Ocular surface disease in moderate-to-severe atopic dermatitis patients and the effect of biological therapy

Roselie Achten1, Judith Thijs1, Marlot van der Wal2

  • 1Department of Dermatology and Allergology, National Expertise Center for Atopic Dermatitis, University Medical Center Utrecht, Utrecht, The Netherlands.

Insights

Most moderate-to-severe atopic dermatitis (AD) patients have ocular surface disease (OSD) before treatment. Dupilumab therapy can cause or worsen OSD, necessitating ophthalmologist consultation.

Area of Science:

  • Ophthalmology
  • Dermatology
  • Immunology

Background:

  • Atopic dermatitis (AD) is a chronic inflammatory skin condition with increasing targeted therapy options.
  • Ocular surface disease (OSD) is frequently observed in AD patients, often preceding targeted treatments.
  • Understanding OSD in moderate-to-severe AD is crucial due to reported increased rates during new therapies.

Purpose of the Study:

  • To review the prevalence and characteristics of OSD in moderate-to-severe AD patients.
  • To investigate the development and potential mechanisms of dupilumab-associated OSD (DAOSD).
  • To provide clinical recommendations for managing OSD in AD patients undergoing targeted therapy.

Main Methods:

  • Literature review of studies on OSD in AD patients.
  • Analysis of OSD prevalence and risk factors in moderate-to-severe AD.
  • Examination of DAOSD occurrence, clinical presentation, and potential pathomechanisms during dupilumab treatment.

Main Results:

  • Most moderate-to-severe AD patients exhibit OSD characteristics before initiating targeted therapy.
  • OSD in AD is linked to reduced conjunctival goblet cells, high disease activity, and specific biomarkers.
  • DAOSD affects approximately one-third of dupilumab-treated AD patients, potentially linked to pre-existing ocular conditions and reduced Mucin 5AC expression.

Conclusions:

  • OSD is common in moderate-to-severe AD, often present before treatment.
  • Dupilumab treatment can lead to new-onset or worsening OSD, with potential mechanisms involving goblet cell function.
  • Clinicians should proactively screen for OSD in AD patients and refer to ophthalmology when indicated.