Evidence map›Paper›PMID 24289455›Full record

ArticleLipids in health and disease2013

Association of angiotensin converting enzyme gene insertion/deletion polymorphism and familial hypercholesterolemia in the Saudi population.

Khalid K Alharbi, Tarek S Kashour, Wejdan Al-Hussaini, May Salem Al-Nbaheen, Sarar Mohamed, Rana M W Hasanato, Waleed Tamimi, Mohammed Yahya Al-Naami, Imran Ali Khan

Open access · goldAbstract read
In one paragraph

Article in Lipids in health and disease, 2013. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 7 papers.

0numbers the graph read from it
0cells of the map it votes in
7citing papers in PubMed
1.2field-weighted citation impact, top 20% 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

7 citing papers in PubMed, 15 citations in OpenAlex.

  1. Association ofSaudi journal of biological sciences · 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

9 authors at 3 institutions in 1 country.

Khalid K Alharbi
Tarek S Kashour
Wejdan Al-Hussaini
May Salem Al-Nbaheen
Sarar Mohamed
Rana M W Hasanato
Waleed Tamimi
Mohammed Yahya Al-Naami
Imran Ali KhanDepartment of Clinical Laboratory Sciences, College of Applied Medical Sciences, King Saud University, P,O, Box 10219, Riyadh 11433, Kingdom of Saudi Arabia. imkhan@ksu.edu.sa.
King Saud University · SAKing Khalid University Hospital · SAKing Khalid University · SA

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundThe study of the association between genotype and phenotype is of great importance for the prediction of multiple diseases and pathophysiological conditions. The relationship between angiotensin converting enzyme (ACE) Insertion/Deletion (I/D) polymorphism and Familial Hypercholesterolemia (FH) has been not fully investigated in all the ethnicities. In this study we sought to determine the frequency of I/D polymorphism genotypes of ACE gene in Saudi patients with FH.

resultsThis is a case-control study carried out purely in Saudi population. Genomic DNA was isolated from 128 subjects who have participated in this study. ACE gene I/D polymorphism was analyzed by polymerase chain reaction in 64 FH cases and 64 healthy controls. There was no statistically significant difference between the groups with respect to genotype distribution. Furthermore, we did not find any significant difference in the frequency of ACE I/D polymorphism in FH subjects when stratified by gender (p = 0.43).

conclusionOur data suggest that ACE gene I/D polymorphism examined in this study has no role in predicting the occurrence and diagnosis of FH.

Indexed as

Base SequenceMutagenesis, InsertionalPolymorphism, GeneticSequence DeletionAdultAllelesArabsCase-Control StudiesFemaleGene FrequencyGenetic Predisposition to DiseaseHumansHyperlipoproteinemia Type IIMaleMiddle AgedMolecular Sequence DataACE protein, humanPeptidyl-Dipeptidase A

Identifiers

PMID24289455
PMCPMC4220775
OpenAlexW2140018799

What OpenQuestion holds

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LicenceCC BY
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Registered trials

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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.