Prevalence of Cerebral Microhemorrhage following Chronic Blast-Related Mild Traumatic Brain Injury in Military Service Members Using Susceptibility-Weighted MRI ================================================================================================================================================================ * E. Lotan * C. Morley * J. Newman * M. Qian * D. Abu-Amara * C. Marmar * Y.W. Lui ## Abstract **BACKGROUND AND PURPOSE:** Cerebral microhemorrhages are a known marker of mild traumatic brain injury. Blast-related mild traumatic brain injury relates to a propagating pressure wave, and there is evidence that the mechanism of injury in blast-related mild traumatic brain injury may be different from that in blunt head trauma. Two recent reports in mixed cohorts of blunt and blast-related traumatic brain injury in military personnel suggest that the prevalence of cerebral microhemorrhages is lower than in civilian head injury. In this study, we aimed to characterize the prevalence of cerebral microhemorrhages in military service members specifically with chronic blast-related mild traumatic brain injury. **MATERIALS AND METHODS:** Participants were prospectively recruited and underwent 3T MR imaging. Susceptibility-weighted images were assessed by 2 neuroradiologists independently for the presence of cerebral microhemorrhages. **RESULTS:** Our cohort included 146 veterans (132 men) who experienced remote blast-related mild traumatic brain injury (mean, 9.4 years; median, 9 years after injury). Twenty-one (14.4%) reported loss of consciousness for <30 minutes. Seventy-seven subjects (52.7%) had 1 episode of blast-related mild traumatic brain injury; 41 (28.1%) had 2 episodes; and 28 (19.2%) had >2 episodes. No cerebral microhemorrhages were identified in any subject, as opposed to the frequency of SWI-detectable cerebral microhemorrhages following blunt-related mild traumatic brain injury in the civilian population, which has been reported to be as high as 28% in the acute and subacute stages. **CONCLUSIONS:** Our results may reflect differences in pathophysiology and the mechanism of injury between blast- and blunt-related mild traumatic brain injury. Additionally, the chronicity of injury may play a role in the detection of cerebral microhemorrhages. ## ABBREVIATIONS: CMH : cerebral microhemorrhages CTE : chronic traumatic encephalopathy mTBI : mild traumatic brain injury TBI : traumatic brain injury Blast-related traumatic brain injury (TBI) is of considerable interest in the study of military head trauma due to ongoing United States military deployments in the Middle East and the frequency of exposure to improvised explosive devices.1,2 Ten-to-twenty percent of veterans returning from Iraq and Afghanistan are estimated to have had TBI with blast exposure, with >75% of these classified as mild traumatic brain injury (mTBI) by the American Congress of Rehabilitative Medicine criteria.2⇓–4 Blast-related TBI results from blast wave–induced changes in atmospheric pressure.5 It is clear from several recent studies that blast-related mTBI is associated with remarkable clinical impact,6 and chronic traumatic encephalopathy (CTE) has been described on postmortem examinations in individuals with exposure to repeat episodes.7 How a pressure wave damages the brain is the subject of debate dating back to the post-World War II period.8⇓–10 A few recent reports using in vivo diffusion MR imaging showed a reduction in white matter fractional anisotropy in patients with blast-related mTBI11⇓⇓⇓–15 in a pattern that may be distinct from civilian blunt-related mTBI.16 It has been suggested that blast-related mTBI represents a unique injury mechanism distinct from blunt head trauma.9,17,18 There is current interest in specifically characterizing patients who have experienced blast-related mTBI and in determining whether there are unique features of this type of injury. Cerebral microhemorrhage is a clear imaging biomarker associated with mTBI seen distinctly on conventional MR imaging using