Evidence map›Paper›PMID 26261636›Full record

ArticleInternational journal of clinical and experimental pathology2015

Associations of common SNPs in the SORT1, GCKR, LPL, APOA1, CETP, LDLR, APOE genes with lipid trait levels in an Algerian population sample.

Djabaria Naïma Meroufel, Sounnia Mediene-Benchekor, Sarah Aïcha Lardjam-Hetraf, Hadjira Ouhaïbi-Djellouli, Houssam Boulenouar, Imane Hamani-Medjaoui, Xavier Hermant, Nadhira Saïdi-Mehtar, Philippe Amouyel, Leïla Houti and 2 more

Open access · greenAbstract read
In one paragraph

Article in International journal of clinical and experimental pathology, 2015. 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
2.0field-weighted citation impact, top 12% 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, 11 citations in OpenAlex.

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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

12 authors at 3 institutions in 2 countries.

Djabaria Naïma MeroufelLaboratoire de Génétique Moléculaire et Cellulaire, Université des Sciences et de Technologie d'Oran Mohamed Boudiaf BP 1505 El M'Naouer 31000, Oran, Algeria.
Sounnia Mediene-BenchekorLaboratoire de Génétique Moléculaire et Cellulaire, Université des Sciences et de Technologie d'Oran Mohamed Boudiaf BP 1505 El M'Naouer 31000, Oran, Algeria ; Département de Biotechnologie, Faculté des Sciences de la Nature et de la Vie, Université d'Oran BP 1524 El M'Naouer 31000, Oran, Algeria.
Sarah Aïcha Lardjam-HetrafLaboratoire de Génétique Moléculaire et Cellulaire, Université des Sciences et de Technologie d'Oran Mohamed Boudiaf BP 1505 El M'Naouer 31000, Oran, Algeria.
Hadjira Ouhaïbi-DjellouliLaboratoire de Génétique Moléculaire et Cellulaire, Université des Sciences et de Technologie d'Oran Mohamed Boudiaf BP 1505 El M'Naouer 31000, Oran, Algeria ; Département de Biotechnologie, Faculté des Sciences de la Nature et de la Vie, Université d'Oran BP 1524 El M'Naouer 31000, Oran, Algeria.
Houssam BoulenouarLaboratoire de Génétique Moléculaire et Cellulaire, Université des Sciences et de Technologie d'Oran Mohamed Boudiaf BP 1505 El M'Naouer 31000, Oran, Algeria.
Imane Hamani-MedjaouiLaboratoire de Génétique Moléculaire et Cellulaire, Université des Sciences et de Technologie d'Oran Mohamed Boudiaf BP 1505 El M'Naouer 31000, Oran, Algeria ; Caisse Nationale des Assurances Sociales des travailleurs salariés, Clinique Spécialisée en Orthopédie et Rééducation des Victimes des Accidents de Travail Oran, Algeria.
Xavier HermantINSERM, U1167, Institut Pasteur de Lille, Université de Lille 1 rue du Pr. Calmette, BP 245, F-59019 Lille Cedex, France.
Nadhira Saïdi-MehtarLaboratoire de Génétique Moléculaire et Cellulaire, Université des Sciences et de Technologie d'Oran Mohamed Boudiaf BP 1505 El M'Naouer 31000, Oran, Algeria.
Philippe AmouyelINSERM, U1167, Institut Pasteur de Lille, Université de Lille 1 rue du Pr. Calmette, BP 245, F-59019 Lille Cedex, France.
Leïla HoutiLaboratoire de Génétique Moléculaire et Cellulaire, Université des Sciences et de Technologie d'Oran Mohamed Boudiaf BP 1505 El M'Naouer 31000, Oran, Algeria ; Faculté de Médecine, Université Djillali Liabes de Sidi Bel Abbes Sidi Bel Abbes, Algeria ; Laboratoire des Systèmes d'Information en Santé, Université d'Oran Oran, Algeria.
Aline MeirhaegheINSERM, U1167, Institut Pasteur de Lille, Université de Lille 1 rue du Pr. Calmette, BP 245, F-59019 Lille Cedex, France.
Louisa GoumidiINSERM, U1167, Institut Pasteur de Lille, Université de Lille 1 rue du Pr. Calmette, BP 245, F-59019 Lille Cedex, France.
Université des Sciences et de la Technologie d'Oran Mohamed Boudiaf · DZInserm · FRUniversité Oran 1 Ahmed Ben Bella · DZ

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Genome-wide association studies have identified many lipid-associated loci primarily in European and Asian populations. In view of the differences between ethnic groups in terms of the frequency and impact of these variants, our objective was to evaluate the relationships between eight lipid-associated variants (considered individually and in combination) and fasting serum triglyceride, total cholesterol, HDL- and LDL-cholesterol levels in an Algerian population sample (ISOR study, n = 751). Three SNPs (in SORT1, CETP and GCKR) were individually associated with lipid level variations. Moreover, the risk allele scores for total cholesterol, triglyceride and LDL-C levels (encompassing between three and six SNPs) were associated with their corresponding lipid traits. Our study is the first to show that some of the lipid-associated loci in European populations are associated with lipid traits in Algerians. Although our results will have to be confirmed in other North African populations, this study contributes to a better understanding of genetic susceptibility to lipid traits in Algeria.

Indexed as

Polymorphism, Single NucleotideAdaptor Proteins, Signal TransducingAdaptor Proteins, Vesicular TransportAlgeriaApolipoprotein A-IApolipoproteins EBiomarkersBlack PeopleCholesterol Ester Transfer ProteinsGene FrequencyGenetic Association StudiesGenotypeHumansLipidsLipoprotein LipasePhenotypeAdaptor Proteins, Signal TransducingAdaptor Proteins, Vesicular TransportAPOA1 protein, humanApolipoprotein A-IApolipoproteins EBiomarkersCETP protein, humanCholesterol Ester Transfer ProteinsGCKR protein, humanLDLR protein, humanLipidsLipoprotein LipaseLPL protein, humanReceptors, LDLSortilinAlgeriacombined risk allele scoreISOR studylipidNorth African populationpolymorphism

Identifiers

PMID26261636
PMCPMC4525970
OpenAlexW2417108154

What OpenQuestion holds

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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.