Evidence for an Interaction Between Familial Liability and Prenatal Exposure to Infection in the Causation of Schizophrenia

Objective: The authors sought to determine whether prenatal exposure to infection and a positive family history of psychotic disorders interact synergistically to increase the risk of later developing schizophrenia. Method: The authors linked two national registers, the Medical Birth Register and th...

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Veröffentlicht in:The American journal of psychiatry 2009-09, Vol.166 (9), p.1025-1030
Hauptverfasser: Clarke, Mary C., Tanskanen, Antti, Huttunen, Matti, Whittaker, John C., Cannon, Mary
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container_end_page 1030
container_issue 9
container_start_page 1025
container_title The American journal of psychiatry
container_volume 166
creator Clarke, Mary C.
Tanskanen, Antti
Huttunen, Matti
Whittaker, John C.
Cannon, Mary
description Objective: The authors sought to determine whether prenatal exposure to infection and a positive family history of psychotic disorders interact synergistically to increase the risk of later developing schizophrenia. Method: The authors linked two national registers, the Medical Birth Register and the Finnish Population Register, to identify all women in Helsinki who received hospital treatment during pregnancy for an upper urinary tract infection (N=9,596) between 1947 and 1990. The Finnish Hospital Discharge Register was used to ascertain psychiatric outcomes in adulthood of offspring exposed to infection prenatally. Family history of psychotic disorders was determined by linking the Hospital Discharge Register and the Population Register. The authors used an additive statistical interaction model to calculate the amount of biological synergism between positive family history and prenatal exposure to infection. Results: Prenatal exposure to infection did not significantly increase the risk of schizophrenia. However, the effect of prenatal exposure to pyelonephritis was five times greater in those who had a family history of psychosis compared to those who did not. The synergy analysis suggested that an estimated 38%-46% of the offspring who developed schizophrenia and had both prenatal exposure to infection and a positive family history of psychotic disorders did so as a result of the synergistic action of both risk factors. Conclusions: These findings support a mechanism of gene-environment interaction in the causation of schizophrenia.
doi_str_mv 10.1176/appi.ajp.2009.08010031
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Method: The authors linked two national registers, the Medical Birth Register and the Finnish Population Register, to identify all women in Helsinki who received hospital treatment during pregnancy for an upper urinary tract infection (N=9,596) between 1947 and 1990. The Finnish Hospital Discharge Register was used to ascertain psychiatric outcomes in adulthood of offspring exposed to infection prenatally. Family history of psychotic disorders was determined by linking the Hospital Discharge Register and the Population Register. The authors used an additive statistical interaction model to calculate the amount of biological synergism between positive family history and prenatal exposure to infection. Results: Prenatal exposure to infection did not significantly increase the risk of schizophrenia. However, the effect of prenatal exposure to pyelonephritis was five times greater in those who had a family history of psychosis compared to those who did not. The synergy analysis suggested that an estimated 38%-46% of the offspring who developed schizophrenia and had both prenatal exposure to infection and a positive family history of psychotic disorders did so as a result of the synergistic action of both risk factors. Conclusions: These findings support a mechanism of gene-environment interaction in the causation of schizophrenia.</description><identifier>ISSN: 0002-953X</identifier><identifier>EISSN: 1535-7228</identifier><identifier>DOI: 10.1176/appi.ajp.2009.08010031</identifier><identifier>PMID: 19487391</identifier><identifier>CODEN: AJPSAO</identifier><language>eng</language><publisher>Arlington, VA: American Psychiatric Association</publisher><subject>Adult ; Adult and adolescent clinical studies ; Biological and medical sciences ; Cohort Studies ; Confidence intervals ; Cross-Sectional Studies ; Denmark - epidemiology ; E coli ; Family - psychology ; Female ; Genetic Markers ; Genetic Predisposition to Disease ; Health risk assessment ; Humans ; Infection - epidemiology ; Influenza ; Male ; Maternal Exposure - statistics &amp; numerical data ; Medical sciences ; Pregnancy ; Pregnancy Complications, Infectious - epidemiology ; Prenatal development ; Prenatal exposure ; Prenatal Exposure Delayed Effects - epidemiology ; Prevalence ; Psychiatry ; Psychology. 