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Search: id:"swepub:oai:lup.lub.lu.se:85a3970c-8fe0-4d31-8b5d-2ee6b2130ceb" > Refining the Defini...

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LIBRIS Formathandbok  (Information om MARC21)
FältnamnIndikatorerMetadata
00004323naa a2200445 4500
001oai:lup.lub.lu.se:85a3970c-8fe0-4d31-8b5d-2ee6b2130ceb
003SwePub
008231206s2023 | |||||||||||000 ||eng|
024a https://lup.lub.lu.se/record/85a3970c-8fe0-4d31-8b5d-2ee6b2130ceb2 URI
024a https://doi.org/10.2337/dc22-19602 DOI
040 a (SwePub)lu
041 a engb eng
042 9 SwePub
072 7a art2 swepub-publicationtype
072 7a ref2 swepub-contenttype
100a Frohnert, Brigitte I.u University of Colorado4 aut
2451 0a Refining the Definition of Stage 1 Type 1 Diabetes : An Ontology-Driven Analysis of the Heterogeneity of Multiple Islet Autoimmunity
264 c 2023-03-02
264 1b American Diabetes Association,c 2023
300 a 9 s.
520 a OBJECTIVE To estimate the risk of progression to stage 3 type 1 diabetes based on varying definitions of multiple islet autoantibody positivity (mIA). RESEARCH DESIGN AND METHODS Type 1 Diabetes Intelligence (T1DI) is a combined prospective data set of children from Finland, Germany, Sweden, and the U.S. who have an increased genetic risk for type 1 diabetes. Analysis included 16,709 infants-toddlers enrolled by age 2.5 years and comparison between groups using Kaplan-Meier survival analysis. RESULTS Of 865 (5%) children with mIA, 537 (62%) progressed to type 1 diabetes. The 15-year cumulative incidence of diabetes varied from the most stringent definition (mIA/ Persistent/2: two or more islet autoantibodies positive at the same visit with two or more antibodies persistent at next visit; 88% [95% CI 85–92%]) to the least stringent (mIA/Any: positivity for two islet autoantibodies without co-occurring positivity or persistence; 18% [5–40%]). Progression in mIA/Persistent/2 was significantly higher than all other groups (P < 0.0001). Intermediate stringency definitions showed intermediate risk and were significantly different than mIA/Any (P < 0.05); however, differences waned over the 2-year follow-up among those who did not subsequently reach higher stringency. Among mIA/Persistent/2 individuals with three autoantibodies, loss of one autoantibody by the 2-year follow-up was associated with accelerated progression. Age was significantly associated with time from seroconversion to mIA/ Persistent/2 status and mIA to stage 3 type 1 diabetes. CONCLUSIONS The 15-year risk of progression to type 1 diabetes risk varies markedly from 18 to 88% based on the stringency of mIA definition. While initial categorization identifies highest-risk individuals, short-term follow-up over 2 years may help stratify evolving risk, especially for those with less stringent definitions of mIA.
650 7a MEDICIN OCH HÄLSOVETENSKAPx Klinisk medicinx Endokrinologi och diabetes0 (SwePub)302052 hsv//swe
650 7a MEDICAL AND HEALTH SCIENCESx Clinical Medicinex Endocrinology and Diabetes0 (SwePub)302052 hsv//eng
700a Ghalwash, Mohamedu Ain Shams University,IBM Thomas J. Watson Research Center4 aut
700a Li, Yingu IBM Thomas J. Watson Research Center4 aut
700a Ng, Kenneyu IBM Thomas J. Watson Research Center4 aut
700a Dunne, Jessica L.u Juvenile Diabetes Research Foundation4 aut
700a Lundgren, Markusu Lund University,Lunds universitet,Pediatrisk endokrinologi,Forskargrupper vid Lunds universitet,Paediatric Endocrinology,Lund University Research Groups,Central Hospital Kristianstad4 aut0 (Swepub:lu)med-mn2
700a Hagopian, Williamu Pacific Northwest Research Institute4 aut
700a Lou, Oliviau Juvenile Diabetes Research Foundation4 aut
700a Winkler, Christianeu Helmholtz Zentrum München4 aut
700a Toppari, Jormau Turku University Hospital4 aut
700a Veijola, Riittau University of Oulu4 aut
700a Anand, Vibhau IBM Thomas J. Watson Research Center4 aut
710a University of Coloradob Ain Shams University4 org
710a T1DI Study Group
773t Diabetes Cared : American Diabetes Associationg 46:10, s. 1753-1761q 46:10<1753-1761x 0149-5992x 1935-5548
856u http://dx.doi.org/10.2337/dc22-1960x freey FULLTEXT
8564 8u https://lup.lub.lu.se/record/85a3970c-8fe0-4d31-8b5d-2ee6b2130ceb
8564 8u https://doi.org/10.2337/dc22-1960

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