Alopecia areata (AA) is a condition of hair loss with an immune-mediated cause. The efficacy of switching to a different JAK inhibitor in a patient who has failed to respond to one JAK inhibitor for AA is also unknown. This review is to examine the efficacy and safety of baricitinib in patients' inadequate response to tofacitinib. This is a retrospective study of 26 patients with AA who were switched from tofacitinib to baricitinib because of insufficient response, side effects or disease relapse. The patients had a mean age of 31 years, with 65% being female. The SALT score was reduced from 90 ± 19 to 68 ± 31 (p < 0.05) in an average of 16 months of tofacitinib treatment. However, the SALT score was reduced from 68 ± 31 to 50 ± 31 (p < 0.05) in about 7 months of baricitinib treatment. 34.6% of patients taking tofacitinib and 19.2% of patients receiving baricitinib did not respond to the treatment; however, 66.66% of the tofacitinib non-responders had improvement with baricitinib. Of the five patients with unchanged SALT scores after tofacitinib, four (80%) had an average reduction of 58.25 points with baricitinib. Baricitinib induced eyebrow and eyelash regrowth in 60% of AU (Alopecia Universalis) patients. Both treatments brought down SALT scores in pediatric cases. Adverse effects were mild and were noted in 30.76% of patients on tofacitinib and 3.84% of patients on baricitinib treatment. Oral baricitinib is safe with minimal side effects and also effective for both pediatric and adult AA patients who are inadequate responders to tofacitinib. These findings need to be confirmed by further research.
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http://dx.doi.org/10.1007/s00403-025-04035-y | DOI Listing |
J Clin Aesthet Dermatol
February 2025
Drs. Desir, Encarnacion, and Mollanazar are with the Department of Dermatology at Perelman School of Medicine at the University of Pennsylvania in Philadelphia, Pennsylvania.
Objective: Oral Janus kinase inhibitors (JAKi) have demonstrated high levels of efficacy with acceptable safety in patients with atopic dermatitis (AD), yet there remains significant hesitancy among the dermatologic community to use JAKi in elderly populations due to the potential increased risk of serious adverse events in this population. We aimed to perform a retrospective review to describe real-world outcomes for the use of selective JAK-1 inhibitors in patients with AD aged 65 years or older.
Methods: We conducted a multicenter retrospective review.
PLoS Biol
March 2025
Department of Cell and Developmental Biology, University College London, London, United Kingdom.
Stem cells have the unique ability among adult cells to give rise to cells of different identities. To do so, they must change gene expression in response to environmental signals. Much work has focused on how transcription is regulated to achieve these changes; however, in many cell types, transcripts and proteins correlate poorly, indicating that post-transcriptional regulation is important.
View Article and Find Full Text PDFArch Dermatol Res
February 2025
Autoimmune Bullous Diseases Research Center, Razi Hospital, Tehran University of Medical Sciences, Tehran, Iran.
Alopecia areata (AA) is a condition of hair loss with an immune-mediated cause. The efficacy of switching to a different JAK inhibitor in a patient who has failed to respond to one JAK inhibitor for AA is also unknown. This review is to examine the efficacy and safety of baricitinib in patients' inadequate response to tofacitinib.
View Article and Find Full Text PDFArch Dermatol Res
February 2025
The Kimberly and Eric J. Waldman Department of Dermatology, Icahn School of Medicine at Mount Sinai Hospital, New York, NY, USA.
J Clin Med
January 2025
Dermatology Unit, Department of Medicine and Surgery, University of Parma, I-43121 Parma, Italy.
: Psoriasis (PSO) and atopic dermatitis (AD) have traditionally been considered distinct diseases, respectively, mediated by T-helper 1 (Th1) and the T-helper 2 (Th2) immune pathway. In recent years, there has been a growing body of evidence highlighting an overlap between the two conditions, such as Asian AD, pediatric PSO, or "psoriasis dermatitis/PSOREMA". Moreover, psoriasis dermatitis can be induced by therapeutic interventions.
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