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Abstract

Background: Lichen sclerosus (LS) is an acquired, non-communicable, chronic inflammatory disease that predominantly affects the genital area and may lead to substantial impairment in quality of life. While some studies reported elevated rates of depression and anxiety among patients with LS, the available evidence is limited by often small sample sizes, cross-sectional designs, narrow matching, and limited consideration of sex- or race-disparities. Moreover, the risk of a broader spectrum of psychiatric disorders remains insufficiently characterized. Objective: To evaluate the risk of a larger spectrum of psychiatric disorders following a diagnosis of LS in a retrospective cohort study. Methods: The US Collaborative Network of TriNetX was used to create a propensity-score-matched cohort of individuals with LS and non-LS controls (n = 42,581 per cohort). Risk of psychiatric disorders following the index events was analyzed in a retrospective cohort study. Several sensitivity analyses were conducted to assess robustness of the findings. Subgroup analyses were performed to identify potential sex- or racial-disparities. Results: Within 5 years, 3.92% of patients with LS as opposed to 3.43% of controls were subsequently diagnosed with a depressive episode (HR 1.31, CI 1.22–1.40, p < 0.0001). Furthermore, risks of recurrent major depression (HR 1.71, CI 1.48–1.98, p < 0.0001) and reaction to severe stress (HR 1.62, CI 1.45–1.80, p < 0.0001) were increased in patients with LS. These risks seemed more pronounced in those of White ethnicity and in women. Risks for suicidal ideations, suicide attempts, and schizophrenia were not different between patients and matched controls. Conclusion: Patients with LS are at a moderately increased risk of depression and stress-related psychiatric disorders.

OriginalspracheEnglisch
Aufsatznummer1653347
ZeitschriftFrontiers in medicine
Jahrgang12
ISSN2296-858X
DOIs
PublikationsstatusVeröffentlicht - 2025

Fördermittel

The author(s) declare that financial support was received for the research and/or publication of this article. This work was supported by the Cluster of Excellence Precision Medicine in Chronic Inflammation (EXC 2167), Individual Research Grant LU 877/25-1, by the Deutsche Forschungsgemeinschaft and the Schleswig-Holstein Excellence-Chair Program from the State of Schleswig-Holstein. PC was supported by Region Stockholm, Karolinska Institutet, Hudfonden, and the Tore Nilson Foundation.

TrägerTrägernummer
Schleswig-Holstein
Deutsche Forschungsgemeinschaft
Karolinska Institutet
Tore Nilsons Stiftelse för Medicinsk Forskning
HudFonden

    UN SDGs

    Dieser Output leistet einen Beitrag zu folgendem(n) Ziel(en) für nachhaltige Entwicklung

    1. SDG 3 – Gesundheit und Wohlergehen
      SDG 3 – Gesundheit und Wohlergehen

    Strategische Forschungsbereiche und Zentren

    • Forschungsschwerpunkt: Infektion und Entzündung - Zentrum für Infektions- und Entzündungsforschung Lübeck (ZIEL)
    • Zentren: Center for Research on Inflammation of the Skin (CRIS)

    DFG-Fachsystematik

    • 2.21-05 Immunologie
    • 2.22-19 Dermatologie
    • 2.23-10 Klinische Psychiatrie, Psychotherapie und Kinder- und Jugendpsychiatrie

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