alterations resulting from symptomatology, such as decreased overall activity level, as well as increased systemic inflammation, similar to that which may be observed in other predominantly cutaneous diseases, like psoriasis.Limitations of the study include the retrospective methodology: only recorded comorbid diagnoses, BMI and laboratory data collected in the electronic medical record were available for review. We were unable to grade the severity of LS or associated comorbidities or assess the effect of LS-specific treatments on the risk of cardiovascular comorbidities. Our patient population came from a tertiary referral centre and was overwhelming composed of white women, which may limit generalizability. Additionally, the matched cohort was selected from dermatology and gynaecology outpatients who did not carry a diagnosis of LS, rather than the general population, although how these populations may differ, including rates of cardiovascular comorbidities, is uncertain. Further prospective investigation is warranted to more precisely determine the pathogenesis of these risks and the effect of intervention on risk reduction.