susceptibility-weighted imaging.19,20 Studies in civilians following acute and subacute blunt mTBI have reported that the frequency of SWI-detected cerebral microhemorrhages (CMH) ranged from 19% to 28%.21⇓⇓–24 A few recent works have suggested a lower prevalence in military personnel with chronic mTBI compared with civilians,3,25,26 though these studies were of mixed cohorts, including both blast- and blunt-related TBI and a range of injury severity.3,25 Riedy et al3 and Liu et al25 found an approximately 3%–4% prevalence of CMH in subjects with a mixed history of blast- and blunt-related mTBI. The true prevalence of CMH in blast-related mTBI is not known. The purpose of the current study was to characterize CMH in military service members with chronic blast-related mTBI. ## Materials and Methods ### Participants and Measures Subjects in this study were drawn from an ongoing prospective study of military veterans performed at the NYU Langone Medical Center. The study was approved by the local institutional review board. All participants provided written informed consent. Inclusion criteria for this study were the following: military service in Operation Enduring Freedom, Operation Iraqi Freedom, and/or Operation New Dawn; between 18 and 70 years; and clinical diagnosis of mTBI in conjunction with close proximity to a blast explosion without concomitant blunt traumatic head injury based on the Department of Veterans Affairs and the Department of Defense definition of mTBI27 (including altered mental state for <24 hours and no or <30 minutes loss of consciousness) as elicited by the Ohio State University TBI Identification Method–Short Form.28 Subjects were excluded with a history of comorbid major neurologic disorder or systemic illness, a history of severe drug use disorder, psychosis, suicidality, homicidality, a history of prior moderate or severe head injury, or contraindications to MR imaging. All participants completed a formal, self-report measure of postconcussion symptoms. Symptom severity and quantity were measured using the Concussion Symptom Inventory, a list of 12 symptoms that are graded in severity by the patient on a 7-point Likert scale.29 The maximum Concussion Symptom Inventory score is 72, indicating maximum overall symptom severity. Additionally, to assess the impact of headache, we used the Headache Impact Test-6 score.30 This score ranges between 36 and 78, with larger scores reflecting greater impact and a score of >50 considered an abnormal finding. All participants were administered the 2-factor model from the Wechsler Adult Intelligence Scale, 2nd ed,31 which uses vocabulary and matrix reasoning subtests to estimate intelligence quotient. ### MR Imaging Participants were imaged at 3T (Skyra; Siemens, Erlangen, Germany) using a 20-channel head coil. SWI was performed with the following parameters: TR = 29 ms, TE = 20 ms, flip angle = 15°, slice thickness = 2 mm, intersection gap = 0 mm, FOV = 158 × 220 mm, matrix = 261 × 448, generalized autocalibrating partially parallel acquisition factor = 2. Conventional MR imaging, including T1-weighted imaging, T2-weighted imaging, T2-weighted FLAIR imaging, and diffusion-weighted imaging, was also performed. SWI and conventional MR imaging sequences were reviewed independently by 2 neuroradiologists (1 second-year neuroradiology fellow [E.L] and 1 attending neuroradiologist with >10 years of experience [Y.W.L]). Susceptibility-weighted images were reviewed for quality in terms of susceptibility seen in expected locations such as venous structures and calcification of the choroid plexus, or for the presence of any artifacts. The presence of CMH was determined using the Greenberg criteria, including a round or ovoid signal at least half surrounded by brain parenchyma with a dipole effect on SWI phase imaging and distinct from other potential mimics (calcium deposits, bone, air, or vessel flow voids).32,33 ## Results One-hundred forty-six subjects were identified with a history of blast-related mTBI (132 men, 14 women). Demographic