钠-葡萄糖共转运蛋白2抑制剂:缺血性卒中管理的一种新兴治疗方法。

IF 7.4 2区 医学 Q1 CLINICAL NEUROLOGY
Yiwei Huang, Xinyuan Yu, Changxin Li
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引用次数: 0

摘要

钠-葡萄糖共转运蛋白2抑制剂(SGLT2i)是2型糖尿病(T2DM)和心力衰竭的基础疗法,正在成为缺血性卒中(IS)治疗的一个有前途的治疗类别。鉴于T2DM是is的重要危险因素,了解SGLT2i的潜在神经保护作用具有重要的临床意义。本综述从动物模型的基础临床前研究开始,对目前的证据进行了系统和逻辑结构的综合,这些研究一致证明了梗死面积的减少和神经系统预后的改善。然后,我们转向广泛的临床证据,主要来自大规模的现实世界观察性研究,这些证据证实了卒中风险的显著降低,特别是在高风险的T2DM人群中。对该证据基础的优势和局限性进行了严格的评估,强调了研究结果的稳健性,同时承认数据主要是观察性的,并且在主要试验中缺乏中风特异性的主要终点。SGLT2i的神经保护作用似乎是多因素的;这篇综述深入探讨了潜在的机制,强调了改善高血糖诱导的神经毒性的基础的、葡萄糖依赖的途径,这是一套多效性的、葡萄糖独立的作用的补充,包括诱导轻度酮症、神经炎症的衰减和神经血管单位的保存。最后,我们讨论了其应用的关键临床挑战,如血糖酮症酸中毒的管理,并概述了未来研究的关键方向,强调了专门的随机试验的必要性。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Sodium-Glucose Cotransporter 2 Inhibitors: An Emerging Therapeutic Approach for Ischemic Stroke Management.

Sodium-glucose cotransporter 2 inhibitors (SGLT2i), a cornerstone therapy for type 2 diabetes mellitus (T2DM) and heart failure, are emerging as a promising therapeutic class for the management of ischemic stroke (IS). Given that T2DM is a significant risk factor for IS, understanding the potential neuroprotective role of SGLT2i is of paramount clinical importance. This review provides a systematic and logically structured synthesis of the current evidence, beginning with foundational preclinical studies in animal models that consistently demonstrate a reduction in infarct volume and improved neurological outcomes. We then transition to the extensive clinical evidence, primarily from large-scale real-world observational studies, that has confirmed a significant reduction in stroke risk, particularly in high-risk T2DM populations. The strengths and limitations of this evidence base are critically appraised, highlighting the robustness of the findings while acknowledging the predominantly observational nature of the data and the lack of stroke-specific primary endpoints in major trials. The neuroprotective benefits of SGLT2i appear to be multifactorial; this review delves into the potential mechanisms, emphasizing a foundational, glucose-dependent pathway of ameliorating hyperglycemia-induced neurotoxicity, which is complemented by a suite of pleiotropic, glucose-independent effects, including the induction of mild ketosis, attenuation of neuroinflammation, and preservation of the neurovascular unit. Finally, we address the key clinical challenges to their application, such as the management of euglycemic ketoacidosis, and outline crucial directions for future research, underscoring the need for dedicated randomized trials.

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来源期刊
CNS drugs
CNS drugs 医学-精神病学
CiteScore
12.00
自引率
3.30%
发文量
82
审稿时长
6-12 weeks
期刊介绍: CNS Drugs promotes rational pharmacotherapy within the disciplines of clinical psychiatry and neurology. The Journal includes: - Overviews of contentious or emerging issues. - Comprehensive narrative reviews that provide an authoritative source of information on pharmacological approaches to managing neurological and psychiatric illnesses. - Systematic reviews that collate empirical evidence to answer a specific research question, using explicit, systematic methods as outlined by the PRISMA statement. - Adis Drug Reviews of the properties and place in therapy of both newer and established drugs in neurology and psychiatry. - Original research articles reporting the results of well-designed studies with a strong link to clinical practice, such as clinical pharmacodynamic and pharmacokinetic studies, clinical trials, meta-analyses, outcomes research, and pharmacoeconomic and pharmacoepidemiological studies. Additional digital features (including animated abstracts, video abstracts, slide decks, audio slides, instructional videos, infographics, podcasts and animations) can be published with articles; these are designed to increase the visibility, readership and educational value of the journal’s content. In addition, articles published in CNS Drugs may be accompanied by plain language summaries to assist readers who have some knowledge of, but not in-depth expertise in, the area to understand important medical advances.
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