Traumatic microbleeds suggest vascular injury and predict disability in traumatic brain injury

被引:85
|
作者
Griffin, Allison D. [1 ,2 ]
Turtzo, L. Christine [2 ]
Parikh, Gunjan Y. [3 ,4 ]
Tolpygo, Alexander [5 ]
Lodato, Zachary [1 ,5 ]
Moses, Anita D. [1 ,2 ]
Nair, Govind [6 ]
Perl, Daniel P. [1 ,7 ]
Edwards, Nancy A. [8 ]
Dardzinski, Bernard J. [1 ,7 ]
Armstrong, Regina C. [1 ,7 ]
Ray-Chaudhury, Abhik [8 ]
Mitra, Partha P. [5 ]
Latour, Lawrence L. [1 ,2 ,6 ]
机构
[1] Ctr Neurosci & Regenerat Med, Bethesda, MD USA
[2] Natl Inst Neurol Disorders & Stroke, Acute Cerebrovasular Diagnost Unit, Bethesda, MD USA
[3] Univ Maryland, Sch Med, R Adams Cowley Shock Trauma Ctr, Program Trauma, Baltimore, MD 21201 USA
[4] Univ Maryland, Sch Med, Dept Neurol, Div Neurocrit Care & Emergency Neurol, Baltimore, MD 21201 USA
[5] Cold Spring Harbor Lab, Cold Spring Harbor, NY 11724 USA
[6] Natl Inst Neurol Disorders & Stroke, Bethesda, MD USA
[7] Uniformed Serv Univ Hlth Sci, Bethesda, MD 20814 USA
[8] Natl Inst Neurol Disorders & Stroke, Surg Neurol Branch, Bethesda, MD USA
关键词
radiological-pathological analysis; MRI biomarkers of traumatic brain injury; traumatic vascular injury; traumatic microbleeds; mild traumatic brain injury; DIFFUSE AXONAL INJURY; LONG-TERM DISABILITY; CEREBRAL MICROBLEEDS; UNITED-STATES; HEAD-INJURY; LESIONS; MICROHEMORRHAGES; CHILDREN; RECOVERY; DISEASE;
D O I
10.1093/brain/awz290
中图分类号
R74 [神经病学与精神病学];
学科分类号
摘要
Traumatic microbleeds are small foci of hypointensity seen on T-2*-weighted MRI in patients following head trauma that have previously been considered a marker of axonal injury. The linear appearance and location of some traumatic microbleeds suggests a vascular origin. The aims of this study were to: (i) identify and characterize traumatic microbleeds in patients with acute traumatic brain injury; (ii) determine whether appearance of traumatic microbleeds predict clinical outcome; and (iii) describe the pathology underlying traumatic microbleeds in an index patient. Patients presenting to the emergency department following acute head trauma who received a head CT were enrolled within 48 h of injury and received a research MRI. Disability was defined using Glasgow Outcome Scale-Extended <= 6 at follow-up. All magnetic resonance images were interpreted prospectively and were used for subsequent analysis of traumatic microbleeds. Lesions on T-2* MRI were stratified based on 'linear' streak-like or 'punctate' petechial-appearing traumatic microbleeds. The brain of an enrolled subject imaged acutely was procured following death for evaluation of traumatic microbleeds using MRI targeted pathology methods. Of the 439 patients enrolled over 78 months, 31% (134/439) had evidence of punctate and/or linear traumatic microbleeds on MRI. Severity of injury, mechanism of injury, and CT findings were associated with traumatic microbleeds on MRI. The presence of traumatic microbleeds was an independent predictor of disability (P < 0.05; odds ratio = 2.5). No differences were found between patients with punctate versus linear appearing microbleeds. Post-mortem imaging and histology revealed traumatic microbleed co-localization with iron-laden macrophages, predominately seen in perivascular space. Evidence of axonal injury was not observed in co-localized histopathological sections. Traumatic microbleeds were prevalent in the population studied and predictive of worse outcome. The source of traumatic microbleed signal on MRI appeared to be iron-laden macrophages in the perivascular space tracking a network of injured vessels. While axonal injury in association with traumatic microbleeds cannot be excluded, recognizing traumatic microbleeds as a form of traumatic vascular injury may aid in identifying patients who could benefit from new therapies targeting the injured vasculature and secondary injury to parenchyma.
引用
收藏
页码:3550 / 3564
页数:15
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