Sørensen Holger J, Mortensen Erik L, Reinisch June M, Mednick Sarnoff A
Danish Epidemiology Science Center, Institute of Preventive Medicine, Copenhagen University Hospital, University of Copenhagen, Copenhagen, Denmark.
Schizophr Bull. 2009 May;35(3):631-7. doi: 10.1093/schbul/sbn121. Epub 2008 Oct 1.
Recent research suggests that prenatal exposure to nonviral infection may be associated with increased risk of schizophrenia, and we hypothesized an association between maternal bacterial infection during pregnancy and elevated offspring risk of schizophrenia. Data on maternal infections from the Copenhagen Perinatal Cohort were linked with the Danish National Psychiatric Register. Offspring cases of narrowly defined schizophrenia (International Classification of Diseases, Eighth Revision [ICD-8]) and more broadly defined schizophrenia (ICD-8 and ICD-10) were identified before the ages of 32-34 and 45-47 years, respectively. The effect of prenatal exposure to bacterial infections was adjusted for prenatal exposure to analgesics and parental social status. In a risk set of 7941 individuals, 85 cases (1.1%) of ICD-8 schizophrenia were identified by the age of 32-34 years and 153 cases (1.9%) of more broadly defined schizophrenia by the age of 45-47 years. First-trimester exposure conferred an elevated risk of ICD-8 schizophrenia (odds ratio 2.53; 95% confidence interval [CI] 1.07-5.96) and also of broadly defined schizophrenia (odds ratio 2.14; 95% CI 1.06-4.31). Second-trimester exposure also conferred a significantly elevated risk of schizophrenia but only in unadjusted analyses. These findings suggest a relationship between maternal bacterial infection in pregnancy and offspring risk of schizophrenia, and this effect was somewhat stronger for ICD-8 schizophrenia with earlier onset. Post hoc analyses showed that upper respiratory tract and gonococcal infections were associated with elevated risk of the disease. An association between risk of schizophrenia and prenatal exposure to bacterial infections might be mediated through transplacental passage of maternally produced cytokines in response to bacterial infections.
近期研究表明,产前暴露于非病毒感染可能与精神分裂症风险增加有关,我们推测孕期母亲细菌感染与后代精神分裂症风险升高之间存在关联。来自哥本哈根围产期队列的母亲感染数据与丹麦国家精神病学登记册相关联。分别在32 - 34岁和45 - 47岁之前确定了狭义精神分裂症(《国际疾病分类》第八版[ICD - 8])和广义精神分裂症(ICD - 8和ICD - 10)的后代病例。对产前暴露于细菌感染进行了调整,以考虑产前暴露于镇痛药和父母社会地位的因素。在一组7941名个体的风险队列中,到32 - 34岁时确定了85例(1.1%)ICD - 8精神分裂症病例以及到45 - 47岁时确定了153例(1.9%)广义精神分裂症病例。孕早期暴露使患ICD - 8精神分裂症的风险升高(优势比2.53;95%置信区间[CI] 1.07 - 5.96),也使患广义精神分裂症的风险升高(优势比2.14;95% CI 1.06 - 4.31)。孕中期暴露也使精神分裂症风险显著升高,但仅在未调整分析中如此。这些发现表明孕期母亲细菌感染与后代精神分裂症风险之间存在关联,且这种效应对于发病较早的ICD - 8精神分裂症更强。事后分析表明,上呼吸道感染和淋球菌感染与该疾病风险升高有关。精神分裂症风险与产前暴露于细菌感染之间的关联可能是通过母体产生的细胞因子经胎盘传递以应对细菌感染来介导的。