Long-Term Use of

acne lipid droplet proteins microcomedones phytotherapy real-life study sebum

Journal

Journal of personalized medicine
ISSN: 2075-4426
Titre abrégé: J Pers Med
Pays: Switzerland
ID NLM: 101602269

Informations de publication

Date de publication:
31 Dec 2022
Historique:
received: 21 11 2022
revised: 16 12 2022
accepted: 19 12 2022
entrez: 21 1 2023
pubmed: 22 1 2023
medline: 22 1 2023
Statut: epublish

Résumé

Homeostasis in the differentiation programme of sebaceous stem cells has been identified as a key step in comedogenesis and should be a target for acne-prone skin care. To report on a multicentre, year-long/real-life use study of a patented natural product containing An open-label multicentric international study, with a 12 month follow-up, included 54 teenage and young adult subjects with mild to moderate facial acne. The study was aimed at reproducing a real-life use context. Total lesion count mean was 88.3 at inclusion. There was a sustained, highly significant decrease over the months of clinical lesion counts (45.6% improvement after 6 months and 59.6% at 12 months) and on other efficacy markers, associated with a significant decrease in global microcomedone quantity on cyanoacrylate superficial skin surface biopsies. Importantly, the study protocol allowed the dermatologist to prescribe, if needed as in real life, any of the acne drugs registered in the acne guidelines. The exposure to these acne drugs during the whole year was calculated as a percentage of The association with routine prescription acne drugs when needed, even if limited, does not allow a full evaluation of the intrinsic quantitative efficacy of This open, real-life, year-long multicentre study confirms a previous 48-week proof of concept study and qualifies the use of

Sections du résumé

BACKGROUND BACKGROUND
Homeostasis in the differentiation programme of sebaceous stem cells has been identified as a key step in comedogenesis and should be a target for acne-prone skin care.
OBJECTIVE OBJECTIVE
To report on a multicentre, year-long/real-life use study of a patented natural product containing
METHODS METHODS
An open-label multicentric international study, with a 12 month follow-up, included 54 teenage and young adult subjects with mild to moderate facial acne. The study was aimed at reproducing a real-life use context.
RESULTS RESULTS
Total lesion count mean was 88.3 at inclusion. There was a sustained, highly significant decrease over the months of clinical lesion counts (45.6% improvement after 6 months and 59.6% at 12 months) and on other efficacy markers, associated with a significant decrease in global microcomedone quantity on cyanoacrylate superficial skin surface biopsies. Importantly, the study protocol allowed the dermatologist to prescribe, if needed as in real life, any of the acne drugs registered in the acne guidelines. The exposure to these acne drugs during the whole year was calculated as a percentage of
LIMITATIONS CONCLUSIONS
The association with routine prescription acne drugs when needed, even if limited, does not allow a full evaluation of the intrinsic quantitative efficacy of
CONCLUSION CONCLUSIONS
This open, real-life, year-long multicentre study confirms a previous 48-week proof of concept study and qualifies the use of

Identifiants

pubmed: 36675757
pii: jpm13010096
doi: 10.3390/jpm13010096
pmc: PMC9862999
pii:
doi:

Types de publication

Journal Article

Langues

eng

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Auteurs

Jean-Hilaire Saurat (JH)

Department of Clinical Pharmacology and Toxicology, University of Geneva, 1205 Geneva, Switzerland.

Pascal Reygagne (P)

Sabouraud Clinical Research Center, St Louis University Hospital, 75010 Paris, France.

Gwendal Josse (G)

Research & Development, Pierre Fabre Dermo-Cosmétique et Personal Care, 31035 Toulouse, France.

Zhorha Hamidou (Z)

Sabouraud Clinical Research Center, St Louis University Hospital, 75010 Paris, France.

Sophie Bianovici (S)

Sabouraud Clinical Research Center, St Louis University Hospital, 75010 Paris, France.

Francoise Ramel (F)

Independent Researcher, 75010 Paris, France.

Elizabeth Durbise (E)

Independent Researcher, 31000 Toulouse, France.

Chiara Lovati (C)

Independent Researcher, 20122 Milano, Italy.

Eleonora Bellani (E)

Independent Researcher, 20122 Milano, Italy.

Dorota Bystrzanowska (D)

Evimed Centrum Medyczne, Private Dermatologic Practice, JP Woronicza 16, 02-625 Warsaw, Poland.

Ewa Chlebus (E)

Evimed Centrum Medyczne, Private Dermatologic Practice, JP Woronicza 16, 02-625 Warsaw, Poland.

Elzbieta Kowalska-Oledzka (E)

Evimed Centrum Medyczne, Private Dermatologic Practice, JP Woronicza 16, 02-625 Warsaw, Poland.
LDermatology Department, Uczelnia Medyczna im. Marii Skłodowskiej Curie, 02-093 Warsaw, Poland.

Guillaume D'Auzers (G)

Research & Development, Pierre Fabre Dermo-Cosmétique et Personal Care, 31035 Toulouse, France.

Jimmy Le Digabel (J)

Research & Development, Pierre Fabre Dermo-Cosmétique et Personal Care, 31035 Toulouse, France.

Jerome Filiol (J)

Research & Development, Pierre Fabre Dermo-Cosmétique et Personal Care, 31035 Toulouse, France.

Christophe Lauze (C)

Research & Development, Pierre Fabre Dermo-Cosmétique et Personal Care, 31035 Toulouse, France.

Ariadna Ortiz-Brugues (A)

Laboratoires Dermatologiques Avène, 81500 Lavaur, France.

Therese Nocera (T)

Research & Development, Pierre Fabre Dermo-Cosmétique et Personal Care, 31035 Toulouse, France.
Dermatology Department, University Hospital, 31000 Toulouse, France.

Classifications MeSH