Læknablaðið : fylgirit - 01.08.2003, Blaðsíða 79

Læknablaðið : fylgirit - 01.08.2003, Blaðsíða 79
POSTERS / 27TH NORDIC PSYCHIATRIC CONGRESS I P - 73 Friday 15/8,14:00-15:00 The effects of influenza on risk of developing schizophrenia Haukur Freyr Gylfason MA, Faculty of Social Scicnce, University of Iceland, 101 Reykjavík, Iceland. Stefánsson B, Smári J, Tómasson H. haukurgy@hi.is Background: The first opportunity to study the effects of influenza on schizophrenia was after the influenza epidemic in 1918. That is because it was not until the late 18th century that Kraepelin de- scribed the symptoms of schizophrenia. In 1926 Menninger dis- covered that schizophrenia was the most frequent mental illness that followed the influenza epidemic eight years earlier, and by doing so started a debate that is yet to be decided. Method: Data from the Icelandic State Social Security Institute was used to test the hypothesis that exposure to influenza during the second trimester of pregnancy would increase the risk for adult schizophrenia. Participants in this study were almost the total popu- lation of Iceland, and all those who had been diagnosed with schizo- phrenia and received disabilities for the last half a century. Analysis of transition data was used to record the sequence of states that were occupied and the times at which movements between them occurred (not diagnosed with schizophrenia - diagnosed with schizophrenia). Results: The main results were that if there was an increased likeli- hood for maternal influenza infection in the second trimester then the child was at more risk of being diagnosed with schizophrenia later in life. Condusion: The research supports the hypothesis that maternal influenza during pregnancy is a risk factor for schizophrenia. P - 74 Friday 15/8,14:00-15:00 Parental age and risk for schizophrenia: A nested case- control study Mujella Byrne1, MSc, PhD, Esben Agerbo1, MSc, Henrik EwalcR, DMSc, William W. Eaton-\ PhD, Preben Bo Mortensen1, MD, DMSc. •National Centre for Register-Based Research, Aarhus University, Taasingegade 1, DK-8000 Aarhus C, Denmark, ^lnstitute for Basic Psychiatric Research, Psychiatric Hospital in Aarhus, Skovagervej 2, DK-8240 Risskov, Denmark, -^Department of Mental Hygiene, School of Hygiene and Public Health, Johns Hopkins University, 615 N. Wolfe Street, Baltimore, MD 21205, USA. We investigated the reported association between advanced pater- nal age and risk for schizophrenia. Unlike previous studies we in- vestigated whether this association could be explained by social factors or family history of psychiatric illness. A national population-based nested case-control study based on Danish longitudinal register data was conducted. The sample inclu- ded 7704 first admissions to or contacts with Danish psychiatric ser- vices between 1981 and 1998 with an ICD-8 (until end of December 1993) or ICD-10 (from January 1994) diagnosis of schizophrenia, and 192590 individually time-, age-, and sex- matched population controls, their parents and siblings. Paternal age was categorised into the following age groups: <20 years, 20-24 years, 25-29 years, 30-34 years, 35-39 years, 40-44 years, 45-49 years, 50-54 years, and >= 55 years. Maternal age was defined as: <20 years, 20-24 years, 25-29 years, 30-34 years, 35-39 years, 40- 44 years, and >= 45 years. The risk for schizophrenia associated with parental age was investigated by conditional logistic regression. Adjusting for socioeconomic and demographic factors and family psychiatric history, increased risk for schizophrenia was identified in those with paternal age >= 55 (Incidence Rate Ratio (IRR) 2.27; 95% CI 1.57-3.29). Significant sex interactions were ob- served. Sex specific analyses suggested that females were at higher risk from raised paternal age than males who were also at risk. Increased risk for schizophrenia was associated with advanced paternal age. The interactions between sex and age of the parent of origin suggests that de novo genetic mutations occurring on the X chromosome might be involved in the aetiology of schizophrenia in males and females of older parents. The study was funded by the Theodore and Vada Stanley Foun- dation and by NIMH Grant #MH53188. NCRR is funded by the Danish National Research Foundation. P - 75 Friday 15/8,14:00-15:00 Mortality in schizophrenia over the last 60 years in the township of Malmö Lise-Lotte Nilsson. PhD, BSc in Social Work, Department of Psychiatry, University Hospital of Malmö, Lund University, Sege Park 8 A, 205 02 Malmö, Svveden. Bcngt Lögdberg. lise-lotte.nilsson@swipnet.se The mortality and the standardized mortality ratio (SMR) for patients with the diagnosis of schizophrenia, and between 25-64 years of age, in the township of Malmö (population about 250 000) in Southern Sweden were studied from about 1935 until 2003, by analyses of patients’ records. Data will be presented from the time period 1940-2000. From about 1940-1960 most of the patients diagnosed with schizophrenia were living at mental hospital, and the mortality was similar to the general population, i.e. the standardized mortality ratio was about 1. Over the ensuing decades, the standardized mor- tality ratio increased about from 2 to 3 between 1960-1980, remained unchanged around 2 between 1980-1990, but then increased again from about 3 to 5 between 1990-2000, concomitant with the full sectorization and the final closure of the mental hospital. Analyses of relationships between trends in standardized morta- lity ratio and organizational changes in psychiatry as well as societal changes will be presented and discussed. P - 76 Friday 15/8,14:00-15:00 Schizoaffective disorders in Denmark 1970-2000 Thomas Munk Laursen, Researcher, MSc, National Centre for Register-based Research, Taasingegade I, 8000 Aarhus C, Denmark. Rodrigo Labouriau, Aksel Bertelsen, Rasmus Licht, Preben Bo Mortensen. tml@ncrr.dk Background: Schizoaffective disorder is related to both schizophre- nia and to affective disorders. To our knowledge, however, no population-based study has investigated the association between the risk of schizoaffective disorders and familial aggregation of schizophrenia and affective disorders. Læknablaðið / FYLGIRIT 48 2003/89 79
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