Evidence map›Paper›PMID 26668049›Full record

ArticleReproductive sciences (Thousand Oaks, Calif.)2016

Improved Murine Blastocyst Quality and Development in a Single Culture Medium Compared to Sequential Culture Media.

Justin M Hennings, Randall L Zimmer, Henda Nabli, J Wade Davis, Peter Sutovsky, Miriam Sutovsky, Kathy L Sharpe-Timms

Abstract readComparative Study
In one paragraph

Article in Reproductive sciences (Thousand Oaks, Calif.), 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

0numbers the graph read from it
0cells of the map it votes in
1citing papers in PubMed
–field-weighted citation impact
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

1 citing paper in PubMed.

  1. 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.

Justin M HenningsDivision of Reproductive and Perinatal Research, Department of Obstetrics, Gynecology and Women's Health, School of Medicine, Columbia, MO, USA Division of Animal Sciences, College of Agriculture, Food and Natural Resources, Columbia, MO, USA.
Randall L ZimmerDivision of Reproductive and Perinatal Research, Department of Obstetrics, Gynecology and Women's Health, School of Medicine, Columbia, MO, USA.
Henda NabliDivision of Reproductive and Perinatal Research, Department of Obstetrics, Gynecology and Women's Health, School of Medicine, Columbia, MO, USA.
J Wade DavisDepartment of Health Management and Informatics, School of Medicine, The University of Missouri, Columbia, MO, USA Department of Statistics, College of Arts and Sciences, The University of Missouri, Columbia, MO, USA Biostatistics and Research Design, Galena Hall, Columbia, MO, USA.
Peter SutovskyDivision of Reproductive and Perinatal Research, Department of Obstetrics, Gynecology and Women's Health, School of Medicine, Columbia, MO, USA Division of Animal Sciences, College of Agriculture, Food and Natural Resources, Columbia, MO, USA.
Miriam SutovskyDivision of Animal Sciences, College of Agriculture, Food and Natural Resources, Columbia, MO, USA.
Kathy L Sharpe-TimmsDivision of Reproductive and Perinatal Research, Department of Obstetrics, Gynecology and Women's Health, School of Medicine, Columbia, MO, USA Division of Animal Sciences, College of Agriculture, Food and Natural Resources, Columbia, MO, USA timmsk@health.missouri.edu.

Funding

Mechanisms of Reduced Fecundity in Endometriosis: A role for MMPs and TIMPsR01HD057445 · NICHD · UNIVERSITY OF MISSOURI-COLUMBIA · PI TIMMS, KATHY L · 2008 to 2012
$1.6M
NICHD NIH HHS R01 HD057445
6 · The paper itself

Abstract

objectiveValidate single versus sequential culture media for murine embryo development.

designProspective laboratory experiment.

settingAssisted Reproduction Laboratory. ANIMALS: Murine embryos.

interventionsThawed murine zygotes cultured for 3 or 5 days (d3 or d5) in single or sequential embryo culture media developed for human in vitro fertilization.

main outcome measuresOn d3, zygotes developing to the 8 cell (8C) stage or greater were quantified using 4',6-diamidino-2-phenylindole (DAPI), and quality was assessed by morphological analysis. On d5, the number of embryos reaching the blastocyst stage was counted. DAPI was used to quantify total nuclei and inner cell mass nuclei. Localization of ubiquitin C-terminal hydrolase L1 (UCHL1) and ubiquitin C-terminal hydrolase L3 (UCHL3) was reference points for evaluating cell quality.

resultsComparing outcomes in single versus to sequential media, the odds of embryos developing to the 8C stage on d3 were 2.34 time greater (P = .06). On d5, more embryos reached the blastocyst stage (P = <.0001), hatched, and had significantly more trophoblast cells (P = .005) contributing to the increased total cell number. Also at d5, localization of distinct cytoplasmic UCHL1 and nuclear UCHL3 was found in high-quality hatching blastocysts. Localization of UCHL1 and UCHL3 was diffuse and inappropriately dispersed throughout the cytoplasm in low-quality nonhatching blastocysts.

conclusionsSingle medium yields greater cell numbers, an increased growth rate, and more hatching of murine embryos. Cytoplasmic UCHL1 and nuclear UHCL3 localization patterns were indicative of embryo quality. Our conclusions are limited to murine embryos but one might speculate that single medium may also be more beneficial for human embryo culture. Human embryo studies are needed.

Indexed as

AnimalsBlastocystCulture MediaEmbryo Culture TechniquesEmbryonic DevelopmentFemaleHumansMaleMiceMice, Inbred C57BLCulture MediacultureembryomediaUCHL1UCHL3

Identifiers

PMID26668049
PMCPMC5933093

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Registered trials

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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.