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            <r:String xml:lang="sv">Omgivningsfaktorers betydelse för uppkomst av diabetes hos barn - TEDDY: uppföljningsstudie</r:String>
            <r:String xml:lang="en">The Environmental Determinants of Diabetes in the Young - TEDDY: follow up study</r:String>
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            <r:String xml:lang="sv">Omgivningsfaktorers betydelse för uppkomst av diabetes hos barn - TEDDY</r:String>
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            <a:FirstGiven>Åke</a:FirstGiven>
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        <r:String xml:lang="sv">DiabetesPrediktion i Skåne - DiPiS</r:String>
        <r:String xml:lang="en">Diabetes Prediction in Scania - DiPiS</r:String>
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          <r:String xml:lang="sv">Lunds universitet</r:String>
          <r:String xml:lang="en">Lund University</r:String>
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      <r:Publisher>
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          <r:String xml:lang="sv">Lunds universitet</r:String>
          <r:String xml:lang="en">Lund University</r:String>
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      <r:Content xml:lang="sv">DiabetesPrediktion i Skåne (DiPiS) syftar till att ta reda på varför barn får typ 1 diabetes. Genom att kunna förutsäga vilka barn som utvecklar diabetes är förhoppningen att i framtiden kunna förhindra att sjukdomen bryter ut. DiPiS genomfördes i två steg:

Steg 1. Undersökning av ärftlig risk för typ 1 diabetes hos alla nyfödda barn i Skåne. Detta steg pågick från september 2000 till september 2004.  I detta steg undersöktes nästan 36 000 barn. 
Steg 2. Uppföljning hos en grupp barn med ärftlig risk. Ungefär 5 000 barn följdes upp. Deltagarna i uppföljningsstudien lämnade blodprov en gång om året och fick även fylla i en enkät. Barn med flera antikroppar har en förhöjd risk att utveckla typ 1 diabetes och följdes därför med tätare intervall. Barnen följdes upp till och med 15 års ålder.

Syfte:

Att bestämma faktorer som kan förutsäga autoimmun (typ 1) diabetes hos barn.</r:Content>
      <r:Content xml:lang="en">Diabetes Prediction in Scania (DiPiS) aims to determine why children develop type 1 diabetes. By being able to predict which children are at risk of developing diabetes, the hope is to prevent the onset of the disease in the future. DiPiS was conducted in two stages:

Stage 1: Examination of the hereditary risk for type 1 diabetes in all newborns in Scania. This stage took place from September 2000 to September 2004. During this stage, almost 36,000 children were examined.

Stage 2: Follow-up of a group of children with hereditary risk. Approximately 5,000 children were followed. Participants in the follow-up study provided blood samples once a year and also completed a questionnaire. Children with multiple antibodies are at an increased risk of developing type 1 diabetes and were therefore monitored more frequently. The children were followed until the age of 15.

Objective:
To determine factors that can predict autoimmune (type 1) diabetes in children.</r:Content>
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