Evidence map›Paper›PMID 34582652›Full record

ArticleAsian Pacific journal of cancer prevention : APJCP2021

Significance of Hereditary Hemochromatosis Gene (HFE) Mutations in Chronic Hepatitis C and Hepatocellular Carcinoma Patients in Egypt: A Pilot Study.

Reham M Dawood, Mai Abd El Meguid, Walied Elrobe, Ghada M Salum, Naglaa Zayed, Sherief Mousa, Eman Medhat

Open access · goldAbstract read
In one paragraph

Article in Asian Pacific journal of cancer prevention : APJCP, 2021. 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
0.4field-weighted citation impact, top 36% 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

3 citing papers in PubMed, 6 citations in OpenAlex.

  1. Article
  2. Review
  3. TGF-Β1, PNPLA3 Genetic Variants and the Risk of Hepatic Fibrosis: Correspondence.Asian Pacific journal of cancer prevention : APJCP · 2021
    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

7 authors at 2 institutions in 1 country.

Reham M DawoodDepartment of Microbial Biotechnology, Genetic Engineering Division, National Research Center, Giza, Egypt.
Mai Abd El MeguidDepartment of Microbial Biotechnology, Genetic Engineering Division, National Research Center, Giza, Egypt.
Walied ElrobeDepartment of Endemic Medicine, Faculty of Medicine, Cairo University, Cairo, Egypt.
Ghada M SalumDepartment of Microbial Biotechnology, Genetic Engineering Division, National Research Center, Giza, Egypt.
Naglaa ZayedDepartment of Endemic Medicine, Faculty of Medicine, Cairo University, Cairo, Egypt.
Sherief MousaDepartment of Endemic Medicine, Faculty of Medicine, Cairo University, Cairo, Egypt.
Eman MedhatDepartment of Endemic Medicine, Faculty of Medicine, Cairo University, Cairo, Egypt.
Cairo University · EGNational Research Centre · EG

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundHereditary hemochromatosis is a genetic disease defined by enhanced overloading of iron and associated with Chronic Hepatitis C (CHC). This study aims to evaluate the correlation of the HFE gene mutations on Egyptian CHC with liver disease progression and the risk of HCC development.

methodsThe HFE mutations (C282Y and H63D) were genotyped on 100 CHC patients and 50 healthy individuals by a hybridization assay. The serum iron content was also measured for all subjects.

resultsA significant elevation of the serum iron, ferritin, and TIBC in HCV-infected patients (p≤0.05). The H63D mutation was detected in 23% of the all studied samples. The serum iron and the H63D heterozygosity were correlated significantly between non-cirrhotic and cirrhotic without HCC patients.

conclusionThe H63D heterozygosity might have a potential role in iron accumulation. Moreover, HFE mutations did not tend to be associated with an increased risk of HCC in cirrhotic patients.

Indexed as

MutationCarcinoma, HepatocellularEgyptFemaleGenotypeHemochromatosisHepatitis C, ChronicHumansLiver NeoplasmsMaleMiddle AgedPilot ProjectsHemochromatosisHepatitis CHFE gene polymorphismIron

Identifiers

PMID34582652
PMCPMC8850884
OpenAlexW3204751443

What OpenQuestion holds

Textmetadata
LicenceCC BY
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Registered trials

None linked

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.