Evidence map›Paper›PMID 27565903›Full record

ArticlePhysiological reports2016

Increasing fetal ovine number per gestation alters fetal plasma clinical chemistry values.

Micaela Zywicki, Sharon E Blohowiak, Ronald R Magness, Jeffrey L Segar, Pamela J Kling

Open access · goldAbstract read
In one paragraph

Article in Physiological reports, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 7 papers.

0numbers the graph read from it
0cells of the map it votes in
7citing papers in PubMed
2.6field-weighted citation impact, top 9% 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

7 citing papers in PubMed, 6 citations in OpenAlex.

  1. Article
  2. Review
  3. Article
  4. Article
  5. Impact of the ovarian cycle and pregnancy on plasma chemistry values in ewes.Journal of veterinary diagnostic investigation : official publication of the American Association of Veterinary Laboratory Diagnosticians, Inc · 2018
    Article
  6. Article
  7. 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

5 authors at 3 institutions in 1 country.

Micaela ZywickiDepartments of Pediatrics, University of Wisconsin-Madison School of Medicine and Public Health, Madison, WI, USA.
Sharon E BlohowiakDepartments of Pediatrics, University of Wisconsin-Madison School of Medicine and Public Health, Madison, WI, USA.
Ronald R MagnessDepartments of Pediatrics, University of Wisconsin-Madison School of Medicine and Public Health, Madison, WI, USA Obstetrics and Gynecology Perinatal Research Laboratories, University of Wisconsin-Madison School of Medicine and Public Health, Madison, WI, USA.
Jeffrey L SegarDepartment of Pediatrics, University of Iowa Children's Hospital, Iowa, IA, USA.
Pamela J KlingDepartments of Pediatrics, University of Wisconsin-Madison School of Medicine and Public Health, Madison, WI, USA pkling@pediatrics.wisc.edu.
University of Wisconsin–Madison · USUniversity of Iowa Stead Family Children’s Hospital · USWisconsin Division of Public Health · US

Funding

Endothelial Function in a Model of IUGR Induced by Uterine Space RestrictionR01HL117341 · NHLBI · UNIVERSITY OF WISCONSIN-MADISON · PI MAGNESS, RONALD R · 2014 to 2017
$1.8M
NHLBI NIH HHS R01 HL117341
6 · The paper itself

Abstract

Intrauterine growth restriction (IUGR) is interconnected with developmental programming of lifelong pathophysiology. IUGR is seen in human multifetal pregnancies, with stepwise rises in fetal numbers interfering with placental nutrient delivery. It remains unknown whether fetal blood analyses would reflect fetal nutrition, liver, and excretory function in the last trimester of human or ovine IUGR In an ovine model, we hypothesized that fetal plasma biochemical values would reflect progressive placental, fetal liver, and fetal kidney dysfunction as the number of fetuses per gestation rose. To determine fetal plasma biochemical values in singleton, twin, triplet, and quadruplet/quintuplet ovine gestation, we investigated morphometric measures and comprehensive metabolic panels with nutritional measures, liver enzymes, and placental and fetal kidney excretory measures at gestational day (GD) 130 (90% gestation). As anticipated, placental dysfunction was supported by a stepwise fall in fetal weight, fetal plasma glucose, and triglyceride levels as fetal number per ewe rose. Fetal glucose and triglycerides were directly related to fetal weight. Plasma creatinine, reflecting fetal renal excretory function, and plasma cholesterol, reflecting placental excretory function, were inversely correlated with fetal weight. Progressive biochemical disturbances and growth restriction accompanied the rise in fetal number. Understanding the compensatory and adaptive responses of growth-restricted fetuses at the biochemical level may help explain how metabolic pathways in growth restriction can be predetermined at birth. This physiological understanding is important for clinical care and generating interventional strategies to prevent altered developmental programming in multifetal gestation.

Indexed as

Pregnancy, AnimalAnimalsChemistry, ClinicalFemaleFetal BloodFetal DevelopmentFetal Growth RetardationFetusGestational AgeOrgan SizePlacentaPregnancyPregnancy, MultipleSheepSheep, DomesticFetalnutritionovineplacenta

Identifiers

PMID27565903
PMCPMC5002913
OpenAlexW2516306283

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.