Skip to main content
Erschienen in: Endocrine 1/2010

01.08.2010 | Original Article

Co-morbidities, management and clinical outcome of auto-immune Addison’s disease

verfasst von: Lalantha Leelarathna, Louise Breen, James K. Powrie, Stephen M. Thomas, Rustom Guzder, Barbara McGowan, Paul V. Carroll

Erschienen in: Endocrine | Ausgabe 1/2010

Einloggen, um Zugang zu erhalten

Abstract

There are no consensus guidelines on the optimum long-term care of patients with primary adrenal failure. Published data suggest increased morbidity and mortality in patients treated with current therapy. Investigations of bone mineral density (BMD) in adults with adrenal failure have reported conflicting results. The objectives of this study were to determine the prevalence of auto-immune and other co-morbidities, describe the treatment regimens and to assess the BMD of adults with auto-immune Addison’s disease (AAD). A retrospective, cohort study of adults with primary adrenal failure was used. Electronic and paper records were used to collect demographic, biochemical, BMD data and details of other co-morbidities. 48 patients (35% male; 65% female; 50 ± 16, years, mean ± SD) with primary adrenal failure were identified. There was high prevalence of other auto-immune co-morbidities (hypothyroidism 58%, vitamin B12 deficiency 29%, type 1 diabetes 10%). The presence of cardiovascular risk factors including dyslipidaemia (65% had total cholesterol >5 mmol/l) and excess weight (65% had a BMI >25 kg/m2) were high. Using WHO criteria, 17.9 and 53.5% of patients had spinal osteoporosis and osteopenia, respectively, at the spine. This did not relate to the duration or dose of glucocorticoid replacement. Our data shows a high prevalence of both auto-immune and non-autoimmune co-morbidities in patients with AAD. In addition to common auto-immune diseases, patients should be screened for other cardiovascular risk factors. Further studies are needed to assess the cause of the observed increased prevalence of reduced BMD at the lumbar spine. There is a need for internationally agreed long-term management guidelines.
Literatur
2.
Zurück zum Zitat K. Lovas, E.S. Husebye, High prevalence and increasing incidence of Addison’s disease in western Norway. Clin. Endocrinol. (Oxf) 56(6), 787–791 (2002)CrossRef K. Lovas, E.S. Husebye, High prevalence and increasing incidence of Addison’s disease in western Norway. Clin. Endocrinol. (Oxf) 56(6), 787–791 (2002)CrossRef
3.
Zurück zum Zitat L. Leelarathna, J.K. Powrie, P.V. Carroll, Thomas Addison’s disease after 154 years: modern diagnostic perspectives on an old condition. Q. J. Med. (QJM) 102(8), 569–573 (2009) L. Leelarathna, J.K. Powrie, P.V. Carroll, Thomas Addison’s disease after 154 years: modern diagnostic perspectives on an old condition. Q. J. Med. (QJM) 102(8), 569–573 (2009)
4.
Zurück zum Zitat K. Lovas, J.H. Loge, E.S. Husebye, Subjective health status in Norwegian patients with Addison’s disease. Clin. Endocrinol. (Oxf) 56(5), 581–588 (2002)CrossRef K. Lovas, J.H. Loge, E.S. Husebye, Subjective health status in Norwegian patients with Addison’s disease. Clin. Endocrinol. (Oxf) 56(5), 581–588 (2002)CrossRef
5.
Zurück zum Zitat S. Hahner, M. Loeffler, M. Fassnacht et al., Impaired subjective health status in 256 patients with adrenal insufficiency on standard therapy based on cross-sectional analysis 2007. J. Clin. Endocrinol. Metab. 92(10), 3912–3922 (2007)CrossRefPubMed S. Hahner, M. Loeffler, M. Fassnacht et al., Impaired subjective health status in 256 patients with adrenal insufficiency on standard therapy based on cross-sectional analysis 2007. J. Clin. Endocrinol. Metab. 92(10), 3912–3922 (2007)CrossRefPubMed
6.
Zurück zum Zitat M.M. Erichsen, K. Løvås, B. Skinningsrud et al., Clinical, immunological, and genetic features of autoimmune primary adrenal insufficiency: observations from a Norwegian registry. J. Clin. Endocrinol. Metab. 94(12), 4882–4890 (2009)CrossRefPubMed M.M. Erichsen, K. Løvås, B. Skinningsrud et al., Clinical, immunological, and genetic features of autoimmune primary adrenal insufficiency: observations from a Norwegian registry. J. Clin. Endocrinol. Metab. 94(12), 4882–4890 (2009)CrossRefPubMed
7.
