Lichen planus autoimmune comorbidities: A retrospective case control study.
Dermatol Online J 2026 Jan 05; 31(6).

Abstract

PURPOSE

To assess whether patients with lichen planus (LP) show increased prevalence and odds of autoimmune and viral comorbidities compared with matched controls using real-world data.

METHODS

We analyzed TriNetX Linked Network electronic health records and claims data from 2016 to 2024 (more than 112 million patients). LP was defined by at least 2 International Classification of Diseases, Tenth Revision, Clinical Modification codes (excluding drug-induced variants) and matched 1:1 to controls on age, sex, and race. We calculated odds ratios (ORs), 95% confidence intervals, prevalence, and absolute risk differences (ARDs).

RESULTS

The matched cohort included 43 458 LP and control patients (mean age, 53.8 years; 64.4% female). LP was associated with higher prevalence of autoimmune conditions, including psoriasis (6.59% versus 2.54%; ARD, 4.05%; OR, 2.71), lupus erythematosus (2.87% versus 1.13%; ARD, 1.74%; OR, 2.58), and autoimmune thyroiditis (3.09% versus 1.61%; ARD, 1.48%; OR, 1.95). Associations were also seen for Sjögren syndrome, alopecia areata, localized scleroderma, and vitiligo. Hepatitis C virus was more common in LP (2.95% versus 2.03%; ARD, 0.92%) but with a lower OR (1.47).

CONCLUSION

LP was associated with substantially higher odds and prevalence of several autoimmune comorbidities, exceeding those for viral infections such as hepatitis C. These findings inform LP pathogenesis and comorbidity patterns but do not support changes to clinical management.

Authors+Show Affiliations

Rosenberg ALDepartment of Dermatology, University of Texas Southwestern Medical Center, Dallas, TX, USA.
Wu ADepartment of Dermatology, University of Texas Southwestern Medical Center, Dallas, TX, USA.
DeBusk LDepartment of Dermatology, University of Texas Southwestern Medical Center, Dallas, TX, USA.
Mehta AColumbia University Vagelos College of Physicians and Surgeons, New York, NY, USA.
Bartley BDepartment of Dermatology, University of Texas Southwestern Medical Center, Dallas, TX, USA.
McAleer LDepartment of Dermatology, University of Texas Southwestern Medical Center, Dallas, TX, USA.
Dominguez RDepartment of Dermatology, University of Texas Southwestern Medical Center, Dallas, TX, USA.
Rigel DDepartment of Dermatology, University of Texas Southwestern Medical Center, Dallas, TX, USA. Department of Dermatology, NYU Grossman School of Medicine, New York, NY, USA.
Mauskar MDepartment of Dermatology, University of Texas Southwestern Medical Center, Dallas, TX, USA. Department of Obstetrics and Gynecology, UT Southwestern Medical Center, Dallas, TX, USA.
Merola JFDepartment of Dermatology, University of Texas Southwestern Medical Center, Dallas, TX, USA. Department of Dermatology, Division of Rheumatology, University of Texas Southwestern Medical Center, Dallas, TX, USA.
Nezafati KDepartment of Dermatology, University of Texas Southwestern Medical Center, Dallas, TX, USA.

Pub Type(s)

Journal Article

Language

eng

PubMed ID

42246344