Evidence map›Paper›PMID 41346392›Full record

ArticleBiological psychiatry global open science2025

Investigating Irritability as a Potentially Causal Risk Pathway to Depression Using Two Genetically Informed Designs.

Amy Shakeshaft, Olakunle Oginni, Joanna Martin, Charlotte A Dennison, Olga Eyre, Ellen Leibenluft, Sebastian Lundström, Evie Stergiakouli, Henrik Larsson, Paul Lichtenstein and 4 more

Abstract read
In one paragraph

Article in Biological psychiatry global open science, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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0citing papers in PubMed
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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

14 authors.

Amy ShakeshaftWolfson Centre for Young People's Mental Health, Cardiff University, Cardiff, United Kingdom.
Olakunle OginniWolfson Centre for Young People's Mental Health, Cardiff University, Cardiff, United Kingdom.
Joanna MartinWolfson Centre for Young People's Mental Health, Cardiff University, Cardiff, United Kingdom.
Charlotte A DennisonWolfson Centre for Young People's Mental Health, Cardiff University, Cardiff, United Kingdom.
Olga EyreWolfson Centre for Young People's Mental Health, Cardiff University, Cardiff, United Kingdom.
Ellen LeibenluftOffice of the Scientific Director, National Institute of Mental Health, Bethesda, Maryland.
Sebastian LundströmGillberg Neuropsychiatry Centre, University of Gothenburg, Gothenburg, Sweden.
Evie StergiakouliMRC Integrative Epidemiology Unit, Population Health Sciences, University of Bristol, Bristol, United Kingdom.
Henrik LarssonDepartment of Medical Epidemiology and Biostatistics, Karolinska Institute, Stockholm, Sweden.
Paul LichtensteinDepartment of Medical Epidemiology and Biostatistics, Karolinska Institute, Stockholm, Sweden.
Argyris StringarisFaculty of Brain Sciences, Division of Psychiatry and Division of Psychology and Language Sciences, University College London, London, United Kingdom.
Lucy RiglinWolfson Centre for Young People's Mental Health, Cardiff University, Cardiff, United Kingdom.
Mark J TaylorDepartment of Medical Epidemiology and Biostatistics, Karolinska Institute, Stockholm, Sweden.
Anita ThaparWolfson Centre for Young People's Mental Health, Cardiff University, Cardiff, United Kingdom.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Background: Major depressive disorder (MDD) is heterogeneous, with diverse risk pathways leading to illness. Identifying causal routes to depression helps prioritize targets for early intervention and prevention strategies. Although irritability is associated with risk for later depression, this association could be explained by confounders, including genetic confounders. Methods: We used two genetically informed designs to examine whether irritability is causally linked to depression. First, using data from the Child and Adolescent Twin Study in Sweden (CATSS) ( Results: In CATSS, associations were observed between irritability at age 15 (parent-reported odds ratio [OR] = 1.93 [1.61-2.34], Conclusions: These results indicate that self-reported irritability may represent a causal risk pathway to MDD and thus could serve as a potential target for MDD prevention or early intervention.

Indexed as

Causal inferenceDepressionGeneticsIrritabilityMendelian randomizationTwin study

Identifiers

PMID41346392
PMCPMC12673388

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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.