Longitudinal course and predictors of depressive symptoms in atopic dermatitis

J Am Acad Dermatol. 2022 Sep;87(3):582-591. doi: 10.1016/j.jaad.2022.04.061. Epub 2022 May 10.

Abstract

Background: Atopic dermatitis (AD) is associated with eczematous lesions, pruritus, pain, and sleep disturbance, which may negatively impact mental health over time.

Objective: To determine the predictors and longitudinal course of depressive symptoms in adults with AD.

Methods: A prospective, dermatology practice-based study was performed (N = 695). AD signs, symptoms, and severity and patient health questionnaire-9 (PHQ-9) were assessed.

Results: At baseline, of the 695 participants, 454 (65.32%) had minimal, 139 (20.00%) had mild, 57 (8.20%) had moderate, 27 (3.88%) had moderately severe, and 8 (2.59%) had severe depression. Most had fluctuating levels of depressive symptoms. Feeling bad, thoughts of self-harm, difficulty concentrating, and slow movement were most persistent. Predictors of persistent depression included older age, non-White race, male sex, public or no insurance, more severe itch, skin pain, facial erythema, nipple eczema, sleep disturbance, and presence of pityriasis alba.

Limitations: Single center study.

Conclusion: Depressive symptoms are closely related to and fluctuate with AD severity over time. Improved control of AD signs and symptoms, particularly itch, may secondarily improve mental health.

Keywords: atopic dermatitis; depression; eczema; emotional; longitudinal; prospective; pruritus; psychology.

Publication types

  • Research Support, Non-U.S. Gov't
  • Research Support, U.S. Gov't, P.H.S.

MeSH terms

  • Adult
  • Depression / diagnosis
  • Depression / epidemiology
  • Depression / etiology
  • Dermatitis, Atopic* / complications
  • Dermatitis, Atopic* / diagnosis
  • Dermatitis, Atopic* / epidemiology
  • Humans
  • Male
  • Pain / diagnosis
  • Prospective Studies
  • Pruritus / diagnosis
  • Quality of Life
  • Severity of Illness Index
  • Sleep Wake Disorders* / epidemiology
  • Sleep Wake Disorders* / etiology