Background:
Acne is a chronic inflammatory disease and mainly seen in adolescence, but it
can also be seen during the neonatal, infantile, pre-pubertal, and adult periods. Isotretinoin
(13-cis-retinoic acid) is a first-generation retinoid and is the most effective treatment for acne
vulgaris.
Objective:
Serious adverse effects of teratogenicity and spontaneous abortions, skin irritation,
cheilitis, photosensitivity, arthralgias, hypertriglyceridemia, infammatory bowel disease,
pancreatitis, and depression, have all been documented. However, there were very limited
reports about its genotoxicity, carcinogenicity. The present study has been systematically
designed to undertake the toxic, genotoxic, and carcinogenic activities of isotretinoin.
Method: In this study, a systematic approach was followed by focusing on the possible links
between these topics. The search of the databases was carried out by two independent
researchers in accordance with the guidelines of the Centre for Reviews and Dissemination
(2009) developed by York University National Institute of Health Research. The search was
concentrated on the Web of Science, PubMed, Science Direct, Scopus, EBSCO Host, and
Google Scholar databases
Results:
Isotretinoin was found a toxic agent in all studies. All researchers proposed that
apoptosis is the only pathway of adverse effects of isotretinoin. However, genotoxicity,
teratogenicity and carcinogenicity information of isotretinoin is very limited and
controversial.
Conclusion:
More detailed study needs to clarify the genotoxic and carcinogenic potential of
isotretinoin. Patients should be informed correctly, the risks of treatment should be explained,
and awareness should be raised.