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Mortality in patients with pituitary disease
Mark Sherlock1, John Ayuk, Jeremy W Tomlinson
1Centre for Endocrinology, Diabetes, and Metabolism, School of Clinical and Experimental Medicine, College of Medical and Dental Sciences, University of Birmingham, Birmingham B15 2TH, United Kingdom.
Insights
Pituitary diseases increase mortality, mainly from vascular causes. Better control of hormone secretion and cardiovascular risk factors is crucial for improving patient outcomes and reducing death rates.
Area of Science:
- Endocrinology
- Oncology
- Cardiovascular Medicine
Background:
- Pituitary diseases are linked to higher mortality, primarily due to vascular complications.
- Effective management of hormone hypersecretion, such as cortisol and growth hormone (GH), is vital for reducing mortality in Cushing's disease and acromegaly.
- Pituitary hormone deficiencies and treatments like radiotherapy can negatively impact patient outcomes.
Purpose of the Study:
- To review the factors contributing to increased mortality in pituitary disease.
- To highlight the importance of managing hormone secretion and cardiovascular risk factors.
- To identify areas for future research, particularly for craniopharyngioma.
Main Methods:
- Retrospective analysis of mortality data in pituitary disease patients.
- Review of factors influencing outcomes, including hormone control and treatment modalities.
- Identification of specific patient groups with elevated mortality risks.
Main Results:
- Vascular disease is the predominant cause of mortality in pituitary disease.
- Control of cortisol and GH hypersecretion is key for reducing mortality in Cushing's disease and acromegaly.
- Pituitary radiotherapy is associated with increased cerebrovascular mortality.
Conclusions:
- Despite falling mortality rates, pituitary disease patients still face elevated risks.
- Optimizing treatment strategies and further research are needed to improve long-term outcomes.
- Craniopharyngioma patients require focused research to mitigate mortality risks from the tumor and its treatment.
Abstract:
Pituitary disease is associated with increased mortality predominantly due to vascular disease. Control of cortisol secretion and GH hypersecretion (and cardiovascular risk factor reduction) is key in the reduction of mortality in patients with Cushing's disease and acromegaly, retrospectively. For patients with acromegaly, the role of IGF-I is less clear-cut. Confounding pituitary hormone deficiencies such as gonadotropins and particularly ACTH deficiency (with higher doses of hydrocortisone replacement) may have a detrimental effect on outcome in patients with pituitary disease. Pituitary radiotherapy is a further factor that has been associated with increased mortality (particularly cerebrovascular). Although standardized mortality ratios in pituitary disease are falling due to improved treatment, mortality for many conditions are still elevated above that of the general population, and therefore further measures are needed. Craniopharyngioma patients have a particularly increased risk of mortality as a result of the tumor itself and treatment to control tumor growth; this is a key area for future research in order to optimize the outcome for these patients.
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