Morphological Medial Gastrocnemius Muscle Growth in Ambulant Children with Spastic Cerebral Palsy: A Prospective Longitudinal Study

Author:

De Beukelaer Nathalie1ORCID,Vandekerckhove Ines1ORCID,Huyghe Ester1,Molenberghs Geert23ORCID,Peeters Nicky14ORCID,Hanssen Britta14ORCID,Ortibus Els5ORCID,Van Campenhout Anja67ORCID,Desloovere Kaat17

Affiliation:

1. Department of Rehabilitation Sciences, KU Leuven, 3000 Leuven, Belgium

2. Interuniversity Institute for Biostatistics and Statistical Bioinformatics (I-BIOSTAT), KU Leuven, 3000 Leuven, Belgium

3. Interuniversity Institute for Biostatistics and Statistical Bioinformatics (I-BIOSTAT), Data Science Institute, Hasselt University, 3590 Diepenbeek, Belgium

4. Department of Rehabilitation Sciences, Ghent University, 9000 Gent, Belgium

5. Department of Development and Regeneration, KU Leuven, 3000 Leuven, Belgium

6. Department of Orthopedics, University Hospitals Leuven, 3000 Leuven, Belgium

7. Clinical Motion Analysis Laboratory, University Hospitals Leuven, 3000 Leuven, Belgium

Abstract

Only cross-sectional studies have demonstrated muscle deficits in children with spastic cerebral palsy (SCP). The impact of gross motor functional limitations on altered muscle growth remains unclear. This prospective longitudinal study modelled morphological muscle growth in 87 children with SCP (age range 6 months to 11 years, Gross Motor Function Classification System [GMFCS] level I/II/III = 47/22/18). Ultrasound assessments were performed during 2-year follow-up and repeated for a minimal interval of 6 months. Three-dimensional freehand ultrasound was applied to assess medial gastrocnemius muscle volume (MV), mid-belly cross-sectional area (CSA) and muscle belly length (ML). Non-linear mixed models compared trajectories of (normalized) muscle growth between GMFCS-I and GMFCS-II&III. MV and CSA growth trajectories showed a piecewise model with two breakpoints, with the highest growth before 2 years and negative growth rates after 6–9 years. Before 2 years, children with GMFCS-II&III already showed lower growth rates compared to GMFCS-I. From 2 to 9 years, the growth rates did not differ between GMFCS levels. After 9 years, a more pronounced reduction in normalized CSA was observed in GMFCS-II&III. Different trajectories in ML growth were shown between the GMFCS level subgroups. These longitudinal trajectories highlight monitoring of SCP muscle pathology from early ages and related to motor mobility. Treatment planning and goals should stimulate muscle growth.

Funder

KU Leuven

Research Foundation Flanders

Fund for Translational Biomedical Research, Belgium

Publisher

MDPI AG

Subject

General Medicine

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