Depressive symptoms and heart rate variability

Evidence for a shared genetic substrate in a study of twins

Viola Vaccarino, Rachel Lampert, J. Douglas Bremner, Forrester Lee, Shaoyong Su, Carisa Maisano, Nancy V. Murrah, Linda Jones, Farhan Jawed, Nadeem Afzal, Ali Ashraf, Jack Goldberg

Research output: Contribution to journalArticle

47 Citations (Scopus)

Abstract

Objective: To clarify the relationship between depression and heart rate variability (HRV) in a sample of twins. Reduced HRV, a measure of autonomic dysfunction, has been linked to depression but many studies have inadequately controlled for familial and environmental factors. Furthermore, little is known about whether depression and HRV share common genetic pathways. Methods: We performed power spectral analysis on 24-hour ambulatory electrocardiograms in 288 middle-aged male twins. Log-normalized ultra low, very low, low, high frequency, and total power were calculated. A lifetime history of major depressive disorder (MDD) was determined, using the Structured Clinical Interview for Psychiatry Disorders, and current depressive symptoms were measured with the Beck Depression Inventory. Mixed-effect regression models were used to account for intrapair variability and estimate within-pair effects at the same time controlling for potential confounders. Results: Both current depressive symptoms and a history of MDD were significantly associated with lower HRV. There was a graded effect, and power in each frequency band was 29% to 36% lower in the lowest band compared with the highest BDI category. All HRV measures except high frequency remained significantly associated with current depressive symptoms in multivariable analysis, but not with lifetime history of MDD. When analyses were stratified by zygosity, a significant within-pair association between BDI score and HRV was found in the dizygotic but not in the monozygotic twins, suggesting a genetic influence on the association. Conclusions: A shared, genetically influenced biological pathway underlies the association between depression and lower HRV. These two phenotypes may be the expression of a generalized neurobiological perturbation.

Original languageEnglish (US)
Pages (from-to)628-636
Number of pages9
JournalPsychosomatic Medicine
Volume70
Issue number6
DOIs
StatePublished - Jul 1 2008

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Twin Studies
Heart Rate
Depression
Major Depressive Disorder
Monozygotic Twins
Psychiatry
Electrocardiography
Interviews
Phenotype
Equipment and Supplies

Keywords

  • Autonomic function
  • Electrophysiology
  • Genetic factors
  • Psychosocial factors
  • Risk factors

ASJC Scopus subject areas

  • Applied Psychology
  • Psychiatry and Mental health

Cite this

Depressive symptoms and heart rate variability : Evidence for a shared genetic substrate in a study of twins. / Vaccarino, Viola; Lampert, Rachel; Bremner, J. Douglas; Lee, Forrester; Su, Shaoyong; Maisano, Carisa; Murrah, Nancy V.; Jones, Linda; Jawed, Farhan; Afzal, Nadeem; Ashraf, Ali; Goldberg, Jack.

In: Psychosomatic Medicine, Vol. 70, No. 6, 01.07.2008, p. 628-636.

Research output: Contribution to journalArticle

Vaccarino, V, Lampert, R, Bremner, JD, Lee, F, Su, S, Maisano, C, Murrah, NV, Jones, L, Jawed, F, Afzal, N, Ashraf, A & Goldberg, J 2008, 'Depressive symptoms and heart rate variability: Evidence for a shared genetic substrate in a study of twins', Psychosomatic Medicine, vol. 70, no. 6, pp. 628-636. https://doi.org/10.1097/PSY.0b013e31817bcc9e
Vaccarino, Viola ; Lampert, Rachel ; Bremner, J. Douglas ; Lee, Forrester ; Su, Shaoyong ; Maisano, Carisa ; Murrah, Nancy V. ; Jones, Linda ; Jawed, Farhan ; Afzal, Nadeem ; Ashraf, Ali ; Goldberg, Jack. / Depressive symptoms and heart rate variability : Evidence for a shared genetic substrate in a study of twins. In: Psychosomatic Medicine. 2008 ; Vol. 70, No. 6. pp. 628-636.
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AU - Su, Shaoyong

AU - Maisano, Carisa

AU - Murrah, Nancy V.

AU - Jones, Linda

AU - Jawed, Farhan

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AU - Ashraf, Ali

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N2 - Objective: To clarify the relationship between depression and heart rate variability (HRV) in a sample of twins. Reduced HRV, a measure of autonomic dysfunction, has been linked to depression but many studies have inadequately controlled for familial and environmental factors. Furthermore, little is known about whether depression and HRV share common genetic pathways. Methods: We performed power spectral analysis on 24-hour ambulatory electrocardiograms in 288 middle-aged male twins. Log-normalized ultra low, very low, low, high frequency, and total power were calculated. A lifetime history of major depressive disorder (MDD) was determined, using the Structured Clinical Interview for Psychiatry Disorders, and current depressive symptoms were measured with the Beck Depression Inventory. Mixed-effect regression models were used to account for intrapair variability and estimate within-pair effects at the same time controlling for potential confounders. Results: Both current depressive symptoms and a history of MDD were significantly associated with lower HRV. There was a graded effect, and power in each frequency band was 29% to 36% lower in the lowest band compared with the highest BDI category. All HRV measures except high frequency remained significantly associated with current depressive symptoms in multivariable analysis, but not with lifetime history of MDD. When analyses were stratified by zygosity, a significant within-pair association between BDI score and HRV was found in the dizygotic but not in the monozygotic twins, suggesting a genetic influence on the association. Conclusions: A shared, genetically influenced biological pathway underlies the association between depression and lower HRV. These two phenotypes may be the expression of a generalized neurobiological perturbation.

AB - Objective: To clarify the relationship between depression and heart rate variability (HRV) in a sample of twins. Reduced HRV, a measure of autonomic dysfunction, has been linked to depression but many studies have inadequately controlled for familial and environmental factors. Furthermore, little is known about whether depression and HRV share common genetic pathways. Methods: We performed power spectral analysis on 24-hour ambulatory electrocardiograms in 288 middle-aged male twins. Log-normalized ultra low, very low, low, high frequency, and total power were calculated. A lifetime history of major depressive disorder (MDD) was determined, using the Structured Clinical Interview for Psychiatry Disorders, and current depressive symptoms were measured with the Beck Depression Inventory. Mixed-effect regression models were used to account for intrapair variability and estimate within-pair effects at the same time controlling for potential confounders. Results: Both current depressive symptoms and a history of MDD were significantly associated with lower HRV. There was a graded effect, and power in each frequency band was 29% to 36% lower in the lowest band compared with the highest BDI category. All HRV measures except high frequency remained significantly associated with current depressive symptoms in multivariable analysis, but not with lifetime history of MDD. When analyses were stratified by zygosity, a significant within-pair association between BDI score and HRV was found in the dizygotic but not in the monozygotic twins, suggesting a genetic influence on the association. Conclusions: A shared, genetically influenced biological pathway underlies the association between depression and lower HRV. These two phenotypes may be the expression of a generalized neurobiological perturbation.

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