Increased femoral cartilage thickness in acne patients using isotretinoin: could it be a sign of early osteoarthritis?


Journal

Archives of dermatological research
ISSN: 1432-069X
Titre abrégé: Arch Dermatol Res
Pays: Germany
ID NLM: 8000462

Informations de publication

Date de publication:
12 Aug 2024
Historique:
received: 05 06 2024
accepted: 30 07 2024
revised: 24 07 2024
medline: 12 8 2024
pubmed: 12 8 2024
entrez: 12 8 2024
Statut: epublish

Résumé

Vitamin A derivatives have inhibitory effects on cartilage tissue, such as decreasing chondrocyte proliferation and collagen synthesis, and increasing the loss of glycosaminoglycans and proteoglycans. Therefore, isotretinoin (a vitamin A derivative) may play a role in the pathogenesis of cartilage-related diseases like osteoarthritis by affecting the balance of cartilage tissue. The aim of this study was to evaluate the distal femoral cartilage thickness in acne patients under the systemic isotretinoin therapy and to determine whether it constitutes a risk factor for the development of osteoarthritis. The study included 52 patients (42 female, 10 male, mean age 23.31 ± 3.89 years) who were prescribed systemic isotretinoin for acne and completed at least 3 months of treatment, along with 45 healthy controls ((35 female, 10 male, mean age 23.85 ± 4.77 years). Bilateral distal femoral cartilage thickness was measured by ultrasonography before isotretinoin treatment and after the completion of the third month of treatment. After treatment, a statistically significant increase was found in the thickness of the right medial, right lateral, left medial, left lateral, and left intercondylar cartilage (p = 0.014, 0.012, 0.019, 0.027, 0.002, respectively). There was also an increase in the right intercondylar cartilage thickness, but this was not statistically significant (p = 0.1). Systemic isotretinoin seems to make cartilage thicker. The increase in femoral cartilage thickness observed after short-term isotretinoin treatment might be an indicator of very early-stage osteoarthritis. Extended follow-up studies with larger participant pools are necessary to substantiate this result.

Identifiants

pubmed: 39133320
doi: 10.1007/s00403-024-03264-x
pii: 10.1007/s00403-024-03264-x
doi:

Substances chimiques

Isotretinoin EH28UP18IF
Dermatologic Agents 0

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Pagination

512

Informations de copyright

© 2024. The Author(s).

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Auteurs

Sevgi Kulaklı (S)

Department of Dermatology and Venereology, Giresun University Faculty of Medicine, Giresun, 28200, Turkey. sevgi.kulakli@giresun.edu.tr.

Asude Cevher Elmas Telli (AC)

Department of Physical Medicine and Rehabilitation, Giresun University Faculty of Medicine, Giresun, 28200, Turkey.

İlker Fatih Sarı (İF)

Department of Physical Medicine and Rehabilitation, Giresun University Faculty of Medicine, Giresun, 28200, Turkey.

Işıl Deniz Oğuz (ID)

Department of Dermatology and Venereology, Giresun University Faculty of Medicine, Giresun, 28200, Turkey.

Fazıl Kulaklı (F)

Department of Physical Medicine and Rehabilitation, Giresun University Faculty of Medicine, Giresun, 28200, Turkey.

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