Key result
Adiponectin reduces myocardial infarct size and improves hemodynamics in animal models of ischemia-reperfusion injury.
Why the study?
Treatment options for myocardial ischemia-reperfusion injury are limited, and the mechanisms of adiponectin in this setting remain unclear.
Does exogenous adiponectin reduce myocardial infarct size and improve hemodynamics in preclinical animal models of myocardial ischemia-reperfusion injury?
Meta-Analysis (n=426)
Does exogenous adiponectin reduce myocardial infarct size and improve hemodynamics in preclinical animal models of myocardial ischemia-reperfusion injury?
Exogenous adiponectin provides cardioprotection against myocardial ischemia-reperfusion injury in animal models by reducing infarct size and improving hemodynamics.
Adiponectin may protect against ischemia-reperfusion injury; extends animal evidence but leaves human translation open.
BACKGROUND: Myocardial ischemia-reperfusion injury (MIRI) is widespread in the treatment of ischemic heart disease, and its treatment options are currently limited. Adiponectin (APN) is an adipocytokine with cardioprotective properties; however, the mechanisms of APN in MIRI are unclear. Therefore, based on preclinical (animal model) evidence, the cardioprotective effects of APN and the underlying mechanisms were explored. METHODS: The literature was searched for the protective effect of APN on MIRI in six databases until 16 November 2023, and data were extracted according to selection criteria. The outcomes were the size of the myocardial necrosis area and hemodynamics. Markers of oxidation, apoptosis, and inflammation were secondary outcome indicators. The quality evaluation was performed using the animal study evaluation scale recommended by the Systematic Review Center for Laboratory animal Experimentation statement. Stata/MP 14.0 software was used for the summary analysis. RESULTS: In total, 20 papers with 426 animals were included in this study. The pooled analysis revealed that APN significantly reduced myocardial infarct size [weighted mean difference (WMD) = 16.67 (95% confidence interval (CI) = 13.18 to 20.16, P < 0.001)] and improved hemodynamics compared to the MIRI group [Left ventricular end-diastolic pressure: WMD = 5.96 (95% CI = 4.23 to 7.70, P < 0.001); + dP/dtmax: WMD = 1393.59 (95% CI = 972.57 to 1814.60, P < 0.001); -dP/dtmax: WMD = 850.06 (95% CI = 541.22 to 1158.90, P < 0.001); Left ventricular ejection fraction: WMD = 9.96 (95% CI = 7.29 to 12.63, P < 0.001)]. Apoptosis indicators [caspase-3: standardized mean difference (SMD) = 3.86 (95% CI = 2.97 to 4.76, P < 0.001); TUNEL-positive cells: WMD = 13.10 (95% CI = 8.15 to 18.05, P < 0.001)], inflammatory factor levels [TNF-α: SMD = 4.23 (95% CI = 2.48 to 5.98, P < 0.001)], oxidative stress indicators [Superoxide production: SMD = 4.53 (95% CI = 2.39 to 6.67, P < 0.001)], and lactate dehydrogenase levels [SMD = 2.82 (95% CI = 1.60 to 4.04, P < 0.001)] were significantly reduced. However, the superoxide dismutase content was significantly increased [SMD = 1.91 (95% CI = 1.17 to 2.65, P < 0.001)]. CONCLUSION: APN protects against MIRI via anti-inflammatory, antiapoptotic, and antioxidant effects, and this effect is achieved by activating different signaling pathways.
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Yue et al. (2024) conducted a meta-analysis in Myocardial ischemia-reperfusion injury (n=426). Adiponectin vs. Normal saline or carrier was evaluated on Myocardial infarct size (WMD 16.67, 95% CI 13.18 to 20.16, p=<0.001). Adiponectin significantly reduced myocardial infarct size (WMD 16.67) and improved hemodynamics compared to control in animal models of myocardial ischemia-reperfusion injury.
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