Patch testing with glucosides: The North American Contact Dermatitis Group experience, 2009-2018.


Journal

Journal of the American Academy of Dermatology
ISSN: 1097-6787
Titre abrégé: J Am Acad Dermatol
Pays: United States
ID NLM: 7907132

Informations de publication

Date de publication:
11 2022
Historique:
received: 18 02 2022
revised: 04 04 2022
accepted: 30 04 2022
pubmed: 14 5 2022
medline: 20 10 2022
entrez: 13 5 2022
Statut: ppublish

Résumé

Alkyl glucosides are nonionic surfactants that are increasingly used in personal care products. To characterize positive patch test reactions to decyl glucoside (5% petrolatum, tested 2009-2018) and lauryl glucoside (3% petrolatum, tested 2017-2018). Retrospective analysis of patients tested by the North American Contact Dermatitis Group. Of 24,097 patients patch tested to decyl and/or lauryl glucoside, 470 (2.0%) had positive reactions. Compared with glucoside-negative patients, glucoside-positive patients had higher odds of occupational skin disease (13.4% vs 10.1%; P = .0207), history of hay fever (38.5% vs 31.6%; P = .0014), atopic dermatitis (39.0% vs 28.6%; P < .0001), and/or asthma (21.8% vs 16.5%; P = .0023). Most glucoside reactions (83.9%) were currently relevant. The most common source was personal care products (63.0%), especially hair products (16.5%) and skin cleansers (15.2%). Of 4933 patients tested to decyl and lauryl glucoside, 134 (2.7%) were positive to 1 or both; 43.4% (43 of 99) of decyl-positive patients were also positive to lauryl glucoside and 55.1% (43/78) of lauryl glucoside patients were also positive to decyl glucoside. The cohort predominantly reflects a referral population, and follow-up after testing was not captured. Glucoside positivity occurred in 2.0% of the tested patients. Reactions were often clinically relevant and linked to personal care products. Cross-reactivity was >40%.

Sections du résumé

BACKGROUND
Alkyl glucosides are nonionic surfactants that are increasingly used in personal care products.
OBJECTIVE
To characterize positive patch test reactions to decyl glucoside (5% petrolatum, tested 2009-2018) and lauryl glucoside (3% petrolatum, tested 2017-2018).
METHODS
Retrospective analysis of patients tested by the North American Contact Dermatitis Group.
RESULTS
Of 24,097 patients patch tested to decyl and/or lauryl glucoside, 470 (2.0%) had positive reactions. Compared with glucoside-negative patients, glucoside-positive patients had higher odds of occupational skin disease (13.4% vs 10.1%; P = .0207), history of hay fever (38.5% vs 31.6%; P = .0014), atopic dermatitis (39.0% vs 28.6%; P < .0001), and/or asthma (21.8% vs 16.5%; P = .0023). Most glucoside reactions (83.9%) were currently relevant. The most common source was personal care products (63.0%), especially hair products (16.5%) and skin cleansers (15.2%). Of 4933 patients tested to decyl and lauryl glucoside, 134 (2.7%) were positive to 1 or both; 43.4% (43 of 99) of decyl-positive patients were also positive to lauryl glucoside and 55.1% (43/78) of lauryl glucoside patients were also positive to decyl glucoside.
LIMITATIONS
The cohort predominantly reflects a referral population, and follow-up after testing was not captured.
CONCLUSION
Glucoside positivity occurred in 2.0% of the tested patients. Reactions were often clinically relevant and linked to personal care products. Cross-reactivity was >40%.

Identifiants

pubmed: 35551968
pii: S0190-9622(22)00788-5
doi: 10.1016/j.jaad.2022.04.058
pii:
doi:

Substances chimiques

Allergens 0
Cosmetics 0
Glucosides 0
Surface-Active Agents 0
Petrolatum 8009-03-8

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Pagination

1033-1041

Informations de copyright

Copyright © 2022 American Academy of Dermatology, Inc. Published by Elsevier Inc. All rights reserved.

Déclaration de conflit d'intérêts

Conflicts of interest Dr Warshaw reports investigator-initiated grant from WEN by Chaz Dean and has served as a consultant for WEN by Chaz Dean and Noven Pharmaceuticals. Dr Atwater has received a Pfizer Independent Grant for Learning & Change, has consulted for Henkel, and is employed by Eli Lilly and Company. Dr Taylor owns noncontrolling common shares of stock in Astra Zeneca, Cigna, Merck, Johnson & Johnson, and Opko Health; has consulted for Kao Brands and Monsanto (Bayer); is a member of the Cosmetic Ingredient Review Steering Committee; and has a nondependent child employed by Pfizer. Dr Sasseville receives royalties from UpToDate (Wolters Kluwer Health). Author Xiong and Drs DeKoven, Pratt, Maibach, Belsito, Silverberg, Reeder, Zug, Fowler, DeLeo, Houle, and Dunnick have no conflicts of interest to disclose.

Auteurs

Erin M Warshaw (EM)

Department of Dermatology, Park Nicollet/Health Partners Health Services, Minneapolis, Minnesota; Department of Dermatology, University of Minnesota, Minneapolis, Minnesota; Department of Dermatology, Minneapolis Veterans Affairs Medical Center, Minneapolis, Minnesota.

Michelle Xiong (M)

Department of Dermatology, Park Nicollet/Health Partners Health Services, Minneapolis, Minnesota; Warren Alpert Medical School of Brown University, Providence, Rhode Island. Electronic address: michelle_xiong@brown.edu.

Amber R Atwater (AR)

Department of Dermatology, Duke University Medical Center, Durham, North Carolina.

Joel G DeKoven (JG)

Division of Dermatology, Sunnybrook Health Sciences Centre, University of Toronto, Toronto, Ontario, Canada.

Melanie D Pratt (MD)

Division of Dermatology, University of Ottawa, Ottawa, Ontario, Canada.

Howard I Maibach (HI)

Department of Dermatology, University of California San Francisco, San Francisco, California.

James S Taylor (JS)

Department of Dermatology, Cleveland Clinic, Cleveland, Ohio.

Donald V Belsito (DV)

Department of Dermatology, Columbia University Irving Medical School, New York, New York.

Jonathan I Silverberg (JI)

Department of Dermatology, The George Washington University School of Medicine and Health Sciences, Washington, District of Columbia.

Margo J Reeder (MJ)

Department of Dermatology, University of Wisconsin School of Medicine and Public Health, Madison, Wisconsin.

Kathryn A Zug (KA)

Department of Dermatology, Dartmouth-Hitchcock Medical Center, Lebanon, New Hampshire.

Denis Sasseville (D)

Division of Dermatology, Montreal General Hospital, McGill University, Montreal, Québec, Canada.

Joseph F Fowler (JF)

Division of Dermatology, University of Louisville, Louisville, Kentucky.

Vincent A DeLeo (VA)

Department of Dermatology, Keck School of Medicine, Los Angeles, California.

Marie-Claude Houle (MC)

Division of Dermatology, Centre Hospitalier Universitaire Québec, Laval University, Laval, Québec, Canada.

Cory A Dunnick (CA)

Department of Dermatology, University of Colorado, Aurora, Colorado.

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