Evidence map›Paper›PMID 36142493›Full record

ArticleInternational journal of molecular sciences2022

Unravelling the Contribution of the rs7041 and rs4588 Polymorphisms of the

Alberto Hidalgo-Bravo, Berenice Rivera-Paredez, Guadalupe León-Reyes, Nelly Patiño, Manuel Castillejos-López, Jorge Salmerón, Rafael Velázquez-Cruz

Open access · goldAbstract read
In one paragraph

Article in International journal of molecular sciences, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 4 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
4citing papers in PubMed, 1 pooled it
1.3field-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

4 citing papers in PubMed, 1 synthesis or guideline pooled it, 9 citations in OpenAlex.

  1. Pooled it
  2. Article
  3. Observational
  4. Article
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

7 authors at 4 institutions in 1 country.

Alberto Hidalgo-BravoDepartamento de Genética, Instituto Nacional de Rehabilitación (INR), Mexico City 014389, Mexico.ORCID 0000-0003-2506-8784
Berenice Rivera-ParedezCentro de Investigación en Políticas, Población y Salud, Facultad de Medicina, Universidad Nacional Autónoma de México (UNAM), Mexico City 04510, Mexico.
Guadalupe León-ReyesLaboratorio de Genómica del Metabolismo Óseo, Instituto Nacional de Medicina Genómica (INMEGEN), Mexico City 14610, Mexico.
Nelly PatiñoInstituto Nacional de Medicina Genómica (INMEGEN), Mexico City 14610, Mexico.
Manuel Castillejos-LópezDepartamento de Epidemiología, Instituto Nacional de Enfermedades Respiratorias (INER), Mexico City 14080, Mexico.ORCID 0000-0001-8689-9755
Jorge SalmerónCentro de Investigación en Políticas, Población y Salud, Facultad de Medicina, Universidad Nacional Autónoma de México (UNAM), Mexico City 04510, Mexico.ORCID 0000-0002-5113-299X
Rafael Velázquez-CruzLaboratorio de Genómica del Metabolismo Óseo, Instituto Nacional de Medicina Genómica (INMEGEN), Mexico City 14610, Mexico.ORCID 0000-0003-4515-0777
National Institute of Genomic Medicine · MXUniversidad Nacional Autónoma de México · MXInstituto Nacional de Enfermedades Respiratorias · MXInstituto Nacional de Rehabilitación · MX

Funding

Consejo Nacional de Ciencia y Tecnología 7876, 87783, 262233, 26267 M, SALUD-2010-01-139796, SALUD-2011-01-161930, and CB-2013-01-221628Consejo Nacional de Ciencia y Tecnología INFR-2016-01-270405National Institute of Genomic Medicine 346-05/2018/I
6 · The paper itself

Abstract

Metabolic syndrome (MetS) is a multifactorial disorder integrated by a constellation of cardiovascular risk factors. The genetic and environmental determinants of MetS are not fully elucidated. This study investigated the association of two common single nucleotide polymorphisms (SNPs) on

Indexed as

Metabolic SyndromeVitamin D-Binding ProteinAdultCarrier ProteinsFemaleGenetic Predisposition to DiseaseGenotypeHaplotypesHumansPolymorphism, Single NucleotideVitamin DCarrier ProteinsVitamin DVitamin D-Binding ProteinGC genehaplotypemetabolic syndromeserum vitamin D binding proteinsingle nucleotide polymorphism

Identifiers

PMID36142493
PMCPMC9503453
OpenAlexW4296588709

What OpenQuestion holds

Textmetadata
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.