Evidence map›Paper›PMID 29338565›Full record

ArticleThe Journal of international medical research2018

Associations of the lipid genetic variants Thr54 ( FABP2) and -493T ( MTTP) with total cholesterol and low-density lipoprotein cholesterol levels in Mexican subjects.

Karina Gonzalez-Becerra, Omar Ramos-Lopez, Mary Lolis Garcia-Cazarin, Elisa Barron-Cabrera, Arturo Panduro, Erika Martinez-Lopez

Open access · goldAbstract read
In one paragraph

Article in The Journal of international medical research, 2018. 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
0.2field-weighted citation impact, top 48% 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, 5 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

6 authors at 3 institutions in 2 countries.

Karina Gonzalez-Becerra1 Medical Molecular Biology Service, "Fray Antonio Alcalde" Civil Hospital of Guadalajara, Department of Molecular Biology and Genomics, 42571 University Center of Health Sciences, University of Guadalajara , Guadalajara, Jalisco, Mexico.
Omar Ramos-Lopez1 Medical Molecular Biology Service, "Fray Antonio Alcalde" Civil Hospital of Guadalajara, Department of Molecular Biology and Genomics, 42571 University Center of Health Sciences, University of Guadalajara , Guadalajara, Jalisco, Mexico.
Mary Lolis Garcia-Cazarin2 Office of 171302 Disease Prevention, National Institutes of Health , Bethesda, MD, USA.
Elisa Barron-Cabrera1 Medical Molecular Biology Service, "Fray Antonio Alcalde" Civil Hospital of Guadalajara, Department of Molecular Biology and Genomics, 42571 University Center of Health Sciences, University of Guadalajara , Guadalajara, Jalisco, Mexico.
Arturo Panduro1 Medical Molecular Biology Service, "Fray Antonio Alcalde" Civil Hospital of Guadalajara, Department of Molecular Biology and Genomics, 42571 University Center of Health Sciences, University of Guadalajara , Guadalajara, Jalisco, Mexico.
Erika Martinez-Lopez1 Medical Molecular Biology Service, "Fray Antonio Alcalde" Civil Hospital of Guadalajara, Department of Molecular Biology and Genomics, 42571 University Center of Health Sciences, University of Guadalajara , Guadalajara, Jalisco, Mexico.
Hospital Civil de Guadalajara · MXUniversidad de Guadalajara · MXNational Institutes of Health · US

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Objective Mexico has one of the world's highest rates of obesity, which is influenced by lipid-genetic and lifestyle factors. This study aimed to determine whether FABP2 (Ala54Thr) and MTTP (-493 G/T) genetic polymorphisms are associated with metabolic disorders in Mexican subjects. Methods A total of 523 subjects participated in a cross-sectional study. Genotyping for FABP2 and MTTP was performed using real-time RT-PCR. Biochemical and anthropometric data were evaluated. Results The genetically at-risk group (Thr54/-493T) was associated with significantly higher total and low-density lipoprotein cholesterol levels (difference between genetically at-risk group and wild-type group: 10.6 mg/dL and 8.94 mg/dL, respectively). Carriers within the genetically at-risk group had a significantly higher prevalence rate of hypercholesterolaemia (42.5% vs. 32.0%) and higher LDL-C levels (37.6% vs. 26.4%) than did non-carriers. Conclusions Subjects who are genetically at risk (Thr54/-493T) have higher total cholesterol levels, low-density lipoprotein cholesterol levels, and prevalence rate of hypercholesterolaemia. These findings highlight the importance of basing nutritional intervention strategies for preventing and treating chronic diseases on individual genetic characteristics.

Indexed as

Genetic Association StudiesAdultCholesterolDemographyFatty Acid-Binding ProteinsFemaleGenetic Predisposition to DiseaseHumansLipoproteins, LDLMaleMetabolic DiseasesMexicoPolymorphism, Single NucleotideRacial GroupsRisk FactorsCholesterolFABP2 protein, humanFatty Acid-Binding ProteinsLipoproteins, LDLFABP2hypercholesterolaemiaLipid genetic variantsMexicoMTTPpolymorphism

Identifiers

PMID29338565
PMCPMC6091818
OpenAlexW2782670235

What OpenQuestion holds

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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.