and clinical data for the present sample are reported in Tables 1 and 2. The mean age was 32.8 ± 7.4 years (median, 31 years; range, 22–66 years). The time interval from the last injury to MR imaging ranged from 1 to 31 years (mean, 9.4 ± 6.2 years; median, 9 years). Sixty-nine subjects (47.3%) had ≥2 episodes. Twenty-one (14.4%) reported loss of consciousness with their injury of <30 minutes, and 85.6% had altered mental status. Subjects had a normal distribution of IQ and demonstrated mild headache pain and postconcussive symptoms (Tables 1 and 2). No CMH were detected by either neuroradiologist. One subject (1%) had cerebellar ectopia, 7 (5%) had developmental venous anomalies, 48 (33%) had some degree of white matter abnormality (ie, T2 hyperintensity), 3 (2%) had arachnoid cysts, and 54 (37%) had sinus disease. No other structural abnormalities were identified. No images demonstrated artifacts warranting exclusion. View this table: [Table 1:](http://www.ajnr.org/content/39/7/1222/T1) Table 1: Demographic and clinical characteristics (*N* = 146) View this table: [Table 2:](http://www.ajnr.org/content/39/7/1222/T2) Table 2: Demographic and clinical characteristics (*N* = 146)a ## Discussion In this cohort of 146 veterans with exposure to chronic blast-related mTBI, with approximately half exposed to multiple blast episodes in multiple tours during 5 years of deployment time, no foci of CMH were detected at 3T MR imaging using SWI. The overall prevalence of CMH in our cohort of well-characterized subjects with a history of chronic military blast-related mTBI was low compared with previous reports of civilian blunt-related mTBI.21⇓⇓–24,34⇓–36 There is a mix of literature and findings in terms of the mechanism of injury (blunt or mixed population of blunt- and blast-related mTBI), prevalence of CMH, variable cohorts (military or civilian), variable time since injury, and the MR imaging techniques used for CMH detection. The literature is summarized in Table 3.3,21⇓⇓⇓⇓–26,34⇓–36 Our findings are in keeping with Liu et al25 and Riedy et al,3 who reported 3%–4% prevalence of CMH in a mixed group of military service members with a chronic history of either blunt- or blast-related mTBI. Technical differences between the current study and prior studies do not account for differences in CMH prevalence. The acquisition and protocol used in the current study are comparable with those in multiple other recent studies (Table 3). View this table: [Table 3:](http://www.ajnr.org/content/39/7/1222/T3) Table 3: Prevalence of CMH in civilian and military populations The undetectable prevalence of CMH in the current cohort of 146 subjects with blast-related mTBI supports the evolving notion that blast-related mTBI has not only a unique mechanism of injury but also a unique pathophysiology that may be distinct from blunt trauma–induced mTBI.9,17,18 In addition, despite the long-standing idea that brain hemosiderin remains in clusters of iron-laden macrophages in perivascular spaces for the long term,37⇓–39 there may be variability in the detection of CMH relating to the evolution of blood products, particularly in the acute and subacute phases after injury.40 The sensitivity for CMH may diminish with time as has been suggested by Liu et al.25 Furthermore, in an 8-year longitudinal study of nontraumatic CMH using SWI, the hemorrhages persisted across time, with a slight decrease in volume.41 Nevertheless, 2 recently published studies on civilian patients with chronic blunt-related mTBI demonstrated a CMH prevalence of 8%–17%.34,35 This suggests that while CMH may evolve between the acute and chronic phases after injury, the prevalence of chronic blast-related mTBI CMH that we report here remains lower than in previous reports of blunt-related injury. Limitations of this study include a retrospective self-report of injury, though a prospective study including acutely injured subjects is challenging due to the limitations of MR imaging availability in remote military sites. Furthermore, the Ohio State