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Sökning: WFRF:(Vaarala Outi) > (2005-2009) > Progression to type...

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FältnamnIndikatorerMetadata
00005091naa a2200385 4500
001oai:DiVA.org:liu-42864
003SwePub
008091010s2008 | |||||||||||000 ||eng|
009oai:DiVA.org:oru-110291
024a https://urn.kb.se/resolve?urn=urn:nbn:se:liu:diva-428642 URI
024a https://doi.org/10.1111/j.1399-5448.2008.00369.x2 DOI
024a https://urn.kb.se/resolve?urn=urn:nbn:se:oru:diva-1102912 URI
040 a (SwePub)liud (SwePub)oru
041 a engb eng
042 9 SwePub
072 7a ref2 swepub-contenttype
072 7a art2 swepub-publicationtype
100a Gullstrand, Camilla,d 1977-u Linköpings universitet,Pediatrik,Hälsouniversitetet,Division of Pediatrics and Diabetes Research Centre, Department of Molecular and Clinical Medicine, Faculty of Health Sciences, Linköping University, Linköping, Sweden4 aut0 (Swepub:liu)camgu49
2451 0a Progression to type 1 diabetes and autoantibody positivity in relation to HLA-risk genotypes in children participating in the ABIS study
264 1b Hindawi Limited,c 2008
338 a print2 rdacarrier
520 a Background: Autoantibodies against beta-cell antigens together with human leukocyte antigen (HLA)-risk genotypes are used as predictive markers for type 1 diabetes (T1D). In this study, we have investigated the role of HLA-risk and -protective genotypes for development of beta-cell autoantibodies and progression to T1D in healthy children. Methods: T1D-related HLA genotypes and autoantibodies against glutamic acid decarboxylase [glutamic acid decarboxylase antibodies (GADA)] and islet antigen-2 (IA-2A) were studied at 1, 2.5 and 5 yr of age in unselected healthy children and children with T1D participating in the All Babies In Southeast Sweden (ABIS) study. Results: GADA or IA-2A positivity at 5 yr of age was associated with DR4-DQ8 haplotype and DR3-DQ2/DR4-DQ8 genotype. By the age of 6-7 yr, we identified 32 children with T1D among the 17 055 participants in the ABIS study. Eight of 2329 (0.3%) non-diabetic children had permanent autoantibodies, and 143 of 2329 (6%) children had transient autoantibodies. HLA-risk genotypes associated with T1D, whereas protective genotypes were seldom found in children with T1D. Children with permanent autoantibodies had more often risk-associated DR4-DQ8 haplotype than autoantibody-negative children. No associations with HLA-risk or -protective genotypes were found for transient autoantibodies. Conclusions: The strong relation between HLA-risk alleles and T1D once again confirmed that HLA-risk genotypes play an important role for development of T1D. However, HLA genotypes seem not to explain induction of autoantibodies, especially transient autoantibodies, in the general population, emphasizing the role of environmental factors in the initiation of autoimmunity. It seems that HLA-risk genotypes are responsible for maturation of the permanent autoantibody response. © 2008 The Authors Journal compilation © 2008 Blackwell Munksgaard.
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
653 a MEDICINE
653 a MEDICIN
700a Wahlberg Topp, Jeanette,d 1969-u Östergötlands Läns Landsting,Linköpings universitet,Internmedicin,Hälsouniversitetet,Endokrin- och magtarmmedicinska kliniken US,Division of Pediatrics and Diabetes Research Centre, Department of Molecular and Clinical Medicine, Faculty of Health Sciences, Linköping University, Linköping, Sweden; Division of Internal Medicine, Department of Medicine and Care, Faculty of Health Sciences, Linköping University, Linköping, Sweden4 aut0 (Swepub:oru)jewg
700a Ilonen, Jormau Dept of Microbiology Kuopio, Finland,Linköping University, Linköping, Sweden; Department of Clinical Microbiology, University of Kuopio, Kuopio, Finland; Immunogenetics Laboratory, University of Turku, Turku, Finland4 aut
700a Vaarala, Outi,d 1962-u Linköpings universitet,Pediatrik,Hälsouniversitetet,Division of Pediatrics and Diabetes Research Centre, Department of Molecular and Clinical Medicine, Faculty of Health Sciences, Linköping University, Linköping, Sweden4 aut0 (Swepub:liu)outva41
700a Ludvigsson, Johnny,d 1943-u Östergötlands Läns Landsting,Linköpings universitet,Hälsouniversitetet,Pediatrik,Barn- och ungdomskliniken i Linköping,Division of Pediatrics and Diabetes Research Centre, Department of Molecular and Clinical Medicine, Faculty of Health Sciences, Linköping University, Linköping, Sweden4 aut0 (Swepub:liu)johlu29
710a Linköpings universitetb Pediatrik4 org
773t Pediatric Diabetesd : Hindawi Limitedg 9:3 PART 1, s. 182-190q 9:3 PART 1<182-190x 1399-543Xx 1399-5448
8564 8u https://urn.kb.se/resolve?urn=urn:nbn:se:liu:diva-42864
8564 8u https://doi.org/10.1111/j.1399-5448.2008.00369.x
8564 8u https://urn.kb.se/resolve?urn=urn:nbn:se:oru:diva-110291

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