Evidence map›Paper›PMID 41282910›Full record

ArticlemedRxiv : the preprint server for health sciences2025

Machine learning-optimized perinatal depression screening: Maximum impact, minimal burden.

Eric Hurwitz, Caroline Shell, Kritika Chugh, Veerle Bergink, Rena C Patel, Crystal Schiller, Melissa A Haendel

Abstract readPreprint
In one paragraph

Article in medRxiv : the preprint server for health sciences, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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

0 citing papers in PubMed.

No citing paper in PubMed yet.

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.

Eric HurwitzDepartment of Genetics, University of North Carolina at Chapel Hill, Chapel Hill, NC, United States.ORCID 0000-0002-6581-7754
Caroline ShellDepartment of OBGYN, Sinai Hospital of Baltimore, Baltimore, MD, United States.
Kritika ChughDepartment of Psychiatry, University of North Carolina at Chapel Hill, Chapel Hill, NC, United States.
Veerle BerginkDepartment of Psychiatry, Icahn School of Medicine at Mount Sinai, New York, NY, United States.ORCID 0009-0003-4495-4762
Rena C PatelDepartment of Medicine, University of Alabama at Birmingham, Birmingham, AL, United States.ORCID 0000-0001-9893-5856
Crystal SchillerDepartment of Psychiatry, University of North Carolina at Chapel Hill, Chapel Hill, NC, United States.ORCID 0000-0001-6186-701X
Melissa A HaendelDepartment of Genetics, University of North Carolina at Chapel Hill, Chapel Hill, NC, United States.ORCID 0000-0001-9114-8737

Funding

Improvements to the LinkML framework to support the Phenomics First open science resourceRM1HG010860 · NHGRI · UNIV OF NORTH CAROLINA CHAPEL HILL · PI HAENDEL, MELISSA A, MUNGALL, CHRISTOPHER J · 2020 to 2024
$10.3M
The Human Phenotype Ontology: Accelerating Computational Integration of Clinical Data for GenomicsU24HG011449 · NHGRI · JACKSON LABORATORY · PI Peter Nicholas Robinson · 2021 to 2026
$6.7M
NHGRI NIH HHS RM1 HG010860NHGRI NIH HHS U24 HG011449
6 · The paper itself

Abstract

Introduction: Perinatal depression affects up to 30% of pregnant and postpartum women, which has increased since the COVID-19 pandemic, making rapidly identifying affected women a high clinical priority. While screening tools like the Edinburgh Postnatal Depression Scale (EPDS) are widely used, brevity is important for busy clinical practice to reduce administration time and patient burden. Current methods to shorten assessments rely on traditional psychometric approaches, rather than machine learning (ML) methods that could optimize predictive accuracy. Methods: We developed a ML framework using National Clinical Cohort Collaborative (N3C) data to predict full 10-item EPDS scores from shortened question subsets (n=22,924). We evaluated all 2-5 item combinations using linear regression, validating performance across multiple cohorts including postpartum women (n=7,750) and an external non-N3C pregnancy population (n=1,217). For additional validation, we applied our approach to the PHQ-9 (n=398,606) to test generalizability. Binary classification models using clinical thresholds (≥13) determined EPDS screening accuracy. Decision curve analysis was performed to assess the clinical utility of our ML method. Results: The optimal 2-question EPDS combinations Q4+Q8 (anxiety/sadness) and Q5+Q8 (scared/sadness) both achieved R Conclusion/Implications: Our ML framework suggests a reduced assessment burden with two EPDS questions maintains predictive accuracy as the full-item EPDS. With ~3.6 million annual U.S. births, this approach could identify additional positive perinatal depression screens, enhancing screening implementation across clinical settings.

Identifiers

PMID41282910
PMCPMC12633091

What OpenQuestion holds

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LicenceCC BY-NC-ND
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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.