Evidence map›Paper›PMID 39116519›Full record

ArticlePsychoneuroendocrinology2024

Affect regulation and allostatic load over time.

Amanda E Ng, Tara Gruenewald, Robert-Paul Juster, Claudia Trudel-Fitzgerald

Abstract read
In one paragraph

Article in Psychoneuroendocrinology, 2024. 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
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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

4 authors.

Amanda E NgDepartment of Epidemiology, University of Maryland School of Public Health, USA.
Tara GruenewaldDepartment of Psychology, Chapman University, USA.
Robert-Paul JusterDepartment of Psychiatry, Université de Montréal, Canada; Research Center, Institut Universitaire en Santé Mentale de Montréal, Canada.
Claudia Trudel-FitzgeraldResearch Center, Institut Universitaire en Santé Mentale de Montréal, Canada; Department of Psychology, Université du Québec à Trois-Rivières, Canada; Lee Kum Sheung Center for Health and Happiness, Harvard T.H. Chan School of Public Health, USA. Electronic address: claudia.trudel-fitzgerald@uqtr.ca.

Funding

U19 MIDlife in the United States-Diversity Supplement-WellsU19AG051426 · NIA · UNIVERSITY OF WISCONSIN-MADISON · PI CHRISTOPHER L COE · 2016 to 2026
$74.8M
STATISTICS COREP01AG020166 · NIA · UNIVERSITY OF WISCONSIN-MADISON · PI RYFF, CAROL D. · 2002 to 2015
$50.6M
Stress, diet quality, and biological aging across the lifespanR24AG048024 · NIA · UNIVERSITY OF CALIFORNIA, SAN FRANCISCO · PI EPEL, ELISSA S., MENDES, WENDY BERRY · 2014 to 2025
$6.2M
Summer Training Program in Integrative Methods for Mental and Physical HealthR25AT010664 · NCCIH · UNIVERSITY OF MICHIGAN AT ANN ARBOR · PI MEZUK, BRIANA · 2020 to 2023
$1.0M
NCCIH NIH HHS R25 AT010664NIA NIH HHS P01 AG020166NIA NIH HHS R24 AG048024NIA NIH HHS U19 AG051426
6 · The paper itself

Abstract

objectiveEmerging work suggests that affect regulation strategies (e.g., active coping, anger expression) predict disease and mortality risk, with sometimes divergent estimates by sex or education levels. However, few studies have examined potential underlying biological mechanisms. This study assessed the longitudinal association of affect regulation with future allostatic load.

methodIn 2004-2006, 574 participants from the Midlife in the United States study completed validated scales assessing use of nine general and emotion-specific regulatory strategies (e.g., denial, anger expression). As a proxy for how flexibly participants regulate their affect, variability in the use of regulatory strategies was operationalized using a standard deviation-based algorithm and considered categorically (i.e., lower, moderate, greater variability) to assess non-linear effects. Participants also provided data on relevant covariates and 24 allostatic load biomarkers (e.g., cortisol, blood pressure). In 2017-2021, these biomarkers were again collected. Linear regressions modeled betas (β) and 95 % confidence intervals (CI) examining associations of affect regulatory constructs with future allostatic load.

resultsIn fully-adjusted models including initial allostatic load, general regulatory strategies were unrelated to future allostatic load. Yet, greater versus moderate affect regulation variability levels predicted lower allostatic load (β=-0.14; 95 %CI: -0.27, -0.01). Only among more educated participants, greater use of anger expression predicted lower allostatic load, while the reverse was noted with anger control (β

conclusionsWhile general regulatory strategies appeared unrelated to allostatic load, greater variability in their use and anger-related strategies showed predictive value. Subsequent studies should examine these associations in larger, more diverse samples.

Indexed as

Adaptation, PsychologicalAllostasisAngerHydrocortisoneAdultAffectAgedBiomarkersBlood PressureEmotional RegulationFemaleHumansLongitudinal StudiesMaleMiddle AgedStress, PsychologicalBiomarkersHydrocortisoneAffect regulationAllostatic loadAngerCopingCoping variabilityEmotion regulation

Identifiers

PMID39116519
PMCPMC11856246

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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.