Zurück zum Zitat R. Bergthorsdottir, M. Leonsson-Zachrisson, A. Oden et al., Premature mortality in patients with Addison’s disease: a population-based study. J. Clin. Endocrinol. Metab. 91(12), 4849–4853 (2006)CrossRefPubMed R. Bergthorsdottir, M. Leonsson-Zachrisson, A. Oden et al., Premature mortality in patients with Addison’s disease: a population-based study. J. Clin. Endocrinol. Metab. 91(12), 4849–4853 (2006)CrossRefPubMed
8.
Zurück zum Zitat S. Bensing, L. Brandt, F. Tabaroj et al., Increased death risk and altered cancer incidence pattern in patients with isolated or combined autoimmune primary adrenocortical insufficiency. Clin. Endocrinol. (Oxf) 69(5), 697–704 (2008)CrossRef S. Bensing, L. Brandt, F. Tabaroj et al., Increased death risk and altered cancer incidence pattern in patients with isolated or combined autoimmune primary adrenocortical insufficiency. Clin. Endocrinol. (Oxf) 69(5), 697–704 (2008)CrossRef
9.
Zurück zum Zitat J.A. Kanis, L.J. Melton, C. Christiansen et al., The diagnosis of osteoporosis. Bone Miner. Res. 9(8), 1137–1141 (1994)CrossRef J.A. Kanis, L.J. Melton, C. Christiansen et al., The diagnosis of osteoporosis. Bone Miner. Res. 9(8), 1137–1141 (1994)CrossRef
10.
Zurück zum Zitat C.M. Florkowski, S.J. Holmes, J.R. Elliot et al., Bone mineral density is reduced in female but not male subjects with Addison’s disease. N. Z. Med. J. 107(972), 52–53 (1994)PubMed C.M. Florkowski, S.J. Holmes, J.R. Elliot et al., Bone mineral density is reduced in female but not male subjects with Addison’s disease. N. Z. Med. J. 107(972), 52–53 (1994)PubMed
11.
Zurück zum Zitat P.M. Zelissen, R.J. Croughs, P.P. van Rijk et al., Effect of glucocorticoid replacement therapy on bone mineral density in patients with Addison disease. Ann. Intern. Med. 120(3), 207–210 (1994)PubMed P.M. Zelissen, R.J. Croughs, P.P. van Rijk et al., Effect of glucocorticoid replacement therapy on bone mineral density in patients with Addison disease. Ann. Intern. Med. 120(3), 207–210 (1994)PubMed
12.
Zurück zum Zitat E. Jodar, M.P. Valdepenas, G. Martinez, Long-term follow-up of bone mineral density in Addison’s disease. Clin. Endocrinol. (Oxf) 58(5), 617–620 (2003)CrossRef E. Jodar, M.P. Valdepenas, G. Martinez, Long-term follow-up of bone mineral density in Addison’s disease. Clin. Endocrinol. (Oxf) 58(5), 617–620 (2003)CrossRef
13.
Zurück zum Zitat G.D. Braatvedt, M. Joyce, M. Evans, Bone mineral density in patients with treated Addison’s disease. Osteoporos. Int. 10(6), 435–440 (1999)CrossRefPubMed G.D. Braatvedt, M. Joyce, M. Evans, Bone mineral density in patients with treated Addison’s disease. Osteoporos. Int. 10(6), 435–440 (1999)CrossRefPubMed
14.
Zurück zum Zitat E.M. Gurnell, P.J. Hunt, S.E. Curran et al., Long-term DHEA replacement in primary adrenal insufficiency. a randomized, controlled trial. J. Clin. Endocrinol. Metab. 93(2), 400–409 (2008)CrossRefPubMed E.M. Gurnell, P.J. Hunt, S.E. Curran et al., Long-term DHEA replacement in primary adrenal insufficiency. a randomized, controlled trial. J. Clin. Endocrinol. Metab. 93(2), 400–409 (2008)CrossRefPubMed
15.
Zurück zum Zitat G. Johannsson, R. Bergthorsdottir, A.G. Nilsson et al., Improving glucocorticoid replacement therapy using a novel modified-release hydrocortisone tablet: a pharmacokinetic study. Eur. J. Endocrinol. 161(1), 119–130 (2009)CrossRefPubMed G. Johannsson, R. Bergthorsdottir, A.G. Nilsson et al., Improving glucocorticoid replacement therapy using a novel modified-release hydrocortisone tablet: a pharmacokinetic study. Eur. J. Endocrinol. 161(1), 119–130 (2009)CrossRefPubMed
16.
Zurück zum Zitat M. Debono, C. Ghobadi, A. Rostami-Hodjegan et al., Modified-release hydrocortisone to provide circadian cortisol profiles. Clin. Endocrinol. Metab. 94(5), 1548–1554 (2009)CrossRef M. Debono, C. Ghobadi, A. Rostami-Hodjegan et al., Modified-release hydrocortisone to provide circadian cortisol profiles. Clin. Endocrinol. Metab. 94(5), 1548–1554 (2009)CrossRef
Metadaten
Titel
Co-morbidities, management and clinical outcome of auto-immune Addison’s disease
verfasst von
Lalantha Leelarathna
Louise Breen
James K. Powrie
Stephen M. Thomas
Rustom Guzder
Barbara McGowan
Paul V. Carroll
Publikationsdatum
01.08.2010
Verlag
Springer US
Erschienen in
Endocrine / Ausgabe 1/2010
Print ISSN: 1355-008X
Elektronische ISSN: 1559-0100
DOI
https://doi.org/10.1007/s12020-010-9359-8

