Cervical cord deformation in cerebral palsy: Structural signatures of gross motor function and outcomes after selective dorsal rhizotomy

AIM: To identify structural signatures of cerebral palsy (CP) motor impairment and selective dorsal rhizotomy (SDR) outcomes using spinal cord deformation-based morphometry (scDBM). METHOD: This retrospective study quantifies spinal cord structural abnormalities in 39 children with CP, stratified by the baseline motor function (Gross Motor Function Classification System [GMFCS] levels I-II, n = 21 and GMFCS level > II, n = 18). T1-weighted clinical images were non-linearly registered to a healthy normative template. Localized spinal cord tissue volume change was modeled against baseline Gross Motor Function Measure (GMFM-66) and 12-month postSDR improvement. RESULTS: In children with ambulatory impairment (GMFCS level > II, n = 18), lower motor capacity correlated with localized rostral cervical (C1-C4) deformation (p < 0.05); no correlates were identified in GMFCS levels I to II (n = 21). Clinical improvement after SDR was associated with baseline C1 dimensions closer to normative adult values, specifically involving reticulospinal and vestibulospinal tracts (p < 0.05). INTERPRETATION: Spinal cord morphology reflects motor potential and surgical outcomes in CP (GMFCS level > II). Localizing C1 structural deficit, scDBM may provide an objective structural signature of severity to identify presurgical candidates with the necessary reserve to translate spasticity reduction into clinically meaningful motor gains.

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Publication Details

Journal
Developmental Medicine & Child Neurology
Published
2026-10-14
DOI
https://doi.org/10.1111/dmcn.70576
Primary Topic
Cerebral Palsy and Movement Disorders
Type
article
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article

Cervical cord deformation in cerebral palsy: Structural signatures of gross motor function and outcomes after selective dorsal rhizotomy

Golda Milo‐Manson, Timur H. Latypov, Darcy L. Fehlings, Sara C. Breitbart et al.
Developmental Medicine & Child Neurology
Cerebral Palsy and Movement Disorders
article

Cervical cord deformation in cerebral palsy: Structural signatures of gross motor function and outcomes after selective dorsal rhizotomy

Golda Milo‐Manson, Timur H. Latypov, Darcy L. Fehlings, Sara C. Breitbart, Karim Mithani, Jackie Cotton, George M. Ibrahim, Leah Takeuchi, Amber Gill, Juliana Douglas, Aimee Chin‐A‐Young
article en

Abstract

AIM: To identify structural signatures of cerebral palsy (CP) motor impairment and selective dorsal rhizotomy (SDR) outcomes using spinal cord deformation-based morphometry (scDBM). METHOD: This retrospective study quantifies spinal cord structural abnormalities in 39 children with CP, stratified by the baseline motor function (Gross Motor Function Classification System [GMFCS] levels I-II, n = 21 and GMFCS level > II, n = 18). T1-weighted clinical images were non-linearly registered to a healthy normative template. Localized spinal cord tissue volume change was modeled against baseline Gross Motor Function Measure (GMFM-66) and 12-month postSDR improvement. RESULTS: In children with ambulatory impairment (GMFCS level > II, n = 18), lower motor capacity correlated with localized rostral cervical (C1-C4) deformation (p < 0.05); no correlates were identified in GMFCS levels I to II (n = 21). Clinical improvement after SDR was associated with baseline C1 dimensions closer to normative adult values, specifically involving reticulospinal and vestibulospinal tracts (p < 0.05). INTERPRETATION: Spinal cord morphology reflects motor potential and surgical outcomes in CP (GMFCS level > II). Localizing C1 structural deficit, scDBM may provide an objective structural signature of severity to identify presurgical candidates with the necessary reserve to translate spasticity reduction into clinically meaningful motor gains.

Developmental Medicine & Child Neurology
University of Toronto (CA), Hospital for Sick Children (CA), Holland Bloorview Kids Rehabilitation Hospital (CA), Sickkids Research Institute (CA)
Openalex Percentile: Top 12%
Cerebral Palsy and Movement Disorders
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