Evidence map›Paper›PMID 39766785›Full record

ArticleGenes2024

Disentangling the Genetic Landscape of Peripartum Depression: A Multi-Polygenic Machine Learning Approach on an Italian Sample.

Yasmin A Harrington, Lidia Fortaner-Uyà, Marco Paolini, Sara Poletti, Cristina Lorenzi, Sara Spadini, Elisa M T Melloni, Elena Agnoletto, Raffaella Zanardi, Cristina Colombo and 1 more

Abstract read
In one paragraph

Article in Genes, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 4 papers.

0numbers the graph read from it
0cells of the map it votes in
4citing 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

4 citing papers in PubMed.

  1. Review
  2. Review
  3. Article
  4. Article
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

11 authors.

Yasmin A HarringtonVita-Salute San Raffaele University, 20132 Milan, Italy.ORCID 0009-0003-2122-1304
Lidia Fortaner-UyàVita-Salute San Raffaele University, 20132 Milan, Italy.ORCID 0000-0003-2004-5567
Marco PaoliniPsychiatry & Clinical Psychobiology, Division of Neuroscience, IRCCS San Raffaele Hospital, 20132 Milan, Italy.
Sara PolettiVita-Salute San Raffaele University, 20132 Milan, Italy.ORCID 0000-0001-9594-0246
Cristina LorenziPsychiatry & Clinical Psychobiology, Division of Neuroscience, IRCCS San Raffaele Hospital, 20132 Milan, Italy.ORCID 0000-0002-3324-1359
Sara SpadiniPsychiatry & Clinical Psychobiology, Division of Neuroscience, IRCCS San Raffaele Hospital, 20132 Milan, Italy.ORCID 0000-0002-7059-8242
Elisa M T MelloniPsychiatry & Clinical Psychobiology, Division of Neuroscience, IRCCS San Raffaele Hospital, 20132 Milan, Italy.
Elena AgnolettoPsychiatry & Clinical Psychobiology, Division of Neuroscience, IRCCS San Raffaele Hospital, 20132 Milan, Italy.
Raffaella ZanardiVita-Salute San Raffaele University, 20132 Milan, Italy.ORCID 0000-0001-5941-5663
Cristina ColomboVita-Salute San Raffaele University, 20132 Milan, Italy.
Francesco BenedettiVita-Salute San Raffaele University, 20132 Milan, Italy.

Funding

The Italian Ministry of Health project RF-2019-12371066
6 · The paper itself

Abstract

backgroundThe genetic determinants of peripartum depression (PPD) are not fully understood. Using a multi-polygenic score approach, we characterized the relationship between genome-wide information and the history of PPD in patients with mood disorders, with the hypothesis that multiple polygenic risk scores (PRSs) could potentially influence the development of PPD.

methodsWe calculated 341 PRSs for 178 parous mood disorder inpatients affected by major depressive disorder (MDD) or bipolar disorder (BD) with (

resultsThe PLS linear regression in the whole sample defined a model explaining 27.12% of the variance in the presence of PPD history, 56.73% of variance among MDD, and 42.96% of variance in BD. Our findings highlight that multiple genetic factors related to circadian rhythms, inflammation, and psychiatric diagnoses are top contributors to the prediction of PPD. Specifically, in MDD, the top contributing PRS was monocyte count, while in BD, it was chronotype, with PRSs for inflammation and psychiatric diagnoses significantly contributing to both groups.

conclusionsThese results confirm previous literature about the immune system dysregulation in postpartum mood disorders, and shed light on which genetic factors are involved in the pathophysiology of PPD.

Indexed as

Bipolar DisorderMachine LearningMajor Depressive DisorderMultifactorial InheritanceAdultDepression, PostpartumFemaleGenetic Predisposition to DiseaseGenome-Wide Association StudyHumansItalyPeripartum PeriodPregnancybipolar disordermajor depressive disorderpartial least squares regressionperipartum depressionpolygenic risk scores

Identifiers

PMID39766785
PMCPMC11675425

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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.