Evidence map›Paper›PMID 39600173›Full record

ArticleClinical and experimental pediatrics2024

Clinical, biochemical, and genetic study of TACE/TNF-α/ACE signaling pathway in pediatric COVID-19 infection.

Ahmed El-Abd Ahmed, Sawsan M A Abuhamdah, Mohammed H Hassan, Nagwan I Rashwan, Eman A Abd-Elmawgood, Haggagy Mansour, Hoda S Sherkawy, Shymaa G Rizk

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Article in Clinical and experimental pediatrics, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.

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2citing papers in PubMed
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1 · What the graph read from it

What it found

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2 · The registry

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3 · Its place in the literature

Who cites it

2 citing papers in PubMed.

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4 · The record

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5 · Who and what money

Authors and funding

8 authors.

Ahmed El-Abd AhmedDepartment of Pediatrics, Faculty of Medicine, South Valley University, Qena, Egypt.
Sawsan M A AbuhamdahDepartment of Biopharmaceutics and Clinical Pharmacy, School of Pharmacy, The University of Jordan, Amman, Jordan.
Mohammed H HassanDepartment of Medical Biochemistry, Faculty of Medicine, South Valley University, Qena, Egypt.
Nagwan I RashwanDepartment of Pediatrics, Faculty of Medicine, South Valley University, Qena, Egypt.
Eman A Abd-ElmawgoodDepartment of Pediatrics, Faculty of Medicine, South Valley University, Qena, Egypt.
Haggagy MansourDepartment of Chest Diseases and Tuberculosis, Faculty of Medicine, South Valley University, Qena, Egypt.
Hoda S SherkawyDepartment of Medical Biochemistry, Faculty of Medicine, Aswan University, Aswan, Egypt.
Shymaa G RizkDepartment of Pediatrics, Faculty of Medicine, South Valley University, Qena, Egypt.

Funding

Faculty of Medicine, South Valley University
6 · The paper itself

Abstract

backgroundPediatric patients infected with coronavirus disease 2019 (COVID-19) have unique clinical characteristics. Tumor necrosis factor (TNF) is a proinflammatory cytokine that greatly contributes to tumor pathogenesis. PURPOSE: To describe the presenting characteristics of COVID-19 infection among pediatric patients, and investigate the possible role of the TNF-α signaling pathway.

methodsThis prospective case-control study included 50 Egyptian pediatric patients with COVID-19 and 50 healthy controls. Clinical, laboratory, and radiological assessments were performed. Serum TNF-alpha (TNF-α), TNF-α-converting enzyme (TACE), and angiotensin-converting enzyme 2 (ACE2) were measured using enzyme-linked immunosorbent assay. ACE (I/D) (rs4646994), ACE2 rs2285666, and TNF-α-308G/A single nucleotide polymorphisms (SNPs) were performed using conventional polymerase chain reaction techniques with or without restriction fragment length polymorphism.

resultsThe median age was 1 year (interquartile range [IQR], 0.31-2.50 years) in the case group and 1.45 years (IQR, 1.00-3.00) in the control group. The main presenting symptoms were fever (92%), dry cough (74%), and dyspnea (72%). The lymphocytic count was normal in 14 patients (28%), decreased in 16 patients (32%), and increased in 20 patients (40%) of the case group. Positive chest computed tomography finding of COVID-19 infection were demonstrated among 40% of patients using COVID-19 Reporting and Data System categories (ground-glass opacity with or without consolidations in the lungs). There were significant increased serum TACE and TNF-α with decreased ACE2 levels among cases versus controls (P< 0.001). The GG genotype and G allele of the TNF-α-308G/A SNP were significantly higher in patients than in controls (P<0.05 for both), with insignificant differences in genotype and allelic frequencies in the ACE (I/D) (rs4646994) and ACE2 rs2285666 SNPs.

conclusionThe TNF signaling pathway was significantly activated in pediatric COVID-19 infection. Only the TNF-α-308G/A SNP was significantly associated with pediatric COVID-19 infection.

Indexed as

Angiotensin converting enzymePediatric multisystem inflammatory disease, COVID-19 relatedSingle nucleotide polymorphismsTumor Necrosis Factor-alphaTumor Necrosis Factor-alpha Converting Enzyme

Identifiers

PMID39600173
PMCPMC11621736

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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.