University TBI Identification Method is considered a reliable and valid tool for assessing TBI and was selected on the basis of its high interrater reliability.28 An additional limitation is the variability of the time since injury compared with the previous studies, particularly because there is evidence that CMH may evolve. ## Conclusions We found that no individuals in the 146 subjects with chronic blast-related mTBI had evidence of CMH on 3T SWI. This finding may suggest a substantially lower prevalence of CMH in this cohort of subjects with blast-related mTBI compared with previous reports, primarily in civilian chronic blunt-related mTBI,34,35 and may reflect differences in the mechanism and pathophysiology of injury. However, due to possible degradation of CMH with time, the chronicity of injury may play a role in the detection of CMH, and future studies will be needed to assess the prevalence of CMH in the more acute settings. ## Footnotes * Disclosures: The project described was made possible with support by grants from the Steven A. and Alexandra M. Cohen Foundation, Inc. and Cohen Veterans Bioscience, Inc. (CVB) to NYU School of Medicine. The content is solely the responsibility of the authors and does not necessarily represent the official views of the Foundation or CVB. * Eyal Lotan is a recipient of Fellowship Grants from the American Physicians Fellowship for Medicine in Israel and from the Dr. Pinchas Borenstein Talpiot Medical Leadership Program 2013. * Main findings previously presented at: Annual Meeting of the American Society of Neuroradiology and the Foundation of the ASNR Symposium, April 20–27, 2017; Long Beach, California. ## References 1. 1. Shively SB, Perl DP. Traumatic brain injury, shell shock, and posttraumatic stress disorder in the military: past, present, and future. J Head Trauma Rehabil 2012;27:234–39 doi:10.1097/HTR.0b013e318250e9dd pmid:22573042 [CrossRef](http://www.ajnr.org/lookup/external-ref?access_num=10.1097/HTR.0b013e318250e9dd&link_type=DOI) [PubMed](http://www.ajnr.org/lookup/external-ref?access_num=22573042&link_type=MED&atom=%2Fajnr%2F39%2F7%2F1222.atom) 2. 2. Hoge CW, McGurk D, Thomas JL, et al. Mild traumatic brain injury in U.S. soldiers returning from Iraq. N Engl J Med 2008;358:453–63 doi:10.1056/NEJMoa072972 pmid:18234750 [CrossRef](http://www.ajnr.org/lookup/external-ref?access_num=10.1056/NEJMoa072972&link_type=DOI) [PubMed](http://www.ajnr.org/lookup/external-ref?access_num=18234750&link_type=MED&atom=%2Fajnr%2F39%2F7%2F1222.atom) [Web of Science](http://www.ajnr.org/lookup/external-ref?access_num=000252722900003&link_type=ISI) 3. 3. Riedy G, Senseney JS, Liu W, et al. Findings from structural MR imaging in military traumatic brain injury. Radiology 2016;279:207–15 doi:10.1148/radiol.2015150438 pmid:26669604 [CrossRef](http://www.ajnr.org/lookup/external-ref?access_num=10.1148/radiol.2015150438&link_type=DOI) [PubMed](http://www.ajnr.org/lookup/external-ref?access_num=26669604&link_type=MED&atom=%2Fajnr%2F39%2F7%2F1222.atom) 4. 4. Kay T, Harrington DE, Adams R, et al. Definition of mild traumatic brain injury. J Head Trauma Rehabil 1993;8:86–87 doi:10.1097/00001199-199309000-00010 [CrossRef](http://www.ajnr.org/lookup/external-ref?access_num=10.1097/00001199-199309000-00010&link_type=DOI) 5. 5. DePalma RG, Burris DG, Champion HR, et al. Blast injuries. N Engl J Med 2005;352:1335–42 doi:10.1056/NEJMra042083 pmid:15800229 [CrossRef](http://www.ajnr.org/lookup/external-ref?access_num=10.1056/NEJMra042083&link_type=DOI) [PubMed](http://www.ajnr.org/lookup/external-ref?access_num=15800229&link_type=MED&atom=%2Fajnr%2F39%2F7%2F1222.atom) [Web of Science](http://www.ajnr.org/lookup/external-ref?access_num=000227998300010&link_type=ISI) 6. 6. Mac Donald CL, Barber J, Jordan M, et al. Early clinical predictors of 5-year outcome after concussive blast traumatic brain injury. JAMA Neurol 2017;74:821–29 doi:10.1001/jamaneurol.2017.0143 pmid:28459953 [CrossRef](http://www.ajnr.org/lookup/external-ref?access_num=10.1001/jamaneurol.2017.0143&link_type=DOI) [PubMed](http://www.ajnr.org/lookup/external-ref?access_num=28459953&link_type=MED&atom=%2Fajnr%2F39%2F7%2F1222.atom) 7. 