Evidence map›Paper›PMID 39716300›Full record

ArticleAdvances in rheumatology (London, England)2024

Evaluating the role of active TGF-β1 as inflammatory biomarker in Kashmiri (North-Indian) patients with systemic sclerosis: a case-control study.

Sakeena Ayub, Tabasum Shafi, Roohi Rasool, Mushtaq A Dangroo, Muzaffar A Bindroo, Ayaz Gull, Lamya Ahmad Al-Keridis, Nawaf Alshammari, Mohd Saeed, Zafar Amin Shah

Abstract read
In one paragraph

Article in Advances in rheumatology (London, England), 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 3 papers.

0numbers the graph read from it
0cells of the map it votes in
3citing 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

3 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

10 authors.

Sakeena Ayub *Department of Immunology & Molecular Medicine, Sher-I-Kashmir Institute of Medical Sciences (SKIMS), Soura, Srinagar, Jammu and Kashmir, 190011, India.
Tabasum Shafi *Department of Immunology & Molecular Medicine, Sher-I-Kashmir Institute of Medical Sciences (SKIMS), Soura, Srinagar, Jammu and Kashmir, 190011, India.
Roohi RasoolDepartment of Immunology & Molecular Medicine, Sher-I-Kashmir Institute of Medical Sciences (SKIMS), Soura, Srinagar, Jammu and Kashmir, 190011, India.
Mushtaq A DangrooDivision of Rheumatology, Department of Internal Medicine, Sher-I-Kashmir Institute of Medical Sciences (SKIMS), Soura, Srinagar, 190011, India.
Muzaffar A BindrooDivision of Rheumatology, Department of Internal Medicine, Sher-I-Kashmir Institute of Medical Sciences (SKIMS), Soura, Srinagar, 190011, India.
Ayaz GullDepartment of Immunology & Molecular Medicine, Sher-I-Kashmir Institute of Medical Sciences (SKIMS), Soura, Srinagar, Jammu and Kashmir, 190011, India.
Lamya Ahmad Al-KeridisDepartment of Biology, Faculty of Science, Princess Nourah Bint Abdulrahman University, Riyadh, 11671, Saudi Arabia.
Nawaf AlshammariDepartment of Biology, College of Science, University of Hail, Hail, Saudi Arabia.
Mohd SaeedDepartment of Biology, College of Science, University of Hail, Hail, Saudi Arabia.
Zafar Amin ShahDepartment of Immunology & Molecular Medicine, Sher-I-Kashmir Institute of Medical Sciences (SKIMS), Soura, Srinagar, Jammu and Kashmir, 190011, India. zaffaramin@gmail.com.ORCID http://orcid.org/0000-0001-9269-9303

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundAs a master immune system regulator, transforming growth factor β1 (TGF-β1) is closely linked to the complicated pathophysiology and development of systemic sclerosis (SSc), a multisystem fibrotic disease.

objectiveWe aim to evaluate the transcriptional levels of TGF-β1 mRNA in PBMCs, assess the TGF-β1 serum levels of SSc patients, and compare them with those of healthy subjects.

methodsPBMCs were isolated from whole blood of 50 SSc patients and in 30 healthy controls. After total RNA was extracted from isolated PBMCs, complementary DNA (cDNA) synthesis was performed. Afterward, the expression of TGF-β1 mRNA was assessed using quantitative real-time PCR using the SYBR Green, GAPDH, and TGF-β1 specific primers. The serum levels of TGF-β1 were determined using a commercially available ELISA kit.

resultsThere was a significant upregulation of TGF-β1 relative expression (p < 0.0001), when SSc patients were compared to the control group. The diffuse subgroup was more common in patients with elevated TGF-β1 mRNA expression (p < 0.0001). However, an insignificant difference was observed between the disease subsets of SSc. Serum TGF- β1 levels were upregulated in SSc patients (78.35 ± 23.16) compared to healthy subjects (61.06 ± 15.90), and were considerably higher in SSc patients with ILD (p < 0.01) and positive anti-topo-Isomerase antibody (p < 0.0001).

conclusionIn patients with SSc, elevated levels of TGF-β1 in serum and their correlation with clinical symptoms imply that this cytokine may serve as a marker for fibrotic and vascular involvement in SSc.

Indexed as

BiomarkersRNA, MessengerScleroderma, SystemicTransforming Growth Factor beta1AdultCase-Control StudiesDNA Topoisomerases, Type IFemaleHumansIndiaLeukocytes, MononuclearMaleMiddle AgedScleroderma, DiffuseUp-RegulationBiomarkersDNA Topoisomerases, Type IRNA, MessengerTGFB1 protein, humanTransforming Growth Factor beta1ELISAmRNA expressionqRT-PCRSystemic sclerosisTGF-β1

Identifiers

PMID39716300
PMCPMC13488688

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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.