Clinical and Immunological Characteristics of Autoimmune Addison Disease: A Nationwide Swedish Multicenter StudyKarolinska University Hospital, Karolinska Institutet, Stockholm, Sweden.
Karolinska University Hospital, Karolinska Institutet, Stockholm, Sweden.
Karolinska University Hospital, Karolinska Institutet, Stockholm, Sweden.
Karolinska University Hospital, Karolinska Institutet, Stockholm, Sweden.
Karolinska University Hospital, Karolinska Institutet, Stockholm, Sweden.
Karolinska University Hospital, Karolinska Institutet, Stockholm, Sweden.
Umeå University, Umeå , Sweden.
Karolinska University Hospital, Karolinska Institutet, Stockholm, Sweden.
Karolinska University Hospital, Karolinska Institutet, Stockholm, Sweden.
Uppsala University, Uppsala, Sweden.
Uppsala University, Uppsala, Sweden.
Uppsala University, Uppsala, Sweden.
Karolinska University Hospital, Karolinska Institutet, Stockholm, Sweden.
Karolinska Institutet, Stockholm, Sweden.
Karolinska University Hospital, Karolinska Institutet, Stockholm, Sweden.
Department of Pediatrics, Faculty of Medicine and Health, Örebro University, Örebro, Sweden.
Linköping University, Linköping, Sweden.
Karolinska University Hospital, Karolinska Institutet, Stockholm, Sweden; Sahlgrenska University Hospital, Sahlgrenska Academy, University of Gothenburg, Gothenburg, Sweden.
Karolinska University Hospital, Karolinska Institutet, Stockholm, Sweden; Sahlgrenska University Hospital, Sahlgrenska Academy, University of Gothenburg, Gothenburg, Sweden.
Karolinska University Hospital, Karolinska Institutet, Stockholm, Sweden.
Skåne University Hospital, Lund, Sweden.
Lund University, Lund, Sweden.
Skåne University Hospital, Lund, Sweden.
Karolinska University Hospital, Karolinska Institutet, Stockholm, Sweden.
Karolinska University Hospital, Karolinska Institutet, Stockholm, Sweden.
Karolinska University Hospital, Karolinska Institutet, Stockholm, Sweden.
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2017 (English)In: Journal of Clinical Endocrinology and Metabolism, ISSN 0021-972X, E-ISSN 1945-7197, Vol. 102, no 2, p. 379-389Article in journal (Refereed) Published
Abstract [en]
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.
Place, publisher, year, edition, pages
Oxford University Press, 2017. Vol. 102, no 2, p. 379-389
National Category
Endocrinology and Diabetes
Identifiers
URN: urn:nbn:se:oru:diva-110272DOI: 10.1210/jc.2016-2522ISI: 000397240900009PubMedID: 27870550Scopus ID: 2-s2.0-85012097745OAI: oai:DiVA.org:oru-110272DiVA, id: diva2:1819921
Funder
Swedish Research CouncilRagnar Söderbergs stiftelseTorsten Söderbergs stiftelseEU, FP7, Seventh Framework Programme, 201167Region StockholmKarolinska InstituteEU, European Research CouncilSwedish Society for Medical Research (SSMF)Swedish Society of MedicineMarianne and Marcus Wallenberg FoundationNovo Nordisk FoundationTore Nilsons Stiftelse för medicinsk forskningÅke Wiberg Foundation2023-12-152023-12-152024-01-31Bibliographically approved