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The mechanisms of action and use of botulinum neurotoxin type A in aesthetics: Key Clinical Postulates II

BACKGROUND: The literature on botulinum neurotoxin type A (BoNT‐A) is extensive, often contradictory, and confounded by a competitive market of products and research attempting to distinguish brand individuality. METHODS: A comprehensive review of literature on the principles of BoNT‐A in aesthetics...

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Detalles Bibliográficos
Autores principales: Nestor, Mark S., Arnold, David, Fischer, Daniel
Formato: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley and Sons Inc. 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7693297/
https://www.ncbi.nlm.nih.gov/pubmed/32866999
http://dx.doi.org/10.1111/jocd.13702
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author Nestor, Mark S.
Arnold, David
Fischer, Daniel
author_facet Nestor, Mark S.
Arnold, David
Fischer, Daniel
author_sort Nestor, Mark S.
collection PubMed
description BACKGROUND: The literature on botulinum neurotoxin type A (BoNT‐A) is extensive, often contradictory, and confounded by a competitive market of products and research attempting to distinguish brand individuality. METHODS: A comprehensive review of literature on the principles of BoNT‐A in aesthetics as well as clinical examples. RESULTS: In 2017, the Eight Key Clinical Postulates were formulated as a guide for the aesthetic practitioner in understanding BoNT‐A pharmacodynamics and to compare different toxins. These are now updated to include (a) All type A toxins act identically; (b) The mathematical relationship between toxin and receptor is the basis of efficacy, and clinical efficacy is influenced by molecular potency and patient attributes including muscle mass, gender, age, and ethnicity; (c) Efficacy, onset, and duration are functions of “molecular potency” defined as the number of active 150 kDa molecules available for binding; (d) “Molecular potency” is difficult to objectively quantify for commercially available toxins; (e) Up to a point, increased molecular potency decreases time to onset and increases duration of effect, and the “Molecular Potency Quotient” is a construct for comparing molecular potency commercial cost; (f) The area of effect of a toxin injection is dependent upon molecular potency, diffusion (passive), and spread (active); (g) Differing reconstitution volumes; and (h) Increased number of injection sites can affect spread, onset, and duration of effect. CONCLUSIONS: The principles of BoNT‐A use in aesthetics are complex yet understandable as outlined in the framework of the updated Eight Key Clinical Postulates and serves as a useful tool for providing the most effective treatment and interpreting research on present and future toxin formulations.
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spelling pubmed-76932972020-12-11 The mechanisms of action and use of botulinum neurotoxin type A in aesthetics: Key Clinical Postulates II Nestor, Mark S. Arnold, David Fischer, Daniel J Cosmet Dermatol Review Articles BACKGROUND: The literature on botulinum neurotoxin type A (BoNT‐A) is extensive, often contradictory, and confounded by a competitive market of products and research attempting to distinguish brand individuality. METHODS: A comprehensive review of literature on the principles of BoNT‐A in aesthetics as well as clinical examples. RESULTS: In 2017, the Eight Key Clinical Postulates were formulated as a guide for the aesthetic practitioner in understanding BoNT‐A pharmacodynamics and to compare different toxins. These are now updated to include (a) All type A toxins act identically; (b) The mathematical relationship between toxin and receptor is the basis of efficacy, and clinical efficacy is influenced by molecular potency and patient attributes including muscle mass, gender, age, and ethnicity; (c) Efficacy, onset, and duration are functions of “molecular potency” defined as the number of active 150 kDa molecules available for binding; (d) “Molecular potency” is difficult to objectively quantify for commercially available toxins; (e) Up to a point, increased molecular potency decreases time to onset and increases duration of effect, and the “Molecular Potency Quotient” is a construct for comparing molecular potency commercial cost; (f) The area of effect of a toxin injection is dependent upon molecular potency, diffusion (passive), and spread (active); (g) Differing reconstitution volumes; and (h) Increased number of injection sites can affect spread, onset, and duration of effect. CONCLUSIONS: The principles of BoNT‐A use in aesthetics are complex yet understandable as outlined in the framework of the updated Eight Key Clinical Postulates and serves as a useful tool for providing the most effective treatment and interpreting research on present and future toxin formulations. John Wiley and Sons Inc. 2020-09-16 2020-11 /pmc/articles/PMC7693297/ /pubmed/32866999 http://dx.doi.org/10.1111/jocd.13702 Text en © 2020 The Authors. Journal of Cosmetic Dermatology published by Wiley Periodicals LLC This is an open access article under the terms of the http://creativecommons.org/licenses/by-nc-nd/4.0/ License, which permits use and distribution in any medium, provided the original work is properly cited, the use is non‐commercial and no modifications or adaptations are made.
spellingShingle Review Articles
Nestor, Mark S.
Arnold, David
Fischer, Daniel
The mechanisms of action and use of botulinum neurotoxin type A in aesthetics: Key Clinical Postulates II
title The mechanisms of action and use of botulinum neurotoxin type A in aesthetics: Key Clinical Postulates II
title_full The mechanisms of action and use of botulinum neurotoxin type A in aesthetics: Key Clinical Postulates II
title_fullStr The mechanisms of action and use of botulinum neurotoxin type A in aesthetics: Key Clinical Postulates II
title_full_unstemmed The mechanisms of action and use of botulinum neurotoxin type A in aesthetics: Key Clinical Postulates II
title_short The mechanisms of action and use of botulinum neurotoxin type A in aesthetics: Key Clinical Postulates II
title_sort mechanisms of action and use of botulinum neurotoxin type a in aesthetics: key clinical postulates ii
topic Review Articles
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7693297/
https://www.ncbi.nlm.nih.gov/pubmed/32866999
http://dx.doi.org/10.1111/jocd.13702
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