# The Relative Effects of Monotherapies for Psoriatic Nails: A Network Meta‐Analysis Study

**Authors:** Aditya K. Gupta, Mary A. Bamimore, Tong Wang, Mesbah Talukder

PMC · DOI: 10.1111/jocd.70657 · Journal of Cosmetic Dermatology · 2026-01-07

## TL;DR

This study compares the effectiveness of different single treatments for nail psoriasis using advanced statistical methods to help guide treatment choices.

## Contribution

The study provides a Bayesian network meta-analysis comparing monotherapies for nail psoriasis, including some that have never been directly compared.

## Key findings

- Tofacitinib 10 mg twice daily was most effective for reducing nail psoriasis severity based on NAPSI scores.
- Ixekizumab 160 mg at week 0 followed by 80 mg every 4 weeks was most effective for achieving clear or almost clear nails.
- The study produced comparative evidence for 22 active treatments, including biologics and non-biologics.

## Abstract

Various treatments exist for nail psoriasis (NP). We determined the relative efficacy of various monotherapies through Bayesian network meta‐analyses (NMAs).

We systematically reviewed the literature to identify eligible studies which—within the patient, intervention, comparator, outcome (PICO) context—determined the impact of biologic monotherapies on NP in terms of two outcome measures, namely, (1) the 16 to 24‐week mean change in the Nail Psoriasis Severity Index (NAPSI) (i.e., outcome 1), and (2) the proportion who attained a Physician Global Assessment of fingernails (PGA‐f) of “0” or “1” (i.e., “clear” or “almost clear”) between 16 and 24 weeks (i.e., outcome 2). Our NMAs estimated the surface under the cumulative ranking curve (SUCRA) values and pairwise relative effects. We also determined relative effects of comparators that had never been compared for this condition, including “deucravacitinib 6mg daily”, “risankizumab 150 mg at weeks 0, 4, 16”, and “golimumab 2mg/kg at weeks 0, 4, then every 8 weeks”.

We identified 22 active comparators; “tofacitinib 10 mg twice daily” was ranked most efficacious in terms of 16 to 24‐week mean change in NAPSI (SUCRA = 99.71%)—while “ixekizumab 160 mg at week 0 followed by 80 mg every 4 weeks” was ranked most efficacious (SUCRA = 95.67%) for proportion attaining PGA‐f of 0 or 1 (i.e., outcome 2). Our analyses produced comparative evidence for the relative efficacy of monotherapies with various agents, including biologics and non‐biologics. Our findings would guide clinical decision‐making.

## Linked entities

- **Chemicals:** deucravacitinib (PubChem CID 134821691), tofacitinib (PubChem CID 9926791)
- **Diseases:** psoriasis (MONDO:0005083)

## Full-text entities

- **Diseases:** Psoriatic (MESH:D015535), NP (MESH:D011565)
- **Chemicals:** golimumab (MESH:C529000), deucravacitinib (MESH:C000628674), ixekizumab (MESH:C549079), tofacitinib (MESH:C479163), risankizumab (MESH:C000601773)
- **Species:** Homo sapiens (human, species) [taxon 9606]

## Full text

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## Figures

7 figures with captions in the complete paper: https://tomesphere.com/paper/PMC12780300/full.md

## References

40 references — full list in the complete paper: https://tomesphere.com/paper/PMC12780300/full.md

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Source: https://tomesphere.com/paper/PMC12780300