Millennium award recipient contribution. Identification of children with early onset and high incidence of anti-islet autoantibodies

A total of 21,000 general population newborns (NECs) and 693 young siblings-offspring of patients with type 1A diabetes (SOCs) were class II genotyped and 293 NECs and 72 SOCs with the high-risk genotype, DR3/4, DQB1*0302 have been prospectively evaluated. Seventeen individuals who converted to pers...

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Veröffentlicht in:Clinical immunology (Orlando, Fla.). - 1999. - 102(2002), 3 vom: 22. März, Seite 217-24
1. Verfasser: Robles, David T (VerfasserIn)
Weitere Verfasser: Eisenbarth, George S, Wang, Tianbao, Erlich, Henry A, Bugawan, Teodorica L, Babu, Sunanda R, Barriga, Kathy, Norris, Jill M, Hoffman, Michelle, Klingensmith, Georgeanna, Yu, Liping, Rewers, Marian, Diabetes Autoimmunity Study in the Young
Format: Aufsatz
Sprache:English
Veröffentlicht: 2002
Zugriff auf das übergeordnete Werk:Clinical immunology (Orlando, Fla.)
Schlagworte:Journal Article Research Support, Non-U.S. Gov't Research Support, U.S. Gov't, P.H.S. Autoantibodies HLA-A Antigens HLA-DQ Antigens HLA-DQ beta-Chains HLA-DQB1 antigen HLA-DR3 Antigen HLA-DR4 Antigen mehr... Histocompatibility Antigens Class I Histocompatibility Antigens Class II Insulin
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100 1 |a Robles, David T  |e verfasserin  |4 aut 
245 1 0 |a Millennium award recipient contribution. Identification of children with early onset and high incidence of anti-islet autoantibodies 
264 1 |c 2002 
336 |a Text  |b txt  |2 rdacontent 
337 |a ohne Hilfsmittel zu benutzen  |b n  |2 rdamedia 
338 |a Band  |b nc  |2 rdacarrier 
500 |a Date Completed 17.04.2002 
500 |a Date Revised 17.11.2011 
500 |a published: Print 
500 |a Citation Status MEDLINE 
520 |a A total of 21,000 general population newborns (NECs) and 693 young siblings-offspring of patients with type 1A diabetes (SOCs) were class II genotyped and 293 NECs and 72 SOCs with the high-risk genotype, DR3/4, DQB1*0302 have been prospectively evaluated. Seventeen individuals who converted to persistent autoantibody positivity and two autoantibody-negative control groups (35 SOCs and 24 NECs) were typed for HLA-A class I alleles. The A1, A2 genotype was significantly increased among the autoantibody-positive subjects (47%) compared to autoantibody-negative SOCs (14%, P = 0.01) and NECs (13%, P = 0.02). Life-table analysis of DR3/4, DQB1*0302 siblings revealed a risk of 75% for development of islet autoantibodies by the age of 2 years for those with A1, A2. The HLA-A2 phenotype frequency was increased among an independent DR3/4, DQB1*0302 young diabetes cohort (64% versus 33% for autoantibody-negative NECs). These results suggest that a high incidence and early appearance of islet autoantibodies for siblings of patients with type 1A diabetes are associated with DR3/4, DQB1*0302 and potentially increased with HLA-A genotype A1, A2 
650 4 |a Journal Article 
650 4 |a Research Support, Non-U.S. Gov't 
650 4 |a Research Support, U.S. Gov't, P.H.S. 
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650 7 |a HLA-A Antigens  |2 NLM 
650 7 |a HLA-DQ Antigens  |2 NLM 
650 7 |a HLA-DQ beta-Chains  |2 NLM 
650 7 |a HLA-DQB1 antigen  |2 NLM 
650 7 |a HLA-DR3 Antigen  |2 NLM 
650 7 |a HLA-DR4 Antigen  |2 NLM 
650 7 |a Histocompatibility Antigens Class I  |2 NLM 
650 7 |a Histocompatibility Antigens Class II  |2 NLM 
650 7 |a Insulin  |2 NLM 
700 1 |a Eisenbarth, George S  |e verfasserin  |4 aut 
700 1 |a Wang, Tianbao  |e verfasserin  |4 aut 
700 1 |a Erlich, Henry A  |e verfasserin  |4 aut 
700 1 |a Bugawan, Teodorica L  |e verfasserin  |4 aut 
700 1 |a Babu, Sunanda R  |e verfasserin  |4 aut 
700 1 |a Barriga, Kathy  |e verfasserin  |4 aut 
700 1 |a Norris, Jill M  |e verfasserin  |4 aut 
700 1 |a Hoffman, Michelle  |e verfasserin  |4 aut 
700 1 |a Klingensmith, Georgeanna  |e verfasserin  |4 aut 
700 1 |a Yu, Liping  |e verfasserin  |4 aut 
700 1 |a Rewers, Marian  |e verfasserin  |4 aut 
700 0 |a Diabetes Autoimmunity Study in the Young  |e verfasserin  |4 aut 
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