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Drug Intake and Actinic Keratosis: A Case-Control Study

BACKGROUND: Actinic keratosis (AK) is a form of premalignant keratinocyte dysplasia. Recently, the role of photosensitizing drugs in the development of AK has been postulated. OBJECTIVE: This study evaluated a possible association between the use of photosensitizing drugs and the development of AK....

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Autores principales: Sechi, Andrea, di Altobrando, Ambra, Cerciello, Eugenio, Maietti, Elisa, Patrizi, Annalisa, Savoia, Francesco
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Mattioli 1885 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8060000/
https://www.ncbi.nlm.nih.gov/pubmed/33954014
http://dx.doi.org/10.5826/dpc.1102a31
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author Sechi, Andrea
di Altobrando, Ambra
Cerciello, Eugenio
Maietti, Elisa
Patrizi, Annalisa
Savoia, Francesco
author_facet Sechi, Andrea
di Altobrando, Ambra
Cerciello, Eugenio
Maietti, Elisa
Patrizi, Annalisa
Savoia, Francesco
author_sort Sechi, Andrea
collection PubMed
description BACKGROUND: Actinic keratosis (AK) is a form of premalignant keratinocyte dysplasia. Recently, the role of photosensitizing drugs in the development of AK has been postulated. OBJECTIVE: This study evaluated a possible association between the use of photosensitizing drugs and the development of AK. A secondary aim was to identify a possible association between any medication other than those primarily examined and AK. METHODS: A single-center, case-control study assessed the cumulative drug exposure of 90 patients with AK and 90 controls visiting a dermatology service for other skin ailments. Before the visit, patients were interviewed to collect data on daily therapy and the lag-time of discontinued drugs within the last 2 years, and to record the drug’s active ingredient, dosage, and duration of therapy. In addition, sociodemographic characteristics including age, sex, educational level, skin phototype, and cumulative sun exposure habits were gathered. RESULTS: By logistic regression, exposures to angiotensin II receptor blockers (ARBs) and antiplatelet agents were identified as independent risk factors for the development of AK. ARB intake was associated with AK only at high exposure (OR = 13.6; 95% CI, 2.0–93.8). The use of antiplatelet drugs was borderline, yet not significant, at low exposure (OR = 3.31; 95% CI, 0.86–12.7), but increased in a dose-dependent manner. The strongest correlation was found at the highest cumulative dose (>1100 dose unit-years (OR = 4.38; 95% CI, 1.16–16.6). CONCLUSIONS: High exposure to ARBs and antiplatelet agents may promote AK carcinogenesis in at-risk patients.
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spelling pubmed-80600002021-05-04 Drug Intake and Actinic Keratosis: A Case-Control Study Sechi, Andrea di Altobrando, Ambra Cerciello, Eugenio Maietti, Elisa Patrizi, Annalisa Savoia, Francesco Dermatol Pract Concept Research BACKGROUND: Actinic keratosis (AK) is a form of premalignant keratinocyte dysplasia. Recently, the role of photosensitizing drugs in the development of AK has been postulated. OBJECTIVE: This study evaluated a possible association between the use of photosensitizing drugs and the development of AK. A secondary aim was to identify a possible association between any medication other than those primarily examined and AK. METHODS: A single-center, case-control study assessed the cumulative drug exposure of 90 patients with AK and 90 controls visiting a dermatology service for other skin ailments. Before the visit, patients were interviewed to collect data on daily therapy and the lag-time of discontinued drugs within the last 2 years, and to record the drug’s active ingredient, dosage, and duration of therapy. In addition, sociodemographic characteristics including age, sex, educational level, skin phototype, and cumulative sun exposure habits were gathered. RESULTS: By logistic regression, exposures to angiotensin II receptor blockers (ARBs) and antiplatelet agents were identified as independent risk factors for the development of AK. ARB intake was associated with AK only at high exposure (OR = 13.6; 95% CI, 2.0–93.8). The use of antiplatelet drugs was borderline, yet not significant, at low exposure (OR = 3.31; 95% CI, 0.86–12.7), but increased in a dose-dependent manner. The strongest correlation was found at the highest cumulative dose (>1100 dose unit-years (OR = 4.38; 95% CI, 1.16–16.6). CONCLUSIONS: High exposure to ARBs and antiplatelet agents may promote AK carcinogenesis in at-risk patients. Mattioli 1885 2021-04-12 /pmc/articles/PMC8060000/ /pubmed/33954014 http://dx.doi.org/10.5826/dpc.1102a31 Text en ©2021 Sechi et al https://creativecommons.org/licenses/by/4.0/This is an open-access article distributed under the terms of the Creative Commons Attribution License BY-NC-4.0, which permits unrestricted noncommercial use, distribution, and reproduction in any medium, provided the original authors and source are credited.
spellingShingle Research
Sechi, Andrea
di Altobrando, Ambra
Cerciello, Eugenio
Maietti, Elisa
Patrizi, Annalisa
Savoia, Francesco
Drug Intake and Actinic Keratosis: A Case-Control Study
title Drug Intake and Actinic Keratosis: A Case-Control Study
title_full Drug Intake and Actinic Keratosis: A Case-Control Study
title_fullStr Drug Intake and Actinic Keratosis: A Case-Control Study
title_full_unstemmed Drug Intake and Actinic Keratosis: A Case-Control Study
title_short Drug Intake and Actinic Keratosis: A Case-Control Study
title_sort drug intake and actinic keratosis: a case-control study
topic Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8060000/
https://www.ncbi.nlm.nih.gov/pubmed/33954014
http://dx.doi.org/10.5826/dpc.1102a31
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