Evidence map›Paper›PMID 39044939›Full record

ArticleJournal of medicine and life2024

Serum visfatin level in β-thalassemia and its correlation with disease severity.

Himadri Shukla, Anurag Singh, Rashmi Kushwaha, Shailendra Prasad Verma, Nishant Verma, Uma Shankar Singh

Abstract read
In one paragraph

Article in Journal of medicine and life, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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0citing papers in PubMed
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1 · What the graph read from it

What it found

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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

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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

0 citing papers in PubMed.

No citing paper in PubMed yet.

4 · The record

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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.

Himadri ShuklaDepartment of Pathology, King George Medical University, Lucknow, India.
Anurag SinghDepartment of Pathology, King George Medical University, Lucknow, India.
Rashmi KushwahaDepartment of Pathology, King George Medical University, Lucknow, India.
Shailendra Prasad VermaDepartment of Clinical Hematology, King George Medical University, Lucknow, India.
Nishant VermaDepartment of Pediatrics, King George Medical University, Lucknow, India.
Uma Shankar SinghDepartment of Pathology, King George Medical University, Lucknow, India.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Thalassemia is a group of genetic hematological conditions characterized by the defective synthesis of one or more hemoglobin chains. This genetic anomaly alters globin chain balance, causing hemolysis, ineffective erythropoiesis, and chronic inflammatory diseases. The proinflammatory adipocytokine visfatin is predominantly produced in visceral adipose tissue. Its evaluation in individuals with thalassemia may provide valuable insights into the assessment of disease severity. The aim of this study was to investigate the potential role of visfatin in the development of β-thalassemia and its association with the severity of the illness. The study included 40 patients with β-thalassemia and ten healthy individuals matched by age and sex. Serum visfatin level was measured using ELISA. We found that individuals with β-thalassemia major had significantly higher levels of serum visfatin than those with β-thalassemia minor and the control group (

Indexed as

beta-ThalassemiaNicotinamide PhosphoribosyltransferaseSeverity of Illness IndexAdolescentAdultCase-Control StudiesCytokinesFemaleHumansMaleROC CurveYoung AdultCytokinesNicotinamide Phosphoribosyltransferasenicotinamide phosphoribosyltransferase, humanbeta-thalassemiahematological disordersinflammationvisfatin

Identifiers

PMID39044939
PMCPMC11262595

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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.