Treatment of Keloid Scars with Botulinum Toxin Type A versus Triamcinolone in an Athymic Nude Mouse Model.


Journal

Plastic and reconstructive surgery
ISSN: 1529-4242
Titre abrégé: Plast Reconstr Surg
Pays: United States
ID NLM: 1306050

Informations de publication

Date de publication:
03 2019
Historique:
pubmed: 3 1 2019
medline: 30 4 2019
entrez: 3 1 2019
Statut: ppublish

Résumé

Keloid scarring is a serious condition that mostly affects patients of African or Asian descent. Often disfiguring, this condition can have devastating psychosocial consequences. To date, no treatment modality has been proven ideal. The authors' objectives were (1) to determine the efficacy of botulin toxin type A injection for the treatment of keloid scars compared to steroid injection and to control saline injection (this was achieved through a basic science animal model using athymic nude mice and implanted human keloid tissue); and (2) to analyze the histopathologic changes that occur in an organized keloid scar following botulinum toxin type A injection as compared to steroid and saline injections. Keloid scars from four patients were excised and implanted subcutaneously into 28 mice. Three small keloid tissue samples were implanted in each of the 28 mice. One week after implantation, each implant received one of three injections: botulinum toxin type A (treatment drug), saline (control), or steroid injection (first-line gold standard). The keloid tissue was extracted 3 weeks after implantation. Weight analysis, immunohistochemistry, and standard hematoxylin and eosin pathologic analysis were performed on each extracted tissue sample. Paired t test analysis of pretreatment and posttreatment tissue weights revealed a statistically significant difference between the treatment and control groups (p < 0.05). Analysis by a blinded pathologist confirmed fewer collagen bundles in the treatment group. Immunohistochemistry with Ki-67, a marker of cell proliferation, revealed significantly less staining in the treatment groups. Botulinum toxin type A could be an effective treatment for keloid scars.

Sections du résumé

BACKGROUND
Keloid scarring is a serious condition that mostly affects patients of African or Asian descent. Often disfiguring, this condition can have devastating psychosocial consequences. To date, no treatment modality has been proven ideal. The authors' objectives were (1) to determine the efficacy of botulin toxin type A injection for the treatment of keloid scars compared to steroid injection and to control saline injection (this was achieved through a basic science animal model using athymic nude mice and implanted human keloid tissue); and (2) to analyze the histopathologic changes that occur in an organized keloid scar following botulinum toxin type A injection as compared to steroid and saline injections.
METHODS
Keloid scars from four patients were excised and implanted subcutaneously into 28 mice. Three small keloid tissue samples were implanted in each of the 28 mice. One week after implantation, each implant received one of three injections: botulinum toxin type A (treatment drug), saline (control), or steroid injection (first-line gold standard). The keloid tissue was extracted 3 weeks after implantation. Weight analysis, immunohistochemistry, and standard hematoxylin and eosin pathologic analysis were performed on each extracted tissue sample.
RESULTS
Paired t test analysis of pretreatment and posttreatment tissue weights revealed a statistically significant difference between the treatment and control groups (p < 0.05). Analysis by a blinded pathologist confirmed fewer collagen bundles in the treatment group. Immunohistochemistry with Ki-67, a marker of cell proliferation, revealed significantly less staining in the treatment groups.
CONCLUSION
Botulinum toxin type A could be an effective treatment for keloid scars.

Identifiants

pubmed: 30601323
doi: 10.1097/PRS.0000000000005323
pii: 00006534-201903000-00020
doi:

Substances chimiques

Acetylcholine Release Inhibitors 0
Glucocorticoids 0
Triamcinolone 1ZK20VI6TY
Botulinum Toxins, Type A EC 3.4.24.69

Types de publication

Comparative Study Journal Article

Langues

eng

Sous-ensembles de citation

IM

Pagination

760-767

Commentaires et corrections

Type : CommentIn

Références

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Auteurs

Amanda Fanous (A)

From the Departments of Otolaryngology, Experimental Surgery, and Otolaryngology, McGill University; McGill Auditory Sciences Laboratory; and the Department of Pathology, McGill University Health Centre.

Aren Bezdjian (A)

From the Departments of Otolaryngology, Experimental Surgery, and Otolaryngology, McGill University; McGill Auditory Sciences Laboratory; and the Department of Pathology, McGill University Health Centre.

Derin Caglar (D)

From the Departments of Otolaryngology, Experimental Surgery, and Otolaryngology, McGill University; McGill Auditory Sciences Laboratory; and the Department of Pathology, McGill University Health Centre.

Aleksander Mlynarek (A)

From the Departments of Otolaryngology, Experimental Surgery, and Otolaryngology, McGill University; McGill Auditory Sciences Laboratory; and the Department of Pathology, McGill University Health Centre.

Nabil Fanous (N)

From the Departments of Otolaryngology, Experimental Surgery, and Otolaryngology, McGill University; McGill Auditory Sciences Laboratory; and the Department of Pathology, McGill University Health Centre.

Stephanie Fay Lenhart (SF)

From the Departments of Otolaryngology, Experimental Surgery, and Otolaryngology, McGill University; McGill Auditory Sciences Laboratory; and the Department of Pathology, McGill University Health Centre.

Sam J Daniel (SJ)

From the Departments of Otolaryngology, Experimental Surgery, and Otolaryngology, McGill University; McGill Auditory Sciences Laboratory; and the Department of Pathology, McGill University Health Centre.

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