Evidence map›Paper›PMID 38223014›Full record

ArticleIndian journal of clinical biochemistry : IJCB2024

Clinical Utility of Pro-inflammatory Oligomeric Glycoprotein Tenascin-C in the Diagnosis of Seropositive and Seronegative Rheumatoid Arthritis.

Sachin Dominic, K S S Sai Baba, N N Sreedevi, Arshi Sanober, Liza Rajasekhar, Siraj Ahmed Khan, Noorjahan Mohammed, M Vijaya Bhaskar, Iyyapu Krishna Mohan

Open access · greenAbstract read
In one paragraph

Article in Indian journal of clinical biochemistry : IJCB, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

0numbers the graph read from it
0cells of the map it votes in
1citing papers in PubMed
0.1field-weighted citation impact, top 53% 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

1 citing paper in PubMed, 1 citations in OpenAlex.

  1. 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

9 authors at 1 institution in 1 country.

Sachin DominicDepartment of Biochemistry, Nizam's Institute of Medical Sciences, Punjagutta, Hyderabad, Telangana 500082 India.
K S S Sai BabaDepartment of Biochemistry, Nizam's Institute of Medical Sciences, Punjagutta, Hyderabad, Telangana 500082 India.
N N SreedeviDepartment of Biochemistry, Nizam's Institute of Medical Sciences, Punjagutta, Hyderabad, Telangana 500082 India.
Arshi SanoberDepartment of Biochemistry, Nizam's Institute of Medical Sciences, Punjagutta, Hyderabad, Telangana 500082 India.
Liza RajasekharDepartment of Clinical Immunology and Rheumatology, Nizam's Institute of Medical Sciences, Punjagutta, Hyderabad, Telangana 500082 India.
Siraj Ahmed KhanDepartment of Biochemistry, Nizam's Institute of Medical Sciences, Punjagutta, Hyderabad, Telangana 500082 India.
Noorjahan MohammedDepartment of Biochemistry, Nizam's Institute of Medical Sciences, Punjagutta, Hyderabad, Telangana 500082 India.
M Vijaya BhaskarDepartment of Biochemistry, Nizam's Institute of Medical Sciences, Punjagutta, Hyderabad, Telangana 500082 India.
Iyyapu Krishna MohanDepartment of Biochemistry, Nizam's Institute of Medical Sciences, Punjagutta, Hyderabad, Telangana 500082 India.ORCID 0000-0002-7478-0375
Nizam's Institute of Medical Sciences · IN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Owing to limited usefulness of Rheumatoid Factor and anti-CCP in rheumatoid arthritis, there is a need to identify a more sensitive and specific biomarker to detect rheumatoid arthritis (RA), particularly seronegative RA cases. Tenascin-C is an extracellular matrix glycoprotein, which has been implicated in the pathophysiology of RA. The objective of our study was to evaluate the diagnostic utility of serum Tenascin-C in seropositive and seronegative rheumatoid arthritis patients. We conducted a cross-sectional case control study. Sixty patients who fulfilled the ACR 2010 criteria for rheumatoid arthritis were included in the study. Thirty patients were found to be positive for RF and/or anti-CCP and 30 were negative for both RF and anti-CCP. Thirty age and gender-matched healthy subjects were taken as controls. Serum Tenascin-C was measured by quantitative sandwich enzyme immunoassay technique. The mean serum concentration of Tenascin-C in controls, seronegative and seropositive cases was 0.66 ng/ml, 20.54 ng/ml and 23.42 ng/ml, respectively. Tenascin-C levels were significantly higher in RA cases compared to controls (

Indexed as

Anti-CCPBiomarkerRheumatoid arthritisRheumatoid factorTenascin-C

Identifiers

PMID38223014
PMCPMC10784432
OpenAlexW4297883923

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.