Evidence map›Paper›PMID 30775605›Full record

ArticleArchives of medical sciences. Atherosclerotic diseases2018

Association of ficolin-2 (FCN2) functional polymorphisms and protein levels with rheumatic fever and rheumatic heart disease: relationship with cardiac function.

Manal F Elshamaa, Hala Hamza, Naglaa Abd El Rahman, Soha Emam, Eman A Elghoroury, Tarek M Farid, Asmaa Zakareya Zaher, Mona H Ibrahim, Solaf Kamel, Doaa Abd El-Aziz

Open access · diamondAbstract read
In one paragraph

Article in Archives of medical sciences. Atherosclerotic diseases, 2018. 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
1.4field-weighted citation impact, top 17% 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, 9 citations in OpenAlex.

  1. Selected SNPs ofGenes · 2023
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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 at 2 institutions in 1 country.

Manal F ElshamaaPediatrics Department, National Research Centre (NRC), Cairo, Egypt.
Hala HamzaPediatrics Department, Faculty of Medicine, Cairo University, Cairo, Egypt.
Naglaa Abd El RahmanPediatrics Department, Faculty of Medicine, Cairo University, Cairo, Egypt.
Soha EmamPediatrics Department, Faculty of Medicine, Cairo University, Cairo, Egypt.
Eman A ElghorouryClinical and Chemical Pathology Department, National Research Centre, Cairo, Egypt.
Tarek M FaridPediatrics Department, National Research Centre (NRC), Cairo, Egypt.
Asmaa Zakareya ZaherPediatrics Department, Faculty of Medicine, Cairo University, Cairo, Egypt.
Mona H IbrahimClinical and Chemical Pathology Department, National Research Centre, Cairo, Egypt.
Solaf KamelClinical and Chemical Pathology Department, National Research Centre, Cairo, Egypt.
Doaa Abd El-AzizPediatrics Department, 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

introductionA role for ficolin (FCN) 2 gene polymorphisms in the pathogenesis of recurrent severe streptococcal infections and rheumatic carditis has been suggested. The aim of the study was to evaluate a possible relationship between single nucleotide polymorphisms located at positions -602 and -4 of the FCN2 gene and FCN2 serum levels and risk of development of rheumatic fever (RF) and rheumatic heart disease (RHD). MATERIAL AND

methodsSeventy-seven Caucasian Egyptian patients with RF were recruited with a control group of 43 healthy subjects. DNA was extracted for analysis of the FCN2 gene at positions -602 and -4 and serum protein level was measured by ELISA.

resultsFCN2 AA genotype at the -4 position was more frequently observed in RF and RHD patients, as compared to healthy subjects (

conclusionsPolymorphisms linked to low levels of L-ficolin may render an individual at risk of recurrent and/or severe streptococcal infection. The -4 AA genotype and -602/-4

Indexed as

FCN2 geneL-ficolin (ficolin-2)polymorphismrheumatic feverrheumatic heart disease

Identifiers

PMID30775605
PMCPMC6374577
OpenAlexW2909419719

What OpenQuestion holds

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LicenceCC BY-NC-SA
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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.