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Stress related disorders and subsequent risk of life threatening infections: population based sibling controlled cohort study

Stress related disorders and subsequent risk of life threatening infections: population based sibling controlled cohort study


Titill: Stress related disorders and subsequent risk of life threatening infections: population based sibling controlled cohort study
Höfundur: Song, Huan
Fall, Katja
Fang, Fang
Erlendsdóttir, Helga
Lu, Donghao
Mataix-Cols, David
Fernández de la Cruz, Lorena
D’Onofrio, Brian M.
Lichtenstein, Paul
Gottfredsson, Magnus   orcid.org/0000-0003-2465-0422
... 2 fleiri höfundar Sýna alla höfunda
Útgáfa: 2019-10-23
Tungumál: Enska
Umfang: l5784
Háskóli/Stofnun: Háskóli Íslands
University of Iceland
Svið: Heilbrigðisvísindasvið (HÍ)
School of Health Sciences (UI)
Deild: Læknadeild (HÍ)
Faculty of Medicine (UI)
Birtist í: BMJ;367
ISSN: 0959-8138
1756-1833 (eISSN)
DOI: 10.1136/bmj.l5784
Efnisorð: Trauma; Infection; PTSD; Sálræn áföll; Áfallastreita; Sýkingar
URI: https://hdl.handle.net/20.500.11815/1899

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Tilvitnun:

Song Huan, Fall Katja, Fang Fang, Erlendsdóttir Helga, Lu Donghao, Mataix-Cols David et al. Stress related disorders and subsequent risk of life threatening infections: population based sibling controlled cohort study BMJ 2019; 367 :l5784

Útdráttur:

Objective: To assess whether severe psychiatric reactions to trauma and other adversities are associated with subsequent risk of life threatening infections. Design: Population and sibling matched cohort study. Setting: Swedish population. Participants: 144 919 individuals with stress related disorders (post-traumatic stress disorder (PTSD), acute stress reaction, adjustment disorder, and other stress reactions) identified from 1987 to 2013 compared with 184 612 full siblings of individuals with a diagnosed stress related disorder and 1 449 190 matched individuals without such a diagnosis from the general population. Main outcome measures: A first inpatient or outpatient visit with a primary diagnosis of severe infections with high mortality rates (ie, sepsis, endocarditis, and meningitis or other central nervous system infections) from the Swedish National Patient Register, and deaths from these infections or infections of any origin from the Cause of Death Register. After controlling for multiple confounders, Cox models were used to estimate hazard ratios of these life threatening infections. Results: The average age at diagnosis of a stress related disorder was 37 years (55 541, 38.3% men). During a mean follow-up of eight years, the incidence of life threatening infections per 1000 person years was 2.9 in individuals with a stress related disorder, 1.7 in siblings without a diagnosis, and 1.3 in matched individuals without a diagnosis. Compared with full siblings without a diagnosis of a stress related disorder, individuals with such a diagnosis were at increased risk of life threatening infections (hazard ratio for any stress related disorder was 1.47 (95% confidence intervals1.37 to 1.58) and for PTSD was 1.92 (1.46 to 2.52)). Corresponding estimates in the population based analysis were similar (1.58 (1.51 to 1.65) for any stress related disorder, P=0.09 for difference between sibling and population based comparison, and 1.95 (1.66 to 2.28) for PTSD, P=0.92 for difference). Stress related disorders were associated with all studied life threatening infections, with the highest relative risk observed for meningitis (sibling based analysis 1.63 (1.23 to 2.16)) and endocarditis (1.57 (1.08 to 2.30)). Younger age at diagnosis of a stress related disorder and the presence of psychiatric comorbidity, especially substance use disorders, were associated with higher hazard ratios, whereas use of selective serotonin reuptake inhibitors in the first year after diagnosis of a stress related disorder was associated with attenuated hazard ratios. Conclusion: In the Swedish population, stress related disorders were associated with a subsequent risk of life threatening infections, after controlling for familial background and physical or psychiatric comorbidities.

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This is an Open Access article distributed in accordance with the Creative Commons Attribution Non Commercial (CC BY-NC 4.0) license, which permits others to distribute, remix, adapt, build upon this work non-commercially, and license their derivative works on different terms, provided the original work is properly cited and the use is non-commercial. See: http://creativecommons.org/licenses/by-nc/4.0/.

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