Weitere Artikel der Ausgabe 1/2010

Endocrine 1/2010 Zur Ausgabe

Leitlinien kompakt für die Innere Medizin

Mit medbee Pocketcards sicher entscheiden.

Seit 2022 gehört die medbee GmbH zum Springer Medizin Verlag

„Jeder Fall von plötzlichem Tod muss obduziert werden!“

17.05.2024 Plötzlicher Herztod Nachrichten

Ein signifikanter Anteil der Fälle von plötzlichem Herztod ist genetisch bedingt. Um ihre Verwandten vor diesem Schicksal zu bewahren, sollten jüngere Personen, die plötzlich unerwartet versterben, ausnahmslos einer Autopsie unterzogen werden.

Hirnblutung unter DOAK und VKA ähnlich bedrohlich

17.05.2024 Direkte orale Antikoagulanzien Nachrichten

Kommt es zu einer nichttraumatischen Hirnblutung, spielt es keine große Rolle, ob die Betroffenen zuvor direkt wirksame orale Antikoagulanzien oder Marcumar bekommen haben: Die Prognose ist ähnlich schlecht.

Schlechtere Vorhofflimmern-Prognose bei kleinem linken Ventrikel

17.05.2024 Vorhofflimmern Nachrichten

Nicht nur ein vergrößerter, sondern auch ein kleiner linker Ventrikel ist bei Vorhofflimmern mit einer erhöhten Komplikationsrate assoziiert. Der Zusammenhang besteht nach Daten aus China unabhängig von anderen Risikofaktoren.

Semaglutid bei Herzinsuffizienz: Wie erklärt sich die Wirksamkeit?

17.05.2024 Herzinsuffizienz Nachrichten

Bei adipösen Patienten mit Herzinsuffizienz des HFpEF-Phänotyps ist Semaglutid von symptomatischem Nutzen. Resultiert dieser Benefit allein aus der Gewichtsreduktion oder auch aus spezifischen Effekten auf die Herzinsuffizienz-Pathogenese? Eine neue Analyse gibt Aufschluss.

Update Innere Medizin

Bestellen Sie unseren Fach-Newsletter und bleiben Sie gut informiert.