Associations between depression and cardiometabolic health: A 27-year longitudinal study.


Journal

Psychological medicine
ISSN: 1469-8978
Titre abrégé: Psychol Med
Pays: England
ID NLM: 1254142

Informations de publication

Date de publication:
10 2022
Historique:
pubmed: 13 1 2021
medline: 5 1 2023
entrez: 12 1 2021
Statut: ppublish

Résumé

Clarifying the relationship between depression symptoms and cardiometabolic and related health could clarify risk factors and treatment targets. The objective of this study was to assess whether depression symptoms in midlife are associated with the subsequent onset of cardiometabolic health problems. The study sample comprised 787 male twin veterans with polygenic risk score data who participated in the Harvard Twin Study of Substance Abuse ('baseline') and the longitudinal Vietnam Era Twin Study of Aging ('follow-up'). Depression symptoms were assessed at baseline [mean age 41.42 years (s.d. = 2.34)] using the Diagnostic Interview Schedule, Version III, Revised. The onset of eight cardiometabolic conditions (atrial fibrillation, diabetes, erectile dysfunction, hypercholesterolemia, hypertension, myocardial infarction, sleep apnea, and stroke) was assessed via self-reported doctor diagnosis at follow-up [mean age 67.59 years (s.d. = 2.41)]. Total depression symptoms were longitudinally associated with incident diabetes (OR 1.29, 95% CI 1.07-1.57), erectile dysfunction (OR 1.32, 95% CI 1.10-1.59), hypercholesterolemia (OR 1.26, 95% CI 1.04-1.53), and sleep apnea (OR 1.40, 95% CI 1.13-1.74) over 27 years after controlling for age, alcohol consumption, smoking, body mass index, C-reactive protein, and polygenic risk for specific health conditions. In sensitivity analyses that excluded somatic depression symptoms, only the association with sleep apnea remained significant (OR 1.32, 95% CI 1.09-1.60). A history of depression symptoms by early midlife is associated with an elevated risk for subsequent development of several self-reported health conditions. When isolated, non-somatic depression symptoms are associated with incident self-reported sleep apnea. Depression symptom history may be a predictor or marker of cardiometabolic risk over decades.

Sections du résumé

BACKGROUND
Clarifying the relationship between depression symptoms and cardiometabolic and related health could clarify risk factors and treatment targets. The objective of this study was to assess whether depression symptoms in midlife are associated with the subsequent onset of cardiometabolic health problems.
METHODS
The study sample comprised 787 male twin veterans with polygenic risk score data who participated in the Harvard Twin Study of Substance Abuse ('baseline') and the longitudinal Vietnam Era Twin Study of Aging ('follow-up'). Depression symptoms were assessed at baseline [mean age 41.42 years (s.d. = 2.34)] using the Diagnostic Interview Schedule, Version III, Revised. The onset of eight cardiometabolic conditions (atrial fibrillation, diabetes, erectile dysfunction, hypercholesterolemia, hypertension, myocardial infarction, sleep apnea, and stroke) was assessed via self-reported doctor diagnosis at follow-up [mean age 67.59 years (s.d. = 2.41)].
RESULTS
Total depression symptoms were longitudinally associated with incident diabetes (OR 1.29, 95% CI 1.07-1.57), erectile dysfunction (OR 1.32, 95% CI 1.10-1.59), hypercholesterolemia (OR 1.26, 95% CI 1.04-1.53), and sleep apnea (OR 1.40, 95% CI 1.13-1.74) over 27 years after controlling for age, alcohol consumption, smoking, body mass index, C-reactive protein, and polygenic risk for specific health conditions. In sensitivity analyses that excluded somatic depression symptoms, only the association with sleep apnea remained significant (OR 1.32, 95% CI 1.09-1.60).
CONCLUSIONS
A history of depression symptoms by early midlife is associated with an elevated risk for subsequent development of several self-reported health conditions. When isolated, non-somatic depression symptoms are associated with incident self-reported sleep apnea. Depression symptom history may be a predictor or marker of cardiometabolic risk over decades.

Identifiants

pubmed: 33431106
doi: 10.1017/S003329172000505X
pii: S003329172000505X
pmc: PMC8547283
mid: NIHMS1720499
doi:

Types de publication

Journal Article Research Support, N.I.H., Extramural Research Support, Non-U.S. Gov't

Langues

eng

Sous-ensembles de citation

IM

Pagination

3007-3017

Subventions

Organisme : NIA NIH HHS
ID : R01 AG022982
Pays : United States
Organisme : NIA NIH HHS
ID : R01 AG059329
Pays : United States
Organisme : NIA NIH HHS
ID : P01 AG055367
Pays : United States
Organisme : NIA NIH HHS
ID : R56 AG037985
Pays : United States
Organisme : NCATS NIH HHS
ID : KL2 TR001444
Pays : United States
Organisme : NIA NIH HHS
ID : K01 AG063805
Pays : United States
Organisme : NIA NIH HHS
ID : F31 AG064834
Pays : United States
Organisme : NIA NIH HHS
ID : R01 AG022381
Pays : United States
Organisme : NIA NIH HHS
ID : R01 AG050595
Pays : United States

Auteurs

Hillary L Ditmars (HL)

Department of Psychological and Brain Sciences, Boston University, Boston, MA, USA.

