Evidence map›Paper›PMID 41909688›Full record

ArticleFrontiers in immunology2026

Vitiligo secondary to immunosuppressants: a pharmacovigilance study of the FDA Adverse Event Reporting System.

Ying Jia, Hanzhang Xie, Yixuan Yang, Bingnan Cui, Junhui Wang, Zhanshuo Xiao

Abstract read
In one paragraph

Article in Frontiers in immunology, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

0numbers the graph read from it
0cells of the map it votes in
0citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

0 citing papers in PubMed.

No citing paper in PubMed yet.

4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

6 authors.

Ying Jia *Department of Dermatology, Guang'anmen Hospital, China Academy of Chinese Medical Sciences, Beijing, China.
Hanzhang Xie *Beijing University of Chinese Medicine, Beijing, China.
Yixuan Yang *Department of Dermatology, Guang'anmen Hospital, China Academy of Chinese Medical Sciences, Beijing, China.
Bingnan CuiDepartment of Dermatology, Guang'anmen Hospital, China Academy of Chinese Medical Sciences, Beijing, China.
Junhui WangDepartment of Dermatology, Guang'anmen Hospital, China Academy of Chinese Medical Sciences, Beijing, China.
Zhanshuo XiaoDepartment of Dermatology, Guang'anmen Hospital, China Academy of Chinese Medical Sciences, Beijing, China.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Background: Vitiligo is an acquired depigmentation disorder affecting individuals worldwide. The potential link between immunosuppressants and the onset or exacerbation of vitiligo remains a topic of clinical concern. Objective: This study aims to evaluate the association between various immunosuppressants and vitiligo using data from the FDA Adverse Event Reporting System (FAERS). Methods: A retrospective pharmacovigilance analysis was conducted using FAERS data from January 2004 to June 2024. Vitiligo cases were identified through the Medical Dictionary for Regulatory Activities (MedDRA) terminology. Disproportionality analysis was performed using the Reporting Odds Ratio (ROR), Proportional Reporting Ratio (PRR), Bayesian Confidence Propagation Neural Network (BCPNN), and Empirical Bayes Geometric Mean (EBGM) to detect significant drug-event associations. Results: A total of 435 vitiligo-related adverse event (AE) reports were identified. The United States, Canada, France, Germany, and Brazil contributed the most reports. Vitiligo reports were more frequent in female patients, particularly within the 18-65 age group. The primary indications for immunosuppressant use included psoriasis, rheumatoid arthritis, psoriatic arthropathy, Crohn's disease, and ulcerative colitis. Adalimumab (74 cases) and secukinumab (52 cases) accounted for the highest number of reports. Significant signals were detected for alemtuzumab, ixekizumab, ustekinumab, secukinumab, guselkumab, and risankizumab. Conclusion: This study highlights the importance of continuous pharmacovigilance in monitoring potential adverse events associated with immunosuppressants. The observed association between specific immunosuppressants and vitiligo suggests a need for further research to elucidate underlying mechanisms and develop strategies to mitigate these potential AEs.

Indexed as

Adverse Drug Reaction Reporting SystemsImmunosuppressive AgentsVitiligoAdolescentAdultAgedChildChild, PreschoolFemaleHumansMaleMiddle AgedPharmacovigilanceRetrospective StudiesUnited StatesUnited States Food and Drug AdministrationImmunosuppressive Agentsadverse eventdrug-induced vitiligoFAERSpharmacovigilance studyvitiligo

Identifiers

PMID41909688
PMCPMC13017276

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.