Evidence map›Paper›PMID 34364844›Full record

ArticleAmerican journal of obstetrics and gynecology2022

Effects of early daily alcohol exposure on placental function and fetal growth in a rhesus macaque model.

Jamie O Lo, Matthias C Schabel, Victoria H J Roberts, Terry K Morgan, Suzanne S Fei, Lina Gao, Karina G Ray, Katherine S Lewandowski, Natali P Newman, Jacqueline A Bohn and 3 more

Open access · greenAbstract read
In one paragraph

Article in American journal of obstetrics and gynecology, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 14 papers.

0numbers the graph read from it
0cells of the map it votes in
14citing papers in PubMed
4.7field-weighted citation impact, top 5% 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

14 citing papers in PubMed, 17 citations in OpenAlex.

  1. Article
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  8. Review
  9. Fetal alcohol spectrum disorders.Nature reviews. Disease primers · 2023
    Review
  10. Article
  11. Article
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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

13 authors at 2 institutions in 1 country.

Jamie O LoDepartment of Obstetrics and Gynecology, Oregon Health & Science University, Portland, OR; Division of Reproductive and Developmental Sciences, Oregon National Primate Research Center, Oregon Health & Science University, Beaverton, OR. Electronic address: loj@ohsu.edu.
Matthias C SchabelAdvanced Imaging Research Center, Oregon Health & Science University, Portland, OR.
Victoria H J RobertsDivision of Reproductive and Developmental Sciences, Oregon National Primate Research Center, Oregon Health & Science University, Beaverton, OR.
Terry K MorganDepartment of Pathology, Oregon Health & Science University, Portland, OR.
Suzanne S FeiBioinformatics and Biostatistics Core, Oregon National Primate Research Center, Oregon Health & Science University, Beaverton, OR.
Lina GaoBioinformatics and Biostatistics Core, Oregon National Primate Research Center, Oregon Health & Science University, Beaverton, OR.
Karina G RayBioinformatics and Biostatistics Core, Oregon National Primate Research Center, Oregon Health & Science University, Beaverton, OR.
Katherine S LewandowskiDivision of Reproductive and Developmental Sciences, Oregon National Primate Research Center, Oregon Health & Science University, Beaverton, OR.
Natali P NewmanDivision of Neuroscience, Oregon National Primate Research Center, Oregon Health & Science University, Beaverton, OR.
Jacqueline A BohnDepartment of Obstetrics and Gynecology, Oregon Health & Science University, Portland, OR.
Kathleen A GrantDivision of Neuroscience, Oregon National Primate Research Center, Oregon Health & Science University, Beaverton, OR.
Antonio E FriasDepartment of Obstetrics and Gynecology, Oregon Health & Science University, Portland, OR; Division of Reproductive and Developmental Sciences, Oregon National Primate Research Center, Oregon Health & Science University, Beaverton, OR.
Christopher D KroenkeAdvanced Imaging Research Center, Oregon Health & Science University, Portland, OR; Division of Neuroscience, Oregon National Primate Research Center, Oregon Health & Science University, Beaverton, OR.
Oregon National Primate Research Center · USOregon Health & Science University · US

Funding

Upgrade of confocal microscopy at the Oregon National Primate Research CenterP51OD011092 · OD · OREGON HEALTH & SCIENCE UNIVERSITY · PI Bonnie J. Nagel · 2012 to 2026
$203.9M
REPRODUCTIVE SCIENTIST TRAINING PROGRAMK12HD000849 · NICHD · WASHINGTON UNIVERSITY · PI Danny J Schust · 1988 to 2026
$33.2M
Development and validation of MR imaging methods for in vivo assessment of placental perfusion and oxygenationR01HD086331 · NICHD · OREGON HEALTH & SCIENCE UNIVERSITY · PI FRIAS, ANTONIO E · 2015 to 2019
$2.6M
Characterizing the FASD cerebral cortex in utero with DTIR01AA021981 · NIAAA · OREGON HEALTH & SCIENCE UNIVERSITY · PI KROENKE, CHRISTOPHER D · 2013 to 2017
$2.3M
NIAAA NIH HHS R01 AA021981NICHD NIH HHS K12 HD000849NICHD NIH HHS R01 HD086331NIH HHS P51 OD011092
6 · The paper itself

Abstract

backgroundPrenatal alcohol exposure is the most common cause of birth defects and intellectual disabilities and can increase the risk of stillbirth and negatively impact fetal growth.

objectiveTo determine the effect of early prenatal alcohol exposure on nonhuman primate placental function and fetal growth. We hypothesized that early chronic prenatal alcohol would alter placental perfusion and oxygen availability that adversely affects fetal growth. STUDY

designRhesus macaques self-administered 1.5 g/kg/d of ethanol (n=12) or isocaloric maltose-dextrin (n=12) daily before conception through the first 60 days of gestation (term is approximately 168 days). All animals were serially imaged with Doppler ultrasound to measure fetal biometry, uterine artery volume blood flow, and placental volume blood flow. Following Doppler ultrasound, all animals underwent both blood oxygenation level-dependent magnetic resonance imaging to characterize placental blood oxygenation and dynamic contrast-enhanced magnetic resonance imaging to quantify maternal placental perfusion. Animals were delivered by cesarean delivery for placental collection and fetal necropsy at gestational days 85 (n=8), 110 (n=8), or 135 (n=8). Histologic and RNA-sequencing analyses were performed on collected placental tissue.

resultsPlacental volume blood flow was decreased at all gestational time points in ethanol-exposed vs control animals, but most significantly at gestational day 110 by Doppler ultrasound (P<.05). A significant decrease in total volumetric blood flow occurred in ethanol-exposed vs control animals on dynamic contrast-enhanced magnetic resonance imaging at both gestation days 110 and 135 (P<.05); moreover, a global reduction in T

conclusionEarly chronic prenatal alcohol exposure significantly diminished placental perfusion at mid to late gestation and also significantly decreased the oxygen supply to the fetal vasculature throughout pregnancy, these findings were associated with the presence of microscopic placental infarctions in the nonhuman primate. Although placental adaptations may compensate for early environmental perturbations to fetal growth, placental blood flow and oxygenation were reduced, consistent with the evidence of placental ischemic injury.

Indexed as

Macaca mulattaAnimalsDisease Models, AnimalEthanolFemaleFetal DevelopmentHumansPlacentaPregnancyPrenatal Exposure Delayed EffectsEthanolfetal alcohol spectrum disorderfetal alcohol syndromematernal drinkingplacental perfusion and oxygenationprenatal alcohol exposure

Identifiers

PMID34364844
PMCPMC8748286
OpenAlexW3187874307

What OpenQuestion holds

Textmetadata
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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.