Evidence map›Paper›PMID 25395450›Full record

ArticleFASEB journal : official publication of the Federation of American Societies for Experimental Biology2015

Essential nutrient supplementation prevents heritable metabolic disease in multigenerational intrauterine growth-restricted rats.

Danielle Goodspeed, Maxim D Seferovic, William Holland, Robert A Mcknight, Scott A Summers, D Ware Branch, Robert H Lane, Kjersti M Aagaard

Open access · greenAbstract read
In one paragraph

Article in FASEB journal : official publication of the Federation of American Societies for Experimental Biology, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 18 papers.

0numbers the graph read from it
0cells of the map it votes in
18citing papers in PubMed
8.1field-weighted citation impact, top 3% 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

18 citing papers in PubMed, 33 citations in OpenAlex.

  1. Article
  2. Review
  3. Review
  4. Review
  5. Interaction between Metformin, Folate and Vitamin BInternational journal of molecular sciences · 2021
    Review
  6. Review
  7. Article
  8. Article
  9. Article
  10. Article
  11. Review
  12. Methyl donor supplementation alters cognitive performance and motivation in female offspring from high-fat diet-fed dams.FASEB journal : official publication of the Federation of American Societies for Experimental Biology · 2017
    Article
  13. Article
  14. Developmental Origins of Common Disease: Epigenetic Contributions to Obesity.Annual review of genomics and human genetics · 2016
    Review
  15. Article
  16. Article
  17. Article
  18. The growing problem of obesity: mechanisms, consequences, and therapeutic approaches.Arteriosclerosis, thrombosis, and vascular biology · 2015
    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 4 institutions in 2 countries.

Danielle Goodspeed*Department of Obstetrics and Gynecology, Baylor College of Medicine, Houston, Texas, USA; Department of Internal Medicine, Department of Pediatrics, and Department of Obstetrics and Gynecology, University of Utah, Salt Lake City, Utah, USA; Program in Cardiovascular and Metabolic Diseases, Duke-National University of Singapore Graduate Medical School, Singapore; and Department of Pediatrics, Medical College of Wisconsin and Children's Hospital of Wisconsin, Milwaukee, Wisconsin, USA.
Maxim D Seferovic*Department of Obstetrics and Gynecology, Baylor College of Medicine, Houston, Texas, USA; Department of Internal Medicine, Department of Pediatrics, and Department of Obstetrics and Gynecology, University of Utah, Salt Lake City, Utah, USA; Program in Cardiovascular and Metabolic Diseases, Duke-National University of Singapore Graduate Medical School, Singapore; and Department of Pediatrics, Medical College of Wisconsin and Children's Hospital of Wisconsin, Milwaukee, Wisconsin, USA.
William Holland*Department of Obstetrics and Gynecology, Baylor College of Medicine, Houston, Texas, USA; Department of Internal Medicine, Department of Pediatrics, and Department of Obstetrics and Gynecology, University of Utah, Salt Lake City, Utah, USA; Program in Cardiovascular and Metabolic Diseases, Duke-National University of Singapore Graduate Medical School, Singapore; and Department of Pediatrics, Medical College of Wisconsin and Children's Hospital of Wisconsin, Milwaukee, Wisconsin, USA.
Robert A Mcknight*Department of Obstetrics and Gynecology, Baylor College of Medicine, Houston, Texas, USA; Department of Internal Medicine, Department of Pediatrics, and Department of Obstetrics and Gynecology, University of Utah, Salt Lake City, Utah, USA; Program in Cardiovascular and Metabolic Diseases, Duke-National University of Singapore Graduate Medical School, Singapore; and Department of Pediatrics, Medical College of Wisconsin and Children's Hospital of Wisconsin, Milwaukee, Wisconsin, USA.
Scott A Summers*Department of Obstetrics and Gynecology, Baylor College of Medicine, Houston, Texas, USA; Department of Internal Medicine, Department of Pediatrics, and Department of Obstetrics and Gynecology, University of Utah, Salt Lake City, Utah, USA; Program in Cardiovascular and Metabolic Diseases, Duke-National University of Singapore Graduate Medical School, Singapore; and Department of Pediatrics, Medical College of Wisconsin and Children's Hospital of Wisconsin, Milwaukee, Wisconsin, USA.
D Ware Branch*Department of Obstetrics and Gynecology, Baylor College of Medicine, Houston, Texas, USA; Department of Internal Medicine, Department of Pediatrics, and Department of Obstetrics and Gynecology, University of Utah, Salt Lake City, Utah, USA; Program in Cardiovascular and Metabolic Diseases, Duke-National University of Singapore Graduate Medical School, Singapore; and Department of Pediatrics, Medical College of Wisconsin and Children's Hospital of Wisconsin, Milwaukee, Wisconsin, USA.
Robert H Lane*Department of Obstetrics and Gynecology, Baylor College of Medicine, Houston, Texas, USA; Department of Internal Medicine, Department of Pediatrics, and Department of Obstetrics and Gynecology, University of Utah, Salt Lake City, Utah, USA; Program in Cardiovascular and Metabolic Diseases, Duke-National University of Singapore Graduate Medical School, Singapore; and Department of Pediatrics, Medical College of Wisconsin and Children's Hospital of Wisconsin, Milwaukee, Wisconsin, USA.
Kjersti M Aagaard*Department of Obstetrics and Gynecology, Baylor College of Medicine, Houston, Texas, USA; Department of Internal Medicine, Department of Pediatrics, and Department of Obstetrics and Gynecology, University of Utah, Salt Lake City, Utah, USA; Program in Cardiovascular and Metabolic Diseases, Duke-National University of Singapore Graduate Medical School, Singapore; and Department of Pediatrics, Medical College of Wisconsin and Children's Hospital of Wisconsin, Milwaukee, Wisconsin, USA aagaardt@bcm.tmc.edu.
Baylor College of Medicine · USUniversity of Utah · USChildren's Hospital of Wisconsin · USNational University of Singapore · SG

