Josephine Egan
Johns Hopkins University School of Medicine
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Journal of Clinical Oncology | 2006
Milena Braga-Basaria; Adrian S. Dobs; Denis C. Muller; Michael A. Carducci; Majnu John; Josephine Egan; Shehzad Basaria
PURPOSEnProstate cancer (PCa) is one of the most common cancers in men. Men with recurrent or metastatic PCa are treated with androgen-deprivation therapy (ADT), resulting in profound hypogonadism. Because male hypogonadism is a risk factor for metabolic syndrome and men with PCa have high cardiovascular mortality, we evaluated the prevalence of metabolic syndrome in men undergoing long-term ADT.nnnPATIENTS AND METHODSnThis was a cross-sectional study. We evaluated 58 men, including 20 with PCa undergoing ADT for at least 12 months (ADT group), 18 age-matched men with nonmetastatic PCa who had received local treatment and were recently found to have an increasing prostate-specific antigen (non-ADT group), and 20 age-matched controls (control group). Men in the non-ADT and control groups were eugonadal. Metabolic syndrome was defined according to the Adult Treatment Panel III criteria.nnnRESULTSnMean age was similar among the groups. Men on ADT had significantly higher body mass index and lower total and free testosterone levels. The prevalence of metabolic syndrome was higher in the ADT group compared with the non-ADT (P < .01) and control (P = .03) groups. Among the components of metabolic syndrome, men on ADT had a higher prevalence of abdominal obesity and hyperglycemia. Androgen-deprived men also had elevated triglycerides compared with controls (P = .02). The prevalence of hypertension and low high-density lipoprotein levels were similar.nnnCONCLUSIONnThese data suggest that metabolic syndrome was present in more than 50% of the men undergoing long-term ADT, predisposing them to higher cardiovascular risk. Abdominal obesity and hyperglycemia were responsible for this higher prevalence. We recommend prospective studies to further delineate this association.
Journal of the American Geriatrics Society | 2006
Marcello Maggio; Fulvio Lauretani; Gian Paolo Ceda; Stefania Bandinelli; Shehzad Basaria; Alessandro Ble; Josephine Egan; Giuseppe Paolisso; Samer S. Najjar; E. Jeffrey Metter; Giorgio Valenti; Jack M. Guralnik; Luigi Ferrucci
OBJECTIVES: To determine whether low levels of testosterone, sex hormone binding globulin (SHBG), insulin‐like growth factor‐1 (IGF‐1), and dehydroepiandrosterone sulfate (DHEAS) and high levels of cortisol and leptin would be associated with metabolic syndrome (MS).
Archive | 1999
Josephine Egan; Riccardo Perfetti; Antonino Passaniti; Nigel H. Greig; Harold Holloway; Joel F. Habener; Doris A. Stoffers
Gastroenterology | 1996
Michael E. Zenilman; Thomas H. Magnuson; Kevin Swinson; Josephine Egan; Riccardo Perfetti; Alan R. Shuldiner
Archive | 2005
Josephine Egan; Maire Doyle
Archive | 2015
Alice S. Ryan; Denis C. Muller; Dariush Elahi; S. Meneilly; Josephine Egan; Dora M. Berman; Barbara J. Nicklas; Madhur K. Sinha; Ronald L. Gingerich; Graydon S. Meneilly; Nigel H. Greig; Hugh D. Tildesley; Joel F. Habener
Archive | 2013
Nigel H. Greig; ニゲル・エイチ・グレイグ; Josephine Egan; ジョセフィン・イーガン; Maire Doyle; マイア・ドイル; Harold Holloway; ハロルド・ホロウェイ; Tracy Ann Perry; トレイシー・アン・ペリー
Archive | 2013
Jennifer L. Fiori; Yu-Kyong Shin; Wook Kim; Susan M. Krzysik-Walker; Olga D. Carlson; Mitesh Sanghvi; Ruin Moaddel; Kathleen Farhang; Maire Doyle; Kevin J. Pearson; Julie A. Mattison; Rafael de Cabo; Josephine Egan
Archive | 2002
Nigel H. Greig; Josephine Egan; Maire Doyle; Harold Holloway; Tracy Ann Perry
Archive | 2002
Maire Doyle; Josephine Egan; Nigel H. Greig; Harold Holloway; Tracy Ann Perry