A Danish National Birth Cohort study of maternal HSV-2 antibodies as a risk factor for schizophrenia in their offspring

被引:77
|
作者
Mortensen, Preben B. [1 ]
Pedersen, Carsten B. [1 ]
Hougaard, David M. [2 ]
Norgaard-Petersen, Bent [2 ]
Mors, Ole [3 ]
Borglum, Anders D. [4 ]
Yolken, Robert H. [5 ]
机构
[1] Univ Aarhus, Fac Social Sci, Natl Ctr Register Based Res, DK-8000 Aarhus C, Denmark
[2] Statens Serum Inst, DK-2300 Copenhagen S, Denmark
[3] Hosp Psychiat, Aarhus Univ Hosp, Ctr Psychiat Res, DK-8240 Risskov, Denmark
[4] Univ Aarhus, Inst Human Genet, DK-8000 Aarhus C, Denmark
[5] Johns Hopkins Univ, Sch Med, Stanley Neurovirol Lab, Baltimore, MD 21287 USA
关键词
Schizophrenia; Herpes simplex 2; Neonatal; National birth cohort; HERPES-SIMPLEX-VIRUS; PRENATAL EXPOSURE; ADULT SCHIZOPHRENIA; INFECTION; PSYCHOSIS; TYPE-2; AGE; REGISTER; DENMARK; CYTOMEGALOVIRUS;
D O I
10.1016/j.schres.2010.06.010
中图分类号
R749 [精神病学];
学科分类号
100205 ;
摘要
Background: Several studies have implicated early infections, including maternal infection with herpes simplex virus 2 (HSV-2), as an environmental risk factor for schizophrenia. Methods: A case-control study nested within the national Danish birth cohort constituted by the PKU Biobank covering all children born in Denmark since 1981. 602 cases of schizophrenia (ICD-10 F20) were ascertained in the Danish Psychiatric Central Register, covering all in- and out-patient contacts in Denmark, and 602 controls were matched individually on gender, exact date of birth and living in Denmark on the date the case became a case. Incidence rate ratio for schizophrenia was estimated using conditional logistic regression. Main exposure was HSV-2 IgG antibody levels. Confounders and potential interacting factors included family history of mental illness, place of birth and gestational age at time of birth. Results: Elevated levels of maternal HSV-2 IgG were associated with schizophrenia risk (IRR 1.56; 95% CI 1.17-2.07, p = 0.002). This association was not confounded by a maternal or sibling history of psychiatric illness, place of birth, parental age, gestational age, or immigrant status of the parents. However, adjustment for paternal psychiatric history reduced risk slightly (IRR 1.43; 95% CI 1.06-1.92, p = 0.02). Conclusions: The study replicates an association between maternal HSV-2 IgG levels and schizophrenia risk. Since the confounding by familial risk factors is confined to paternal mental illnesses not belonging to the schizophrenia spectrum, we hypothesize that this confounding may be partly due to other risk factors, e.g., other sexually transmitted infections, rather than reflecting variations in genetic liability to develop schizophrenia. (C) 2010 Elsevier B.V. All rights reserved.
引用
收藏
页码:257 / 263
页数:7
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