Multimodal Analysis of Secondary Cerebellar Alterations After Pediatric Traumatic Brain Injury

Author:

Keleher Finian1,Lindsey Hannah M.12,Kerestes Rebecca3,Amiri Houshang4,Asarnow Robert F.567,Babikian Talin58,Bartnik-Olson Brenda9,Bigler Erin D.11011,Caeyenberghs Karen12,Esopenko Carrie13,Ewing-Cobbs Linda14,Giza Christopher C.81516,Goodrich-Hunsaker Naomi J.1210,Hodges Cooper B.1017,Hoskinson Kristen R.1819,Irimia Andrei2021,Königs Marsh22,Max Jeffrey E.2324,Newsome Mary R.25,Olsen Alexander262728,Ryan Nicholas P.122930,Schmidt Adam T.31,Stein Dan J.3233,Suskauer Stacy J.343536,Ware Ashley L.137,Wheeler Anne L.3839,Zielinski Brandon A.1404142,Thompson Paul M.4344454647,Harding Ian H.348,Tate David F.1210,Wilde Elisabeth A.1225,Dennis Emily L.12

Affiliation:

1. TBI and Concussion Center, Department of Neurology, University of Utah School of Medicine, Salt Lake City

2. George E. Wahlen Veterans Affairs Medical Center, Salt Lake City, Utah

3. Department of Neuroscience, Central Clinical School, Monash University, Melbourne, Victoria, Australia

4. Institute of Neuropharmacology, Neuroscience Research Center, Kerman University of Medical Sciences, Kerman, Iran

5. Semel Institute for Neuroscience and Human Behavior, Department of Psychiatry and Biobehavioral Sciences, University of California, Los Angeles

6. Brain Research Institute, University of California, Los Angeles

7. Department of Psychology, University of California, Los Angeles

8. Steve Tisch BrainSPORT Program, University of California, Los Angeles

9. Department of Radiology, Loma Linda University Medical Center, Loma Linda, California

10. Department of Psychology, Brigham Young University, Provo, Utah

11. Neuroscience Center, Brigham Young University, Provo, Utah

12. Cognitive Neuroscience Unit, School of Psychology, Deakin University, Geelong, Victoria, Australia

13. Department of Rehabilitation and Human Performance, Icahn School of Medicine at Mount Sinai, New York, New York

14. Children’s Learning Institute, Department of Pediatrics, University of Texas Health Science Center at Houston

15. Division of Neurology, Department of Pediatrics, Mattel Children’s Hospital University of California, Los Angeles

16. Department of Neurosurgery, David Geffen School of Medicine at the University of California, Los Angeles

17. School of Social and Behavioral Sciences, Andrews University, Berrien Springs, Michigan

18. Center for Biobehavioral Health, The Abigail Wexner Research Institute at Nationwide Children’s Hospital, Columbus, Ohio

19. Department of Pediatrics, The Ohio State University College of Medicine, Columbus

20. Ethel Percy Andrus Gerontology Center, Leonard Davis School of Gerontology, University of Southern California, Los Angeles,

21. Department of Biomedical Engineering, Viterbi School of Engineering, University of Southern California, Los Angeles

22. Emma Neuroscience Group, Emma Children’s Hospital, Amsterdam University Medical Centers, University of Amsterdam, Amsterdam, the Netherlands

23. Department of Psychiatry, University of California, San Diego, La Jolla

24. Department of Psychiatry, Rady Children’s Hospital, San Diego, California

25. H. Ben Taub Department of Physical Medicine and Rehabilitation, Baylor College of Medicine, Houston, Texas

26. Department of Psychology, Norwegian University of Science and Technology, Trondheim, Norway

27. Clinic of Rehabilitation, St Olavs Hospital, Trondheim University Hospital, Trondheim, Norway

28. NorHEAD-Norwegian Centre for Headache Research, Trondheim, Norway

29. Department of Clinical Sciences, Murdoch Children’s Research Institute, Melbourne, Victoria, Australia

30. Department of Paediatrics, The University of Melbourne, Melbourne, Victoria, Australia

31. Department of Psychological Sciences, Texas Tech University, Lubbock

32. South African Medical Research Council Unit on Risk and Resilience in Mental Disorders, Department of Psychiatry, Cape Town University, Cape Town, South Africa

33. South African Medical Research Council Unit on Risk and Resilience in Mental Disorders, Neuroscience Institute, Cape Town University, Cape Town, South Africa

