Infections and severe mental illness: a population-based matched cohort study.

IF 6.6 0 PSYCHIATRY
Sharon L Cadogan, Georgia R Gore-Langton, Kathryn E Mansfield, John Tazare, Seena Fazel, Ian J Douglas, Caroline Morton, Naaheed Mukadam, Charlotte Warren-Gash
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引用次数: 0

Abstract

Background: It is unclear whether acute infections associated with short-term systemic inflammation influence the risk of severe mental illness (SMI).

Objective: To investigate relationships between acute infections and incident SMI using electronic health records from the UK.

Methods: Using data from the Clinical Practice Research Datalink Aurum (1 January 2007 to 15 June 2024), we conducted six matched cohort studies. Adults (≥18 years) with gastroenteritis (GE), lower respiratory tract infection (LRTI), skin and soft tissue infection (SSTI), urinary tract infection (UTI), sepsis and meningitis/encephalitis (positive control exposure) recorded in primary care were matched with up to five individuals without infection on age, sex and practice in calendar date order and followed for incident SMI (schizophrenia, bipolar disorder, other psychoses). We estimated HRs for SMI comparing those with and without each infection using Cox regression, stratified by match set, adjusting for potential confounders (deprivation, Charlson Comorbidity Index, alcohol, smoking, body mass index and ethnicity).

Findings: Our six study cohorts ranged from 2 089 168 adults (391 773 with SSTI, 1 697 395 without) to 106 155 (17 860 with meningitis/encephalitis, 88 295 without). Median follow-up ranged from 4.1 years (IQR 1.9-6.9) in the sepsis cohort to 5.7 years (IQR 2.6-9.8) in the meningitis/encephalitis cohort. After adjustment, each infection was associated with increased SMI risk: SSTI, HR 1.16 (95% CI 1.08 to 1.24); LRTI, 1.28 (95% CI 1.20 to 1.38); UTI, 1.44 (95% CI 1.31 to 1.58); GE, 1.53 (95% CI 1.42 to 1.65); sepsis, 1.69 (95% CI 1.52 to 1.88); and meningitis/encephalitis, 3.36 (95% CI 2.61 to 4.32).

Conclusion: Our findings suggest SMI risk is higher among adults with a range of acute infections compared with those without, with higher risks for the more severe infections meningitis/encephalitis and sepsis.

Clinical implications: Providing timely infection treatment, targeted mental health support following severe infections, and where appropriate offering relevant vaccinations, may limit SMI risk.

感染与严重精神疾病:一项基于人群的匹配队列研究
背景:目前尚不清楚急性感染与短期全身性炎症是否会影响严重精神疾病(SMI)的风险。目的:利用英国的电子健康记录调查急性感染与重度精神分裂症事件之间的关系。方法:使用临床实践研究数据链Aurum(2007年1月1日至2024年6月15日)的数据,我们进行了6项匹配队列研究。在初级保健中记录的患有胃肠炎(GE)、下呼吸道感染(LRTI)、皮肤和软组织感染(SSTI)、尿路感染(UTI)、败血症和脑膜炎/脑炎(阳性对照暴露)的成人(≥18岁)按日历日期顺序与最多5名未感染的个体进行年龄、性别和实践匹配,并随访SMI事件(精神分裂症、双相情感障碍、其他精神病)。我们使用Cox回归方法对患有和未患有每种感染的重度精神分裂症患者的hr进行了比较,并按匹配集分层,调整了潜在的混杂因素(剥夺、查尔森合并症指数、酒精、吸烟、体重指数和种族)。结果:我们的6个研究队列从2089 168名成年人(391 773名患有SSTI, 1 697 395名没有)到106 155名(17 860名患有脑膜炎/脑炎,88 295名没有)。中位随访时间从败血症组的4.1年(IQR 1.9-6.9)到脑膜炎/脑炎组的5.7年(IQR 2.6-9.8)。调整后,每种感染都与SMI风险增加相关:SSTI, HR 1.16 (95% CI 1.08 ~ 1.24);LRTI, 1.28 (95% CI 1.20 ~ 1.38);UTI, 1.44 (95% CI 1.31 - 1.58);GE, 1.53 (95% CI 1.42 - 1.65);脓毒症,1.69 (95% CI 1.52 ~ 1.88);脑膜炎/脑炎,3.36 (95% CI 2.61 - 4.32)。结论:我们的研究结果表明,与没有急性感染的成年人相比,患有一系列急性感染的成年人患SMI的风险更高,其中脑膜炎/脑炎和败血症等严重感染的风险更高。临床意义:提供及时的感染治疗,在严重感染后提供有针对性的心理健康支持,并在适当的情况下提供相关的疫苗接种,可能会限制重度精神分裂症的风险。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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CiteScore
6.80
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