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Association Between Depressive Symptoms and Incident Cardiovascular Diseases.
Harshfield, Eric L; Pennells, Lisa; Schwartz, Joseph E; Willeit, Peter; Kaptoge, Stephen; Bell, Steven; Shaffer, Jonathan A; Bolton, Thomas; Spackman, Sarah; Wassertheil-Smoller, Sylvia; Kee, Frank; Amouyel, Philippe; Shea, Steven J; Kuller, Lewis H; Kauhanen, Jussi; van Zutphen, E M; Blazer, Dan G; Krumholz, Harlan; Nietert, Paul J; Kromhout, Daan; Laughlin, Gail; Berkman, Lisa; Wallace, Robert B; Simons, Leon A; Dennison, Elaine M; Barr, Elizabeth L M; Meyer, Haakon E; Wood, Angela M; Danesh, John; Di Angelantonio, Emanuele; Davidson, Karina W.
Affiliation
  • Harshfield EL; Department of Public Health and Primary Care, University of Cambridge, Cambridge, United Kingdom.
  • Pennells L; Department of Clinical Neurosciences, University of Cambridge, Cambridge, United Kingdom.
  • Schwartz JE; Department of Public Health and Primary Care, University of Cambridge, Cambridge, United Kingdom.
  • Willeit P; Center for Behavioral Cardiovascular Health, Columbia University Medical Center, New York, New York.
  • Kaptoge S; Applied Behavioral Medicine Research Institute, Stony Brook University, Stony Brook, New York.
  • Bell S; Department of Public Health and Primary Care, University of Cambridge, Cambridge, United Kingdom.
  • Shaffer JA; Department of Neurology & Neurosurgery, Medical University of Innsbruck, Innsbruck, Austria.
  • Bolton T; Department of Public Health and Primary Care, University of Cambridge, Cambridge, United Kingdom.
  • Spackman S; Department of Public Health and Primary Care, University of Cambridge, Cambridge, United Kingdom.
  • Wassertheil-Smoller S; Department of Clinical Neurosciences, University of Cambridge, Cambridge, United Kingdom.
  • Kee F; University of Colorado Denver, Denver.
  • Amouyel P; Department of Public Health and Primary Care, University of Cambridge, Cambridge, United Kingdom.
  • Shea SJ; Department of Public Health and Primary Care, University of Cambridge, Cambridge, United Kingdom.
  • Kuller LH; Department of Epidemiology and Population Health, Albert Einstein College of Medicine, Bronx, New York.
  • Kauhanen J; Centre for Public Health, Queens University, Belfast, United Kingdom.
  • van Zutphen EM; Institut Pasteur de Lille, Lille, France.
  • Blazer DG; Columbia Field Center, Columbia University, New York, New York.
  • Krumholz H; Department of Epidemiology, University of Pittsburgh Graduate School of Public Health, Pittsburgh, Pennsylvania.
  • Nietert PJ; Institute of Public Health and Clinical Nutrition, University of Eastern Finland, Kuopio, Finland.
  • Kromhout D; Department of Psychiatry, Amsterdam Public Health Research Institute, Amsterdam UMC at VU University Medical Center, Amsterdam, the Netherlands.
  • Laughlin G; Department of Epidemiology and Biostatistics, Amsterdam Public Health Research Institute, Amsterdam UMC at VU University Medical Center, Amsterdam, the Netherlands.
  • Berkman L; GGZ inGeest Specialized Mental Health Care, Amsterdam, the Netherlands.
  • Wallace RB; Department of Psychiatry and Behavioral Sciences, Duke University, Durham, North Carolina.
  • Simons LA; Yale School of Medicine, New Haven, Connecticut.
  • Dennison EM; Department of Public Health Sciences, Medical University of South Carolina.
  • Barr ELM; Department of Epidemiology, University Medical Centre Groningen, University of Groningen, Groningen, the Netherlands.
  • Meyer HE; Family Medicine & Public Health, University of California, San Diego.
  • Wood AM; Harvard T.H. Chan School of Public Health, Boston, Massachusetts.
  • Danesh J; Department of Epidemiology, University of Iowa College of Public Health.
