Finnish Prenatal Study of Autism and Autism Spectrum Disorders (FIPS-A): Overview and Design / Katja M. LAMPI in Journal of Autism and Developmental Disorders, 41-8 (August 2011)  

Public ISBD [article]  inJournal of Autism and Developmental Disorders > 41-8 (August 2011) . - p.1090-1096 Titre : Finnish Prenatal Study of Autism and Autism Spectrum Disorders (FIPS-A): Overview and Design Type de document : Texte imprimé et/ou numérique Auteurs : Katja M. LAMPI, Auteur ; P. Nina BANERJEE, Auteur ; Mika GISSLER, Auteur ; Susanna HINKKA-YLI-SALOMAKI, Auteur ; Jukka HUTTUNEN, Auteur ; Ulla KULMALA, Auteur ; Jarna LINDROOS, Auteur ; Solja NIEMELA, Auteur ; Maria RIHKO, Auteur ; Terja RISTKARI, Auteur ; Kristiina SAANAKORPI, Auteur ; Tanja SARLIN, Auteur ; Lauri SILLANMAKI, Auteur ; Ian W. MCKEAGUE, Auteur ; Heljä-Marja SURCEL, Auteur ; Hans HELENIUS, Auteur ; Alan S. BROWN, Auteur ; Andre SOURANDER, Auteur Année de publication : 2011 Article en page(s) : p.1090-1096 Langues : Anglais (eng) Mots-clés : Autism  Register study  Prenatal risk factors  Epidemiology  Methodology Index. décimale : PER Périodiques Résumé : This article presents an overview of the Finnish Prenatal Study of Autism and Autism Spectrum Disorders (FIPS-A), a new study designed to examine the relationship between prenatal serologic factors, mediating and moderating developmental antecedents, and risk of autism spectrum disorders (ASD). The FIPS-A is based on register linkages between births from 1987 to 2005 ascertained from the Finnish Medical Birth Register (FMBR) and other national registers on treatment for this group of disorders. All subjects were members of the Finnish Maternity Cohort (FMC), which consists of virtually all births in Finland from 1983 to the present, and which includes archived maternal serum samples. This study also capitalizes on other registry information, such as systematically collected data on pregnancy, prenatal and neonatal complications and manual data collection from well-child clinics providing developmental data from birth to the age of 7 years. In this paper, we describe the methods used in the FIPS-A study, including a description of the national registers, available data and case ascertainment procedures. Finally, we discuss implications of the data for future work on uncovering putative aetiologies of ASD and key strengths and limitations of the design. En ligne : http://dx.doi.org/10.1007/s10803-010-1132-6 Permalink : https://www.cra-rhone-alpes.org/cid/opac_css/index.php?lvl=notice_display&id=132 [article] Finnish Prenatal Study of Autism and Autism Spectrum Disorders (FIPS-A): Overview and Design [Texte imprimé et/ou numérique] / Katja M. LAMPI, Auteur ; P. Nina BANERJEE, Auteur ; Mika GISSLER, Auteur ; Susanna HINKKA-YLI-SALOMAKI, Auteur ; Jukka HUTTUNEN, Auteur ; Ulla KULMALA, Auteur ; Jarna LINDROOS, Auteur ; Solja NIEMELA, Auteur ; Maria RIHKO, Auteur ; Terja RISTKARI, Auteur ; Kristiina SAANAKORPI, Auteur ; Tanja SARLIN, Auteur ; Lauri SILLANMAKI, Auteur ; Ian W. MCKEAGUE, Auteur ; Heljä-Marja SURCEL, Auteur ; Hans HELENIUS, Auteur ; Alan S. BROWN, Auteur ; Andre SOURANDER, Auteur . - 2011 . - p.1090-1096. Langues : Anglais (eng) in Journal of Autism and Developmental Disorders > 41-8 (August 2011) . - p.1090-1096 Mots-clés : Autism  Register study  Prenatal risk factors  Epidemiology  Methodology Index. décimale : PER Périodiques Résumé : This article presents an overview of the Finnish Prenatal Study of Autism and Autism Spectrum Disorders (FIPS-A), a new study designed to examine the relationship between prenatal serologic factors, mediating and moderating developmental antecedents, and risk of autism spectrum disorders (ASD). The FIPS-A is based on register linkages between births from 1987 to 2005 ascertained from the Finnish Medical Birth Register (FMBR) and other national registers on treatment for this group of disorders. All subjects were members of the Finnish Maternity Cohort (FMC), which consists of virtually all births in Finland from 1983 to the present, and which includes archived maternal serum samples. This study also capitalizes on other registry information, such as systematically collected data on pregnancy, prenatal and neonatal complications and manual data collection from well-child clinics providing developmental data from birth to the age of 7 years. In this paper, we describe the methods used in the FIPS-A study, including a description of the national registers, available data and case ascertainment procedures. Finally, we discuss implications of the data for future work on uncovering putative aetiologies of ASD and key strengths and limitations of the design. En ligne : http://dx.doi.org/10.1007/s10803-010-1132-6 Permalink : https://www.cra-rhone-alpes.org/cid/opac_css/index.php?lvl=notice_display&id=132

