Evidence map›Paper›PMID 39238035›Full record

ArticleTrials2024

Upadacitinib to improve anxiety in patients with adalimumab-treated psoriatic arthritis: study protocol for a randomized controlled trial.

Junlan Liao, Ziyu Wang, Jianyong Zhang, Haibo Tan, Zhihao Zhang, Shan Zhang, Shasha Hu, Hongling Geng, Zhiying Zhan, Jiaxin Wei and 2 more

Abstract readClinical Trial Protocol
In one paragraph

Article in Trials, 2024. 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

12 authors.

Junlan Liao *Shenzhen Traditional Chinese Medicine Hospital Affiliated to Nanjing University of Chinese Medicine, Shenzhen, China.
Ziyu Wang *The Department of Rheumatology, Shenzhen Traditional Chinese Medicine Hospital, Shenzhen, China.
Jianyong Zhang *Shenzhen Traditional Chinese Medicine Hospital Affiliated to Nanjing University of Chinese Medicine, Shenzhen, China.
Haibo TanShenzhen Traditional Chinese Medicine Hospital Affiliated to Nanjing University of Chinese Medicine, Shenzhen, China.
Zhihao ZhangThe Department of Rheumatology, Shenzhen Traditional Chinese Medicine Hospital, Shenzhen, China.
Shan ZhangShenzhen Traditional Chinese Medicine Hospital Affiliated to Nanjing University of Chinese Medicine, Shenzhen, China.
Shasha HuThe Department of Rheumatology, Shenzhen Traditional Chinese Medicine Hospital, Shenzhen, China.
Hongling GengThe Department of Gynecology, Guangdong Provincial Hospital of Chinese Medicine, the Second Affiliated Hospital of Guangzhou University of Chinese Medicine, Guangzhou, China.
Zhiying ZhanThe Department of Epidemiology and Health Statistics, Fujian Provincial Key Laboratory of Environment Factors and Caner, School of Public Health, Fujian Medical University, Fuzhou, China.
Jiaxin WeiThe Department of Rheumatology, Shenzhen Traditional Chinese Medicine Hospital, Shenzhen, China.
Zhiling LiThe Department of Rheumatology, Shenzhen Traditional Chinese Medicine Hospital, Shenzhen, China.
Ertao JiaThe Department of Rheumatology, Guangdong Provincial Second Hospital of Traditional Chinese Medicine, Guangzhou, China. sailing1980@126.com.ORCID http://orcid.org/0000-0002-0513-1689

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundPatients with psoriatic arthritis (PsA) often suffer from anxiety disorders. While upadacitinib has shown effectiveness in reducing various disease activity indicators in active PsA, its impact on anxiety disorders in PsA patients needs further investigation.

methodsIn this 12-week randomized, open-label, controlled trial, PsA patients with coexisting anxiety were randomly assigned to either the upadacitinib group or the adalimumab group in a 1:1 ratio. The upadacitinib group received a daily dose of 15 mg, while the adalimumab group received 40 mg every 2 weeks. The primary outcome measured the change in Hospital Anxiety Self-Assessment Scale (HADS-A) total scores after the 12-week intervention. Secondary outcomes included changes in the Health Assessment Questionnaire-Disability Index (HAQ-DI), the percentage of participants meeting the ACR20 criteria compared to baseline after 12 weeks, and the percentage of participants achieving a grade 0 or 1 in the psoriasis static Investigator's overall assessment (sPGA) at week 12 with an improvement of at least 2 points from baseline (sPGA 0/1). One-way analysis of variance (ANOVA) was used to compare the means of normally distributed variables between the upadacitinib and adalimumab groups. DISCUSSION: The impact of upadacitinib on anxiety in PsA patients remains uncertain. This 12-week open randomized controlled trial aims to provide insights into disease progression and underscore the importance of addressing PsA-related anxiety during treatment.

trial registrationChiCTR2400079755. Registered on January 11, 2024, with ChiCTR. https://www.chictr.org.cn/showproj.html?proj=216538.

Indexed as

AdalimumabAnxietyArthritis, PsoriaticHeterocyclic Compounds, 3-RingAdultAntirheumatic AgentsFemaleHumansMaleMiddle AgedRandomized Controlled Trials as TopicTime FactorsTreatment OutcomeAdalimumabAntirheumatic AgentsHeterocyclic Compounds, 3-RingupadacitinibAnxietyPsoriatic arthritisRandomized controlled trialUpadacitinib

Identifiers

PMID39238035
PMCPMC11376005

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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.