# Psoriasis Course in Patients with Alopecia Areata Undergoing Baricitinib Therapy

**Authors:** Enrico Matteini, Fabio Artosi, Giacomo Caldarola, Lorenzo Maria Pinto, Alfredo Rossi, Lorenzo Ala, Gaetana Costanza, Luca Bianchi, Elena Campione, Laura Diluvio

PMC · DOI: 10.3390/clinpract16020028 · 2026-01-28

## TL;DR

This study examines how baricitinib affects psoriasis in patients with alopecia areata, finding it effective for hair loss but uncertain for psoriatic arthritis.

## Contribution

The study provides insights into the use of baricitinib for managing coexisting alopecia areata and psoriasis.

## Key findings

- Baricitinib achieved complete remission in one patient and significant improvement in two others with alopecia areata.
- Psoriasis remained stable in patients treated with baricitinib.
- One patient with psoriatic arthritis worsened and discontinued treatment.

## Abstract

Background/Objectives: Alopecia areata (AA) and psoriasis are immune-mediated diseases that can coexist, suggesting shared pathogenic mechanisms. While Janus kinase inhibitors (JAKi) are approved for AA treatment, their role in managing concomitant psoriasis and psoriatic arthritis (PsA) remains unclear. This study evaluates the efficacy and safety of baricitinib in patients with severe AA and coexisting psoriasis and/or PsA. Materials and Methods: A retrospective case series of five patients (mean age 53.2 years) with severe AA (SALT > 80) or alopecia universalis (AU) and concomitant psoriasis (n = 2) and/or PsA (n = 3) was conducted in the Dermatology Unit of Policlinico of Tor Vergata, Catholic University of the Sacred Heart and La Sapienza University of Rome, Italy. Patients received baricitinib 4 mg/day and were assessed at weeks 4, 24, and 52 using SALT, PASI, and pVAS scores. Results: At week 52, one patient achieved complete AA remission, while two improved to SALT < 20 (mean SALT 83 to 8.75). Psoriasis remained stable (mean PASI 1.4 to 0.5). However, one PsA patient worsened (pVAS 9) and discontinued the treatment. Conclusions: Baricitinib was effective for AA, with potential benefits for psoriasis, but it may not be optimal for PsA. Further studies are needed to define its role in multiple immune diseases.

## Linked entities

- **Chemicals:** baricitinib (PubChem CID 44205240)
- **Diseases:** Alopecia Areata (MONDO:0004907), psoriasis (MONDO:0005083), psoriatic arthritis (MONDO:0011849)

## Full-text entities

- **Genes:** IL13 (interleukin 13) [NCBI Gene 3596] {aka IL-13, P600}, JAK2 (Janus kinase 2) [NCBI Gene 3717] {aka JTK10}, IFNG (interferon gamma) [NCBI Gene 3458] {aka IFG, IFI, IMD69}, IL4 (interleukin 4) [NCBI Gene 3565] {aka BCGF-1, BCGF1, BSF-1, BSF1, IL-4}, IL23A (interleukin 23 subunit alpha) [NCBI Gene 51561] {aka IL-23, IL-23A, IL23P19, P19, SGRF}, IL6 (interleukin 6) [NCBI Gene 3569] {aka BSF-2, BSF2, CDF, HGF, HSF, IFN-beta-2}, IL17A (interleukin 17A) [NCBI Gene 3605] {aka CTLA-8, CTLA8, IL-17, IL-17A, IL17, ILA17}, JAK1 (Janus kinase 1) [NCBI Gene 3716] {aka AIIDE, JAK1A, JAK1B, JTK3}, IL12B (interleukin 12B) [NCBI Gene 3593] {aka CLMF, CLMF2, IL-12B, IMD28, IMD29, NKSF}, IL15 (interleukin 15) [NCBI Gene 3600] {aka IL-15}, TYK2 (tyrosine kinase 2) [NCBI Gene 7297] {aka IMD35, JTK1}, JAK3 (Janus kinase 3) [NCBI Gene 3718] {aka JAK-3, JAK3_HUMAN, JAKL, L-JAK, LJAK}, TNF (tumor necrosis factor) [NCBI Gene 7124] {aka DIF, IMD127, TNF-alpha, TNFA, TNFSF2, TNLG1F}
- **Diseases:** bacterial infections (MESH:D001424), type II diabetes mellitus (MESH:D003924), depression (MESH:D003866), AD (MESH:D003876), synovial hyperplasia (MESH:D006965), AA (MESH:D000506), PASI (MESH:D045169), arthritis (MESH:D001168), ophiasis (MESH:C536159), rheumatoid arthritis (MESH:D001172), hypothyroidism (MESH:D007037), hypertension (MESH:D006973), cardiovascular diseases (MESH:D002318), synovitis (MESH:D013585), immune diseases (MESH:D007154), joint disease (MESH:D007592), enthesitis (MESH:D001171), dermatologic diseases (MESH:D000168), joint pain (MESH:D018771), bone erosions (MESH:D014077), cutaneous (MESH:D018366), autoimmune and (MESH:D001327), Alopecia (MESH:D000505), metabolic disorders (MESH:D008659), AU (MESH:C537055), PsA (MESH:D015535), Erythrodermic psoriasis (MESH:D011565), inflammation (MESH:D007249), injury to (MESH:D014947), Pain (MESH:D010146), inflammatory dermatoses (MESH:D012871), cutaneous and/or articular psoriasis (MESH:D056587), vitiligo (MESH:D014820), anxiety (MESH:D001007)
- **Chemicals:** ATP (MESH:D000255), steroids (MESH:D013256), Brodalumab (MESH:C571216), Baricitinib (MESH:C000596027), -Rheumatic Drugs (-), cyclosporine (MESH:D016572), Deucravacitinib (MESH:C000628674), Ixekizumab (MESH:C549079), Upadacitinib (MESH:C000613732), tofacitinib (MESH:C479163)
- **Species:** Homo sapiens (human, species) [taxon 9606]

## Figures

2 figures with captions in the complete paper: https://tomesphere.com/paper/PMC12939786/full.md

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Source: https://tomesphere.com/paper/PMC12939786