创伤性脑损伤
医学
生物标志物
胶质纤维酸性蛋白
部分各向异性
弥漫性轴索损伤
辐射冠(胚胎学)
病理
磁共振弥散成像
麻醉
炎症
治疗效果
成像生物标志物
外伤
作者
Samuel S. Shin,Kevin D. Browne,Angela N. Viaene,Garrett Keim,Daniel J. Han,Rinat Degani,Vanessa Mazandi,Sarah U. Morton,Jonathan Starr,Katie Weeks,Nicholas J. Widmann,Lucas J. Hobson,Hunter Gaudio,Tiffany S. Ko,Rodrigo M. Forti,David H. Jang,D. Kacy Cullen,Todd J. Kilbaugh,Shih-Han Kao
标识
DOI:10.1177/08977151251401236
摘要
Given the heterogeneity of traumatic brain injury (TBI), the development of a therapeutic strategy has been difficult despite decades of research. To develop an accurate classification system to guide individualized treatment, new protein biomarkers of TBI have been studied. We explored if different subtypes of TBI have unique biomarker profiles and histological findings using four pig models of TBI: moderate rotational injury (100-110 r/s), mild rotational injury (85-95 r/s), moderate contusional injury (8-9 mm), and mild contusional injury (6-7 mm). Among these groups, we identified unique profile of plasma neurofilament light (NFL) and glial fibrillary acidic protein (GFAP): whereas moderate contusion animals had early peak of NFL (2-3 days) and GFAP (1 day), mild contusion animals had delayed peak of NFL (8 days) and GFAP (3 days). Diffusion tensor imaging analysis found reduced fractional anisotropy in corona radiata for contusional injured animals but rotational injured animals showed no significant changes compared to control animals. Histological analysis showed prominent vascular inflammation and axonal injury in the pericontusional cortex in contusional injured animals. In rotational injured animals, prominent axonal injury was found in perivascular white matter. Future studies for mechanistic underpinning of biomarker changes are needed to establish therapeutic targets, predict severity of injury, and determine clinical trial enrollment and therapeutic response.
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