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Method: The authors linked two national registers, the Medical Birth Register and the Finnish Population Register, to identify all women in Helsinki who received hospital treatment during pregnancy for an upper urinary tract infection (N=9,596) between 1947 and 1990. The Finnish Hospital Discharge Register was used to ascertain psychiatric outcomes in adulthood of offspring exposed to infection prenatally. Family history of psychotic disorders was determined by linking the Hospital Discharge Register and the Population Register. The authors used an additive statistical interaction model to calculate the amount of biological synergism between positive family history and prenatal exposure to infection. Results: Prenatal exposure to infection did not significantly increase the risk of schizophrenia. However, the effect of prenatal exposure to pyelonephritis was five times greater in those who had a family history of psychosis compared to those who did not. The synergy analysis suggested that an estimated 38%-46% of the offspring who developed schizophrenia and had both prenatal exposure to infection and a positive family history of psychotic disorders did so as a result of the synergistic action of both risk factors. Conclusions: These findings support a mechanism of gene-environment interaction in the causation of schizophrenia.</description><subject>Adult</subject><subject>Adult and adolescent clinical studies</subject><subject>Biological and medical sciences</subject><subject>Cohort Studies</subject><subject>Confidence intervals</subject><subject>Cross-Sectional Studies</subject><subject>Denmark - epidemiology</subject><subject>E coli</subject><subject>Family - psychology</subject><subject>Female</subject><subject>Genetic Markers</subject><subject>Genetic Predisposition to Disease</subject><subject>Health risk assessment</subject><subject>Humans</subject><subject>Infection - epidemiology</subject><subject>Influenza</subject><subject>Male</subject><subject>Maternal Exposure - statistics &amp; numerical data</subject><subject>Medical sciences</subject><subject>Pregnancy</subject><subject>Pregnancy Complications, Infectious - epidemiology</subject><subject>Prenatal development</subject><subject>Prenatal exposure</subject><subject>Prenatal Exposure Delayed Effects - epidemiology</subject><subject>Prevalence</subject><subject>Psychiatry</subject><subject>Psychology. Psychoanalysis. Psychiatry</subject><subject>Psychopathology. Psychiatry</subject><subject>Psychoses</subject><subject>Pyelonephritis - epidemiology</subject><subject>Risk Factors</subject><subject>Schizophrenia</subject><subject>Schizophrenia - epidemiology</subject><subject>Schizophrenia - etiology</subject><subject>Schizophrenia - genetics</subject><issn>0002-953X</issn><issn>1535-7228</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2009</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNqFkMFuEzEQhi1ERUPhFSoLieMGj531ro8QpbRSJJDaStysWa-tOEq8i-0FCi9fpwnlyMGyZ_T9M9ZHyCWwOUAjP-A4-jluxzlnTM1Zy4AxAS_IDGpRVw3n7UsyY4zxStXi2zl5ndK2lEw0_BU5B7VoG6FgRv6sfvjeBmOpGyLFQG9CthFN9kOgn2z-aW2gV7j3O487uvbYlVd-KGRPv0YbMJf26tc4pClamoeSd_aY9oHmjaVLnBI-NQZHb83G_x7GTUl6fEPOHO6SfXu6L8j91epueV2tv3y-WX5cV7hoZK5E13cCrQTsjFQtB4l9DVg3TIHpWmGFA1arFkVveldL49AsAKRsOtsqrMUFeXecO8bh-2RT1tthiqGs1JyzRQOtUAWSR8jEIaVonR6j32N80MD0Qbk-KNdFuT4o13-Vl-DlafrU7W3_L3ZyXID3JwCTwZ2LGIxPzxwHxcs5cOLIPS16_uJ_1j8CfHedlg</recordid><startdate>20090901</startdate><enddate>20090901</enddate><creator>Clarke, Mary C.</creator><creator>Tanskanen, Antti</creator><creator>Huttunen, Matti</creator><creator>Whittaker, John C.</creator><creator>Cannon, Mary</creator><general>American Psychiatric Association</general><scope>IQODW</scope><scope>CGR</scope><scope>CUY</scope><scope>CVF</scope><scope>ECM</scope><scope>EIF</scope><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>K9.</scope><scope>NAPCQ</scope></search><sort><creationdate>20090901</creationdate><title>Evidence for an Interaction Between Familial Liability and Prenatal Exposure to Infection in the Causation of Schizophrenia</title><author>Clarke, Mary C. ; Tanskanen, Antti ; Huttunen, Matti ; Whittaker, John C. ; Cannon, Mary</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-a476t-3bdb3ae61abc698216ad51a57091cb83e3f10598a3dcdf56cfac411667be89a53</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2009</creationdate><topic>Adult</topic><topic>Adult and adolescent clinical studies</topic><topic>Biological and medical sciences</topic><topic>Cohort Studies</topic><topic>Confidence intervals</topic><topic>Cross-Sectional Studies</topic><topic>Denmark - epidemiology</topic><topic>E coli</topic><topic>Family - psychology</topic><topic>Female</topic><topic>Genetic Markers</topic><topic>Genetic Predisposition to Disease</topic><topic>Health risk