Oct 2026· MedComm· Vol 7· 0 citations· 428 references
Medicine
TL;DR
This review systematically compares the epidemiology, shared molecular pathways, and emerging therapeutic strategies for secondary brain injury after ischemic stroke and traumatic brain injury to guide the development of more effective, personalized treatments for secondary brain injury.
Abstract
Ischemic stroke and traumatic brain injury are two leading causes of death and long‐term disability worldwide. Despite their different primary insults, both conditions trigger a complex cascade of secondary brain injury that largely determines neurological outcome. This review systematically compares the epidemiology, shared molecular pathways, and emerging therapeutic strategies for secondary brain injury after ischemic stroke and traumatic brain injury. We focus on three interconnected pathological cascades spanning blood–brain barrier disruption, neuroinflammation, and neuronal death driven by excitotoxicity, oxidative stress, and multiple forms of programmed cell death. For each pathway, we highlight convergent and divergent mechanisms between the two disorders. We then summarize emerging preclinical interventions ranging from small molecule inhibitors and repurposed drugs to nanomedicine, extracellular vesicles, and neuromodulation techniques. In parallel, we review recent and ongoing clinical trials targeting these pathways, emphasizing mechanism‐based strategies. Finally, we discuss current challenges and offer future perspectives on biomarker‐driven patient stratification, innovative drug delivery systems bypassing the blood–brain barrier, and multitarget combination regimens. By providing a unified framework that compares ischemic stroke and traumatic brain injury side by side, this review aims to guide the development of more effective, personalized treatments for secondary brain injury.
Traumatic brain injury (TBI) is among the leading causes of mortality and long-term disability worldwide, particularly in younger populations. Despite extensive research, there are currently no clinically effective neuroprotective therapies capable of fully preventing secondary neurological damage after TBI. The pathol...
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INTRODUCTION
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