Treatment of Acne with Isotretinoin Should Be Avoided in Patients with Hidradenitis Suppurativa "Conglobata Phenotype".

Acne conglobata Acne vulgaris Hidradenitis suppurativa Isotretinoin Phenotypes

Journal

Dermatology (Basel, Switzerland)
ISSN: 1421-9832
Titre abrégé: Dermatology
Pays: Switzerland
ID NLM: 9203244

Informations de publication

Date de publication:
2023
Historique:
received: 10 02 2022
accepted: 31 03 2023
pubmed: 26 7 2023
medline: 26 7 2023
entrez: 25 7 2023
Statut: ppublish

Résumé

Acne conglobata (AC) and nodulocystic acne have long been confused clinically, despite the presentation and the response to treatment being different. AC and hidradenitis suppurativa (HS) resemble each other; a subtype of HS called "conglobata phenotype" has recently been reported in a large Dutch cohort. Acne vulgaris and HS are often associated. Isotretinoin is typically ineffective in treating HS and may even aggravate it, but it is often indispensable in treating acne vulgaris. The aim of the study was to assess whether isotretinoin may be used safely in adults with both HS and acne vulgaris and when it might be contraindicated. Belgian HS patients from the European Registry for Hidradenitis Suppurativa Registry (ERHS) reporting a history of severe acne of the face and/or the back, and who have ever used isotretinoin for their acne, were all selected. Patients whose acne worsened on isotretinoin were compared to patients whose acne did not worsen (improvement or no change). Among the 82 selected patients, 10 (12.2%) report that their acne was aggravated while taking isotretinoin, while 72 (87.8%) report that their acne was not aggravated on isotretinoin. Of the 10 HS patients whose acne worsened with isotretinoin, 9 (90%) were men (p = 0.04) and 8 (80%) were HS "conglobata phenotype" (p < 0.001). In contrast, 47 (65.3%) of the 72 patients whose acne did not worsen on isotretinoin belonged to the HS "regular phenotype" (p = 0.01). On multivariate analysis, the item most strongly associated with poor response to isotretinoin was the HS "conglobata phenotype," followed by body mass index (BMI) (worse response to isotretinoin if BMI >25 kg/m2). Additionally, of 26 patients who received isotretinoin while their HS had already started, only 6 (23.1%) reported isotretinoin effectiveness on their HS. Subject to confirmation by larger studies, our study suggests that isotretinoin should be avoided in the treatment of acne in HS patients with the HS "conglobata phenotype," as it may worsen the acne, likewise being male or having a BMI above 25 seems to increase this risk of a bad therapeutic outcome. Patients with an HS "regular phenotype" appear to be at a reduced risk of isotretinoin treatment worsening their acne.

Sections du résumé

BACKGROUND BACKGROUND
Acne conglobata (AC) and nodulocystic acne have long been confused clinically, despite the presentation and the response to treatment being different. AC and hidradenitis suppurativa (HS) resemble each other; a subtype of HS called "conglobata phenotype" has recently been reported in a large Dutch cohort. Acne vulgaris and HS are often associated. Isotretinoin is typically ineffective in treating HS and may even aggravate it, but it is often indispensable in treating acne vulgaris.
OBJECTIVE OBJECTIVE
The aim of the study was to assess whether isotretinoin may be used safely in adults with both HS and acne vulgaris and when it might be contraindicated.
MATERIALS AND METHODS METHODS
Belgian HS patients from the European Registry for Hidradenitis Suppurativa Registry (ERHS) reporting a history of severe acne of the face and/or the back, and who have ever used isotretinoin for their acne, were all selected. Patients whose acne worsened on isotretinoin were compared to patients whose acne did not worsen (improvement or no change).
RESULTS RESULTS
Among the 82 selected patients, 10 (12.2%) report that their acne was aggravated while taking isotretinoin, while 72 (87.8%) report that their acne was not aggravated on isotretinoin. Of the 10 HS patients whose acne worsened with isotretinoin, 9 (90%) were men (p = 0.04) and 8 (80%) were HS "conglobata phenotype" (p < 0.001). In contrast, 47 (65.3%) of the 72 patients whose acne did not worsen on isotretinoin belonged to the HS "regular phenotype" (p = 0.01). On multivariate analysis, the item most strongly associated with poor response to isotretinoin was the HS "conglobata phenotype," followed by body mass index (BMI) (worse response to isotretinoin if BMI >25 kg/m2). Additionally, of 26 patients who received isotretinoin while their HS had already started, only 6 (23.1%) reported isotretinoin effectiveness on their HS.
CONCLUSION CONCLUSIONS
Subject to confirmation by larger studies, our study suggests that isotretinoin should be avoided in the treatment of acne in HS patients with the HS "conglobata phenotype," as it may worsen the acne, likewise being male or having a BMI above 25 seems to increase this risk of a bad therapeutic outcome. Patients with an HS "regular phenotype" appear to be at a reduced risk of isotretinoin treatment worsening their acne.

Identifiants

pubmed: 37490871
pii: 000530664
doi: 10.1159/000530664
doi:

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Pagination

738-745

Informations de copyright

© 2023 S. Karger AG, Basel.

Auteurs

Mathieu Daoud (M)

Department of Dermatology, Hôpital Erasme, Université libre de Bruxelles (ULB), Brussels, Belgium.

Mariano Suppa (M)

Department of Dermatology, Hôpital Erasme, Université libre de Bruxelles (ULB), Brussels, Belgium.
Department of Dermatology, Institut Jules Bordet, Brussels, Belgium.

Stephanie Heudens (S)

Department of Dermatology, Hôpital Erasme, Université libre de Bruxelles (ULB), Brussels, Belgium.

Mathilde Daxhelet (M)

Department of Dermatology, Hôpital Erasme, Université libre de Bruxelles (ULB), Brussels, Belgium.

Hassane Njimi (H)

Department of Dermatology, Hôpital Erasme, Université libre de Bruxelles (ULB), Brussels, Belgium.

Laura Nobile (L)

Department of Dermatology, Hôpital Erasme, Université libre de Bruxelles (ULB), Brussels, Belgium.

Julio Tannous (J)

Department of Dermatology, Hôpital Erasme, Université libre de Bruxelles (ULB), Brussels, Belgium.

Claire Van Damme (C)

Department of Dermatology, Hôpital Erasme, Université libre de Bruxelles (ULB), Brussels, Belgium.

Jalila Karama (J)

Department of Dermatology, Hôpital Erasme, Université libre de Bruxelles (ULB), Brussels, Belgium.

Jonathan M White (JM)

Department of Dermatology, Hôpital Erasme, Université libre de Bruxelles (ULB), Brussels, Belgium.

Jean Revuz (J)

Private practice, Paris, France.

Farida Benhadou (F)

Department of Dermatology, Hôpital Erasme, Université libre de Bruxelles (ULB), Brussels, Belgium.

Veronique Del Marmol (V)

Department of Dermatology, Hôpital Erasme, Université libre de Bruxelles (ULB), Brussels, Belgium.

Classifications MeSH