024 Dec;36(12):1261-1267. doi: 10.3760/cma.j.cn121430-20231011-00862.
To systematically evaluate the impact of aspirin on the pulmonary inflammatory response in animal models of acute lung injury/acute respiratory distress syndrome (ALI/ARDS).
Experimental research on aspirin therapy or prevention of ALI/ARDS in animal models were searched in PubMed, Web of Science, Cochrane library, Embase, China biology medicine, CNKI, Wanfang, VIP. The search time limit was from the establishment of the database to July 17, 2023. The control group established the ALI/ARDS model without any pharmacological intervention. The intervention group was given aspirin or aspirin-derived compounds or polymeric-aspirin (Poly-A) at different time points before and after the preparation of the model, of which there was no restriction on the dosage form, dosage, mode of administration, or number of doses. The primary outcome indicators included bronchoalveolar lavage fluid (BALF) or lung tissue myeloperoxidase (MPO) activity, interleukin-1β (IL-1β), tumour necrosis factor-α (TNF-α) and the counts of neutrophils in BALF. Two researchers screened the literature and extracted information based on inclusion and exclusion criteria. Literature quality was assessed by the bias risk assessment tool SYRCLE. RevMan 5.3 software was used for data synthesis and statistical analysis.
A total of 17 papers were eventually included, involving a total of 449 animal models, all of which were murine. One paper was at high risk of bias and the rest 16 papers were at moderate risk of bias. Meta-analysis showed that compared with the control group, the neutrophil count in BALF [standardized mean difference (SMD) = -5.06, 95% confidence interval (95%CI) was -7.00 to -3.12, P < 0.000 01], the myeloperoxidase (MPO) activity in BALF or lung tissue (SMD = -3.45, 95%CI was -4.43 to -2.47, P < 0.000 01), the TNF-α level in BALF or lung tissue (SMD = -2.78, 95%CI was -3.58 to -1.98, P < 0.000 01), and the IL-1β level in BALF or lung tissue (SMD = -3.12, 95%CI was -4.56 to -1.69, P < 0.000 1) were significantly decreased in the ALI/ARDS model of the intervention group.
Aspirin reduces the level of lung inflammation in animal models of ALI/ARDS. However, there are problems of poor quality and significant heterogeneity of the included studies, which still need our further validation.
系统评价阿司匹林对急性肺损伤/急性呼吸窘迫综合征(ALI/ARDS)动物模型肺炎症反应的影响。
在PubMed、Web of Science、Cochrane图书馆、Embase、中国生物医学文献数据库、中国知网、万方数据库、维普数据库中检索阿司匹林治疗或预防动物模型ALI/ARDS的实验研究。检索时间范围为各数据库建库至2023年7月17日。对照组建立未进行任何药物干预的ALI/ARDS模型。干预组在模型制备前后不同时间点给予阿司匹林或阿司匹林衍生化合物或聚阿司匹林(Poly - A),对剂型、剂量、给药方式或给药次数均无限制。主要结局指标包括支气管肺泡灌洗液(BALF)或肺组织髓过氧化物酶(MPO)活性、白细胞介素 - 1β(IL - 1β)、肿瘤坏死因子 - α(TNF - α)以及BALF中中性粒细胞计数。两名研究人员根据纳入和排除标准筛选文献并提取信息。采用SYRCLE偏倚风险评估工具评估文献质量。使用RevMan 5.3软件进行数据合成和统计分析。
最终纳入17篇论文,共涉及449个动物模型,均为小鼠模型。1篇论文存在高偏倚风险,其余16篇论文存在中度偏倚风险。Meta分析结果显示,与对照组相比,干预组ALI/ARDS模型BALF中的中性粒细胞计数[标准化均数差(SMD)=-5.06,95%置信区间(95%CI)为 - 7.00至 - 3.12,P < 0.000 01]、BALF或肺组织中的髓过氧化物酶(MPO)活性(SMD = - 3.45,95%CI为 - 4.43至 - 2.47,P < 0.000 01)、BALF或肺组织中的TNF - α水平(SMD = - 2.78,95%CI为 - 3.58至 - 1.98,P < 0.000 01)以及BALF或肺组织中的IL - 1β水平(SMD = - 3.12,95%CI为 - 4.56至 - 1.69,P < 0.000 1)均显著降低。
阿司匹林可降低ALI/ARDS动物模型的肺部炎症水平。然而,纳入研究存在质量较差和显著异质性的问题,仍需进一步验证。