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Published on: March 6, 2018
Liver Disease in Men Undergoing Androgen Deprivation Therapy for Prostate Cancer
Philipp Gild1, Alexander P Cole2, Anna Krasnova2
1Center for Surgery and Public Health, Division of Urological Surgery, Brigham and Women's Hospital, Harvard Medical School, Boston, Massachusetts; Department of Urology, University Medical Center Hamburg-Eppendorf, Hamburg, Germany.
Purpose:
Androgen deprivation therapy is associated with the development of diabetes and metabolic syndrome. To our knowledge its effect on the development of nonalcoholic fatty liver disease, a condition which frequently co-occurs with metabolic syndrome and other subsequent liver conditions such as liver cirrhosis, hepatic necrosis or any liver disease, has not been investigated.
Materials And Methods:
We identified 82,938 men 66 years old or older who were diagnosed with localized prostate cancer in the SEER (Surveillance, Epidemiology and End Results)-Medicare database from 1992 to 2009. Men with preexisting nonalcoholic fatty liver disease, liver disease, diabetes or metabolic syndrome were excluded from study. Propensity score adjusted, competing risk regression models were created to compare the risk of nonalcoholic fatty liver disease in men who were vs were not treated with androgen deprivation. We also explored the influence of cumulative exposure to androgen deprivation therapy, calculated as monthly equivalent doses of gonadotropin-releasing hormone agonists/antagonists (fewer than 7, 7 to 11 or more than 11 doses).
Results:
Overall 37.5% of men underwent androgen deprivation therapy. They were more likely to be diagnosed with nonalcoholic fatty liver disease (HR 1.54, 95% CI 1.40-1.68), liver cirrhosis (HR 1.35, 95% CI 1.12-1.60), liver necrosis (HR 1.41, 95% CI 1.15-1.72) and any liver disease (HR 1.47, 95% CI 1.35-1.60). A dose-response relationship was observed between the number of androgen deprivation therapy doses, and nonalcoholic fatty liver disease and any liver disease.
Conclusions:
Androgen deprivation therapy in men with prostate cancer is associated with the diagnosis of nonalcoholic fatty liver disease. The usual limitations of an observational study design apply, including possible inaccuracy in defining outcomes in a population based registry.
Insights
Androgen deprivation therapy for prostate cancer increases the risk of nonalcoholic fatty liver disease and other liver conditions. Higher doses of this therapy correlate with a greater risk of developing these liver diseases.
Area of Science:
- Oncology
- Hepatology
- Endocrinology
Background:
- Androgen deprivation therapy (ADT) is a standard treatment for prostate cancer.
- ADT is known to be associated with metabolic syndrome and diabetes.
- The impact of ADT on nonalcoholic fatty liver disease (NAFLD) has not been previously studied.
Purpose of the Study:
- To investigate the association between androgen deprivation therapy and the development of nonalcoholic fatty liver disease in men with prostate cancer.
- To examine the risk of other liver conditions, including liver cirrhosis, hepatic necrosis, and any liver disease, in relation to ADT.
Main Methods:
- Retrospective analysis of 82,938 men aged 66+ diagnosed with localized prostate cancer (1992-2009) using the SEER-Medicare database.
- Exclusion of men with pre-existing NAFLD, liver disease, diabetes, or metabolic syndrome.
- Propensity score adjustment and competing risk regression models were used to compare NAFLD risk between men treated and not treated with ADT, considering cumulative ADT exposure.
Main Results:
- 37.5% of men received ADT.
- ADT was associated with a significantly higher risk of NAFLD (HR 1.54), liver cirrhosis (HR 1.35), liver necrosis (HR 1.41), and any liver disease (HR 1.47).
- A dose-response relationship was observed between cumulative ADT exposure and the risk of NAFLD and any liver disease.
Conclusions:
- Androgen deprivation therapy in prostate cancer patients is linked to an increased incidence of nonalcoholic fatty liver disease.
- The findings suggest ADT may contribute to the development of various liver conditions.
- Limitations include the observational nature of the study and potential inaccuracies in outcome ascertainment from registry data.
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