Mark W Logue (MW)

Research Service, VA Boston Healthcare System, Boston, MA, USA.
Biomedical Genetics Program, Boston University School of Medicine, Boston, MA, USA.
Department of Biostatistics, Boston University School of Public Health, Boston, MA, USA.

Rosemary Toomey (R)

Department of Psychological and Brain Sciences, Boston University, Boston, MA, USA.

Ruth E McKenzie (RE)

Department of Psychological and Brain Sciences, Boston University, Boston, MA, USA.
School of Education and Social Policy, Merrimack College, North Andover, MA, USA.

Carol E Franz (CE)

Department of Psychiatry, School of Medicine, University of California, San Diego, La Jolla, CA, USA.
Center for Behavior Genetics of Aging, University of California, San Diego, La Jolla, CA, USA.

Matthew S Panizzon (MS)

Department of Psychiatry, School of Medicine, University of California, San Diego, La Jolla, CA, USA.
Center for Behavior Genetics of Aging, University of California, San Diego, La Jolla, CA, USA.

Chandra A Reynolds (CA)

Department of Psychology, University of California, Riverside, Riverside, CA, USA.

Kristy N Cuthbert (KN)

Department of Psychological and Brain Sciences, Boston University, Boston, MA, USA.

Richard Vandiver (R)

Department of Psychological and Brain Sciences, Boston University, Boston, MA, USA.

Daniel E Gustavson (DE)

Department of Medicine, Vanderbilt University Medical Center, Nashville, TN, USA.

Graham M L Eglit (GML)

Department of Psychiatry, School of Medicine, University of California, San Diego, La Jolla, CA, USA.
Center for Behavior Genetics of Aging, University of California, San Diego, La Jolla, CA, USA.
VA San Diego Healthcare System, San Diego, CA, USA.

Jeremy A Elman (JA)

Department of Psychiatry, School of Medicine, University of California, San Diego, La Jolla, CA, USA.
Center for Behavior Genetics of Aging, University of California, San Diego, La Jolla, CA, USA.

Mark Sanderson-Cimino (M)

Department of Psychiatry, School of Medicine, University of California, San Diego, La Jolla, CA, USA.
San Diego State University/UC San Diego Joint Doctoral Program in Clinical Psychology, San Diego, CA, USA.

McKenna E Williams (ME)

Department of Psychiatry, School of Medicine, University of California, San Diego, La Jolla, CA, USA.
San Diego State University/UC San Diego Joint Doctoral Program in Clinical Psychology, San Diego, CA, USA.

Ole A Andreassen (OA)

NORMENT, KG Jebsen Centre for Psychosis Research, Institute of Clinical Medicine University of Oslo, Oslo, Norway.
Division of Mental Health and Addiction, Oslo University Hospital Oslo, Oslo, Norway.

Anders M Dale (AM)

Department of Radiology, School of Medicine, University of California, San Diego, La Jolla, CA, USA.
Department of Neurosciences, University of California, San Diego, La Jolla, CA, USA.

Lisa T Eyler (LT)

Department of Psychiatry, School of Medicine, University of California, San Diego, La Jolla, CA, USA.

Christine Fennema-Notestine (C)

Department of Psychiatry, School of Medicine, University of California, San Diego, La Jolla, CA, USA.
Department of Radiology, School of Medicine, University of California, San Diego, La Jolla, CA, USA.

Nathan A Gillespie (NA)

Department of Psychiatry, Virginia Institute for Psychiatric and Behavioral Genetics, Virginia Commonwealth University, Richmond, VA, USA.

Richard L Hauger (RL)

Department of Psychiatry, School of Medicine, University of California, San Diego, La Jolla, CA, USA.
Center for Behavior Genetics of Aging, University of California, San Diego, La Jolla, CA, USA.
Center of Excellence for Stress and Mental Health, VA San Diego Healthcare System, San Diego, CA, USA.

Amy J Jak (AJ)

Department of Psychiatry, School of Medicine, University of California, San Diego, La Jolla, CA, USA.
Center of Excellence for Stress and Mental Health, VA San Diego Healthcare System, San Diego, CA, USA.

Michael C Neale (MC)

Department of Psychiatry, Virginia Institute for Psychiatric and Behavioral Genetics, Virginia Commonwealth University, Richmond, VA, USA.
Department of Human and Molecular Genetics, Virginia Institute for Psychiatric and Behavioral Genetics, Virginia Commonwealth University, Richmond, VA, USA.

Xin M Tu (XM)

Department of Family Medicine and Public Health, VA San Diego Healthcare System, San Diego, CA, USA.

Nathan Whitsel (N)

Department of Psychiatry, School of Medicine, University of California, San Diego, La Jolla, CA, USA.

Hong Xian (H)

Department of Epidemiology & Biostatistics, Saint Louis University College for Public Health & Social Justice, Saint Louis, MO, USA.

William S Kremen (WS)

Department of Psychiatry, School of Medicine, University of California, San Diego, La Jolla, CA, USA.
Center for Behavior Genetics of Aging, University of California, San Diego, La Jolla, CA, USA.
Center of Excellence for Stress and Mental Health, VA San Diego Healthcare System, San Diego, CA, USA.

Michael J Lyons (MJ)

Department of Psychological and Brain Sciences, Boston University, Boston, MA, USA.

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Classifications MeSH