Literature DB >> 22723331

Genetic determinants of 21-hydroxylase autoantibodies amongst patients of the Type 1 Diabetes Genetics Consortium.

Peter Baker1, Pam Fain, Heinrich Kahles, Liping Yu, John Hutton, Janet Wenzlau, Marian Rewers, Klaus Badenhoop, George Eisenbarth.   

Abstract

BACKGROUND: Autoantibodies to 21-hydroxylase (21OH-AA) precede the onset of autoimmune Addison's disease (AD) and are found in 1.5% of individuals with type 1 diabetes mellitus (T1DM). The greatest genetic risk for both disorders is found in the major histocompatibility complex (MHC), suggesting a common pathophysiology between AD and T1DM. Screening for 21OH-AA in newly diagnosed T1DM patients is a valuable prognostic tool, made stronger when MHC genotype is considered.
METHODS: The Type 1 Diabetes Genetics Consortium has collected genotype data in T1DM subjects with tissue-specific autoantibody typing. Genotype and phenotype data in individuals positive and negative for 21OH-AA are compared.
RESULTS: Major genetic risk for 21OH-AA is in the MHC haplotypes DRB1*04-DQB1*0302 (primarily DRB1*0404) and DRB1*0301-DQB1*0201. Protective effects in class II MHC haplotypes DRB1*0101-DQB1*0501 and DRB1*0701-DQB1*0202 also were detected. There is no difference in the presence of HLA-B15 and little difference in the presence of HLA-B8 (after class II effects are accounted for) in T1DM patients with 21OH-AA compared with known associations (HLA-B8 positive and HLA-B15 negative) in AD.
CONCLUSIONS: In 21OH-AA(+) subjects, genetic risk is found mainly in MHC class II haplotypes DR3 and DR4 but not class I alleles (HLA-B8 or HLA-B15). This suggests a difference between autoantibody formation (class II dependent) and progression to overt disease (class I dependent) in AD.

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Year:  2012        PMID: 22723331      PMCID: PMC3410257          DOI: 10.1210/jc.2011-2824

Source DB:  PubMed          Journal:  J Clin Endocrinol Metab        ISSN: 0021-972X            Impact factor:   5.958


  17 in total

1.  Dominant suppression of Addison's disease associated with HLA-B15.

Authors:  Peter R Baker; Erin E Baschal; Pam R Fain; Priyaanka Nanduri; Taylor M Triolo; Janet C Siebert; Taylor K Armstrong; Sunanda R Babu; Marian J Rewers; Peter A Gottlieb; Jennifer M Barker; George S Eisenbarth
Journal:  J Clin Endocrinol Metab       Date:  2011-05-11       Impact factor: 5.958

2.  Microsatellite polymorphism of the MHC class I chain-related (MIC-A and MIC-B) genes marks the risk for autoimmune Addison's disease.

Authors:  G Gambelunghe; A Falorni; M Ghaderi; S Laureti; C Tortoioli; F Santeusanio; P Brunetti; C B Sanjeevi
Journal:  J Clin Endocrinol Metab       Date:  1999-10       Impact factor: 5.958

3.  An autoimmune disease, APECED, caused by mutations in a novel gene featuring two PHD-type zinc-finger domains.

Authors: 
Journal:  Nat Genet       Date:  1997-12       Impact factor: 38.330

4.  Endocrine and immunogenetic testing in individuals with type 1 diabetes and 21-hydroxylase autoantibodies: Addison's disease in a high-risk population.

Authors:  Jennifer M Barker; Akane Ide; Corey Hostetler; Liping Yu; Dongmei Miao; Pamela R Fain; George S Eisenbarth; Peter A Gottlieb
Journal:  J Clin Endocrinol Metab       Date:  2004-10-13       Impact factor: 5.958

5.  Newborn screening for HLA markers associated with IDDM: diabetes autoimmunity study in the young (DAISY).

Authors:  M Rewers; T L Bugawan; J M Norris; A Blair; B Beaty; M Hoffman; R S McDuffie; R F Hamman; G Klingensmith; G S Eisenbarth; H A Erlich
Journal:  Diabetologia       Date:  1996-07       Impact factor: 10.122

6.  Preliminary evidence that an endogenous retroviral long-terminal repeat (LTR13) at the HLA-DQB1 gene locus confers susceptibility to Addison's disease.

Authors:  Michael A Pani; Christian Seidl; Katrin Bieda; Jochen Seissler; Maren Krause; Erhard Seifried; Klaus-H Usadel; Klaus Badenhoop
Journal:  Clin Endocrinol (Oxf)       Date:  2002-06       Impact factor: 3.478

7.  DRB1*04 and DQ alleles: expression of 21-hydroxylase autoantibodies and risk of progression to Addison's disease.

Authors:  L Yu; K W Brewer; S Gates; A Wu; T Wang; S R Babu; P A Gottlieb; B M Freed; J Noble; H A Erlich; M J Rewers; G S Eisenbarth
Journal:  J Clin Endocrinol Metab       Date:  1999-01       Impact factor: 5.958

8.  Susceptibility and resistance alleles of human leukocyte antigen (HLA) DQA1 and HLA DQB1 are shared in endocrine autoimmune disease.

Authors:  K Badenhoop; P G Walfish; H Rau; S Fischer; A Nicolay; U Bogner; H Schleusener; K H Usadel
Journal:  J Clin Endocrinol Metab       Date:  1995-07       Impact factor: 5.958

9.  High diagnostic accuracy for idiopathic Addison's disease with a sensitive radiobinding assay for autoantibodies against recombinant human 21-hydroxylase.

Authors:  A Falorni; A Nikoshkov; S Laureti; E Grenbäck; A L Hulting; G Casucci; F Santeusanio; P Brunetti; H Luthman; A Lernmark
Journal:  J Clin Endocrinol Metab       Date:  1995-09       Impact factor: 5.958

10.  Analysis of extended human leukocyte antigen haplotype association with Addison's disease in three populations.

Authors:  Z Gombos; R Hermann; M Kiviniemi; S Nejentsev; K Reimand; V Fadeyev; P Peterson; R Uibo; J Ilonen
Journal:  Eur J Endocrinol       Date:  2007-12       Impact factor: 6.664

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  1 in total

1.  Effects of dextrose and lipopolysaccharide on the corrosion behavior of a Ti-6Al-4V alloy with a smooth surface or treated with double-acid-etching.

Authors:  Leonardo P Faverani; Wirley G Assunção; Paulo Sérgio P de Carvalho; Judy Chia-Chun Yuan; Cortino Sukotjo; Mathew T Mathew; Valentim A Barao
Journal:  PLoS One       Date:  2014-03-26       Impact factor: 3.240

  1 in total

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