34. Kennedy Krieger Institute, Baltimore, Maryland

35. Department of Physical Medicine and Rehabilitation, Johns Hopkins University School of Medicine, Baltimore, Maryland

36. Department of Pediatrics, Johns Hopkins University School of Medicine, Baltimore, Maryland

37. Department of Psychology, Georgia State University, Atlanta

38. Neuroscience and Mental Health Program, Hospital for Sick Children, Toronto, Ontario, Canada

39. Physiology Department, University of Toronto, Toronto, Ontario, Canada

40. Department of Pediatrics, University of Florida, Gainesville

41. Department of Pediatrics, University of Utah School of Medicine, Salt Lake City

42. Department of Neurology, University of Florida, Gainesville

43. Imaging Genetics Center, Stevens Neuroimaging & Informatics Institute, Keck School of Medicine of the University of Southern California, Marina del Rey

44. Department of Neurology, University of Southern California, Los Angeles

45. Department of Pediatrics, University of Southern California, Los Angeles

46. Department of Psychiatry, University of Southern California, Los Angeles

47. Department of Radiology, University of Southern California, Los Angeles

48. Monash Biomedical Imaging, Monash University, Melbourne, Victoria, Australia

Abstract

ImportanceTraumatic brain injury (TBI) is known to cause widespread neural disruption in the cerebrum. However, less is known about the association of TBI with cerebellar structure and how such changes may alter executive functioning.ObjectiveTo investigate alterations in subregional cerebellum volume and cerebral white matter microstructure after pediatric TBI and examine subsequent changes in executive function.Design, Setting, and ParticipantsThis retrospective cohort study combined 12 data sets (collected between 2006 and 2020) from 9 sites in the Enhancing Neuroimaging Genetics Through Meta-Analysis Consortium Pediatric TBI working group in a mega-analysis of cerebellar structure. Participants with TBI or healthy controls (some with orthopedic injury) were recruited from trauma centers, clinics, and institutional trauma registries, some of which were followed longitudinally over a period of 0.7 to 1.9 years. Healthy controls were recruited from the surrounding community. Data analysis occurred from October to December 2022.ExposureAccidental mild complicated-severe TBI (msTBI) for those in the TBI group. Some controls received a diagnosis of orthopedic injury.Main Outcomes and MeasuresVolume of 18 cerebellar lobules and vermal regions were estimated from 3-dimensional T1-weighted magnetic resonance imaging (MRI) scans. White matter organization in 28 regions of interest was assessed with diffusion tensor MRI. Executive function was measured by parent-reported scores from the Behavior Rating Inventory of Executive Functioning.ResultsA total of 598 children and adolescents (mean [SD] age, 14.05 [3.06] years; range, 5.45-19.70 years; 386 male participants [64.5%]; 212 female participants [35.5%]) were included in the study, with 314 participants in the msTBI group, and 284 participants in the non-TBI group (133 healthy individuals and 151 orthopedically injured individuals). Significantly smaller total cerebellum volume (d = −0.37; 95% CI, −0.52 to −0.22; P < .001) and subregional cerebellum volumes (eg, corpus medullare; d = −0.43; 95% CI, −0.58 to −0.28; P < .001) were observed in the msTBI group. These alterations were primarily seen in participants in the chronic phase (ie, >6 months postinjury) of injury (total cerebellar volume, d = −0.55; 95% CI, −0.75 to −0.35; P < .001). Smaller cerebellum volumes were associated with higher scores on the Behavior Rating Inventory of Executive Functioning Global Executive Composite score (β = −208.9 mm3; 95% CI, −319.0 to −98.0 mm3; P = .008) and Metacognition Index score (β = −202.5 mm3; 95% CI, −319.0 to −85.0 mm3; P = .02). In a subset of 185 participants with longitudinal data, younger msTBI participants exhibited cerebellum volume reductions (β = 0.0052 mm3; 95% CI, 0.0013 to 0.0090 mm3; P = .01), and older participants slower growth rates. Poorer white matter organization in the first months postinjury was associated with decreases in cerebellum volume over time (β=0.52 mm3; 95% CI, 0.19 to 0.84 mm3; P = .005).Conclusions and RelevanceIn this cohort study of pediatric msTBI, our results demonstrated robust cerebellar volume alterations associated with pediatric TBI, localized to the posterior lobe. Furthermore, longitudinal cerebellum changes were associated with baseline diffusion tensor MRI metrics, suggesting secondary cerebellar atrophy. These results provide further understanding of secondary injury mechanisms and may point to new opportunities for intervention.

Publisher

American Medical Association (AMA)

Subject

General Medicine

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