The prevalence of acromegaly is higher than previously reported: Changes over a three-decade period

Charlotte Aagaard, Amanda S, Christophersen, Susanne Finnerup, Christian Rosendal, Helga A. Gulisano, Kåre S. Ettrup, Peter Vestergaard, Jesper Karmisholt, Eigil Husted Nielsen, Jakob Dal*


Publikation: Bidrag til tidsskriftTidsskriftartikelForskningpeer review

5 Citationer (Scopus)
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Objective: To study time-related changes in the prevalence and patient characteristics of acromegaly, as well as to assess the impact of changes in treatment on disease control. Methods: A total of 107 patients with acromegaly were identified by healthcare registries and subsequently validated by patient chart review over a three-decade period (1992–2021). A systematic literature review focusing on the incidence and prevalence of acromegaly was performed identifying 31 studies. Results: The prevalence of acromegaly significantly increased throughout the study period (R 2 = 0.94, p <.001) and was 122 cases/10 6 persons in 2021 whereas the annual incidence remained constant at 4.6 cases/10 6 persons. The age at the first sign of acromegaly and the age at diagnosis significantly increased during the study period, whereas growth hormone and insulin-like growth factor I decreased. Incidentalomas constituted 32% of all cases diagnosed with acromegaly in the last decade. Primary surgery was used in 93% of all cases, and repeated surgery decreased from 24% to 10% during the three decades. The use of first-generation somatostatin analogues (21%–48%) and second-line medical treatment (4%–20%) increased with a concomitant improvement of biochemical disease control (58%–91%). Conclusion: The prevalence of acromegaly is higher than previously reported and the clinical presentation has shifted towards a milder phenotype. Modern treatment of acromegaly enables individualized treatment and disease control in the majority of patients.

TidsskriftClinical Endocrinology
Udgave nummer6
Sider (fra-til)773-782
Antal sider10
StatusUdgivet - dec. 2022

Bibliografisk note

© 2022 The Authors. Clinical Endocrinology published by John Wiley & Sons Ltd.


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