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Cerebral Microbleeds and Structural White Matter Integrity in Patients With Traumatic Brain Injury-A Diffusion Tensor Imaging Study




TekijätDahl Juho, Tenovuo Olli, Posti Jussi P., Hirvonen Jussi, Katila Ari J., Frantzen Janek, Maanpää Henna-Riikka, Takala Riikka, Löyttyniemi Eliisa, Tallus Jussi, Newcombe Virginia, Menon David K., Hutchinson Peter J., Mohammadian Mehrbod

KustantajaFRONTIERS MEDIA SA

Julkaisuvuosi2022

JournalFrontiers in Neurology

Tietokannassa oleva lehden nimiFRONTIERS IN NEUROLOGY

Lehden akronyymiFRONT NEUROL

Artikkelin numero 888815

Vuosikerta13

Sivujen määrä11

ISSN1664-2295

eISSN1664-2295

DOIhttps://doi.org/10.3389/fneur.2022.888815

Verkko-osoitehttps://doi.org/10.3389/fneur.2022.888815

Rinnakkaistallenteen osoitehttps://research.utu.fi/converis/portal/detail/Publication/175938374


Tiivistelmä
Diffuse axonal injury (DAI) is a common neuropathological manifestation of traumatic brain injury (TBI), presenting as traumatic alterations in the cerebral white matter (WM) microstructure and often leading to long-term neurocognitive impairment. These WM alterations can be assessed using diffusion tensor imaging (DTI). Cerebral microbleeds (CMBs) are a common finding on head imaging in TBI and are often considered a visible sign of DAI, although they represent diffuse vascular injury. It is poorly known how they associate with long-term white matter integrity. This study included 20 patients with TBI and CMBs, 34 patients with TBI without CMBs, and 11 controls with orthopedic injuries. DTI was used to assess microstructural WM alterations. CMBs were detected using susceptibility-weighted imaging (SWI) and graded according to their location in the WM and total lesion load was counted. Patients underwent SWI within 2 months after injury. DTI and clinical outcome assessment were performed at an average of eight months after injury. Outcome was assessed using the extended Glasgow Outcome Scale (GOSe). The Glasgow Coma Scale (GCS) and length of post-traumatic amnesia (PTA) were used to assess clinical severity of the injury. We found that CMB grading and total lesion load were negatively associated with fractional anisotropy (FA) and positively associated with mean diffusivity (MD). Patients with TBI and CMBs had decreased FA and increased MD compared with patients with TBI without CMBs. CMBs were also associated with worse clinical outcome. When adjusting for the clinical severity of the injury, none of the mentioned associations were found. Thus, the difference in FA and MD is explained by patients with TBI and CMBs having more severe injuries. Our results suggest that CMBs are not associated with greater WM alterations when adjusting for the clinical severity of TBI. Thus, CMBs and WM alterations may not be strongly associated pathologies in TBI.

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Last updated on 2024-26-11 at 21:18