Risk Factors for Lichen Sclerosus: A Case-Control Study of 43,000 Finnish Women

Author:

Halonen Pia1,Heikinheimo Oskari1,Hadkhale Kishor2,Gissler Mika3,Pukkala Eero4,Jakobsson Maija5

Affiliation:

1. Department of Obstetrics and Gynecology, University of Helsinki and Helsinki University Hospital, Helsinki, Finland

2. Health Sciences Unit, Faculty of Social Sciences, Tampere University, Tampere, Finland

3. Department of Knowledge Brokers, Finnish Institute for Health and Welfare, Helsinki, Finland; Department of Molecular Medicine and Surgery, Karolinska Institutet, Stockholm, Sweden; Region Stockholm, Academic Primary Health Care Centre, Stockholm, Sweden

4. Finnish Cancer Registry, Institute for Statistical and Epidemiological Cancer Research, Helsinki, Finland; Health Sciences Unit, Faculty of Social Sciences, Tampere University, Tampere, Finland

5. Department of Obstetrics and Gynecology, Hyvinkää Hospital and University of Helsinki, Hyvinkää, Finland

Abstract

Objectives Lichen sclerosus (LS) is an inflammatory skin disease probably arising from an interplay of genetics, local irritation, and autoimmune processes. We identified potential risk factors for the disease using data from nationwide Finnish registries. Methods We identified all women diagnosed with LS within specialized health care during 1998–2016 (n = 10,692) and selected 3 age-matched population control women for each case. We calculated odds ratios (ORs) for possible risk factors using conditional logistic regression. Results Dermatological autoimmune conditions were strongly associated with LS (OR = 15.1, 95% confidence interval [CI] = 13.6–16.7 for morphea; OR = 10.3, 95% CI = 5.02–19.0 for lichen planus; OR = 6.86, 95% CI = 5.65–8.33 for alopecia; OR = 2.20, 95% CI = 1.88–2.56 for vitiligo). A diagnosis of Crohn or celiac disease increased the odds of LS (OR = 1.80, 95% CI = 1.71–1.89; OR = 1.49, 95% CI = 1.28–1.73, respectively) as did urge and stress incontinence (OR = 1.79, 95% CI = 1.71–1.87; OR = 1.28, 95% CI = 1.22–1.35, respectively). The odds of LS were lower in women after a diagnosis of type 1 diabetes (OR = 0.43, 95% CI = 0.41–0.45), coronary artery disease (OR = 0.41, 95% CI = 0.38–0.43), and rheumatoid arthritis (OR = 0.38, 95% CI = 0.36–0.41). Parous women had higher odds of LS (OR = 1.11, 95% CI = 1.04–1.17) than nulliparous ones, but increasing number of births decreased the risk. Lichen sclerosus was not associated with socioeconomic status nor the urbanicity level of the place of residence. Conclusions Certain autoimmune diseases and urinary incontinence were associated with LS.

Publisher

Ovid Technologies (Wolters Kluwer Health)

Reference23 articles.

1. Does treatment of vulvar lichen sclerosus influence its prognosis?;Arch Dermatol,2004

2. Long-term management of adult vulvar lichen sclerosus;JAMA Dermatol,2015

3. Vulvar lichen sclerosus: effect of long-term topical application of a potent steroid on the course of the disease;Arch Dermatol,2004

4. The risk of developing squamous cell carcinoma in patients with anogenital lichen sclerosis: a systematic review;Gynecol Oncol,2020

5. Lichen sclerosus: an autoimmunopathogenic and genomic enigma with emerging genetic and immune targets;Int J Biol Sci,2019

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