Evidence map›Paper›PMID 31617239›Full record

ArticleJournal of clinical laboratory analysis2020

Oxidative stress enhances the immune response to oxidatively modified catalase enzyme in patients with Graves' disease.

Bochra Gargouri, Malek Mseddi, Fatma Mnif, Mohamed Abid, Hamadi Attia, Saloua Lassoued

Abstract read
In one paragraph

Article in Journal of clinical laboratory analysis, 2020. 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

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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.

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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.

Bochra GargouriFaculty of Sciences of Sfax Tunisia, Sfax, Tunisia.
Malek MseddiLaboratory LR11ES45, Research Group "Biotechnology and Pathology", National School of Engineers of Sfax, Sfax, Tunisia.ORCID https://orcid.org/0000-0002-7462-4305
Fatma MnifDepartment of endocrinology, Hedi Chaker Hospital, Sfax, Tunisia.
Mohamed AbidDepartment of endocrinology, Hedi Chaker Hospital, Sfax, Tunisia.
Hamadi AttiaLaboratory LR11ES45, Research Group "Biotechnology and Pathology", National School of Engineers of Sfax, Sfax, Tunisia.
Saloua LassouedLaboratory LR11ES45, Research Group "Biotechnology and Pathology", National School of Engineers of Sfax, Sfax, Tunisia.

Funding

Research Group "Biotechnology and Pathology", National School of Engineers of Sfax, Tunisia. Laboratory LR11ES45
6 · The paper itself

Abstract

backgroundOxidative stress is associated with several autoimmune disorders and oxidative modification of proteins that may result in autoimmune response. This study aims to evaluate the catalase (CAT) activity and the autoimmune response against the native CAT and the oxidatively modified enzyme in patients with Graves' disease (GD) and healthy controls in a comparative way.

methodsThe CAT activity was evaluated via spectrophotometric method. Using enzyme-linked immunosorbent assay, the reactivities of autoantibody toward native, malondialdehyde (MDA) and hydrogen peroxide (H

resultsReduced CAT activity was found in patients compared with controls (P < .05). It was proved that levels of IgG antibodies against MDA-modified CAT were higher than against unmodified ones (P < .001). No changes were found for the reactivities to H

conclusionOur findings incriminate the MDA in the autoantibodies reactivity to oxidatively modified CAT leading to a disturbed oxidative profile and/or the progression of GD pathology.

Indexed as

AdultAutoantibodiesCase-Control StudiesCatalaseFemaleGraves DiseaseHumansHydrogen PeroxideMaleMalondialdehydeMiddle AgedOxidative StressAutoantibodiesCatalaseHydrogen PeroxideMalondialdehydeautoantibodycatalaseGraves' diseasehydrogen peroxidemalondialdehydeoxidative stress

Identifiers

PMID31617239
PMCPMC7031633

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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.