7. Mayer AR, Quinn DK, Master CL. The spectrum of mild traumatic brain injury: a review. Neurology 2017;89:623–32 doi:10.1212/WNL.0000000000004214 pmid:28701496 [Abstract/FREE Full Text](http://www.ajnr.org/lookup/ijlink/YTozOntzOjQ6InBhdGgiO3M6MTQ6Ii9sb29rdXAvaWpsaW5rIjtzOjU6InF1ZXJ5IjthOjQ6e3M6ODoibGlua1R5cGUiO3M6NDoiQUJTVCI7czoxMToiam91cm5hbENvZGUiO3M6OToibmV1cm9sb2d5IjtzOjU6InJlc2lkIjtzOjg6Ijg5LzYvNjIzIjtzOjQ6ImF0b20iO3M6MjA6Ii9ham5yLzM5LzcvMTIyMi5hdG9tIjt9czo4OiJmcmFnbWVudCI7czowOiIiO30=) 8. 8. Denny-Brown D. Cerebral concussion. Physiol Rev 1945;25:296–325 doi:10.1152/physrev.1945.25.2.296 [CrossRef](http://www.ajnr.org/lookup/external-ref?access_num=10.1152/physrev.1945.25.2.296&link_type=DOI) [Web of Science](http://www.ajnr.org/lookup/external-ref?access_num=A1945UM45800004&link_type=ISI) 9. 9. Elder GA, Stone JR, Ahlers ST. Effects of low-level blast exposure on the nervous system: is there really a controversy? Front Neurol 2014;5:269 doi:10.3389/fneur.2014.00269 pmid:25566175 [CrossRef](http://www.ajnr.org/lookup/external-ref?access_num=10.3389/fneur.2014.00269&link_type=DOI) [PubMed](http://www.ajnr.org/lookup/external-ref?access_num=25566175&link_type=MED&atom=%2Fajnr%2F39%2F7%2F1222.atom) 10. 10. Courtney A, Courtney M. The complexity of biomechanics causing primary blast-induced traumatic brain injury: a review of potential mechanisms. Front Neurol 2015;6:221 doi:10.3389/fneur.2015.00221 pmid:26539158 [CrossRef](http://www.ajnr.org/lookup/external-ref?access_num=10.3389/fneur.2015.00221&link_type=DOI) [PubMed](http://www.ajnr.org/lookup/external-ref?access_num=26539158&link_type=MED&atom=%2Fajnr%2F39%2F7%2F1222.atom) 11. 11. Ivanov I, Fernandez C, Mitsis EM, et al. Blast exposure, white matter integrity, and cognitive function in Iraq and Afghanistan combat veterans. Front Neurol 2017;8:127 doi:10.3389/fneur.2017.00127 pmid:28484418 [CrossRef](http://www.ajnr.org/lookup/external-ref?access_num=10.3389/fneur.2017.00127&link_type=DOI) [PubMed](http://www.ajnr.org/lookup/external-ref?access_num=28484418&link_type=MED&atom=%2Fajnr%2F39%2F7%2F1222.atom) 12. 12. Mac Donald CL, Barber J, Andre J, et al. 5-Year imaging sequelae of concussive blast injury and relation to early clinical outcome. Neuroimage Clin 2017;14:371–78 doi:10.1016/j.nicl.2017.02.005 pmid:28243574 [CrossRef](http://www.ajnr.org/lookup/external-ref?access_num=10.1016/j.nicl.2017.02.005&link_type=DOI) [PubMed](http://www.ajnr.org/lookup/external-ref?access_num=28243574&link_type=MED&atom=%2Fajnr%2F39%2F7%2F1222.atom) 13. 13. Trotter BB, Robinson ME, Milberg WP, et al. Military blast exposure, ageing and white matter integrity. Brain 2015;138:2278–92 doi:10.1093/brain/awv139 pmid:26033970 [CrossRef](http://www.ajnr.org/lookup/external-ref?access_num=10.1093/brain/awv139&link_type=DOI) [PubMed](http://www.ajnr.org/lookup/external-ref?access_num=26033970&link_type=MED&atom=%2Fajnr%2F39%2F7%2F1222.atom) 14. 14. Mac Donald CL, Johnson AM, Cooper D, et al. Detection of blast-related traumatic brain injury in U.S. military personnel. N Engl J Med 2011;364:2091–100 doi:10.1056/NEJMoa1008069 pmid:21631321 [CrossRef](http://www.ajnr.org/lookup/external-ref?access_num=10.1056/NEJMoa1008069&link_type=DOI) [PubMed](http://www.ajnr.org/lookup/external-ref?access_num=21631321&link_type=MED&atom=%2Fajnr%2F39%2F7%2F1222.atom) [Web of Science](http://www.ajnr.org/lookup/external-ref?access_num=000291200700007&link_type=ISI) 15. 15. Taber KH, Hurley RA, Haswell CC, et al. White matter compromise in veterans exposed to primary blast forces. J Head Trauma Rehabil 2015;30:E15–25 doi:10.1097/HTR.0000000000000030 pmid:24590156 [CrossRef](http://www.ajnr.org/lookup/external-ref?access_num=10.1097/HTR.0000000000000030&link_type=DOI) [PubMed](http://www.ajnr.org/lookup/external-ref?access_num=24590156&link_type=MED&atom=%2Fajnr%2F39%2F7%2F1222.atom) 16. 