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Mortality in acromegaly: a 20-year follow-up study
Elina Ritvonen1, Eliisa Löyttyniemi2, Pia Jaatinen3
1Division of EndocrinologyAbdominal Center, University of Helsinki and Helsinki University Hospital, Helsinki, Finland.
Mortality remains elevated in acromegaly patients, particularly women. Over 20 years, death causes shifted from cardiovascular to cancer, indicating a need for targeted monitoring in acromegaly care.
Area of Science:
- Endocrinology
- Oncology
- Epidemiology
Background:
- Acromegaly, a condition of excess growth hormone, has uncertain long-term mortality risks.
- Gender-specific differences in acromegaly outcomes require further investigation.
Purpose of the Study:
- To dynamically assess long-term mortality and causes of death in a nationwide cohort of acromegaly patients.
- To investigate potential gender-related differences in acromegaly mortality.
Main Methods:
- A nationwide cohort study compared standardized mortality ratios (SMRs) and causes of death in 333 acromegaly patients versus 4995 age- and gender-matched controls.
- Follow-up extended up to 33 years, dynamically assessing outcomes.
Main Results:
- Acromegaly patients exhibited increased all-cause mortality (OR 1.6) and SMR (1.9) compared to controls over 20 years.
- Causes of death shifted from predominantly cardiovascular to cancer deaths within the acromegaly cohort over time.
- Increased mortality was observed in women with acromegaly compared to controls, but not in men.
Conclusions:
- Mortality is increased in acromegaly, with a notable rise in cancer-related deaths over time.
- Women with acromegaly face higher mortality risks compared to controls, unlike men.
- Men with acromegaly are diagnosed and die at younger ages than women.
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