A Study of Botulinum Toxin A for Ultraviolet-Induced Hyperpigmentation: A Randomized Controlled Trial

BACKGROUNDUltraviolet (UV) exposure contributes to skin hyperpigmentation. Recently, botulinum neurotoxin type A (BoNT-A) showed a promising protective effect on UVB-induced hyperpigmentation in both in vitro and animal models.OBJECTIVEThe study aimed to investigate the preventive effect of BoNT-A a...

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Main Authors: Vasanop Vachiramon, Chaninan Kositkuljorn, Kanchana Leerunyakul, Teeraphong Rattananukrom, Natthachat Jurairattanaporn
Other Authors: Faculty of Medicine Ramathibodi Hospital, Mahidol University
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Published: 2022
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Online Access:https://repository.li.mahidol.ac.th/handle/123456789/78239
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spelling th-mahidol.782392022-08-04T16:25:18Z A Study of Botulinum Toxin A for Ultraviolet-Induced Hyperpigmentation: A Randomized Controlled Trial Vasanop Vachiramon Chaninan Kositkuljorn Kanchana Leerunyakul Teeraphong Rattananukrom Natthachat Jurairattanaporn Faculty of Medicine Ramathibodi Hospital, Mahidol University Medicine BACKGROUNDUltraviolet (UV) exposure contributes to skin hyperpigmentation. Recently, botulinum neurotoxin type A (BoNT-A) showed a promising protective effect on UVB-induced hyperpigmentation in both in vitro and animal models.OBJECTIVEThe study aimed to investigate the preventive effect of BoNT-A against UVB-induced hyperpigmentation in human subjects.MATERIALS AND METHODSA prospective, double-blinded, randomized controlled trial was performed in 15 healthy participants. Four separate square areas on the abdomen were randomly injected intradermally with different dilutions of BoNT-A (1:2.5, 1:5, 1:7.5) and normal saline (control). Two weeks after injection, hyperpigmented spots were induced by UVB irradiation at the experimental sites. The lightness index and hyperpigmentation scores from blinded physician and participants were evaluated.RESULTSFifteen participants completed the study. One week after UVB irradiation, all BoNT-A-treated sites had a significantly lower degree of hyperpigmentation than the control site in lightness index and hyperpigmentation scores from blinded physician and participants (p <.05). However, no statistically significant difference was observed between different concentrations of BoNT-A. No side effects were observed throughout the study period.CONCLUSIONIntradermal BoNT-A injection provided a protective effect from UVB-induced hyperpigmentation. It may be used for other hyperpigmentation disorders that are aggravated by UVB. 2022-08-04T09:25:18Z 2022-08-04T09:25:18Z 2021-05-01 Article Dermatologic Surgery. Vol.47, No.5 (2021), E174-E178 10.1097/DSS.0000000000002943 15244725 10760512 2-s2.0-85105834172 https://repository.li.mahidol.ac.th/handle/123456789/78239 Mahidol University SCOPUS https://www.scopus.com/inward/record.uri?partnerID=HzOxMe3b&scp=85105834172&origin=inward
institution Mahidol University
building Mahidol University Library
continent Asia
country Thailand
Thailand
content_provider Mahidol University Library
collection Mahidol University Institutional Repository
topic Medicine
spellingShingle Medicine
Vasanop Vachiramon
Chaninan Kositkuljorn
Kanchana Leerunyakul
Teeraphong Rattananukrom
Natthachat Jurairattanaporn
A Study of Botulinum Toxin A for Ultraviolet-Induced Hyperpigmentation: A Randomized Controlled Trial
description BACKGROUNDUltraviolet (UV) exposure contributes to skin hyperpigmentation. Recently, botulinum neurotoxin type A (BoNT-A) showed a promising protective effect on UVB-induced hyperpigmentation in both in vitro and animal models.OBJECTIVEThe study aimed to investigate the preventive effect of BoNT-A against UVB-induced hyperpigmentation in human subjects.MATERIALS AND METHODSA prospective, double-blinded, randomized controlled trial was performed in 15 healthy participants. Four separate square areas on the abdomen were randomly injected intradermally with different dilutions of BoNT-A (1:2.5, 1:5, 1:7.5) and normal saline (control). Two weeks after injection, hyperpigmented spots were induced by UVB irradiation at the experimental sites. The lightness index and hyperpigmentation scores from blinded physician and participants were evaluated.RESULTSFifteen participants completed the study. One week after UVB irradiation, all BoNT-A-treated sites had a significantly lower degree of hyperpigmentation than the control site in lightness index and hyperpigmentation scores from blinded physician and participants (p <.05). However, no statistically significant difference was observed between different concentrations of BoNT-A. No side effects were observed throughout the study period.CONCLUSIONIntradermal BoNT-A injection provided a protective effect from UVB-induced hyperpigmentation. It may be used for other hyperpigmentation disorders that are aggravated by UVB.
author2 Faculty of Medicine Ramathibodi Hospital, Mahidol University
author_facet Faculty of Medicine Ramathibodi Hospital, Mahidol University
Vasanop Vachiramon
Chaninan Kositkuljorn
Kanchana Leerunyakul
Teeraphong Rattananukrom
Natthachat Jurairattanaporn
format Article
author Vasanop Vachiramon
Chaninan Kositkuljorn
Kanchana Leerunyakul
Teeraphong Rattananukrom
Natthachat Jurairattanaporn
author_sort Vasanop Vachiramon
title A Study of Botulinum Toxin A for Ultraviolet-Induced Hyperpigmentation: A Randomized Controlled Trial
title_short A Study of Botulinum Toxin A for Ultraviolet-Induced Hyperpigmentation: A Randomized Controlled Trial
title_full A Study of Botulinum Toxin A for Ultraviolet-Induced Hyperpigmentation: A Randomized Controlled Trial
title_fullStr A Study of Botulinum Toxin A for Ultraviolet-Induced Hyperpigmentation: A Randomized Controlled Trial
title_full_unstemmed A Study of Botulinum Toxin A for Ultraviolet-Induced Hyperpigmentation: A Randomized Controlled Trial
title_sort study of botulinum toxin a for ultraviolet-induced hyperpigmentation: a randomized controlled trial
publishDate 2022
url https://repository.li.mahidol.ac.th/handle/123456789/78239
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