Evidence map›Paper›PMID 39046072›Full record

ArticleHuman brain mapping2024

Within-person biological mechanisms of mood variability in childhood and adolescence.

Yara J Toenders, Marleen H M de Moor, Renske van der Cruijsen, Kayla Green, Michelle Achterberg, Eveline A Crone

Abstract readTwin Study
In one paragraph

Article in Human brain mapping, 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

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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.

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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

6 authors.

Yara J ToendersDevelopmental and Educational Psychology, Leiden University, Leiden, The Netherlands.ORCID 0000-0002-4117-1143
Marleen H M de MoorDepartment of Psychology, Education and Child Studies, Erasmus University Rotterdam, Rotterdam, The Netherlands.
Renske van der CruijsenBehavioral Science Institute, Radboud University Nijmegen, Nijmegen, The Netherlands.
Kayla GreenErasmus School of Social and Behavioral Sciences, Erasmus University Rotterdam, Rotterdam, The Netherlands.
Michelle AchterbergDepartment of Psychology, Education and Child Studies, Erasmus University Rotterdam, Rotterdam, The Netherlands.
Eveline A CroneDevelopmental and Educational Psychology, Leiden University, Leiden, The Netherlands.

Funding

Nederlandse Organisatie voor Wetenschappelijk Onderzoek 024.001.003Nederlandse Organisatie voor Wetenschappelijk Onderzoek 453-14-001Netherlands Organisation for Scientific Research 2013-2023 024.001.003Netherlands Organisation for Scientific Research NWO-VICI 453-14-001
6 · The paper itself

Abstract

Mood variability, the day-to-day fluctuation in mood, differs between individuals and develops during adolescence. Because adolescents show higher mood variability and average mood than children and adults, puberty might be a potential biological mechanism underlying this increase. The goal of this preregistered developmental study was to examine the neural and hormonal underpinnings of adolescent-specific within-person changes in mood variability, with a specific focus on testosterone, cortisol, pubertal status, and resting-state functional brain connectivity. Data from two longitudinal cohorts were used: the L-CID twin study (aged 7-13, N at the first timepoint = 258) and the accelerated Leiden Self-Concept study (SC; aged 11-21, N at the first timepoint = 138). In both studies resting-state functional magnetic resonance imaging (rs-fMRI) data was collected, as well as daily mood. Additionally, in the SC study self-reported puberty testosterone and cortisol were collected. Random intercept cross-lagged panel models (RI-CLPM) were used to study the within-person relations between these biological measures and mood variability and average mood. Mood variability and average mood peaked in adolescence and testosterone levels and self-reported puberty also showed an increase. Connectivity between prefrontal cortex (dlPFC and vmPFC) and subcortical regions (caudate, amygdala) decreased across development. Moreover, higher testosterone predicted average negative mood at the next time point, but not vice versa. Further, stronger vmPFC-amygdala functional connectivity predicted decreases in mood variability. Here, we show that brain connectivity during development is an important within-person biological mechanism of the development of mood in adolescents. PRACTITIONER POINTS: Mood variability peaks in adolescence. Within-person changes in testosterone predict within-person changes in mood. Within-person changes in vmPFC-amygdala connectivity predict within-person changes in mood variability.

Indexed as

Adolescent DevelopmentAffectAdolescentAdultAmygdalaBrainChildConnectomeFemaleHumansHydrocortisoneLongitudinal StudiesMagnetic Resonance ImagingMalePrefrontal CortexPubertyHydrocortisoneTestosteroneadolescencemood variabilitypubertyrandom intercept cross‐lagged panel modelsresting‐state fMRItestosterone

Identifiers

PMID39046072
PMCPMC11267453

What OpenQuestion holds

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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.