Brachial Plexus Birth Injury Causes Location-Dependent Detriments in Glenohumeral Trabecular Bone Microstructure

Emily B Fawcett1, Nikhil N Dixit2, Katherine R Saul2

  • 1Lampe Joint Department of Biomedical Engineering, University of North Carolina, Chapel Hill, NC, and North Carolina State University, Raleigh, NC, USA.

Insights

Brachial plexus birth injury (BPBI) can cause lifelong arm impairment. This study reveals injury location and limb disuse significantly impact bone microstructure and morphology, with preganglionic injuries causing greater bone deficits.

Area of Science:

  • Orthopedics
  • Pediatric Neurology
  • Biomedical Engineering

Background:

  • Brachial plexus birth injury (BPBI) affects 30-40% of affected infants, leading to lifelong arm impairment.
  • The impact of BPBI on bone microstructure and morphology, and the role of injury location and limb disuse, remain unclear.

Purpose of the Study:

  • To investigate how different brachial plexus birth injury locations and limb disuse affect bone microstructure and morphology in a rat model.
  • To differentiate the effects of preganglionic versus postganglionic BPBI and disuse on the proximal humerus and distal scapula.

Main Methods:

  • Utilized two rat models of BPBI (postganglionic and preganglionic) and a disuse model (disarticulation).
  • Characterized trabecular bone microstructure and glenohumeral morphology in the proximal humerus and distal scapula.

Main Results:

  • Trabecular bone deficits were most pronounced near the joint articulating surfaces.
  • Preganglionic BPBI resulted in greater bone deficits than postganglionic BPBI.
  • Disuse effects aligned more with postganglionic injuries, with greater impacts on the scapula than the humerus.

Conclusions:

  • Injury location and limb disuse have differential effects on bone microstructure and morphology following BPBI.
  • Effects of limb disuse are most prominent in the postganglionic injury group and the distal scapula.
  • Distinct injury mechanisms may drive preganglionic and postganglionic BPBI, influencing macro- and microstructural bone alterations.