Evidence map›Paper›PMID 36582513›Full record

ArticleFrontiers in pediatrics2022

Revealing the impact of lifestyle stressors on the risk of adverse pregnancy outcomes with multitask machine learning.

Martin Becker, Jennifer Dai, Alan L Chang, Dorien Feyaerts, Ina A Stelzer, Miao Zhang, Eloise Berson, Geetha Saarunya, Davide De Francesco, Camilo Espinosa and 22 more

Abstract read
In one paragraph

Article in Frontiers in pediatrics, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 3 papers.

0numbers the graph read from it
0cells of the map it votes in
3citing 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

3 citing papers in PubMed.

  1. Article
  2. Review
  3. Review
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

32 authors.

Martin BeckerDepartment of Anesthesiology, Perioperative and Pain Medicine, Stanford University, Palo Alto, CA, United States.
Jennifer DaiDepartment of Anesthesiology, Perioperative and Pain Medicine, Stanford University, Palo Alto, CA, United States.
Alan L ChangDepartment of Anesthesiology, Perioperative and Pain Medicine, Stanford University, Palo Alto, CA, United States.
Dorien FeyaertsDepartment of Anesthesiology, Perioperative and Pain Medicine, Stanford University, Palo Alto, CA, United States.
Ina A StelzerDepartment of Anesthesiology, Perioperative and Pain Medicine, Stanford University, Palo Alto, CA, United States.
Miao ZhangDepartment of Anesthesiology, Perioperative and Pain Medicine, Stanford University, Palo Alto, CA, United States.
Eloise BersonDepartment of Anesthesiology, Perioperative and Pain Medicine, Stanford University, Palo Alto, CA, United States.
Geetha SaarunyaDepartment of Anesthesiology, Perioperative and Pain Medicine, Stanford University, Palo Alto, CA, United States.
Davide De FrancescoDepartment of Anesthesiology, Perioperative and Pain Medicine, Stanford University, Palo Alto, CA, United States.
Camilo EspinosaDepartment of Anesthesiology, Perioperative and Pain Medicine, Stanford University, Palo Alto, CA, United States.
Yeasul KimDepartment of Anesthesiology, Perioperative and Pain Medicine, Stanford University, Palo Alto, CA, United States.
Ivana MarićDepartment of Anesthesiology, Perioperative and Pain Medicine, Stanford University, Palo Alto, CA, United States.
Samson MatarasoDepartment of Anesthesiology, Perioperative and Pain Medicine, Stanford University, Palo Alto, CA, United States.
Seyedeh Neelufar PayrovnaziriDepartment of Anesthesiology, Perioperative and Pain Medicine, Stanford University, Palo Alto, CA, United States.
Thanaphong PhongpreechaDepartment of Anesthesiology, Perioperative and Pain Medicine, Stanford University, Palo Alto, CA, United States.
Neal G RavindraDepartment of Anesthesiology, Perioperative and Pain Medicine, Stanford University, Palo Alto, CA, United States.
Sayane ShomeDepartment of Anesthesiology, Perioperative and Pain Medicine, Stanford University, Palo Alto, CA, United States.
Yuqi TanDepartment of Microbiology & Immunology, Stanford University, Palo Alto, CA, United States.
Melan ThuraiappahDepartment of Anesthesiology, Perioperative and Pain Medicine, Stanford University, Palo Alto, CA, United States.
Lei XueDepartment of Anesthesiology, Perioperative and Pain Medicine, Stanford University, Palo Alto, CA, United States.
Jonathan A MayoDepartment of Pediatrics, Stanford University, Palo Alto, CA, United States.
Cecele C QuaintanceDepartment of Pediatrics, Stanford University, Palo Alto, CA, United States.
Ana LabordeDepartment of Pediatrics, Stanford University, Palo Alto, CA, United States.
Lucy S KingDepartment of Psychology, Stanford University, Palo Alto, CA, United States.
Firdaus S DhabharDepartment of Psychiatry & Behavioral Science, University of Miami, Miami, FL, United States.
Ian H GotlibDepartment of Psychology, Stanford University, Palo Alto, CA, United States.
Ronald J WongDepartment of Biomedical Data Science, Stanford University, Palo Alto, CA, United States.
Martin S AngstDepartment of Anesthesiology, Perioperative and Pain Medicine, Stanford University, Palo Alto, CA, United States.
Gary M ShawDepartment of Pediatrics, Stanford University, Palo Alto, CA, United States.
David K StevensonDepartment of Pediatrics, Stanford University, Palo Alto, CA, United States.
Brice GaudilliereDepartment of Anesthesiology, Perioperative and Pain Medicine, Stanford University, Palo Alto, CA, United States.
Nima AghaeepourDepartment of Anesthesiology, Perioperative and Pain Medicine, Stanford University, Palo Alto, CA, United States.

Funding

Neuromodulation of maternal immune adaptations in pregnancyK99HD105016 · NICHD · STANFORD UNIVERSITY · PI STELZER, INA · 2021 to 2022
$263k
NICHD NIH HHS K99 HD105016
6 · The paper itself

Abstract

Psychosocial and stress-related factors (PSFs), defined as internal or external stimuli that induce biological changes, are potentially modifiable factors and accessible targets for interventions that are associated with adverse pregnancy outcomes (APOs). Although individual APOs have been shown to be connected to PSFs, they are biologically interconnected, relatively infrequent, and therefore challenging to model. In this context, multi-task machine learning (MML) is an ideal tool for exploring the interconnectedness of APOs on the one hand and building on joint combinatorial outcomes to increase predictive power on the other hand. Additionally, by integrating single cell immunological profiling of underlying biological processes, the effects of stress-based therapeutics may be measurable, facilitating the development of precision medicine approaches. Objectives: The primary objectives were to jointly model multiple APOs and their connection to stress early in pregnancy, and to explore the underlying biology to guide development of accessible and measurable interventions. Materials and Methods: In a prospective cohort study, PSFs were assessed during the first trimester with an extensive self-filled questionnaire for 200 women. We used MML to simultaneously model, and predict APOs (severe preeclampsia, superimposed preeclampsia, gestational diabetes and early gestational age) as well as several risk factors (BMI, diabetes, hypertension) for these patients based on PSFs. Strongly interrelated stressors were categorized to identify potential therapeutic targets. Furthermore, for a subset of 14 women, we modeled the connection of PSFs to the maternal immune system to APOs by building corresponding ML models based on an extensive single cell immune dataset generated by mass cytometry time of flight (CyTOF). Results: Jointly modeling APOs in a MML setting significantly increased modeling capabilities and yielded a highly predictive integrated model of APOs underscoring their interconnectedness. Most APOs were associated with mental health, life stress, and perceived health risks. Biologically, stressors were associated with specific immune characteristics revolving around CD4/CD8 T cells. Immune characteristics predicted based on stress were in turn found to be associated with APOs. Conclusions: Elucidating connections among stress, multiple APOs simultaneously, and immune characteristics has the potential to facilitate the implementation of ML-based, individualized, integrative models of pregnancy in clinical decision making. The modifiable nature of stressors may enable the development of accessible interventions, with success tracked through immune characteristics.

Indexed as

adverse pregnancy outcomes (APO)immune statesmultitask machine learningpredictionpsychosocial and stress-related factorssingle-cell

Identifiers

PMID36582513
PMCPMC9793100

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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.