Evidence map›Paper›PMID 34660332›Full record

ArticleFrontiers in cellular and infection microbiology2021

Ahmed Abdel-Razik, Walaa Shabana, Ahmed Mohamed El Nakib, Mostafa Abdelsalam, Ahmed Abdelwahab, Ahmad S Hasan, Rasha Elzehery, Rania Elhelaly, Aya Ahmed Fathy, Sally Abdallah Mostafa and 4 more

Open access · goldAbstract read
In one paragraph

Article in Frontiers in cellular and infection microbiology, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 4 papers.

0numbers the graph read from it
0cells of the map it votes in
4citing papers in PubMed
0.7field-weighted citation impact, top 34% 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

4 citing papers in PubMed, 6 citations in OpenAlex.

  1. Review
  2. Review
  3. Article
  4. Review
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

14 authors at 1 institution in 1 country.

Ahmed Abdel-RazikTropical Medicine Department, Faculty of Medicine, Mansoura University, Mansoura City, Egypt.
Walaa ShabanaTropical Medicine Department, Faculty of Medicine, Mansoura University, Mansoura City, Egypt.
Ahmed Mohamed El NakibTropical Medicine Department, Faculty of Medicine, Mansoura University, Mansoura City, Egypt.
Mostafa AbdelsalamNephrology and Dialysis Unit, Internal Medicine Department, Faculty of Medicine, Mansoura University, Mansoura City, Egypt.
Ahmed AbdelwahabNephrology and Dialysis Unit, Internal Medicine Department, Faculty of Medicine, Mansoura University, Mansoura City, Egypt.
Ahmad S HasanClinical Pathology Department, Faculty of Medicine, Mansoura University, Mansoura City, Egypt.
Rasha ElzeheryClinical Pathology Department, Faculty of Medicine, Mansoura University, Mansoura City, Egypt.
Rania ElhelalyClinical Pathology Department, Faculty of Medicine, Mansoura University, Mansoura City, Egypt.
Aya Ahmed FathyPublic Health and Community Department, Faculty of Medicine, Mansoura University, Mansoura City, Egypt.
Sally Abdallah MostafaMedical Biochemistry and Molecular Biology Department, Faculty of Medicine, Mansoura University, Mansoura City, Egypt.
Niveen El-WakeelMedical Microbiology and Immunology Department, Faculty of Medicine, Mansoura University, Mansoura City, Egypt.
Dalia MoemenMedical Microbiology and Immunology Department, Faculty of Medicine, Mansoura University, Mansoura City, Egypt.
Waleed EldarsMedical Microbiology and Immunology Department, Faculty of Medicine, Mansoura University, Mansoura City, Egypt.
Ahmed H YassenTropical Medicine Department, Faculty of Medicine, Mansoura University, Mansoura City, Egypt.
Mansoura University · EG

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Background and Purpose: The advanced glycation end products (AGEs) have been implicated in different diseases' pathogenesis, but their role in hepatocellular carcinoma (HCC) is still a matter of debate. This study aims to investigate the association of AGEs with HCC development in patients with hepatitis C-related cirrhosis. Methods: Only 153 of the 181 non-diabetic patients with cirrhosis were consecutively involved in this pilot cohort prospective study, along with 34 healthy control participants. Demographic characteristics, biochemical parameters, clinical data, and AGEs levels in all subjects at the starting point and every year after that for two years were assessed. Multivariable Cox regression analysis was used to settle variables that could predict HCC development within this period. Results: HCC developed in 13 (8.5%) patients. Univariate Cox regression analysis reported that body mass index (P=0.013), homeostatic model assessment-insulin resistance (P=0.006), alpha-fetoprotein (P <0.001), and AGEs levels (P <0.001) were related to HCC development. After adjusting multiple confounders, the multivariable Cox regression model has revealed that AFP and AGEs were the powerful parameters related to the HCC occurrence (all P<0.05). AGEs at a cutoff value of more than 79.6 ng/ml had 100% sensitivity, 96.4% specificity, and 0.999 area under the curve (all P<0.001), using the receiver operating characteristic curve, for prediction of HCC development. Conclusion: This work suggests that AGEs are associated with an increased incidence of HCC, particularly in cirrhosis, which is encouraging in decreasing the risk of HCC in these patients.

Indexed as

Carcinoma, HepatocellularHepatitis CLiver NeoplasmsGlycation End Products, AdvancedHumansLiver CirrhosisProspective StudiesGlycation End Products, Advancedadvanced glycation end productsdirect-acting antiviralshepatitis C virushepatocellular carcinomaliver cirrhosis

Identifiers

PMID34660332
PMCPMC8517490
OpenAlexW3175991751

What OpenQuestion holds

Textmetadata
LicenceCC BY
Read underepoch 390

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.