Worry and anxiety are associated with an increase in absolute heart rate, while heart rate variability decreases. Low heart rate variability is associated with an active anterior insula. A...Show moreWorry and anxiety are associated with an increase in absolute heart rate, while heart rate variability decreases. Low heart rate variability is associated with an active anterior insula. A hyperactive anterior insula is observed in individuals with anxiety disorders. However, it is not yet known whether a hyperactive anterior insula makes a person vulnerable to developing anxiety disorders or whether the anterior insula becomes hyperactive as a result of the disorder. Therefore, this study aims to investigate these associations in healthy participants. The following research questions were asked, "Is there a correlation between absolute heart rate and trait worry?" and "Is trait worry associated with low heart rate variability?" the same questions are posed in the context of anxiety. Finally, the question "Is trait anxiety associated with a hyperactive insula?" is asked. To examine this, data from the HADS, PSWQ, vectorcardiogram measures of heart rate and the heart rate variability, and the functional connectivity of the salience network from the 30 female participants were used. Results show no significant relationship between absolute heart rate, heart rate variability, and trait worry and anxiety in healthy participants. A significant relationship between the functional connectivity in the anterior insula and trait anxiety was found in our sample (r = .42, p = <.05). The effects of worry and anxiety on cardiac activity are mainly seen in clinically diagnosed individuals under an unpredictable and uncontrollable stressful environment. Our sample were healthy individuals, so symptoms were apparently not severe enough. The effects of trait anxiety are directly reflected in brain connectivity in the anterior insula observed in our analysis. The results can be applied to treatments reducing anxiety and worry.Show less
Background: rumination is both a symptom and predictor of major depressive disorder (MDD). In MDD patients, rumination is correlated with depression severity, and for healthy people rumination is a...Show moreBackground: rumination is both a symptom and predictor of major depressive disorder (MDD). In MDD patients, rumination is correlated with depression severity, and for healthy people rumination is a predictor of the onset and duration of a depressive episode. Recently, rumination was shown to be correlated to functional connectivity in the default mode network (DMN) in the brain. During working memory (WM) tasks, the central executive network (CEN) shows high connectivity and the DMN shows low connectivity, whereas during rest this is the other way around. This ‘switching’ between DMN and CEN connectivity is blunted in MDD patients, but it is still unknown whether this ‘switch’ is affected by acute rumination in healthy participants. The aim of the current study is to determine the effect of acute rumination on the switching between the DMN and the CEN in healthy participants. Methods: 36 healthy females, randomly assigned to the acute-rumination group (n=18) or the no-rumination group (n=18) underwent fMRI assessment during a rest-WM task (alternating rest and WM conditions). Only for the acute-rumination group, an acute rumination phase immediately preceded the rest-WM task. Pearson’s correlation was performed to analyze the correlation between the DMN and the CEN in each participant. A mixed ANOVA was performed to analyze the effects of acute rumination. Results: Negative Pearson correlation coefficients were found between DMN and CEN for both groups. A statistically significant interaction effect was found for network (CEN versus DMN) × condition (rest versus WM). However, no statistically significant main effect was found for group (acute-rumination versus no-rumination). Conclusion: Consistent with previous studies an interaction in the expected direction was found between the DMN and CEN. However, this study does not support the effect of acute rumination on this interaction. The current study contributes to an increased understanding of the effect of rumination, and contributes to research of this prominent symptom of MDD and other psychological disorders.Show less