Association Between Lifetime Affective Symptoms and Premature Mortality.
Journal
JAMA psychiatry
ISSN: 2168-6238
Titre abrégé: JAMA Psychiatry
Pays: United States
ID NLM: 101589550
Informations de publication
Date de publication:
01 08 2020
01 08 2020
Historique:
pubmed:
9
4
2020
medline:
13
2
2021
entrez:
9
4
2020
Statut:
ppublish
Résumé
Associations between affective symptoms and mortality have been evaluated, but studies have not examined timing or cumulative exposure to affective symptoms over the life course. To examine how lifetime accumulation and timing of affective symptoms are associated with mortality and identify potential explanatory factors. Data were obtained from the MRC National Survey of Health and Development (1946 British birth cohort), a socially stratified, population-based sample originally consisting of 5362 singleton births in England, Wales, and Scotland during March 1946. The cohort has been followed up 24 times, most recently in 2014-2015. Eligible participants included those flagged for mortality with affective symptom data available at a minimum of 3 time points (n = 3001). Data analysis was conducted from July 2016 to January 2019. Affective symptoms were assessed at ages 13 to 15 years (teacher-rated questionnaire), 36 years (Present State Examination clinical semistructured interview), 43 years (Psychiatric Symptom Frequency questionnaire), and 53 years (General Health Questionnaire-28). Case-level affective symptoms were determined by those scoring in the top 16th percentile (ie, suggestive of a clinical diagnosis). Mortality data were obtained from the UK National Health Service Central Register from age 53 to 68 years. Of 3001 study members (1509 [50.3%] female, 1492 [49.7%] male), 235 individuals (7.8%) died over a 15-year follow-up. After adjustment for sex, those who experienced case-level affective symptoms 1, 2, and 3 to 4 times had 76%, 87%, and 134% higher rates of premature mortality, respectively, compared with those who never experienced case-level symptoms. Case-level symptoms in adolescence only (ages 13-15 years) were associated with a 94% increased rate of mortality, which was unexplained after full adjustment for covariates (hazard ratio, 1.73; 95% CI, 1.10-2.72). Associations between participants with case-level symptoms multiple (2-4) times and mortality were predominately explained by adult health indicators and behaviors. For example, associations for those with case-level symptoms 3 to 4 times were most strongly attenuated by number of health conditions (32.1%), anxiolytic use (28.4%), lung function (24.6%), physical activity (23.9%), smoking (24.6%), antidepressant use (20.1%), diet (16.4%), pulse rate (12.7%), and adult social class (11.2%). Lifetime accumulation of affective symptoms may be associated with an increased rate of mortality, with explanatory pathways dependent on the duration and timing of symptoms. Future research into causal pathways and potential points of intervention should consider affective symptom history.
Identifiants
pubmed: 32267482
pii: 2763796
doi: 10.1001/jamapsychiatry.2020.0316
pmc: PMC7142795
doi:
Types de publication
Journal Article
Research Support, Non-U.S. Gov't
Langues
eng
Sous-ensembles de citation
IM
Pagination
806-813Subventions
Organisme : Medical Research Council
ID : MC_UU_00019/2
Pays : United Kingdom
Organisme : Medical Research Council
ID : MC_UU_00019/3
Pays : United Kingdom
Organisme : Medical Research Council
ID : MC_UU_00019/4
Pays : United Kingdom
Organisme : Medical Research Council
ID : MC_UU_12019/3
Pays : United Kingdom
Références
Eur J Epidemiol. 2016 Nov;31(11):1135-1147
pubmed: 27995394
Psychol Aging. 2013 Dec;28(4):958-68
pubmed: 24364401
J Affect Disord. 2009 Dec;119(1-3):66-75
pubmed: 19394087
Eur J Ageing. 2013 Jun;10(2):145-157
pubmed: 23637643
Am J Public Health. 1989 Jun;79(6):727-30
pubmed: 2786347
Am J Cardiol. 1998 Apr 15;81(8):988-94
pubmed: 9576158
J Hypertens. 2014 Aug;32(8):1590-8; discussion 1599
pubmed: 24906173
J Psychosom Res. 2015 Dec;79(6):595-603
pubmed: 26299450
Eur J Epidemiol. 2013 Sep;28(9):721-34
pubmed: 23887883
Public Health Nutr. 2014 Dec;17(12):2660-6
pubmed: 24477178
J Chronic Dis. 1978;31(12):741-55
pubmed: 748370
Psychol Med. 2002 May;32(4):609-18
pubmed: 12102375
JAMA. 1984 Oct 12;252(14):1905-7
pubmed: 6471323
Am J Psychiatry. 2007 Jan;164(1):126-33
pubmed: 17202554
Br J Psychiatry. 2000 Dec;177:534-9
pubmed: 11102329
J Child Psychol Psychiatry. 1967 May;8(1):1-11
pubmed: 6033260
J Epidemiol Community Health. 1997 Oct;51(5):549-57
pubmed: 9425466
Psychol Med. 1983 May;13(2):349-53
pubmed: 6878521
Psychol Med. 1978 May;8(2):203-17
pubmed: 652895
J Am Acad Child Adolesc Psychiatry. 2009 Jan;48(1):19-24
pubmed: 19218894
Psychol Med. 2014 Apr;44(5):1077-86
pubmed: 23962416
Br J Psychiatry. 1976 Jul;129:61-7
pubmed: 938806
Psychosom Med. 2013 Apr;75(3):297-304
pubmed: 23533284
Psychol Med. 1997 Jan;27(1):191-7
pubmed: 9122299
Psychosom Med. 1999 Jan-Feb;61(1):6-17
pubmed: 10024062
Psychol Med. 2015 Oct;45(13):2771-9
pubmed: 25936473
Psychol Med. 1977 Aug;7(3):505-16
pubmed: 905467
J Epidemiol Community Health. 2008 Dec;62(12):1051-6
pubmed: 18450766
Lancet. 1994 Nov 19;344(8934):1398-402
pubmed: 7968076
Arch Gen Psychiatry. 1978 Oct;35(10):1181-5
pubmed: 697536
Psychosom Med. 2007 May;69(4):323-31
pubmed: 17470669
Psychol Med. 1979 Feb;9(1):139-45
pubmed: 424481
World Psychiatry. 2017 Jun;16(2):219-220
pubmed: 28498573
BMC Public Health. 2011 Jul 28;11:601
pubmed: 21797992
Br J Psychiatry. 2016 Apr;208(4):337-42
pubmed: 26795425