# From skin clearance to psychological wellbeing: real-world outcomes of biologic therapy in psoriasis

**Authors:** Francesco Cuniberti, Marco Miniotti, Mariagiulia Bailon, Luca Mastorino, Michela Ortoncelli, Angelo Picardi, Simone Ribero, Paolo Leombruni

PMC · DOI: 10.3389/fpsyg.2026.1735777 · Frontiers in Psychology · 2026-02-13

## TL;DR

Biologic therapy for psoriasis significantly improves skin clearance, psychological wellbeing, and quality of life in real-world patients.

## Contribution

Demonstrates the multidimensional benefits of biologic therapy in psoriasis beyond skin clearance in a real-world setting.

## Key findings

- 77.4% of patients achieved complete skin clearance (PASI 100) after 6 months of biologic therapy.
- Psychological distress, including depression and perceived stress, decreased significantly with treatment.
- Baseline psychological symptoms were the strongest predictors of follow-up psychological and quality-of-life outcomes.

## Abstract

Psoriasis impacts psychological and quality-of-life (QoL). While biologic therapies demonstrated robust efficacy in reducing skin lesions, their broader psychosocial impact remains underexplored in real-world settings. This ambispective observational cohort study evaluated clinical, psychological, and health-related QoL (HRQoL) outcomes of biologic therapy in patients with moderate-to-severe plaque psoriasis treated in routine dermatological practice.

A total of 133 patients undergoing biologic therapy at a referral center in Northern Italy were assessed. Baseline data (T0) were retrospectively extracted from medical records, while 6-month follow-up assessments (T1) were conducted prospectively. Clinical severity (PASI), depression (PHQ-9, BSI-18), anxiety and somatization (BSI-18), perceived stress (PSS), dermatology-specific QoL (DLQI), and general HRQoL (WHOQOL-BREF) were evaluated. Regression models identified baseline predictors of T1 psychological and QoL outcomes.

At follow-up, patients reported significant improvements in psychological wellbeing and QoL. PHQ-9 scores decreased markedly (p < 0.001), with the prevalence of moderate-to-severe depressive symptoms dropping from 28.6% to 5.3%. Substantial perceived stress (PSS ≥ 27) declined from 15.0% to 1.5%. DLQI scores showed a large effect size (p < 0.001), with 89.5% reporting minimal impact (DLQI 0–1) at follow-up. Regression analyses identified baseline psychological symptoms as the strongest predictors of follow-up psychological and QoL outcomes. Additional predictors included PASI, female sex, psychiatric comorbidity, and previous biologic therapy. At T1, 77.4% achieved complete skin clearance (PASI 100).

Biologic therapies confer multidimensional benefits in moderate-to-severe psoriasis, extending beyond skin clearance to substantial reductions in psychological distress and improvements in QoL. These findings support a patient-centered model integrating dermatologic and mental health care.

## Linked entities

- **Diseases:** psoriasis (MONDO:0005083)

## Full-text entities

- **Genes:** TNF (tumor necrosis factor) [NCBI Gene 7124] {aka DIF, IMD127, TNF-alpha, TNFA, TNFSF2, TNLG1F}, IL23A (interleukin 23 subunit alpha) [NCBI Gene 51561] {aka IL-23, IL-23A, IL23P19, P19, SGRF}, IL17A (interleukin 17A) [NCBI Gene 3605] {aka CTLA-8, CTLA8, IL-17, IL-17A, IL17, ILA17}, IL6 (interleukin 6) [NCBI Gene 3569] {aka BSF-2, BSF2, CDF, HGF, HSF, IFN-beta-2}
- **Diseases:** DLQI (MESH:D000168), anxiety (MESH:D001007), schizophrenia (MESH:D012559), substance use disorders (MESH:D019966), Psychiatric (MESH:D001523), sleep disturbances (MESH:D012893), skin disease (MESH:D012871), disease (MESH:D004194), inflammation (MESH:D007249), mood and anxiety disorders (MESH:D001008), disability (MESH:D009069), emotional dysregulation (MESH:D021081), psoriatic arthritis (MESH:D015535), Psoriasis (MESH:D011565), fatigue (MESH:D005221), bipolar disorder (MESH:D001714), cutaneous (MESH:D018366), chronic pain (MESH:D059350), Depressive symptoms (MESH:D003866)
- **Chemicals:** guselkumab (MESH:C000588857), cyclosporine (MESH:D016572), infliximab (MESH:D000069285), secukinumab (MESH:C555450), methotrexate (MESH:D008727), adalimumab (MESH:D000068879)
- **Species:** Homo sapiens (human, species) [taxon 9606]

## Full text

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## References

59 references — full list in the complete paper: https://tomesphere.com/paper/PMC12946107/full.md

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Source: https://tomesphere.com/paper/PMC12946107