Parental Age and Risk of Autism Spectrum Disorders in a Finnish National Birth Cohort / Katja M. LAMPI in Journal of Autism and Developmental Disorders, 43-11 (November 2013)  

Public ISBD [article]  inJournal of Autism and Developmental Disorders > 43-11 (November 2013) . - p.2526-2535 Titre : Parental Age and Risk of Autism Spectrum Disorders in a Finnish National Birth Cohort Type de document : Texte imprimé et/ou numérique Auteurs : Katja M. LAMPI, Auteur ; Susanna HINKKA-YLI-SALOMAKI, Auteur ; Venla LEHTI, Auteur ; Hans HELENIUS, Auteur ; Mika GISSLER, Auteur ; Alan S. BROWN, Auteur ; Andre SOURANDER, Auteur Article en page(s) : p.2526-2535 Langues : Anglais (eng) Mots-clés : Epidemiology  Autism spectrum disorders  Parental age Index. décimale : PER Périodiques Résumé : Aim of the study was to examine the associations between parental age and autism spectrum disorders (ASD). Data were based on the FIPS-A (Finnish Prenatal Study of Autism and Autism Spectrum Disorders), a case-control study with a total of 4,713 cases with childhood autism (n = 1,132), Asperger’s syndrome (n = 1,785) or other pervasive developmental disorder (PDD) (n = 1,796), which were ascertained from the Finnish Hospital Discharge Register. Controls were selected from the Finnish Medical Birth Register. Conditional logistic regression models were used for statistical analyses. Advanced paternal age (35–49 years) was associated with childhood autism in offspring, whereas advanced maternal age was associated with both Asperger’s syndrome and PDD in offspring (35 years or more and 40 years or more, respectively). Teenage motherhood (19 years or less) was associated with PDD in offspring. The main finding was that maternal and paternal ages were differentially associated with ASD subtypes. In addition to advanced parental age, teenage pregnancy seems to incur a risk for PDD in offspring. En ligne : http://dx.doi.org/10.1007/s10803-013-1801-3 Permalink : https://www.cra-rhone-alpes.org/cid/opac_css/index.php?lvl=notice_display&id=217 [article] Parental Age and Risk of Autism Spectrum Disorders in a Finnish National Birth Cohort [Texte imprimé et/ou numérique] / Katja M. LAMPI, Auteur ; Susanna HINKKA-YLI-SALOMAKI, Auteur ; Venla LEHTI, Auteur ; Hans HELENIUS, Auteur ; Mika GISSLER, Auteur ; Alan S. BROWN, Auteur ; Andre SOURANDER, Auteur . - p.2526-2535. Langues : Anglais (eng) in Journal of Autism and Developmental Disorders > 43-11 (November 2013) . - p.2526-2535 Mots-clés : Epidemiology  Autism spectrum disorders  Parental age Index. décimale : PER Périodiques Résumé : Aim of the study was to examine the associations between parental age and autism spectrum disorders (ASD). Data were based on the FIPS-A (Finnish Prenatal Study of Autism and Autism Spectrum Disorders), a case-control study with a total of 4,713 cases with childhood autism (n = 1,132), Asperger’s syndrome (n = 1,785) or other pervasive developmental disorder (PDD) (n = 1,796), which were ascertained from the Finnish Hospital Discharge Register. Controls were selected from the Finnish Medical Birth Register. Conditional logistic regression models were used for statistical analyses. Advanced paternal age (35–49 years) was associated with childhood autism in offspring, whereas advanced maternal age was associated with both Asperger’s syndrome and PDD in offspring (35 years or more and 40 years or more, respectively). Teenage motherhood (19 years or less) was associated with PDD in offspring. The main finding was that maternal and paternal ages were differentially associated with ASD subtypes. In addition to advanced parental age, teenage pregnancy seems to incur a risk for PDD in offspring. En ligne : http://dx.doi.org/10.1007/s10803-013-1801-3 Permalink : https://www.cra-rhone-alpes.org/cid/opac_css/index.php?lvl=notice_display&id=217

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