Evidence map›Paper›PMID 38578002›Full record

ArticleImmunity, inflammation and disease2024

Blood MALT1 expression could help predict treatment outcomes in psoriasis patients, especially in those receiving biologics.

Qiaoli Liu, Yanfeng Zhang, Bing Xu, Xiaobo Jin, Tao Yang, Leiqiang Fan

Abstract read
In one paragraph

Article in Immunity, inflammation and disease, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

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1citing papers in PubMed
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1 · What the graph read from it

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3 · Its place in the literature

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1 citing paper in PubMed.

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4 · The record

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5 · Who and what money

Authors and funding

6 authors.

Qiaoli LiuDepartment of Emergency, Chengde Central Hospital, Chengde, China.
Yanfeng ZhangDepartment of Dermatology, Chengde Central Hospital, Chengde, China.
Bing XuDepartment of Dermatology, Chengde Central Hospital, Chengde, China.
Xiaobo JinDepartment of Orthopaedics, Chengde Central Hospital, Chengde, China.
Tao YangDepartment of Clinical Laboratory, Chengde Central Hospital, Chengde, China.
Leiqiang FanDepartment of Dermatology, Chengde Central Hospital, Chengde, China.ORCID 0000-0001-5831-7850

Funding

Project of Health Commission of Hebei Province 20241392
6 · The paper itself

Abstract

introductionMucosa-associated lymphoid tissue 1 (MALT1) modulates T helper cell differentiation, pro-inflammatory cytokine production, and epidermal hyperplasia to participate in the pathology of psoriasis. This study aimed to explore the correlation of blood MALT1 with treatment outcomes in psoriasis patients.

methodsMALT1 was detected in peripheral blood mononuclear cells by reverse transcription-quantitative polymerase chain reaction in 210 psoriasis patients before starting or converting to a new therapy, 50 disease controls, and 50 healthy controls. The psoriasis area severity index (PASI) score was evaluated at month (M)1, M3, and M6 in psoriasis patients.

resultsMALT1 was increased in psoriasis patients versus disease controls and healthy controls (both p < .001); and positively related to body mass index (p = .019) and PASI score (p < .001) in psoriasis patients. PASI75 rate at M1, M3, and M6 was 22.9%, 46.2%, and 71.0%, respectively; while PASI90 rate at M1, M3, and M6 was 3.8%, 29.0%, and 50.5%, respectively, in psoriasis patients. PASI75/90 rates at M1, M3, and M6 were increased in psoriasis patients receiving biologics versus those without (all p < .05). Pretreatment MALT1 was higher in psoriasis patients who achieved PASI75 (p = .001) and PASI90 (p < .001) at M6 compared to those who did not achieve that. Subgroup analyses discovered that pretreatment MALT1 had a stronger ability to predict PASI75 and 90 realizations in psoriasis patients receiving biologics (area under the curve [AUC]: 0.723 and 0.808) versus those without (AUC: 0.594 and 0.675).

conclusionBlood MALT1 measurement may assist in predicting outcomes in psoriasis patients, especially in those receiving biologics.

Indexed as

Biological ProductsMucosa-Associated Lymphoid Tissue Lymphoma Translocation 1 ProteinPsoriasisHumansLeukocytes, MononuclearProspective StudiesTreatment OutcomeBiological ProductsMALT1 protein, humanMucosa-Associated Lymphoid Tissue Lymphoma Translocation 1 Proteinbiologic therapydisease activitymucosa‐associated lymphoid tissue 1psoriasistreatment response

Identifiers

PMID38578002
PMCPMC10996377

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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.