Evidence map›Paper›PMID 38732072›Full record

ArticleInternational journal of molecular sciences2024

Gene Expression Profiling to Unfolded Proteins Response as a Risk Modulator of Patients with Rheumatoid Arthritis.

Aleksandra Kucharska-Lusina, Maciej Skrzypek, Aleksandra Binda, Ireneusz Majsterek

Abstract read
In one paragraph

Article in International journal of molecular sciences, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 4 papers.

0numbers the graph read from it
0cells of the map it votes in
4citing 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

4 citing papers in PubMed.

  1. Observational
  2. Review
  3. Article
  4. Article
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

4 authors.

Aleksandra Kucharska-LusinaDepartment of Clinical Chemistry and Biochemistry, Medical University of Lodz, 92-215 Lodz, Poland.
Maciej SkrzypekDepartment of Clinical Chemistry and Biochemistry, Medical University of Lodz, 92-215 Lodz, Poland.
Aleksandra BindaDepartment of Clinical Chemistry and Biochemistry, Medical University of Lodz, 92-215 Lodz, Poland.ORCID 0009-0007-6173-4525
Ireneusz MajsterekDepartment of Clinical Chemistry and Biochemistry, Medical University of Lodz, 92-215 Lodz, Poland.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Rheumatoid arthritis (RA) is a chronic inflammatory disease. Despite new methods of diagnostics and treatment as well as extensive biological and immunosuppressive treatment, the etiology of RA is not fully understood. Moreover, the problem of diagnosis and treatment of RA patients is still current and affects a large group of patients. It is suggested that endoplasmic reticulum (ER)-related features may impair adaptation to chronic stress, inferring the risk of rheumatoid arthritis. The main goal in this study was evaluation of changes in mRNA translation to determine chronic ER stress conditions in rheumatoid arthritis patients. The study group consist of 86 individuals including a total of 56 rheumatoid arthritis patients and 30 healthy controls. The expression level of mRNA form blood samples of RA patients as well as controls of the unfolded protein response (UPR)-associated genes (

Indexed as

Arthritis, RheumatoideIF-2 KinaseEndoplasmic Reticulum StressGene Expression ProfilingUnfolded Protein ResponseActivating Transcription Factor 4AdultAgedCase-Control StudiesEukaryotic Initiation Factor-2FemaleHumansMaleMiddle AgedRNA, MessengerActivating Transcription Factor 4EIF2AK3 protein, humaneIF-2 KinaseEukaryotic Initiation Factor-2RNA, Messengerendoplasmic reticulum stressER-adaptosomePERK inhibitorrheumatoid arthritisunfolded protein response

Identifiers

PMID38732072
PMCPMC11084936

What OpenQuestion holds

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Registered trials

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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.