Clustering of autoimmune disease in parents of siblings from the Type 1 diabetes Warren repository

Diabetic Medicine

Volumn 21, Issue 4, 2004, Pages 358-362

  Tait, K F ^a   Marshall, T ^a   Berman, J ^a   Carr Smith, J ^a   Rowe, B ^b   Todd, J A ^c   Bain, S C ^a,b   Barnett, A H ^a,b   Gough, S C L ^a,b  

^a UNIVERSITY OF BIRMINGHAM   (United Kingdom)

^b BIRMINGHAM HEARTLANDS HOSPITAL   (United Kingdom)

^c UNIVERSITY OF CAMBRIDGE   (United Kingdom)

Author keywords

Autoimmune disease; Familial clustering; Type 1 diabetes; Warren repository

Indexed keywords

ADOLESCENT; ADULT; AGED; ARTICLE; AUTOIMMUNE DISEASE; CLINICAL FEATURE; FAMILY HISTORY; FEMALE; HUMAN; HYPOTHESIS; INSULIN DEPENDENT DIABETES MELLITUS; MAJOR CLINICAL STUDY; MALE; PARENT; PATHOGENESIS; PREVALENCE; RISK FACTOR; SIBLING; UNITED KINGDOM;

ADULT; AGED; ARTHRITIS, RHEUMATOID; AUTOIMMUNE DISEASES; CLUSTER ANALYSIS; DIABETES MELLITUS, TYPE 1; FATHERS; FEMALE; GREAT BRITAIN; HUMANS; MALE; MIDDLE AGED; MOTHERS; PARENTS; PREVALENCE; SEX DISTRIBUTION; SIBLINGS; THYROID DISEASES;

EID: 1842529365     PISSN: 07423071     EISSN: None     Source Type: Journal    
DOI: 10.1111/j.1464-5491.2004.01162.x     Document Type: Article

References (15)

1. Heward J, Gough SC. Genetic susceptibility to the development of autoimmune disease. Clin Sci (Colch) 1997; 93: 479-491.
2. Vyse TJ, Todd JA. Genetic analysis of autoimmune disease. Cell 1996; 85: 311-18.
3. Ebers GC, Sadovnick AD, Risch NJ. A genetic basis for familial aggregation in multiple sclerosis. Canadian Collaborative Study Group. Nature 1995; 377: 150-151.
4. Marrosu MG, Cocco E, Lai M, Spinicci G, Pischedda MP, Contu P. Patients with multiple sclerosis and risk of type 1 diabetes mellitus in Sardinia, Italy: a cohort study. Lancet 2002; 359: 1461-1465.
5. Payami H, Joe S, Thomson G. Autoimmune thyroid disease in type I diabetic families. Genet Epidemiol 1989; 6: 137-141.
6. Bain SC, Todd JA, Barnett AH. The British Diabetic Association -Warren repository. Autoimmunity 1990; 7: 83-85.
7. Tunbridge WM, Evered DC, Hall R, Appleton D, Brewis M, Clark F et al. The spectrum of thyroid disease in a community: the Whickham survey. Clin Endocrinol (Oxf) 1977; 7: 481-493.
8. Haines JL, Ter-Minassian M, Bazyk A, Gusella JF, Kim DJ, Terwedow H et al. A complete genomic screen for multiple sclerosis underscores a role for the major histocompatability complex. The Multiple Sclerosis Genetics Group. Nat Genet 1996; 13: 469-471.
9. Gillett PM, Gillett HR, Israel DM, Metzger DL, Stewart L, Chanoine JP et al. High prevalence of celiac disease in patients with type 1 diabetes detected by antibodies to endomysium and tissue transglutaminase. Can J Gastroenterol 2001; 15: 297-301.
10. Brown MA, Pile KD, Kennedy LG, Campbell D, Andrew L, March R et al. A genome-wide screen for susceptibility loci in ankylosing spondylitis. Arthritis Rheum 1998; 41: 588-595.
11. Bjoro T, Holmen J, Kruger O, Midthjell K, Hunstad K, Schreiner T et al. Prevalence of thyroid disease, thyroid dysfunction and thyroid peroxidase antibodies in a large, unselected population. The Health Study Nord-Trondelag (HUNT). Eur J Endocrinol 2000; 143: 639-647.
12. Kelly MA, Mijovic CH, Barnett AH. Genetics of type 1 diabetes. Best Pract Res Clin Endocrinol Metab 2001; 15: 279-291.
13. Whitacre CC. Sex differences in autoimmune disease. Nat Immunol 2001; 2: 777-780.
14. Guo SW, Toumilehto, J. Preferential transmission of Type 1 diabetes from parents to offspring: fact or artifact? Genet Epidemiol 2002; 23: 1-12.
15. Brix TH, Kyvik KO, Hegedus L. Validity of self-reported hyperthyroidism and hypothyroidism: comparison of self-reported questionnaire data with medical record review. Thyroid 2001; 11: 769-773.