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White Matter Disruption in Pediatric Traumatic Brain Injury: Results from ENIGMA Pediatric Moderate to Severe Traumatic Brain Injury.
Dennis, Emily L; Caeyenberghs, Karen; Hoskinson, Kristen R; Merkley, Tricia L; Suskauer, Stacy J; Asarnow, Robert F; Babikian, Talin; Bartnik-Olson, Brenda; Bickart, Kevin; Bigler, Erin D; Ewing-Cobbs, Linda; Figaji, Anthony; Giza, Christopher C; Goodrich-Hunsaker, Naomi J; Hodges, Cooper B; Hovenden Aa, Elizabeth S; Irimia, Andrei; Königs, Marsh; Levin, Harvey S; Lindsey, Hannah M; Max, Jeffrey E; Newsome, Mary R; Olsen, Alexander; Ryan, Nicholas P; Schmidt, Adam T; Spruiell, Matthew S; Wade, Benjamin Sc; Ware, Ashley L; Watson, Christopher G; Wheeler, Anne L; Yeates, Keith Owen; Zielinski, Brandon A; Kochunov, Peter; Jahanshad, Neda; Thompson, Paul M; Tate, David F; Wilde, Elisabeth A.
Afiliação
  • Dennis EL; Department of Neurology, University of Utah School of Medicine, Salt Lake City, UT. emily.dennis@hsc.utah.edu.
  • Caeyenberghs K; George E. Wahlen Veterans Affairs Medical Center, Salt Lake City, UT.
  • Hoskinson KR; Cognitive Neuroscience Unit, School of Psychology, Deakin University, Geelong, Australia.
  • Merkley TL; Center for Biobehavioral Health, The Abigail Wexner Research Institute at Nationwide Children's Hospital, Columbus, OH.
  • Suskauer SJ; Department of Pediatrics, The Ohio State University College of Medicine.
  • Asarnow RF; Department of Neurology, University of Utah School of Medicine, Salt Lake City, UT.
  • Babikian T; Department of Psychology, Brigham Young University, Provo, UT.
  • Bartnik-Olson B; Neuroscience Center, Brigham Young University, Provo, UT.
  • Bickart K; Kennedy Krieger Institute, Baltimore, MD.
  • Bigler ED; Johns Hopkins University School of Medicine, Departments of Physical Medicine & Rehabilitation and Pediatrics, Baltimore, MD.
  • Figaji A; Department of Psychiatry and Biobehavioral Sciences, Semel Institute for Neuroscience and Human Behavior, UCLA, Los Angeles, CA.
  • Giza CC; UCLA Steve Tisch BrainSPORT Program, Los Angeles, CA.
  • Goodrich-Hunsaker NJ; Department of Radiology, Loma Linda University Medical Center, Loma Linda, CA.
  • Hodges CB; UCLA Steve Tisch BrainSPORT Program, Los Angeles, CA.
  • Hovenden Aa ES; Department of Neurology, David Geffen School of Medicine at UCLA, Los Angeles, CA.
  • Irimia A; Department of Neurology, University of Utah School of Medicine, Salt Lake City, UT.
  • Königs M; Department of Psychology, Brigham Young University, Provo, UT.
  • Levin HS; Neuroscience Center, Brigham Young University, Provo, UT.
  • Lindsey HM; Department of Pediatrics, Children's Learning Institute, University of Texas Health Science Center at Houston, Houston, TX.
  • Max JE; Division of Neurosurgery, University of Cape Town, Cape Town, South Africa.
  • Newsome MR; Neuroscience Institute, University of Cape Town, Cape Town, South Africa.
  • Olsen A; UCLA Steve Tisch BrainSPORT Program, Los Angeles, CA.
  • Ryan NP; Department of Pediatrics, Division of Neurology, UCLA Mattel Children's Hospital, Los Angeles, CA.
  • Schmidt AT; Department of Neurosurgery, David Geffen School of Medicine at UCLA, Los Angeles, CA.
  • Spruiell MS; Department of Neurology, University of Utah School of Medicine, Salt Lake City, UT.
  • Wade BS; George E. Wahlen Veterans Affairs Medical Center, Salt Lake City, UT.
  • Ware AL; Department of Psychology, Brigham Young University, Provo, UT.
  • Watson CG; Department of Psychology, Brigham Young University, Provo, UT.
  • Wheeler AL; Department of Physical Medicine and Rehabilitation, Virginia Commonwealth University, Richmond, VA.
  • Yeates KO; Department of Neurology, University of Utah School of Medicine, Salt Lake City, UT.
  • Zielinski BA; Ethel Percy Andrus Gerontology Center, Leonard Davis School of Gerontology, University of Southern California, Los Angeles, CA.
  • Kochunov P; Department of Biomedical Engineering, Viterbi School of Engineering, University of Southern California, Los Angeles, CA.
  • Jahanshad N; Emma Children's Hospital, Amsterdam UMC, University of Amsterdam, Emma Neuroscience Group, Amsterdam, The Netherlands.
  • Thompson PM; H. Ben Taub Department of Physical Medicine and Rehabilitation, Baylor College of Medicine, Houston, TX.
  • Tate DF; Michael E. DeBakey Veterans Affairs Medical Center, Houston, TX.
  • Wilde EA; Department of Neurology, University of Utah School of Medicine, Salt Lake City, UT.
Neurology ; 2021 May 28.
Article em En | MEDLINE | ID: mdl-34050006
ABSTRACT

OBJECTIVE:

Our study addressed

aims:

(1) test the hypothesis that moderate-severe TBI in pediatric patients is associated with widespread white matter (WM) disruption; (2) test the hypothesis that age and sex impact WM organization after injury; and (3) examine associations between WM organization and neurobehavioral outcomes.

METHODS:

Data from ten previously enrolled, existing cohorts recruited from local hospitals and clinics were shared with the ENIGMA (Enhancing NeuroImaging Genetics through Meta-Analysis) Pediatric msTBI working group. We conducted a coordinated analysis of diffusion MRI (dMRI) data using the ENIGMA dMRI processing pipeline.

RESULTS:

Five hundred and seven children and adolescents (244 with complicated mild to severe TBI [msTBI] and 263 controls) were included. Patients were clustered into three post-injury intervals acute/subacute - <2 months, post-acute - 2-6 months, chronic - 6+ months. Outcomes were dMRI metrics and post-injury behavioral problems as indexed by the Child Behavior Checklist (CBCL). Our analyses revealed altered WM diffusion metrics across multiple tracts and all post-injury intervals (effect sizes ranging between d=-0.5 to -1.3). Injury severity is a significant contributor to the extent of WM alterations but explained less variance in dMRI measures with increasing time post-injury. We observed a sex-by-group interaction females with TBI had significantly lower fractional anisotropy in the uncinate fasciculus than controls (𝞫=0.043), which coincided with more parent-reported behavioral problems (𝞫=-0.0027).

CONCLUSIONS:

WM disruption after msTBI is widespread, persistent, and influenced by demographic and clinical variables. Future work will test techniques for harmonizing neurocognitive data, enabling more advanced analyses to identify symptom clusters and clinically-meaningful patient subtypes.

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Tipo de estudo: Prognostic_studies Idioma: En Revista: Neurology Ano de publicação: 2021 Tipo de documento: Article

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Tipo de estudo: Prognostic_studies Idioma: En Revista: Neurology Ano de publicação: 2021 Tipo de documento: Article