White Matter Disruption in Pediatric Traumatic Brain Injury Results From ENIGMA Pediatric Moderate to Severe Traumatic Brain Injury

被引:15
|
作者
Dennis, Emily L. [1 ,2 ]
Caeyenberghs, Karen [3 ]
Hoskinson, Kristen R. [4 ,5 ]
Merkley, Tricia L. [1 ,6 ,7 ]
Suskauer, Stacy J. [8 ,9 ,10 ]
Asarnow, Robert F. [11 ,12 ,13 ]
Babikian, Talin [11 ,14 ]
Bartnik-Olson, Brenda [15 ]
Bickart, Kevin [14 ,16 ]
Bigler, Erin D. [1 ,6 ,7 ]
Ewing-Cobbs, Linda [18 ]
Figaji, Anthony [19 ,20 ]
Giza, Christopher C. [14 ,17 ,21 ]
Goodrich-Hunsaker, Naomi J. [1 ,2 ,6 ]
Hodges, Cooper B. [6 ,22 ]
Hovenden, Elizabeth S. [1 ]
Irimia, Andrei [23 ,24 ]
Konigs, Marsh [25 ]
Levin, Harvey S. [26 ,27 ]
Lindsey, Hannah M. [1 ,2 ,6 ]
Max, Jeffrey E. [28 ,29 ]
Newsome, Mary R. [26 ,27 ]
Olsen, Alexander [30 ,31 ]
Ryan, Nicholas P. [3 ,32 ,33 ]
Schmidt, Adam T. [34 ]
Spruiell, Matthew S. [26 ]
Wade, Benjamin S. C. [1 ,35 ]
Ware, Ashley L. [36 ]
Watson, Christopher G. [18 ]
Wheeler, Anne L. [37 ,38 ]
Yeates, Keith Owen [36 ,39 ,40 ,41 ,42 ]
Zielinski, Brandon A. [1 ,43 ]
Kochunov, Peter [44 ]
Jahanshad, Neda [45 ]
Thompson, Paul M. [45 ,46 ,47 ,48 ,49 ,50 ,51 ]
Tate, David F. [1 ,2 ]
Wilde, Elisabeth A. [1 ,2 ,26 ]
机构
[1] Univ Utah, Sch Med, Dept Neurol, Salt Lake City, UT 84112 USA
[2] George E Warden Vet Affairs Med Ctr, Salt Lake City, UT USA
[3] Deakin Univ, Sch Psychol, Cognit Neurosci Unit, Geelong, Vic, Australia
[4] Nationwide Childrens Hosp, Abigail Wexner Res Inst, Ctr Biobehav Hlth, Columbus, OH USA
[5] Ohio State Univ, Coll Med, Dept Pediat, Columbus, OH 43210 USA
[6] Brigham Young Univ, Dept Psychol, Provo, UT 84602 USA
[7] Brigham Young Univ, Neurosci Ctr, Provo, UT 84602 USA
[8] Johns Hopkins Univ, Sch Med, Kennedy Krieger Inst, Baltimore, MD USA
[9] Johns Hopkins Univ, Sch Med, Dept Phys Med & Rehabil, Baltimore, MD USA
[10] Johns Hopkins Univ, Sch Med, Dept Pediat, Baltimore, MD 21205 USA
[11] Univ Calif Los Angeles, Dept Psychiat & Biobehav Sci, Semel Inst Neurosci & Human Behav, Los Angeles, CA 90024 USA
[12] Univ Calif Los Angeles, Brain Res Inst, Los Angeles, CA USA
[13] Univ Calif Los Angeles, Dept Psychol, Los Angeles, CA USA
[14] Univ Calif Los Angeles, Steve Tisch BrainSPORT Program, Los Angeles, CA USA
[15] Loma Linda Univ, Med Ctr, Dept Radiol, Loma Linda, CA USA
[16] Univ Calif Los Angeles, David Geffen Sch Med, Dept Neurol, Los Angeles, CA 90095 USA
[17] Univ Calif Los Angeles, David Geffen Sch Med, Dept Neurosurg, Los Angeles, CA 90095 USA
[18] Univ Texas Hlth Sci Ctr Houston, Childrens Learning Inst, Dept Pediat, Houston, TX 77030 USA
[19] Univ Cape Town, Div Neurosurg, Cape Town, South Africa
[20] Univ Cape Town, Neurosci Inst, Cape Town, South Africa
[21] Univ Calif Los Angeles, Dept Pediat, Div Neurol, Mattel Childrens Hosp, Los Angeles, CA 90024 USA
[22] Virginia Commonwealth Univ, Dept Phys Med & Rehabil, Richmond, VA USA
[23] Univ Southern Calif, Ethel Percy Andrus Gerontol Ctr, Leonard Davis Sch Gerontol, Los Angeles, CA 90007 USA
[24] Univ Southern Calif, Viterbi Sch Engn, Dept Biomed Engn, Los Angeles, CA 90007 USA
[25] Univ Amsterdam, Amsterdam UMC, Emma Childrens Hosp, Emma Neurosci Grp, Amsterdam, Netherlands
[26] Baylor Coll Med, H Ben Taub Dept Phys Med & Rehabil, Houston, TX 77030 USA
[27] Michael E DeBakey VA Med Ctr, Houston, TX USA