16. Davenport ND, Lim KO, Armstrong MT, et al. Diffuse and spatially variable white matter disruptions are associated with blast-related mild traumatic brain injury. Neuroimage 2012;59:2017–24 doi:10.1016/j.neuroimage.2011.10.050 pmid:22040736 [CrossRef](http://www.ajnr.org/lookup/external-ref?access_num=10.1016/j.neuroimage.2011.10.050&link_type=DOI) [PubMed](http://www.ajnr.org/lookup/external-ref?access_num=22040736&link_type=MED&atom=%2Fajnr%2F39%2F7%2F1222.atom) [Web of Science](http://www.ajnr.org/lookup/external-ref?access_num=000299494000005&link_type=ISI) 17. 17. Bhattacharjee Y. Neuroscience: shell shock revisited—solving the puzzle of blast trauma. Science 2008;319:406–08 doi:10.1126/science.319.5862.406 pmid:18218877 [Abstract/FREE Full Text](http://www.ajnr.org/lookup/ijlink/YTozOntzOjQ6InBhdGgiO3M6MTQ6Ii9sb29rdXAvaWpsaW5rIjtzOjU6InF1ZXJ5IjthOjQ6e3M6ODoibGlua1R5cGUiO3M6NDoiQUJTVCI7czoxMToiam91cm5hbENvZGUiO3M6Mzoic2NpIjtzOjU6InJlc2lkIjtzOjEyOiIzMTkvNTg2Mi80MDYiO3M6NDoiYXRvbSI7czoyMDoiL2FqbnIvMzkvNy8xMjIyLmF0b20iO31zOjg6ImZyYWdtZW50IjtzOjA6IiI7fQ==) 18. 18. Fischer B, Parsons M, Durgerian S, et al. Neural activation during response inhibition differentiates blast from mechanical causes of mild to moderate traumatic brain injury. J Neurotrauma 2014;31:169–79 doi:10.1089/neu.2013.2877 pmid:24020449 [CrossRef](http://www.ajnr.org/lookup/external-ref?access_num=10.1089/neu.2013.2877&link_type=DOI) [PubMed](http://www.ajnr.org/lookup/external-ref?access_num=24020449&link_type=MED&atom=%2Fajnr%2F39%2F7%2F1222.atom) [Web of Science](http://www.ajnr.org/lookup/external-ref?access_num=000329870600003&link_type=ISI) 19. 19. Haacke EM, Mittal S, Wu Z, et al. Susceptibility-weighted imaging: technical aspects and clinical applications, part 1. AJNR Am J Neuroradiol 2009;30:19–30 doi:10.3174/ajnr.A1400 pmid:19039041 [Abstract/FREE Full Text](http://www.ajnr.org/lookup/ijlink/YTozOntzOjQ6InBhdGgiO3M6MTQ6Ii9sb29rdXAvaWpsaW5rIjtzOjU6InF1ZXJ5IjthOjQ6e3M6ODoibGlua1R5cGUiO3M6NDoiQUJTVCI7czoxMToiam91cm5hbENvZGUiO3M6NDoiYWpuciI7czo1OiJyZXNpZCI7czo3OiIzMC8xLzE5IjtzOjQ6ImF0b20iO3M6MjA6Ii9ham5yLzM5LzcvMTIyMi5hdG9tIjt9czo4OiJmcmFnbWVudCI7czowOiIiO30=) 20. 20. Bigler ED, Maxwell WL. Neuropathology of mild traumatic brain injury: relationship to neuroimaging findings. Brain Imaging Behav 2012;6:108–36 doi:10.1007/s11682-011-9145-0 pmid:22434552 [CrossRef](http://www.ajnr.org/lookup/external-ref?access_num=10.1007/s11682-011-9145-0&link_type=DOI) [PubMed](http://www.ajnr.org/lookup/external-ref?access_num=22434552&link_type=MED&atom=%2Fajnr%2F39%2F7%2F1222.atom) [Web of Science](http://www.ajnr.org/lookup/external-ref?access_num=000305908900002&link_type=ISI) 21. 21. Yuh EL, Mukherjee P, Lingsma HF, et al; TRACK-TBI Investigators. Magnetic resonance imaging improves 3-month outcome prediction in mild traumatic brain injury. Ann Neurol 2013;73:224–35 doi:10.1002/ana.23783 pmid:23224915 [CrossRef](http://www.ajnr.org/lookup/external-ref?access_num=10.1002/ana.23783&link_type=DOI) [PubMed](http://www.ajnr.org/lookup/external-ref?access_num=23224915&link_type=MED&atom=%2Fajnr%2F39%2F7%2F1222.atom) 22. 22. Huang YL, Kuo YS, Tseng YC, et al. Susceptibility-weighted MRI in mild traumatic brain injury. Neurology 2015;84:580–85 doi:10.1212/WNL.0000000000001237 pmid:25576634 [CrossRef](http://www.ajnr.org/lookup/external-ref?access_num=10.1212/WNL.0000000000001237&link_type=DOI) [PubMed](http://www.ajnr.org/lookup/external-ref?access_num=25576634&link_type=MED&atom=%2Fajnr%2F39%2F7%2F1222.atom) 23. 23. Wang X, Wei XE, Li MH, et al. Microbleeds on susceptibility-weighted MRI in depressive and non-depressive patients after mild traumatic brain injury. Neurol Sci 2014;35:1533–39 doi:10.1007/s10072-014-1788-3 pmid:24740482 [CrossRef](http://www.ajnr.org/lookup/external-ref?access_num=10.1007/s10072-014-1788-3&link_type=DOI) [PubMed](http://www.ajnr.org/lookup/external-ref?access_num=24740482&link_type=MED&atom=%2Fajnr%2F39%2F7%2F1222.atom) 24. 