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Infraslow fluctuations of sustained attention in mood disorders

Published online by Cambridge University Press:  12 March 2025

Tommaso Viola
Affiliation:
Biosciences Institute, Faculty of Medical Sciences, Newcastle University, Newcastle upon Tyne, UK
Quoc C. Vuong
Affiliation:
Biosciences Institute, Faculty of Medical Sciences, Newcastle University, Newcastle upon Tyne, UK School of Psychology, Faculty of Medical Sciences, Newcastle University, Newcastle upon Tyne, UK
Stuart Watson
Affiliation:
Translational and Clinical Research Institute, Faculty of Medical Sciences, Newcastle University, Newcastle upon Tyne, UK Northern Centre for Mood Disorders, Newcastle University, Newcastle upon Tyne, UK Cumbria, Northumberland, Tyne and Wear NHS Trust, Newcastle upon Tyne, UK
Richard J. Porter
Affiliation:
Department of Psychological Medicine, University of Otago, Christchurch, New Zealand Te Whatu Ora, Specialist Mental Health Services, Christchurch, New Zealand
Allan H. Young
Affiliation:
Department of Psychological Medicine, Institute of Psychiatry, Psychology and Neuroscience, King’s College London, London, UK
Peter Gallagher*
Affiliation:
Translational and Clinical Research Institute, Faculty of Medical Sciences, Newcastle University, Newcastle upon Tyne, UK Northern Centre for Mood Disorders, Newcastle University, Newcastle upon Tyne, UK
*
Corresponding author: Peter Gallagher; Email: peter.gallagher@newcastle.ac.uk
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Abstract

Background

Sustained attention is integral to goal-directed tasks in everyday life. It is a demanding and effortful process prone to failure. Deficits are particularly prevalent in mood disorders. However, conventional methods of assessment, rooted in overall measures of performance, neglect the nuanced temporal dimensions inherent in sustained attention, necessitating alternative analytical approaches.

Methods

This study investigated sustained attention deficits and temporal patterns of attentional fluctuation in a large clinical cohort of patients with bipolar depression (BPd, n = 33), bipolar euthymia (BPe, n = 84), major depression (MDd, n = 38) and controls (HC, n = 138) using a continuous performance task (CPT). Longitudinal and spectral analyses were employed to examine trial-level reaction time (RT) data.

Results

Longitudinal analysis revealed a significant worsening of performance over time (vigilance decrement) in BPd, whilst spectral analysis unveiled attentional fluctuations concentrated in the frequency range of 0.077 Hz (1/12.90 s)–0.049 Hz (1/20.24 s), with BPd and MDd demonstrating greater spectral power compared to BPe and controls.

Conclusions

Although speculative, the increased variability in this frequency range may have an association with the dysfunctional activity of the Default Mode Network, which has been shown to oscillate at a similar timescale. These findings underscore the importance of considering the temporal dimensions of sustained attention and show the potential of spectral analysis of RT in future clinical research.

Information

Type
Original Article
Creative Commons
Creative Common License - CCCreative Common License - BY
This is an Open Access article, distributed under the terms of the Creative Commons Attribution licence (http://creativecommons.org/licenses/by/4.0), which permits unrestricted re-use, distribution and reproduction, provided the original article is properly cited.
Copyright
© The Author(s), 2025. Published by Cambridge University Press
Figure 0

Figure 1. Spectral analysis transforms RT data from the time domain (A, seconds or trials) to the frequency domain (B), potentially revealing oscillatory behavior.

Figure 1

Table 1. Participant demographics

Figure 2

Figure 2. Differences in coefficient of variation (CoV) between groups. (a) CoV of reaction times modeled for the 4 groups and across blocks of trials. Dots represent the individual participants, whilst the lines are the model predictions. (b) Coefficient of Variation by group.

Figure 3

Table 2. Standardised parameters of the mixed effect model

Figure 4

Table 3. Summary statistics of CoV RT across blocks for the 4 groups of participants, mean (SD)

Figure 5

Figure 3. Frequency analysis of reaction time data and investigation of differences between the clinical groups. (a) averaged power curves for each experimental group. (b) functional F-test between the power curves; the dotted line represents the critical F-value; the grayed area is where the F-test is considered significant. (c) average absolute power for each group within the frequency range where the F-test was significant. (d) functional t-tests following the significant F-test; the dotted horizontal line represents uncorrected critical t-value whilst the solid line is the Bonferroni corrected value.