Evidence map›Paper›PMID 31154934›Full record

ArticleGut microbes2020

Variants in genes of innate immunity, appetite control and energy metabolism are associated with host cardiometabolic health and gut microbiota composition.

Esteban L Ortega-Vega, Sandra J Guzmán-Castañeda, Omer Campo, Eliana P Velásquez-Mejía, Jacobo de la Cuesta-Zuluaga, Gabriel Bedoya, Juan S Escobar

Open access · goldAbstract read
In one paragraph

Article in Gut microbes, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 6 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
6citing papers in PubMed, 1 pooled it
0.7field-weighted citation impact, top 31% 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

6 citing papers in PubMed, 1 synthesis or guideline pooled it, 15 citations in OpenAlex.

  1. Pooled it
  2. Article
  3. Article
  4. Review
  5. Review
  6. 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 2 institutions in 1 country.

Esteban L Ortega-VegaGrupo de Investigación en Genética Molecular (GENMOL), Sede de Investigación Universitaria, Universidad de Antioquia , Medellin, Colombia.
Sandra J Guzmán-CastañedaGrupo de Investigación en Genética Molecular (GENMOL), Sede de Investigación Universitaria, Universidad de Antioquia , Medellin, Colombia.
Omer CampoGrupo de Investigación en Genética Molecular (GENMOL), Sede de Investigación Universitaria, Universidad de Antioquia , Medellin, Colombia.
Eliana P Velásquez-MejíaVidarium-Nutrition, Health and Wellness Research Center, Grupo Empresarial Nutresa , Medellin, Colombia.
Jacobo de la Cuesta-ZuluagaGrupo de Investigación en Genética Molecular (GENMOL), Sede de Investigación Universitaria, Universidad de Antioquia , Medellin, Colombia.ORCID 0000-0002-7369-992X
Gabriel BedoyaGrupo de Investigación en Genética Molecular (GENMOL), Sede de Investigación Universitaria, Universidad de Antioquia , Medellin, Colombia.ORCID 0000-0002-4820-6679
Juan S EscobarVidarium-Nutrition, Health and Wellness Research Center, Grupo Empresarial Nutresa , Medellin, Colombia.ORCID 0000-0001-7304-917X
Universidad de Antioquia · COFundación Con Vida · CO

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Identifying the genetic and non-genetic determinants of obesity and related cardiometabolic dysfunctions is cornerstone for their prevention, treatment, and control. While genetic variants contribute to the cardiometabolic syndrome (CMS), non-genetic factors, such as the gut microbiota, also play key roles. Gut microbiota is intimately associated with CMS and its composition is heritable. However, associations between this microbial community and host genetics are understudied. We contribute filling this gap by genotyping 60 variants in 39 genes of three modules involved in CMS risk, measuring cardiometabolic risk factors, and characterizing gut microbiota in a cohort of 441 Colombians. We hypothesized that CMS risk variants were correlated with detrimental levels of clinical parameters and with the abundance of disease-associated microbes. We found several polymorphisms in genes of innate immunity, appetite control, and energy metabolism that were associated with metabolic dysregulation and microbiota composition; the associations between host genetics and cardiometabolic health were independent of the participants' gut microbiota, and those between polymorphisms and gut microbes were independent of the CMS risk. Associations were also independent of the host genetic ancestry, diet and lifestyle. Most microbes explaining genetic-microbiota associations belonged to the families

Indexed as

Gastrointestinal MicrobiomeAdultAppetite RegulationBody Mass IndexCohort StudiesCross-Sectional StudiesEnergy MetabolismFemaleGene-Environment InteractionGenotypeHost Microbial InteractionsHumansImmunity, InnateMaleMetabolic SyndromeMiddle AgedRNA, Ribosomal, 16SColombiagastrointestinal tractGenetic polymorphismLatin Americamestizometabolic syndromemicrobiomeobesitySNP

Identifiers

PMID31154934
PMCPMC7524339
OpenAlexW2948727206

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.