24. van der Horn HJ, de Haan S, Spikman JM, et al. Clinical relevance of microhemorrhagic lesions in subacute mild traumatic brain injury. Brain Imaging Behav 2017 Jun 29. [Epub ahead of print] doi:10.1007/s11682-017-9743-6 pmid:28664231 [CrossRef](http://www.ajnr.org/lookup/external-ref?access_num=10.1007/s11682-017-9743-6&link_type=DOI) [PubMed](http://www.ajnr.org/lookup/external-ref?access_num=28664231&link_type=MED&atom=%2Fajnr%2F39%2F7%2F1222.atom) 25. 25. Liu W, Soderlund K, Senseney JS, et al. Imaging cerebral microhemorrhages in military service members with chronic traumatic brain injury. Radiology 2016;278:536–55 doi:10.1148/radiol.2015150160 pmid:26371749 [CrossRef](http://www.ajnr.org/lookup/external-ref?access_num=10.1148/radiol.2015150160&link_type=DOI) [PubMed](http://www.ajnr.org/lookup/external-ref?access_num=26371749&link_type=MED&atom=%2Fajnr%2F39%2F7%2F1222.atom) 26. 26. Tate DF, Gusman M, Kini J, et al. Susceptibility weighted imaging and white matter abnormality findings in service members with persistent cognitive symptoms following mild traumatic brain injury. Mil Med 2017;182:e1651–58 doi:10.7205/MILMED-D-16-00132 pmid:28290939 [CrossRef](http://www.ajnr.org/lookup/external-ref?access_num=10.7205/MILMED-D-16-00132&link_type=DOI) [PubMed](http://www.ajnr.org/lookup/external-ref?access_num=28290939&link_type=MED&atom=%2Fajnr%2F39%2F7%2F1222.atom) 27. 27. O'Neil ME, Carlson K, Storzbach D, et al. Complications of mild traumatic brain injury in veterans and military personnel: a systematic review [Internet]. Washington, DC: Department of Veterans Affairs; 2013 28. 28. Corrigan JD, Bogner J. Initial reliability and validity of the Ohio State University TBI Identification Method. J Head Trauma Rehabil 2007;22:318–29 doi:10.1097/01.HTR.0000300227.67748.77 pmid:18025964 [CrossRef](http://www.ajnr.org/lookup/external-ref?access_num=10.1097/01.HTR.0000300227.67748.77&link_type=DOI) [PubMed](http://www.ajnr.org/lookup/external-ref?access_num=18025964&link_type=MED&atom=%2Fajnr%2F39%2F7%2F1222.atom) [Web of Science](http://www.ajnr.org/lookup/external-ref?access_num=000251181500002&link_type=ISI) 29. 29. Randolph C, Millis S, Barr WB, et al. Concussion Symptom Inventory: an empirically-derived scale for monitoring resolution of symptoms following sports-related concussion. Arch Clin Neuropsychol 2009;24:219–29 doi:10.1093/arclin/acp025 pmid:19549721 [CrossRef](http://www.ajnr.org/lookup/external-ref?access_num=10.1093/arclin/acp025&link_type=DOI) [PubMed](http://www.ajnr.org/lookup/external-ref?access_num=19549721&link_type=MED&atom=%2Fajnr%2F39%2F7%2F1222.atom) [Web of Science](http://www.ajnr.org/lookup/external-ref?access_num=000269001900003&link_type=ISI) 30. 30. Kosinski M, Bayliss MS, Bjorner JB, et al. A six-item short-form survey for measuring headache impact: the HIT-6. Qual Life Res 2003;12:963–74 doi:10.1023/A:1026119331193 pmid:14651415 [CrossRef](http://www.ajnr.org/lookup/external-ref?access_num=10.1023/A:1026119331193&link_type=DOI) [PubMed](http://www.ajnr.org/lookup/external-ref?access_num=14651415&link_type=MED&atom=%2Fajnr%2F39%2F7%2F1222.atom) [Web of Science](http://www.ajnr.org/lookup/external-ref?access_num=000185977800006&link_type=ISI) 31. 31. Wechsler D. Wechsler Test of Adult Reading: WTAR. San Antonio; Psychological Corporation; 2001 32. 32. Greenberg SM, Vernooij MW, Cordonnier C, et al; Microbleed Study Group. Cerebral microbleeds: a guide to detection and interpretation. Lancet Neurol 2009;8:165–74 doi:10.1016/S1474-4422(09)70013-4 pmid:19161908 [CrossRef](http://www.ajnr.org/lookup/external-ref?access_num=10.1016/S1474-4422(09)70013-4&link_type=DOI) [PubMed](http://www.ajnr.org/lookup/external-ref?access_num=19161908&link_type=MED&atom=%2Fajnr%2F39%2F7%2F1222.atom) [Web of Science](http://www.ajnr.org/lookup/external-ref?access_num=000262752000015&link_type=ISI) 33. 33. Greenberg SM, Finklestein SP, Schaefer PW. Petechial hemorrhages accompanying lobar hemorrhage: detection by gradient-echo MRI. Neurology 1996;46:1751–54 doi:10.1212/WNL.46.6.1751 pmid:8649586 [Abstract/FREE Full Text](http://www.ajnr.org/lookup/ijlink/YTozOntzOjQ6InBhdGgiO3M6MTQ6Ii9sb29rdXAvaWpsaW5rIjtzOjU6InF1ZXJ5IjthOjQ6e3M6ODoibGlua1R5cGUiO3M6NDoiQUJTVCI7czoxMToiam91cm5hbENvZGUiO3M6OToibmV1cm9sb2d5IjtzOjU6InJlc2lkIjtzOjk6IjQ2LzYvMTc1MSI7czo0OiJhdG9tIjtzOjIwOiIvYWpuci8zOS83LzEyMjIuYXRvbSI7fXM6ODoiZnJhZ21lbnQiO3M6MDoiIjt9) 34. 