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系统评价 - 酮体对哺乳动物中枢神经系统急性损伤的神经保护作用:荟萃分析。

Systematic Review - Neuroprotection of ketosis in acute injury of the mammalian central nervous system: A meta-analysis.

机构信息

Department of Cardiothoracic Surgery, Weill Cornell Medicine, New York, NY, USA.

Bristol Translational Biomedical Research Centre, University of Bristol, Bristol, UK.

出版信息

J Neurochem. 2021 Jul;158(2):105-118. doi: 10.1111/jnc.15341. Epub 2021 Apr 4.

Abstract

To evaluate the neuroprotection exerted by ketosis against acute damage of the mammalian central nervous system (CNS). Search engines were interrogated to identify experimental studies comparing the mitigating effect of ketosis (intervention) versus non-ketosis (control) on acute CNS damage. Primary endpoint was a reduction in mortality. Secondary endpoints were a reduction in neuronal damage and dysfunction, and an 'aggregated advantage' (composite of all primary and secondary endpoints). Hedges' g was the effect measure. Subgroup analyses evaluated the modulatory effect of age, insult type, and injury site. Meta-regression evaluated timing, type, and magnitude of intervention as predictors of neuroprotection. The selected publications were 49 experimental murine studies (period 1979-2020). The intervention reduced mortality (g 2.45, SE 0.48, p < .01), neuronal damage (g 1.96, SE 0.23, p < .01) and dysfunction (g 0.99, SE 0.10, p < .01). Reduction of mortality was particularly pronounced in the adult subgroup (g 2.71, SE 0.57, p < .01). The aggregated advantage of ketosis was stronger in the pediatric (g 3.98, SE 0.71, p < .01), brain (g 1.96, SE 0.18, p < .01), and ischemic insult (g 2.20, SE 0.23, p < .01) subgroups. Only the magnitude of intervention was a predictor of neuroprotection (g 0.07, SE 0.03, p 0.01 per every mmol/L increase in ketone levels). Ketosis exerts a potent neuroprotection against acute damage to the mammalian CNS in terms of reduction of mortality, of neuronal damage and dysfunction. Hematic levels of ketones are directly proportional to the effect size of neuroprotection.

摘要

评估生酮对哺乳动物中枢神经系统 (CNS) 急性损伤的神经保护作用。使用搜索引擎检索比较生酮(干预)与非生酮(对照)对急性 CNS 损伤缓解作用的实验研究。主要终点是降低死亡率。次要终点是减少神经元损伤和功能障碍,以及“综合优势”(所有主要和次要终点的综合)。Hedges' g 是效应量。亚组分析评估了年龄、损伤类型和损伤部位的调节作用。Meta 回归评估了干预的时间、类型和幅度作为神经保护的预测因子。所选出版物为 49 项实验性啮齿动物研究(1979-2020 年期间)。干预降低了死亡率(g 2.45,SE 0.48,p<.01)、神经元损伤(g 1.96,SE 0.23,p<.01)和功能障碍(g 0.99,SE 0.10,p<.01)。在成年亚组中,死亡率的降低尤为明显(g 2.71,SE 0.57,p<.01)。生酮的综合优势在儿科(g 3.98,SE 0.71,p<.01)、大脑(g 1.96,SE 0.18,p<.01)和缺血性损伤(g 2.20,SE 0.23,p<.01)亚组中更强。只有干预的幅度是神经保护的预测因子(g 0.07,SE 0.03,p 每增加每毫摩尔血酮水平 0.01)。生酮在降低死亡率、神经元损伤和功能障碍方面对哺乳动物 CNS 的急性损伤具有强大的神经保护作用。血酮水平与神经保护的效应大小成正比。

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