[28] Univ Calif San Diego, Dept Psychiat, La Jolla, CA 92093 USA
[29] Rady Childrens Hosp, Dept Psychiat, San Diego, CA USA
[30] Norwegian Univ Sci & Technol, Dept Psychol, Trondheim, Norway
[31] Trondheim Reg & Univ Hosp, St Olavs Hosp, Dept Phys Med & Rehabil, Trondheim, Norway
[32] Univ Melbourne, Murdoch Childrens Res Inst, Dept Clin Sci, Melbourne, Vic, Australia
[33] Univ Melbourne, Dept Paediat, Melbourne, Vic, Australia
[34] Texas Tech Univ, Dept Psychol Sci, Lubbock, TX 79409 USA
[35] Univ Calif Los Angeles, Dept Neurol, Ahmanson Lovelace Brain Mapping Ctr, Los Angeles, CA 90024 USA
[36] Univ Calgary, Dept Psychol, Calgary, AB, Canada
[37] Univ Toronto, Hosp Sick Children, Neurosci & Mental Hlth Program, Toronto, ON, Canada
[38] Univ Toronto, Physiol Dept, Toronto, ON, Canada
[39] Univ Calgary, Alberta Childrens Hosp Res Inst, Calgary, AB, Canada
[40] Univ Calgary, Hotchkiss Brain Inst, Calgary, AB, Canada
[41] Univ Calgary, Dept Pediat, Calgary, AB, Canada
[42] Univ Calgary, Dept Clin Neurosci, Calgary, AB, Canada
[43] Univ Utah, Sch Med, Dept Pediat, Salt Lake City, UT USA
[44] Univ Maryland, Sch Med, Maryland Psychiat Res Ctr, Baltimore, MD 21201 USA
[45] USC, Keck Sch Med, Stevens Neuroimaging & Informat Inst, Imaging Genet Ctr, Marina Del Rey, CA USA
[46] USC, Dept Neurol, Los Angeles, CA USA
[47] USC, Dept Pediat, Los Angeles, CA USA
[48] USC, Dept Psychiat, Los Angeles, CA USA
[49] USC, Dept Radiol, Los Angeles, CA USA
[50] USC, Dept Engn, Los Angeles, CA USA
基金
英国医学研究理事会;
关键词
BEHAVIOR RELATIONSHIPS; PSYCHIATRIC-DISORDERS; CORPUS-CALLOSUM; DIFFUSION MRI; DTI; CHILDREN; AGE; ADOLESCENCE; ANISOTROPY; CHILDHOOD;
D O I
10.1212/WNL.0000000000012222
中图分类号
R74 [神经病学与精神病学];
学科分类号
摘要
Objective Our study addressed aims (1) to test the hypothesis that moderate-severe traumatic brain injury (TBI) in pediatric patients is associated with widespread white matter (WM) disruption, (2) to test the hypothesis that age and sex affect WM organization after injury, and (3) to examine associations between WM organization and neurobehavioral outcomes. Methods Data from 10 previously enrolled, existing cohorts recruited from local hospitals and clinics were shared with the Enhancing NeuroImaging Genetics Through Meta-Analysis (ENIGMA) Pediatric Moderate/Severe TBI (msTBI) working group. We conducted a coordinated analysis of diffusion MRI (dMRI) data using the ENIGMA dMRI processing pipeline. Results Five hundred seven children and adolescents (244 with complicated msTBI and 263 controls) were included. Patients were clustered into 3 postinjury intervals: acute/subacute, <2 months; postacute, 2 to 6 months; and chronic, >= 6 months. Outcomes were dMRI metrics and postinjury behavioral problems as indexed by the Child Behavior Checklist. Our analyses revealed altered WM diffusion metrics across multiple tracts and all postinjury intervals (effect sizes range 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 after injury. We observed a sex-by-group interaction: female patients with TBI had significantly lower fractional anisotropy in the uncinate fasciculus than controls (beta = 0.043), which coincided with more parent-reported behavioral problems (beta = -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.
引用
收藏
页码:E298 / E309
页数:12
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