Evidence map›Paper›PMID 25603303›Full record

ArticlePloS one2015

Influences of gestational obesity on associations between genotypes and gene expression levels in offspring following maternal gastrointestinal bypass surgery for obesity.

Frédéric Guénard, Maxime Lamontagne, Yohan Bossé, Yves Deshaies, Katherine Cianflone, John G Kral, Picard Marceau, Marie-Claude Vohl

Open access · goldAbstract read
In one paragraph

Article in PloS one, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.

0numbers the graph read from it
0cells of the map it votes in
2citing papers in PubMed
1.7field-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

2 citing papers in PubMed, 6 citations in OpenAlex.

  1. Article
  2. Review
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

8 authors at 3 institutions in 2 countries.

Frédéric GuénardInstitute of Nutrition and Functional Foods (INAF) and Department of Food Science and Nutrition, Laval University, Quebec, Canada; Endocrinology and Nephrology, CHU de Quebec Research Center, Quebec, Canada.
Maxime LamontagneQuebec Heart and Lung Institute, Quebec, Canada.
Yohan BosséQuebec Heart and Lung Institute, Quebec, Canada; Department of Molecular Medicine, Laval University, Quebec, Canada.
Yves DeshaiesQuebec Heart and Lung Institute, Quebec, Canada; Department of Medicine, Laval University, Quebec, Canada.
Katherine CianfloneQuebec Heart and Lung Institute, Quebec, Canada; Department of Medicine, Laval University, Quebec, Canada.
John G KralDepartment of Surgery, SUNY Downstate Medical Center, Brooklyn, New York, United States of America.
Picard MarceauQuebec Heart and Lung Institute, Quebec, Canada; Department of Surgery, Laval University, Quebec, Canada.
Marie-Claude VohlInstitute of Nutrition and Functional Foods (INAF) and Department of Food Science and Nutrition, Laval University, Quebec, Canada; Endocrinology and Nephrology, CHU de Quebec Research Center, Quebec, Canada.
Université Laval · CAMontreal Heart Institute · CASUNY Downstate Health Sciences University · US

Funding

Canadian Institutes of Health Research MOP-209380
6 · The paper itself

Abstract

methodsWhole-genome genotyping and gene expression analyses in blood of 22 BMS and 23 AMS offspring from 19 mothers were conducted using Illumina HumanOmni-5-Quad and HumanHT-12 v4 Expression BeadChips, respectively. Using PLINK we analyzed interactions between offspring gene variations and maternal surgical status on offspring gene expression levels. Altered biological functions and pathways were identified and visualized using DAVID and Ingenuity Pathway Analysis.

resultsSignificant interactions (p ≤ 1.22 x 10(-12)) were found for 525 among the 16,060 expressed transcripts: 1.9% of tested SNPs were involved. Gene function and pathway analysis demonstrated enrichment of transcription and of cellular metabolism functions and overrepresentation of cellular stress and signaling, immune response, inflammation, growth, proliferation and development pathways.

conclusionWe suggest that impaired maternal gestational metabolic fitness interacts with offspring gene variations modulating gene expression levels, providing potential mechanisms explaining improved cardiometabolic risk profiles of AMS offspring related to ameliorated maternal lipid and carbohydrate metabolism.

Indexed as

AdolescentAdultChildChild, PreschoolFemaleGene ExpressionGenotypeHumansMiddle AgedMothersObesityPregnancyYoung Adult

Identifiers

PMID25603303
PMCPMC4300091
OpenAlexW2034601720

What OpenQuestion holds

Textmetadata
LicenceCC BY
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.