Ruminative thinking about negative feelings has been prospectively associated with increases in depressive symptoms and heightened risk for new onsets of major depression. One putative pathophysiological mechanism underlying this link might be represented by autonomic nervous system dysfunction. The objective of this longitudinal study was to evaluate the interplay between rumination, autonomic function (as revealed by heart rate variability (HRV) analysis), and depressive symptoms in healthy young subjects, over a three-year period. Rumination and depressive symptoms were evaluated in twenty-two women and twenty men at three assessment points (Time 0, 1 and 2) by the score on the Ruminative Response Scale, and the Center for Epidemiological Studies Depression Scale, respectively. Vagally-mediated HRV was assessed in a laboratory session (Time 0) and in two ambulatory sessions at Time 1 and Time 2 (~13 and 34months after Time 0, respectively). Ruminative thinking was found to be (i) a stable trait characteristic, (ii) more prevalent in women than men, and (iii) positively correlated with depressive symptoms. Moreover, resting HRV was negatively correlated with both rumination and depressive symptoms. Finally, HRV at Time 1 mediated the relationship between rumination at Time 0 and depressive symptoms at Time 2. We conclude that autonomic dysfunction, specifically low vagal tone, may be prospectively implicated in the generation of depressive symptoms in a non-clinical setting.

Heart rate variability mediates the link between rumination and depressive symptoms: A longitudinal study / Carnevali, Luca; Thayer, Julian F.; Brosschot, Jos F.; Ottaviani, Cristina. - In: INTERNATIONAL JOURNAL OF PSYCHOPHYSIOLOGY. - ISSN 0167-8760. - STAMPA. - 131:(2017), pp. 131-138. [10.1016/j.ijpsycho.2017.11.002]

Heart rate variability mediates the link between rumination and depressive symptoms: A longitudinal study

Ottaviani, Cristina
Ultimo
Conceptualization
2017

Abstract

Ruminative thinking about negative feelings has been prospectively associated with increases in depressive symptoms and heightened risk for new onsets of major depression. One putative pathophysiological mechanism underlying this link might be represented by autonomic nervous system dysfunction. The objective of this longitudinal study was to evaluate the interplay between rumination, autonomic function (as revealed by heart rate variability (HRV) analysis), and depressive symptoms in healthy young subjects, over a three-year period. Rumination and depressive symptoms were evaluated in twenty-two women and twenty men at three assessment points (Time 0, 1 and 2) by the score on the Ruminative Response Scale, and the Center for Epidemiological Studies Depression Scale, respectively. Vagally-mediated HRV was assessed in a laboratory session (Time 0) and in two ambulatory sessions at Time 1 and Time 2 (~13 and 34months after Time 0, respectively). Ruminative thinking was found to be (i) a stable trait characteristic, (ii) more prevalent in women than men, and (iii) positively correlated with depressive symptoms. Moreover, resting HRV was negatively correlated with both rumination and depressive symptoms. Finally, HRV at Time 1 mediated the relationship between rumination at Time 0 and depressive symptoms at Time 2. We conclude that autonomic dysfunction, specifically low vagal tone, may be prospectively implicated in the generation of depressive symptoms in a non-clinical setting.
2017
depressive symptoms; heart rate variability; longitudinal; mediation; rumination
01 Pubblicazione su rivista::01a Articolo in rivista
Heart rate variability mediates the link between rumination and depressive symptoms: A longitudinal study / Carnevali, Luca; Thayer, Julian F.; Brosschot, Jos F.; Ottaviani, Cristina. - In: INTERNATIONAL JOURNAL OF PSYCHOPHYSIOLOGY. - ISSN 0167-8760. - STAMPA. - 131:(2017), pp. 131-138. [10.1016/j.ijpsycho.2017.11.002]
File allegati a questo prodotto
File Dimensione Formato  
carnevali_heart_2017.pdf

solo gestori archivio

Tipologia: Versione editoriale (versione pubblicata con il layout dell'editore)
Licenza: Tutti i diritti riservati (All rights reserved)
Dimensione 478.86 kB
Formato Adobe PDF
478.86 kB Adobe PDF   Contatta l'autore

I documenti in IRIS sono protetti da copyright e tutti i diritti sono riservati, salvo diversa indicazione.

Utilizza questo identificativo per citare o creare un link a questo documento: https://hdl.handle.net/11573/1072512
Citazioni
  • ???jsp.display-item.citation.pmc??? 22
  • Scopus 71
  • ???jsp.display-item.citation.isi??? 65
social impact