Evidence map›Paper›PMID 31207234›Full record

ReviewAmerican journal of obstetrics and gynecology2019

The fetal origins of mental illness.

Benjamin J S Al-Haddad, Elizabeth Oler, Blair Armistead, Nada A Elsayed, Daniel R Weinberger, Raphael Bernier, Irina Burd, Raj Kapur, Bo Jacobsson, Caihong Wang and 3 more

Open access · greenAbstract readReview
In one paragraph

Review in American journal of obstetrics and gynecology, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 141 papers, 6 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
141citing papers in PubMed, 6 pooled it
32.0field-weighted citation impact, top 1% 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

141 citing papers in PubMed, 6 syntheses or guidelines pooled it, 270 citations in OpenAlex.

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81 more citing papers are in PubMed but not listed here.

4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

13 authors at 5 institutions in 3 countries.

Benjamin J S Al-HaddadDepartment of Pediatrics, University of Washington, Seattle, WA.
Elizabeth OlerDepartment of Obstetrics & Gynecology, University of Washington, Seattle, WA.
Blair ArmisteadDepartment of Global Health, University of Washington Seattle, WA; Center for Global Infectious Disease Research, Seattle Children's Research Institute, Seattle, WA.
Nada A ElsayedIntegrated Research Center for Fetal Medicine, Department of Gynecology and Obstetrics, Johns Hopkins University School of Medicine, Baltimore, MD.
Daniel R WeinbergerLieber Institute for Brain Development, Departments of Psychiatry, Neurology, Neuroscience, and McKusick-Nathans Institute of Genetic Medicine, Johns Hopkins University School of Medicine Baltimore, MD.
Raphael BernierDepartment of Psychiatry and Behavioral Sciences, University of Washington, Seattle, WA.
Irina BurdIntegrated Research Center for Fetal Medicine, Department of Gynecology and Obstetrics, Johns Hopkins University School of Medicine, Baltimore, MD; Department of Neurology, Johns Hopkins University School of Medicine, Baltimore, MD.
Raj KapurDepartment of Pediatrics, University of Washington, Seattle Children's Hospital, Seattle, WA.
Bo JacobssonDepartment of Obstetrics and Gynecology, Institute of Clinical Science, Sahlgrenska Academy, University of Gothenburg, Gothenburg, Sweden; Region Västra Götaland, Sahlgrenska University Hospital, Gothenburg, Sweden; Department of Genetics and Bioinformatics, Domain of Health Data and Digitalization, Institute of Public Health, Oslo, Norway.
Caihong WangDepartment of Obstetrics and Gynecology, Center for Reproductive Health Sciences, Washington University School of Medicine, St. Louis, MO.
Indira MysorekarDepartments of Obstetrics and Gynecology and Pathology and Immunology, Center for Reproductive Health Sciences, Washington University School of Medicine, St. Louis, MO.
Lakshmi RajagopalCenter for Innate Immunity and Immune Disease, Department of Pediatrics, University of Washington, Seattle, WA; Center for Global Infectious Disease Research, Seattle Children's Research Institute, Seattle, WA.
Kristina M Adams WaldorfDepartment of Obstetrics & Gynecology and Global Health, Center for Innate Immunity and Immune Disease, Center for Emerging and Reemerging Infectious Diseases, University of Washington, Seattle, WA; Sahlgrenska Academy, University of Gothenburg, Gothenburg, Sweden. Electronic address: adamsk@uw.edu.
University of Washington · USJohns Hopkins University · USCenter for Infectious Disease Research · USNorwegian Institute of Public Health · NOSeattle Children's Hospital · US

