Alcohol intake and early‐onset basal cell carcinoma in a case–control study

Y Zhang, LM Ferrucci, B Cartmel… - British Journal of …, 2014 - academic.oup.com
Y Zhang, LM Ferrucci, B Cartmel, AM Molinaro, DJ Leffell, AE Bale, ST Mayne
British Journal of Dermatology, 2014academic.oup.com
Background Previous epidemiological studies of overall alcohol intake and basal cell
carcinoma (BCC) are inconsistent, with some evidence for differences by type of alcoholic
beverage. While alcohol may enhance the carcinogenicity of ultraviolet (UV) radiation, this
has not been evaluated in existing epidemiological studies. Objectives To evaluate alcohol
intake in relation to early‐onset BCC, and explore potential interactions with UV exposure.
Methods Basal cell carcinoma cases (n= 380) and controls with benign skin conditions (n …
Background
Previous epidemiological studies of overall alcohol intake and basal cell carcinoma (BCC) are inconsistent, with some evidence for differences by type of alcoholic beverage. While alcohol may enhance the carcinogenicity of ultraviolet (UV) radiation, this has not been evaluated in existing epidemiological studies.
Objectives
To evaluate alcohol intake in relation to early‐onset BCC, and explore potential interactions with UV exposure.
Methods
Basal cell carcinoma cases (n =380) and controls with benign skin conditions (n =390) under 40 years of age were identified through Yale Dermatopathology. Participants provided information on lifetime alcohol intake, including type of beverage, during an in‐person interview. Self‐reported data on indoor tanning and outdoor sunbathing were used to categorize UV exposure. We calculated odds ratios (OR) and 95% confidence intervals (CIs) using unconditional multivariate logistic regression in the full sample and in women only.
Results
There was no statistically significant association between lifetime alcohol intake and early‐onset BCC overall [above median intake vs. no regular alcohol intake (OR 1·10, 95% CI 0·69–1·73)] or in women only (OR 1·21, 95% CI 0·73–2·01). Similarly, intake of red wine, white wine, beer or spirits and mixed drinks was not associated with early‐onset BCC. In exploratory analyses, we saw limited evidence for an interaction (Pinteraction = 0·003), with highest risk for high alcohol and high UV exposures, especially in women, but subgroup risk estimates had wide and overlapping CIs.
Conclusions
Overall, we did not observe any clear association between lifetime alcohol intake and early‐onset BCC.
Oxford University Press