34. Trifan G, Gattu R, Haacke EM, et al. MR imaging findings in mild traumatic brain injury with persistent neurological impairment. Magn Reson Imaging 2017;37:243–51 doi:10.1016/j.mri.2016.12.009 pmid:27939436 [CrossRef](http://www.ajnr.org/lookup/external-ref?access_num=10.1016/j.mri.2016.12.009&link_type=DOI) [PubMed](http://www.ajnr.org/lookup/external-ref?access_num=27939436&link_type=MED&atom=%2Fajnr%2F39%2F7%2F1222.atom) 35. 35. Toth A, Kornyei B, Kovacs N, et al. Both hemorrhagic and non-hemorrhagic traumatic MRI lesions are associated with the microstructural damage of the normal appearing white matter. Behav Brain Res 2018;340:106–16 doi:10.1016/j.bbr.2017.02.039 pmid:28249729 [CrossRef](http://www.ajnr.org/lookup/external-ref?access_num=10.1016/j.bbr.2017.02.039&link_type=DOI) [PubMed](http://www.ajnr.org/lookup/external-ref?access_num=28249729&link_type=MED&atom=%2Fajnr%2F39%2F7%2F1222.atom) 36. 36. Topal NB, Hakyemez B, Erdogan C, et al. MR imaging in the detection of diffuse axonal injury with mild traumatic brain injury. Neurol Res 2008;30:974–78 doi:10.1179/016164108X323799 pmid:18691451 [CrossRef](http://www.ajnr.org/lookup/external-ref?access_num=10.1179/016164108X323799&link_type=DOI) [PubMed](http://www.ajnr.org/lookup/external-ref?access_num=18691451&link_type=MED&atom=%2Fajnr%2F39%2F7%2F1222.atom) [Web of Science](http://www.ajnr.org/lookup/external-ref?access_num=000261323000016&link_type=ISI) 37. 37. Shoamanesh A, Kwok CS, Benavente O. Cerebral microbleeds: histopathological correlation of neuroimaging. Cerebrovasc Dis 2011;32:528–34 doi:10.1159/000331466 pmid:22104448 [CrossRef](http://www.ajnr.org/lookup/external-ref?access_num=10.1159/000331466&link_type=DOI) [PubMed](http://www.ajnr.org/lookup/external-ref?access_num=22104448&link_type=MED&atom=%2Fajnr%2F39%2F7%2F1222.atom) 38. 38. Roob G, Fazekas F. Magnetic resonance imaging of cerebral microbleeds. Curr Opin Neurol 2000;13:69–73 doi:10.1097/00019052-200002000-00013 pmid:10719653 [CrossRef](http://www.ajnr.org/lookup/external-ref?access_num=10.1097/00019052-200002000-00013&link_type=DOI) [PubMed](http://www.ajnr.org/lookup/external-ref?access_num=10719653&link_type=MED&atom=%2Fajnr%2F39%2F7%2F1222.atom) [Web of Science](http://www.ajnr.org/lookup/external-ref?access_num=000168284400013&link_type=ISI) 39. 39. Roob G, Lechner A, Schmidt R, et al. Frequency and location of microbleeds in patients with primary intracerebral hemorrhage. Stroke 2000;31:2665–69 doi:10.1161/01.STR.31.11.2665 pmid:11062292 [Abstract/FREE Full Text](http://www.ajnr.org/lookup/ijlink/YTozOntzOjQ6InBhdGgiO3M6MTQ6Ii9sb29rdXAvaWpsaW5rIjtzOjU6InF1ZXJ5IjthOjQ6e3M6ODoibGlua1R5cGUiO3M6NDoiQUJTVCI7czoxMToiam91cm5hbENvZGUiO3M6OToic3Ryb2tlYWhhIjtzOjU6InJlc2lkIjtzOjEwOiIzMS8xMS8yNjY1IjtzOjQ6ImF0b20iO3M6MjA6Ii9ham5yLzM5LzcvMTIyMi5hdG9tIjt9czo4OiJmcmFnbWVudCI7czowOiIiO30=) 40. 40. Toth A, Kovacs N, Tamas V, et al. Microbleeds may expand acutely after traumatic brain injury. Neurosci Lett 2016;617:207–12 doi:10.1016/j.neulet.2016.02.028 pmid:26912192 [CrossRef](http://www.ajnr.org/lookup/external-ref?access_num=10.1016/j.neulet.2016.02.028&link_type=DOI) [PubMed](http://www.ajnr.org/lookup/external-ref?access_num=26912192&link_type=MED&atom=%2Fajnr%2F39%2F7%2F1222.atom) 41. 41. Daugherty AM, Raz N. Incident risk and progression of cerebral microbleeds in healthy adults: a multi-occasion longitudinal study. Neurobiol Aging 2017;59:22–29 doi:10.1016/j.neurobiolaging.2017.07.003 pmid:28800410 [CrossRef](http://www.ajnr.org/lookup/external-ref?access_num=10.1016/j.neurobiolaging.2017.07.003&link_type=DOI) [PubMed](http://www.ajnr.org/lookup/external-ref?access_num=28800410&link_type=MED&atom=%2Fajnr%2F39%2F7%2F1222.atom) * Received February 3, 2018. * Accepted after revision April 4, 2018. * © 2018 by American Journal of Neuroradiology