Literature DB >> 21565792

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

Peter R Baker1, 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.   

Abstract

CONTEXT: Autoimmune Addison's disease (AD) is the major cause of primary adrenal failure in developed nations. Autoantibodies to 21-hydroxylase (21OH-AA) are associated with increased risk of progression to AD. Highest genetic risk is associated with the Major Histocompatibility region (MHC), specifically human leukocyte antigen (HLA)-DR3 haplotypes (containing HLA-B8) and HLA-DR4.
OBJECTIVE: The objective of the study was the further characterization of AD risk associated with MHC alleles. DESIGN, SETTING, AND PARTICIPANTS: MHC genotypes were determined for HLA-DRB1, DQA1, DQB1, MICA, HLA-B, and HLA-A in 168 total individuals with 21OH-AA (85 with AD at referral and 83 with positive 21OH-AA but without AD at referral). MAIN OUTCOME MEASURE(S): Genotype was evaluated in 21OH-AA-positive individuals. Outcomes were compared with general population controls and type 1 diabetes patients.
RESULTS: In HLA-DR4+ individuals, HLA-B15 was found in only one of 55 (2%) with AD vs. 24 of 63 (40%) 21OH-AA-positive nonprogressors (P = 2 × 10(-7)) and 518 of 1558 (33%) HLA-DR4 patients with type 1 diabetes (P = 1 × 10(-8)). On prospective follow-up, none of the HLA-B15-positive, 21-hydroxylase-positive individuals progressed to AD vs. 25% non-HLA-B15 autoantibody-positive individuals by life table analysis (P = 0.03). Single nucleotide polymorphism analysis revealed the HLA-DR/DQ region associated with risk and HLA-B15 were separated by multiple intervening single-nucleotide polymorphism haplotypes.
CONCLUSIONS: HLA-B15 is not associated with protection from 21OH-AA formation but is associated with protection from progression to AD in 21OH-AA-positive individuals. To our knowledge, this is one of the most dramatic examples of genetic disease suppression in individuals who already have developed autoantibodies and of novel dominant suppression of an autoimmune disease by a class I HLA allele.

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Year:  2011        PMID: 21565792      PMCID: PMC3135206          DOI: 10.1210/jc.2010-2964

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


  40 in total

1.  Extreme genetic risk for type 1A diabetes.

Authors:  Theresa A Aly; Akane Ide; Mohamed M Jahromi; Jennifer M Barker; Maria S Fernando; Sunanda R Babu; Liping Yu; Dongmei Miao; Henry A Erlich; Pamela R Fain; Katherine J Barriga; Jill M Norris; Marian J Rewers; George S Eisenbarth
Journal:  Proc Natl Acad Sci U S A       Date:  2006-09-11       Impact factor: 11.205

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.  Haplotype analysis discriminates genetic risk for DR3-associated endocrine autoimmunity and helps define extreme risk for Addison's disease.

Authors:  Peter R Baker; Erin E Baschal; Pam R Fain; Taylor M Triolo; Priyaanka Nanduri; 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:  2010-07-14       Impact factor: 5.958

4.  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

5.  Italian addison network study: update of diagnostic criteria for the etiological classification of primary adrenal insufficiency.

Authors:  Alberto Falorni; Stefano Laureti; Annamaria De Bellis; Renato Zanchetta; Claudio Tiberti; Giorgio Arnaldi; Vittorio Bini; Paolo Beck-Peccoz; Antonio Bizzarro; Francesco Dotta; Franco Mantero; Antonio Bellastella; Corrado Betterle; Fausto Santeusanio
Journal:  J Clin Endocrinol Metab       Date:  2004-04       Impact factor: 5.958

6.  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

Review 7.  Two types of autoimmune Addison's disease associated with different polyglandular autoimmune (PGA) syndromes.

Authors:  M Neufeld; N K Maclaren; R M Blizzard
Journal:  Medicine (Baltimore)       Date:  1981-09       Impact factor: 1.889

8.  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

9.  Anti-interferon autoantibodies in autoimmune polyendocrinopathy syndrome type 1.

Authors:  Anthony Meager; Kumuthini Visvalingam; Pärt Peterson; Kaidi Möll; Astrid Murumägi; Kai Krohn; Petra Eskelin; Jaakko Perheentupa; Eystein Husebye; Yoshihisa Kadota; Nick Willcox
Journal:  PLoS Med       Date:  2006-07       Impact factor: 11.069

10.  Localization of type 1 diabetes susceptibility to the MHC class I genes HLA-B and HLA-A.

Authors:  Sergey Nejentsev; Joanna M M Howson; Neil M Walker; Jeffrey Szeszko; Sarah F Field; Helen E Stevens; Pamela Reynolds; Matthew Hardy; Erna King; Jennifer Masters; John Hulme; Lisa M Maier; Deborah Smyth; Rebecca Bailey; Jason D Cooper; Gloria Ribas; R Duncan Campbell; David G Clayton; John A Todd
Journal:  Nature       Date:  2007-11-14       Impact factor: 49.962

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  3 in total

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

Authors:  Peter Baker; Pam Fain; Heinrich Kahles; Liping Yu; John Hutton; Janet Wenzlau; Marian Rewers; Klaus Badenhoop; George Eisenbarth
Journal:  J Clin Endocrinol Metab       Date:  2012-06-20       Impact factor: 5.958

2.  Predicting the onset of Addison's disease: ACTH, renin, cortisol and 21-hydroxylase autoantibodies.

Authors:  Peter R Baker; Priyaanka Nanduri; Peter A Gottlieb; Liping Yu; Georgeanna J Klingensmith; George S Eisenbarth; Jennifer M Barker
Journal:  Clin Endocrinol (Oxf)       Date:  2012-05       Impact factor: 3.478

3.  Autoantibodies against Cytochrome P450 Side-Chain Cleavage Enzyme in Dogs (Canis lupus familiaris) Affected with Hypoadrenocorticism (Addison's Disease).

Authors:  Alisdair M Boag; Michael R Christie; Kerry A McLaughlin; Harriet M Syme; Peter Graham; Brian Catchpole
Journal:  PLoS One       Date:  2015-11-30       Impact factor: 3.240

  3 in total

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