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Mortality and reduced growth hormone secretion
Kirstine Stochholm1, Jens Christiansen, Torben Laursen
1Department of Endocrinology, Aarhus University Hospital, Aarhus, Denmark. Stochholm@dadlnet.dk
Insights
Mortality rates for growth hormone deficiency (GHD) patients are often increased, particularly in females. While growth hormone (GH) treatment may normalize mortality in some cases, more research is needed.
Area of Science:
- Endocrinology
- Epidemiology
- Public Health
Background:
- Limited data exist on mortality rates for patients with growth hormone deficiency (GHD), though hypopituitary patients show increased mortality compared to the general population.
- Cardiovascular disease is a suspected primary cause of death, with cancer statistics potentially affected by pituitary disease-related malignancies.
- Reported differences in mortality rates between females and males necessitate further investigation.
Purpose of the Study:
- To review and synthesize existing epidemiological data on mortality rates in hypopituitary and GHD patients.
- To identify potential factors influencing mortality, including sex and age of GHD onset.
- To evaluate the impact of growth hormone (GH) treatment on mortality rates.
Main Methods:
- Systematic review and analysis of published epidemiological studies focusing on mortality in hypopituitary and GHD populations.
- Inclusion of studies examining mortality in both treated and untreated GHD patients.
Main Results:
- Most reviewed studies indicate an elevated mortality rate in hypopituitary and GHD patients.
- Female patients generally exhibit higher mortality rates compared to male patients.
- Two studies suggest that GH treatment may lead to mortality rates comparable to the general population, though data are limited.
Conclusions:
- An increased mortality rate in hypopituitary patients is established, but definitive causes require further research.
- Interpreting the impact of GH treatment on mortality must be done cautiously due to limited data and study design constraints.
- Additional high-quality research is essential for accurate mortality estimations and understanding the role of GH therapy.
Background:
Data regarding the mortality rates of patients with growth hormone deficiency (GHD), whether or not treated with growth hormone (GH), are limited, but an increased mortality rate among hypopituitary patients compared with the general population has been documented. Cardiovascular disease has been suggested as a primary cause of death, whereas cancer statistics might be influenced by the number of malignancies causing the pituitary disease. Furthermore, differences in mortality rates in females and males have been reported.
Methods:
Epidemiological studies of mortality in hypopituitary and GHD patients were identified and reviewed.
Results:
Most studies showed an increased mortality rate in hypopituitary and GHD patients and an increased mortality among female compared with male patients. There is a possibility that differences between patients with adult-onset and childhood-onset GHD might also exist. Two studies showed a normal mortality rate in GHD patients treated with GH compared with the general population.
Conclusions:
Although an increased mortality rate in hypopituitary patients is well documented, further research is needed to provide more reliable estimates of the actual causes. Caution should be taken in the interpretation of results regarding mortality and GH treatment due to the limited amount of data and the limitations of the study designs.
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