Evidence map›Paper›PMID 22703775›Full record

ArticleJournal of pediatric surgery2012

Alterations in maternal-fetal cellular trafficking after fetal surgery.

Payam Saadai, Tzong-Hae Lee, Geoanna Bautista, Kelly D Gonzales, Amar Nijagal, Michael P Busch, Chong Jai Kim, Roberto Romero, Hanmin Lee, Shinjiro Hirose and 4 more

Open access · bronzeAbstract read
In one paragraph

Article in Journal of pediatric surgery, 2012. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 11 papers.

0numbers the graph read from it
0cells of the map it votes in
11citing papers in PubMed
4.3field-weighted citation impact, top 6% 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

11 citing papers in PubMed, 21 citations in OpenAlex.

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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

14 authors at 5 institutions in 2 countries.

Payam SaadaiDivision of Pediatric Surgery and Fetal Treatment Center, Department of Surgery, University of California, San Francisco, CA 94143-0570, USA. payam.saadai@ucsfmedctr.org
Tzong-Hae Lee
Geoanna Bautista
Kelly D Gonzales
Amar Nijagal
Michael P Busch
Chong Jai Kim
Roberto Romero
Hanmin Lee
Shinjiro Hirose
Larry Rand
Douglas Miniati
Diana L Farmer
Tippi C MacKenzie
University of California, San Francisco · USBlood Systems Research Institute · USNational Institutes of Health · USSystems Research Institute · PLUnited States Department of Health and Human Services · US

Funding

The Role Of Subclinical Infection And Cytokines In Preterm ParturitionZIAHD002400 · NICHD · EUNICE KENNEDY SHRIVER NATIONAL INSTITUTE OF CHILD HEALTH & HUMAN DEVELOPMENT · PI ROMERO, ROBERTO · 2009 to 2025
$254.4M
Maternal and fetal immune responses to in utero HSC transplantationK08AI085042 · NIAID · UNIVERSITY OF CALIFORNIA, SAN FRANCISCO · PI MACKENZIE, TIPPI · 2010 to 2014
$517k
NHLBI NIH HHS R01-HL-088388NIAID NIH HHS K08 AI085042
6 · The paper itself

Abstract

background/purposeBidirectional trafficking of cells between the mother and the fetus is routine in pregnancy and a component of maternal-fetal tolerance. Changes in fetal-to-maternal cellular trafficking have been reported in prenatal complications, but maternal-to-fetal trafficking has never been studied in the context of fetal intervention. We hypothesized that patients undergoing open fetal surgery would have altered maternal-fetal cellular trafficking.

methodsCellular trafficking was analyzed in patients with myelomeningocele (MMC) who underwent open fetal surgical repair (n = 5), patients with MMC who had routine postnatal repair (n = 6), and healthy control healthy patients (n = 9). As an additional control for the fetal operation, trafficking was also analyzed in patients who were delivered by an ex utero intrapartum treatment procedure (n = 6). Microchimerism in maternal and cord blood was determined using quantitative real-time polymerase chain reaction for nonshared alleles.

resultsMaternal-to-fetal trafficking was significantly increased in patients who underwent open fetal surgery for MMC compared with healthy controls, patients who underwent postnatal MMC repair, and patients who underwent ex utero intrapartum treatment. There were no differences in fetal-to-maternal cell trafficking among groups.

conclusionPatients undergoing open fetal surgery for MMC have elevated levels of maternal microchimerism. These results suggest altered trafficking and/or increased proliferation of maternal cells in fetal blood and may have important implications for preterm labor.

Indexed as

ChimerismFetal TherapiesFetomaternal TransfusionAirway ObstructionCell MovementFemaleFetal BloodHernia, DiaphragmaticHernias, Diaphragmatic, CongenitalHumansHysterotomyInfant, NewbornMeningomyeloceleObstetric Labor, PrematureParturitionPregnancy

Identifiers

PMID22703775
PMCPMC3377979
OpenAlexW2036234485

What OpenQuestion holds

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LicenceTDM
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.