Funding

REPRODUCTIVE SCIENTIST TRAINING PROGRAMK12HD000849 · NICHD · WASHINGTON UNIVERSITY · PI Danny J Schust · 1988 to 2026
$33.2M
Conserved Fetal Epigenomic Signatures in a Primate Model of Maternal ObesityR01DK089201 · NIDDK · BAYLOR COLLEGE OF MEDICINE · PI AAGAARD, KJERSTI MARIE · 2012 to 2021
$5.1M
Characterization of the Fetal Primate Epigenome and Metabolome Under In UteroDP2OD001500 · OD · BAYLOR COLLEGE OF MEDICINE · PI AAGAARD, KJERSTI MARIE · 2007 to 2011
$2.3M
NICHD NIH HHS 5K12HD00849NICHD NIH HHS K12 HD000849NIDDK NIH HHS R01 DK089201NIH HHS DP21DP2OD001500-01NIH HHS DP2 OD001500
6 · The paper itself

Abstract

Intrauterine growth restriction (IUGR) confers heritable alterations in DNA methylation, rendering risk of adult metabolic syndrome (MetS). Because CpG methylation is coupled to intake of essential nutrients along the one-carbon pathway, we reasoned that essential nutrient supplementation (ENS) may abrogate IUGR-conferred multigenerational MetS. Pregnant Sprague-Dawley rats underwent bilateral uterine artery ligation causing IUGR in F1. Among the F2 generation, IUGR lineage rats were underweight at birth (6.7 vs. 8.0 g, P < 0.0001) and obese by adulthood (p160: 613 vs. 510 g; P < 0.0001). Dual energy X-ray absorptiometry studies revealed increased central fat mass (Δ+40 g), accompanied by dyslipidemic (>30% elevated, P < 0.05) serum triglycerides (139 mg/dl), very-LDLs (27.8 mg/dl), and fatty acids (632 µM). Hyperglycemic-euglycemic clamp studies and glucose tolerance testing revealed insulin resistance. Conversely, IUGR lineage ENS-fed rats did not manifest MetS, with significantly lower body weight (p160: 410 g), >5-fold less central fat mass, normal hepatic glucose efflux, and >70% reduced circulating triglycerides and very-LDLs compared with IUGR control-fed F2 offspring (P < 0.01). Moreover, increased methylation of the IGF-1 P2 transcriptional start site among IUGR lineage F2 offspring was reversed in ENS (P < 0.04). This is an initial demonstration that supplementation along the one-carbon pathway abrogates adult morbidity and associated epigenomic modifications of IGF-1 in a rodent model of multigenerational MetS.

Indexed as

Dietary SupplementsDNA MethylationAbsorptiometry, PhotonAnimalsBlood GlucoseFemaleFetal Growth RetardationGlucose Tolerance TestInsulin-Like Growth Factor IMetabolic SyndromePolymerase Chain ReactionPregnancyPrenatal Exposure Delayed EffectsPromoter Regions, GeneticRatsRats, Sprague-DawleyBlood GlucoseInsulin-Like Growth Factor IepigenomicsIGF-1methyl donorsobesityone-carbon pathway

Identifiers

PMID25395450
PMCPMC4422359
OpenAlexW2047758571

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.