  • Di Angelantonio E; Faculty of Medicine, UNSW, Sydney, Australia.
  • Davidson KW; MRC Lifecourse Epidemiology Unit, University of Southampton, Southampton, United Kingdom.
JAMA ; 324(23): 2396-2405, 2020 12 15.
Article in En | MEDLINE | ID: mdl-33320224
Importance: It is uncertain whether depressive symptoms are independently associated with subsequent risk of cardiovascular diseases (CVDs). Objective: To characterize the association between depressive symptoms and CVD incidence across the spectrum of lower mood. Design, Setting, and Participants: A pooled analysis of individual-participant data from the Emerging Risk Factors Collaboration (ERFC; 162 036 participants; 21 cohorts; baseline surveys, 1960-2008; latest follow-up, March 2020) and the UK Biobank (401 219 participants; baseline surveys, 2006-2010; latest follow-up, March 2020). Eligible participants had information about self-reported depressive symptoms and no CVD history at baseline. Exposures: Depressive symptoms were recorded using validated instruments. ERFC scores were harmonized across studies to a scale representative of the Center for Epidemiological Studies Depression (CES-D) scale (range, 0-60; ≥16 indicates possible depressive disorder). The UK Biobank recorded the 2-item Patient Health Questionnaire 2 (PHQ-2; range, 0-6; ≥3 indicates possible depressive disorder). Main Outcomes and Measures: Primary outcomes were incident fatal or nonfatal coronary heart disease (CHD), stroke, and CVD (composite of the 2). Hazard ratios (HRs) per 1-SD higher log CES-D or PHQ-2 adjusted for age, sex, smoking, and diabetes were reported. Results: Among 162 036 participants from the ERFC (73%, women; mean age at baseline, 63 years [SD, 9 years]), 5078 CHD and 3932 stroke events were recorded (median follow-up, 9.5 years). Associations with CHD, stroke, and CVD were log linear. The HR per 1-SD higher depression score for CHD was 1.07 (95% CI, 1.03-1.11); stroke, 1.05 (95% CI, 1.01-1.10); and CVD, 1.06 (95% CI, 1.04-1.08). The corresponding incidence rates per 10 000 person-years of follow-up in the highest vs the lowest quintile of CES-D score (geometric mean CES-D score, 19 vs 1) were 36.3 vs 29.0 for CHD events, 28.0 vs 24.7 for stroke events, and 62.8 vs 53.5 for CVD events. Among 401 219 participants from the UK Biobank (55% were women, mean age at baseline, 56 years [SD, 8 years]), 4607 CHD and 3253 stroke events were recorded (median follow-up, 8.1 years). The HR per 1-SD higher depression score for CHD was 1.11 (95% CI, 1.08-1.14); stroke, 1.10 (95% CI, 1.06-1.14); and CVD, 1.10 (95% CI, 1.08-1.13). The corresponding incidence rates per 10 000 person-years of follow-up among individuals with PHQ-2 scores of 4 or higher vs 0 were 20.9 vs 14.2 for CHD events, 15.3 vs 10.2 for stroke events, and 36.2 vs 24.5 for CVD events. The magnitude and statistical significance of the HRs were not materially changed after adjustment for additional risk factors. Conclusions and Relevance: In a pooled analysis of 563 255 participants in 22 cohorts, baseline depressive symptoms were associated with CVD incidence, including at symptom levels lower than the threshold indicative of a depressive disorder. However, the magnitude of associations was modest.
Subject(s)

Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Cardiovascular Diseases / Depression Type of study: Diagnostic_studies / Etiology_studies / Incidence_studies / Observational_studies / Prognostic_studies / Qualitative_research / Risk_factors_studies Limits: Aged / Female / Humans / Male / Middle aged Language: En Journal: JAMA Year: 2020 Type: Article Affiliation country: United kingdom

Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Cardiovascular Diseases / Depression Type of study: Diagnostic_studies / Etiology_studies / Incidence_studies / Observational_studies / Prognostic_studies / Qualitative_research / Risk_factors_studies Limits: Aged / Female / Humans / Male / Middle aged Language: En Journal: JAMA Year: 2020 Type: Article Affiliation country: United kingdom