Clinical and immunological characteristics of Autoimmune Addison's disease: a nationwide Swedish multicenter study.

Frida Dalin(Science for Life Laboratory), Gabriel Nordling Eriksson, Per Dahlqvist, Åsa Hallgren(Centre of Excellence in Molecular Biology), Jeanette Wahlberg, Olov Ekwall(Institute of Clinical Research), Stefan Söderberg, Johan Rönnelid(Pediatrics and Genetics), Per Olcén, Ola Winqvist, Sergiu‐Bogdan Catrina(Karolinska University Hospital), Berit Kriström(Umeå University), Maria Laudius, Magnus Isaksson, Maria Halldin Stenlid(Uppsala University), Jan Gustafsson(Uppsala University), Gennet Gebre‐Medhin(Uppsala University), Sigríður Björnsdóttir(Karolinska University Hospital), Annika Janson(Karolinska Institutet), Anna‐Karin Åkerman, Jan Åman(Örebro University), Karel Duchén(Linköping University), Ragnhildur Bergthorsdottir(Sahlgrenska University Hospital), Gudmundur Johannsson(Sahlgrenska University Hospital), Emma Lindskog(Institute of Clinical Research), Mona Landin‐Olsson(Skåne University Hospital), Maria Elfving(Lund University), Erik Waldenström(Skåne University Hospital), Anna-Lena Hulting, Olle Kämpe(Karolinska University Hospital), Sophie Bensing(Karolinska University Hospital)
The Journal of Clinical Endocrinology & Metabolism
November 21, 2016
Cited by 79Open Access
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Abstract

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/m2/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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