Surgical treatment and muscle protein analysis of V-pattern exotropia in craniosynostosis

Qingyu Liu1, Yuan Li1, Siying Wang1

  • 1Department of Ophthalmology, Shanghai Children's Hospital, School of Medicine, Shanghai Jiao Tong University, Shanghai, China.

Scientific Reports
|July 7, 2022
PubMed

Insights

Children with craniosynostosis exhibit larger V-pattern exotropia and deviations. Their thinner, weaker extraocular muscles require more surgical recession for correction.

Area of Science:

  • Ophthalmology
  • Genetics
  • Pediatric Surgery

Background:

  • V-pattern exotropia is a common strabismus with specific clinical characteristics.
  • Craniosynostosis, a premature fusion of skull sutures, can be associated with various craniofacial abnormalities, potentially impacting ocular alignment.

Purpose of the Study:

  • To compare V-pattern exotropia characteristics between children with craniosynostosis and healthy controls.
  • To investigate potential differences in extraocular muscle (EOM) structure and protein expression in craniosynostosis.

Main Methods:

  • Comparative study including 19 children with craniosynostosis and 20 controls.
  • Comprehensive ocular examinations, strabismus surgery, and analysis of EOM samples.
  • Proteomic analysis to identify differentially expressed proteins in EOMs.

Main Results:

  • Craniosynostosis group showed larger deviations, increased V-pattern, and more severe inferior oblique overaction.
  • Surgical recession and anterior transposition of EOMs differed significantly between groups.
  • Abnormalities in EOMs were found in 32% of craniosynostosis patients versus 5% of controls.
  • 40 differentially expressed proteins were identified, with increased collagen proteins and decreased tropomodulin noted.

Conclusions:

  • Craniosynostosis is associated with more significant V-pattern exotropia and EOM abnormalities.
  • Thinner, weaker EOMs in craniosynostosis necessitate adjusted surgical approaches.
  • Altered protein expression, particularly involving collagen and tropomodulin, may underlie EOM dysfunction in craniosynostosis.