Funding

MEDICAL SCIENTIST TRAINING PROGRAMT32GM008244 · NIGMS · UNIVERSITY OF MINNESOTA TWIN CITIES · PI SHIMIZU, YOJI · 1988 to 2024
$13.6M
Intellectual and Developmental Disabilities Research CenterU54HD083091 · NICHD · UNIVERSITY OF WASHINGTON · PI DOHERTY, DANIEL · 2014 to 2019
$7.9M
Role of the hyaluronidase in GBS VirulenceR01AI133976 · NIAID · SEATTLE CHILDREN'S HOSPITAL · PI ADAMS WALDORF, KRISTINA M., RAJAGOPAL, LAKSHMI · 2017 to 2021
$4.5M
Safety, Testing/Transmission, and Outcomes in Pregnancy with COVID-19 (STOP-COVID-19 study)R01HD091218 · NICHD · WASHINGTON UNIVERSITY · PI DIAMOND, MICHAEL S, MYSOREKAR, INDIRA U · 2017 to 2022
$4.1M
IL-1β regulation of Zika-mediated adverse perinatal outcomesR01HD097608 · NICHD · UNIVERSITY OF MARYLAND BALTIMORE · PI BURD, IRINA, KLEIN, SABRA L. · 2018 to 2022
$2.9M
ATG16L1 AND MOLECULAR REGULATION OF BACTERIAL PERSISTENCER01DK100644 · NIDDK · WASHINGTON UNIVERSITY · PI MYSOREKAR, INDIRA U · 2013 to 2017
$1.7M
INTERLEUKIN-6 AND AGING: IMPACT ON IMMUNE DEFENSE AND TISSUE REPAIR IN URINARY BLADDERR01AG052494 · NIA · WASHINGTON UNIVERSITY · PI LOWDER, JERRY LANE, MYSOREKAR, INDIRA U · 2016 to 2020
$1.6M
Molecular and neuro-inflammatory biology of aging bladder in normal and disease states: ProjectP20DK119840 · NIDDK · WASHINGTON UNIVERSITY · PI MYSOREKAR, INDIRA U · 2018 to 2019
$612k
NIAID NIH HHS R01 AI133976NIA NIH HHS R01 AG052494NICHD NIH HHS R01 HD091218NICHD NIH HHS R01 HD097608NICHD NIH HHS U54 HD083091NIDDK NIH HHS P20 DK119840NIDDK NIH HHS R01 DK100644NIGMS NIH HHS T32 GM008244
6 · The paper itself

Abstract

The impact of infections and inflammation during pregnancy on the developing fetal brain remains incompletely defined, with important clinical and research gaps. Although the classic infectious TORCH pathogens (ie, Toxoplasma gondii, rubella virus, cytomegalovirus [CMV], herpes simplex virus) are known to be directly teratogenic, emerging evidence suggests that these infections represent the most extreme end of a much larger spectrum of injury. We present the accumulating evidence that prenatal exposure to a wide variety of viral and bacterial infections-or simply inflammation-may subtly alter fetal brain development, leading to neuropsychiatric consequences for the child later in life. The link between influenza infections in pregnant women and an increased risk for development of schizophrenia in their children was first described more than 30 years ago. Since then, evidence suggests that a range of infections during pregnancy may also increase risk for autism spectrum disorder and depression in the child. Subsequent studies in animal models demonstrated that both pregnancy infections and inflammation can result in direct injury to neurons and neural progenitor cells or indirect injury through activation of microglia and astrocytes, which can trigger cytokine production and oxidative stress. Infectious exposures can also alter placental serotonin production, which can perturb neurotransmitter signaling in the developing brain. Clinically, detection of these subtle injuries to the fetal brain is difficult. As the neuropsychiatric impact of perinatal infections or inflammation may not be known for decades after birth, our construct for defining teratogenic infections in pregnancy (eg, TORCH) based on congenital anomalies is insufficient to capture the full adverse impact on the child. We discuss the clinical implications of this body of evidence and how we might place greater emphasis on prevention of prenatal infections. For example, increasing uptake of the seasonal influenza vaccine is a key strategy to reduce perinatal infections and the risk for fetal brain injury. An important research gap exists in understanding how antibiotic therapy during pregnancy affects the fetal inflammatory load and how to avoid inflammation-mediated injury to the fetal brain. In summary, we discuss the current evidence and mechanisms linking infections and inflammation with the increased lifelong risk of neuropsychiatric disorders in the child, and how we might improve prenatal care to protect the fetal brain.

Indexed as

AnimalsAstrocytesAutism Spectrum DisorderBipolar DisorderCytokinesDepressive DisorderFemaleHumansInflammationMental DisordersMicrogliaNeural Stem CellsNeuronsOxidative StressPlacentaPregnancyCytokinesSerotoninautismbraindepressionfetusinfectioninflammationinfluenza virusmicroglianeuronal injurypregnancyschizophreniaseasonality of birth hypothesisTORCHurinary tract infection

Identifiers

PMID31207234
PMCPMC6889013
OpenAlexW2952811277

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.