Evidence map›Paper›PMID 37293321›Full record

ArticleAfrican journal of laboratory medicine2023

Performance of two multiplex flow cytometric assays for antibody detection in Egyptian patients.

Alshymaa A Ahmed, Alia A El Shahawy, Heba M Kadry, Nora M Said

Open access · diamondAbstract read
In one paragraph

Article in African journal of laboratory medicine, 2023. 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, top 76% of its field
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, 0 citations in OpenAlex.

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

4 authors at 1 institution in 1 country.

Alshymaa A AhmedDepartment of Clinical Pathology, Faculty of Medicine, Zagazig University, Zagazig City, Egypt.ORCID https://orcid.org/0000-0002-8695-4037
Alia A El ShahawyDepartment of Medical Microbiology and Immunology, Faculty of Medicine, Zagazig University, Zagazig City, Egypt.ORCID https://orcid.org/0000-0001-7013-9209
Heba M KadryDepartment of Medical Microbiology and Immunology, Faculty of Medicine, Zagazig University, Zagazig City, Egypt.ORCID https://orcid.org/0000-0001-8075-6550
Nora M SaidDepartment of Clinical Pathology, Faculty of Medicine, Zagazig University, Zagazig City, Egypt.ORCID https://orcid.org/0000-0001-6125-1143
Zagazig University · EG

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Background: Autoantibodies are vital biomarkers for the diagnosis, assessment and prognostic determination of various autoimmune disorders. Objective: This study aimed to evaluate the performance of the two AtheNA Multi-Lyte Methods: A total of 105 systemic lupus erythematosus patients, 35 patients with other autoimmune diseases (diseased controls), and 30 healthy volunteers (healthy controls) at Zagazig University Hospitals, Zagazig city, Al Sharqia governorate were tested for anti-double-stranded DNA (anti-dsDNA) antibodies using indirect immunofluorescence (IIF) and the AtheNA Multi-Lyte Results: The AtheNA anti-dsDNA test (98.5%) was more specific than IIF (96.9%) for diagnosing systemic lupus erythematosus, but both tests had the same sensitivity (38.1%). Combining both methods increased sensitivity to 47.6%, while increasing the cut-off of the AtheNA anti-dsDNA test to 134 international units/mL increased specificity to 100%. The AtheNA Multi-Lyte AIV system exhibited substantial agreement with IIF regarding anti-myeloperoxidase testing (κ = 0.65) and almost perfect agreement with ELISA (κ = 0.85). The AtheNA Multi-Lyte Conclusion: AtheNA Multi-Lyte What this study adds: It is necessary to evaluate various autoantibodies detection assays to increase both sensitivity and specificity of autoimmune diseases diagnostic approaches. AtheNA Multi-Lyte

Indexed as

anti-double-stranded DNAanti-neutrophil cytoplasmic antibodiesautoantibodiesmultiplexperformance

Identifiers

PMID37293321
PMCPMC10244819
OpenAlexW4377289791

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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.