TY - JOUR
T1 - The changing landscape of acromegaly - an epidemiological perspective
AU - Rosendal, Christian
AU - Arlien-Søborg, Mai Christiansen
AU - Nielsen, Eigil Husted
AU - Andersen, Marianne Skovsager
AU - Feltoft, Claus Larsen
AU - Kistorp, Caroline
AU - Dekkers, Olaf M
AU - Jørgensen, Jens Otto Lunde
AU - Dal, Jakob
PY - 2024/8
Y1 - 2024/8
N2 - Acromegaly is a rare disease and thus challenging to accurately quantify epidemiologically. In this comprehensive literature review, we compare different approaches to studying acromegaly from an epidemiological perspective and describe the temporal evolution of the disease pertaining to epidemiological variables, clinical presentation and mortality. We present updated epidemiological data from the population-based Danish cohort of patients with acromegaly (AcroDEN), along with meta-analyses of existing estimates from around the world.Based on this, we conclude that the incidence, prevalence and age at acromegaly diagnosis are all steadily increasing, but with considerable variation between studies. An increased number of incidental cases may contribute to the increase in incidence and age at diagnosis, respectively. The clinical features at presentation are trending toward a milder disease phenotype at diagnosis, and advances in therapeutic options have reduced the mortality of patients with acromegaly to a level similar to that of the general population. Moreover, the underlying cause of death has shifted from cardiovascular to malignant neoplastic diseases.
AB - Acromegaly is a rare disease and thus challenging to accurately quantify epidemiologically. In this comprehensive literature review, we compare different approaches to studying acromegaly from an epidemiological perspective and describe the temporal evolution of the disease pertaining to epidemiological variables, clinical presentation and mortality. We present updated epidemiological data from the population-based Danish cohort of patients with acromegaly (AcroDEN), along with meta-analyses of existing estimates from around the world.Based on this, we conclude that the incidence, prevalence and age at acromegaly diagnosis are all steadily increasing, but with considerable variation between studies. An increased number of incidental cases may contribute to the increase in incidence and age at diagnosis, respectively. The clinical features at presentation are trending toward a milder disease phenotype at diagnosis, and advances in therapeutic options have reduced the mortality of patients with acromegaly to a level similar to that of the general population. Moreover, the underlying cause of death has shifted from cardiovascular to malignant neoplastic diseases.
KW - Acromegaly
KW - Epidemiology
KW - Incidence
KW - Mortality
KW - Prevalence
KW - Sex differences
KW - Acromegaly/epidemiology
KW - Denmark/epidemiology
KW - Humans
U2 - 10.1007/s11154-024-09875-z
DO - 10.1007/s11154-024-09875-z
M3 - Journal article
C2 - 38337125
SN - 1389-9155
VL - 25
SP - 691
EP - 705
JO - Reviews in Endocrine and Metabolic Disorders
JF - Reviews in Endocrine and Metabolic Disorders
IS - 4
ER -