assessment</topic><topic>Humans</topic><topic>Infection - epidemiology</topic><topic>Influenza</topic><topic>Male</topic><topic>Maternal Exposure - statistics &amp; numerical data</topic><topic>Medical sciences</topic><topic>Pregnancy</topic><topic>Pregnancy Complications, Infectious - epidemiology</topic><topic>Prenatal development</topic><topic>Prenatal exposure</topic><topic>Prenatal Exposure Delayed Effects - epidemiology</topic><topic>Prevalence</topic><topic>Psychiatry</topic><topic>Psychology. Psychoanalysis. Psychiatry</topic><topic>Psychopathology. Psychiatry</topic><topic>Psychoses</topic><topic>Pyelonephritis - epidemiology</topic><topic>Risk Factors</topic><topic>Schizophrenia</topic><topic>Schizophrenia - epidemiology</topic><topic>Schizophrenia - etiology</topic><topic>Schizophrenia - genetics</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Clarke, Mary C.</creatorcontrib><creatorcontrib>Tanskanen, Antti</creatorcontrib><creatorcontrib>Huttunen, Matti</creatorcontrib><creatorcontrib>Whittaker, John C.</creatorcontrib><creatorcontrib>Cannon, Mary</creatorcontrib><collection>Pascal-Francis</collection><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>ProQuest Health &amp; Medical Complete (Alumni)</collection><collection>Nursing &amp; Allied Health Premium</collection><jtitle>The American journal of psychiatry</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Clarke, Mary C.</au><au>Tanskanen, Antti</au><au>Huttunen, Matti</au><au>Whittaker, John C.</au><au>Cannon, Mary</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Evidence for an Interaction Between Familial Liability and Prenatal Exposure to Infection in the Causation of Schizophrenia</atitle><jtitle>The American journal of psychiatry</jtitle><addtitle>Am J Psychiatry</addtitle><date>2009-09-01</date><risdate>2009</risdate><volume>166</volume><issue>9</issue><spage>1025</spage><epage>1030</epage><pages>1025-1030</pages><issn>0002-953X</issn><eissn>1535-7228</eissn><coden>AJPSAO</coden><abstract>Objective: The authors sought to determine whether prenatal exposure to infection and a positive family history of psychotic disorders interact synergistically to increase the risk of later developing schizophrenia. Method: The authors linked two national registers, the Medical Birth Register and the Finnish Population Register, to identify all women in Helsinki who received hospital treatment during pregnancy for an upper urinary tract infection (N=9,596) between 1947 and 1990. The Finnish Hospital Discharge Register was used to ascertain psychiatric outcomes in adulthood of offspring exposed to infection prenatally. Family history of psychotic disorders was determined by linking the Hospital Discharge Register and the Population Register. The authors used an additive statistical interaction model to calculate the amount of biological synergism between positive family history and prenatal exposure to infection. Results: Prenatal exposure to infection did not significantly increase the risk of schizophrenia. However, the effect of prenatal exposure to pyelonephritis was five times greater in those who had a family history of psychosis compared to those who did not. The synergy analysis suggested that an estimated 38%-46% of the offspring who developed schizophrenia and had both prenatal exposure to infection and a positive family history of psychotic disorders did so as a result of the synergistic action of both risk factors. Conclusions: These findings support a mechanism of gene-environment interaction in the causation of schizophrenia.</abstract><cop>Arlington, VA</cop><pub>American Psychiatric Association</pub><pmid>19487391</pmid><doi>10.1176/appi.ajp.2009.08010031</doi><tpages>6</tpages></addata></record>
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source MEDLINE; American Psychiatric Publishing Journals (1997-Present); Elektronische Zeitschriftenbibliothek - Frei zugängliche E-Journals
subjects Adult
Adult and adolescent clinical studies
Biological and medical sciences
Cohort Studies
Confidence intervals
Cross-Sectional Studies
Denmark - epidemiology
E coli
Family - psychology
Female
Genetic Markers
Genetic Predisposition to Disease
Health risk assessment
Humans
Infection - epidemiology
Influenza
Male
Maternal Exposure - statistics & numerical data
Medical sciences
Pregnancy
Pregnancy Complications, Infectious - epidemiology
Prenatal development
Prenatal exposure
Prenatal Exposure Delayed Effects - epidemiology
Prevalence
Psychiatry
Psychology. Psychoanalysis. Psychiatry
Psychopathology. Psychiatry
Psychoses
Pyelonephritis - epidemiology
Risk Factors
Schizophrenia
Schizophrenia - epidemiology
Schizophrenia - etiology
Schizophrenia - genetics
title Evidence for an Interaction Between Familial Liability and Prenatal Exposure to Infection in the Causation of Schizophrenia
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