4.7 Article

Clinical and Immunological Characteristics of Autoimmune Addison Disease: A Nationwide Swedish Multicenter Study

Journal

JOURNAL OF CLINICAL ENDOCRINOLOGY & METABOLISM
Volume 102, Issue 2, Pages 379-389

Publisher

ENDOCRINE SOC
DOI: 10.1210/jc.2016-2522

Keywords

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Funding

  1. Swedish Research Council
  2. Torsten Soderberg Foundation
  3. Ragnar Soderberg Foundation
  4. European Union Seventh Framework Programme [201167]
  5. EurAdrenal fp7 consortium
  6. Stockholm County Council
  7. Karolinska Institutet
  8. European Union
  9. Swedish Society for Medical Research
  10. Swedish Society of Medicine
  11. Marianne and Marcus Wallenberg Foundation
  12. NovoNordisk Foundation
  13. Tore Nilson's Foundation for Medical Research
  14. Ake Wiberg Foundation
  15. Novo Nordisk Fonden [NNF15OC0015922, NNF14OC0011003, NNF13OC0005975] Funding Source: researchfish

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Context: Studies of the clinical and immunological features of autoimmune Addison disease (AAD) are needed to understand the disease burden and increased mortality. Objective: To provide upgraded data on autoimmune comorbidities, replacement therapy, autoantibody profiles, and cardiovascular risk factors. Design, Setting, and Participants: A cross-sectional, population-based study that included 660 AAD patients from the Swedish Addison Registry (2008-2014). When analyzing the cardiovascular risk factors, 3594 individuals from the population-based survey in Northern Sweden, MONICA (monitoring of trends and determinants of cardiovascular disease), served as controls. Main Outcome Measures: The endpoints were the prevalence of autoimmune comorbidities and cardiovascular risk factors. Autoantibodies against 13 autoantigens were determined. Results: The proportion of 21-hydroxylase autoantibody-positive patients was 83%, and 62% of patients had >= 1 associated autoimmune diseases, more frequently coexisting in females (P, 0.0001). AAD patients had a lower body mass index (P, 0.0001) and prevalence of hypertension (P = 0.027) compared with controls. Conventional hydrocortisone tablets were used by 89% of the patients, with a mean dose of 28.1 +/- 8.5 mg/d. The mean hydrocortisone equivalent dose normalized to the body surface was 14.8 +/- 4.4 mg/m(2)/d. A greater hydrocortisone equivalent dose was associated with a greater incidence of hypertension (P = 0.046). Conclusions: Careful monitoring of AAD patients is warranted to detect associated autoimmune diseases. Contemporary Swedish AAD patients did not have an increased prevalence of overweight, hypertension, type 2 diabetes mellitus, or hyperlipidemia. However, high glucocorticoid replacement doses could be a risk factor for hypertension.

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