Literature DB >> 23465153

Relationship between body mass index and serum testosterone concentration in patients receiving luteinizing hormone-releasing hormone agonist therapy for prostate cancer.

Tim M van der Sluis1, R Jeroen A van Moorselaar, Eric J H Meuleman, Ronald W ter Haar, Hong N Bui, Annemieke C Heijboer, André N Vis.   

Abstract

OBJECTIVE: To evaluate the relationship between the body mass index (BMI) and serum testosterone concentrations in men receiving luteinizing hormone-releasing hormone (LHRH) agonist therapy for prostate cancer.
MATERIALS AND METHODS: A total of 66 white men were included in the present study. All subjects had received LHRH agonist therapy for ≥ 3 months. The BMI was calculated, and the subjects were classified as normal weight (i.e. BMI <25 kg/m(2)), overweight (BMI 25-30 kg/m(2)), or obese (BMI >30 kg/m(2)). The serum testosterone concentration was determined using the highly sensitive isotope dilution-liquid chromatography-tandem mass spectrometry technique. The sex hormone-binding globulin level was determined using an immunometric assay, and the free serum testosterone concentration was calculated.
RESULTS: The median serum testosterone concentration of the patients with a BMI <25 kg/m(2) was 5.5 ng/dL. The patients with a BMI of 25-30 kg/m(2) had a median serum testosterone concentration of 3.8 ng/dL. Those patients with a BMI >30 kg/m(2) had a median concentration of 5.7 ng/dL. No significant difference in the serum testosterone concentrations among the 3 groups was found. The sex hormone-binding globulin levels declined with an increasing BMI. The concentration of free testosterone was significantly greater in the obese men.
CONCLUSION: Using an ultrasensitive technique of serum testosterone measurement, the present data have shown that no difference exists in the serum testosterone concentration in the castrate range among normal weight, overweight, and obese patients receiving LHRH agonist therapy for prostate cancer. From our findings and current knowledge, more stringent follow-up or changes in dosage or dosage intervals of LHRH agonist therapy in those with a greater or high BMI is not warranted.
Copyright © 2013 Elsevier Inc. All rights reserved.

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Year:  2013        PMID: 23465153     DOI: 10.1016/j.urology.2013.01.014

Source DB:  PubMed          Journal:  Urology        ISSN: 0090-4295            Impact factor:   2.649


  3 in total

1.  A semi-mechanistic integrated pharmacokinetic/pharmacodynamic model of the testosterone effects of the gonadotropin-releasing hormone agonist leuprolide in prostate cancer patients.

Authors:  Chay Ngee Lim; Ahmed Hamed Salem
Journal:  Clin Pharmacokinet       Date:  2015-09       Impact factor: 6.447

2.  The prognostic impact of serum testosterone during androgen-deprivation therapy in patients with metastatic prostate cancer and the SRD5A2 polymorphism.

Authors:  M Shiota; N Fujimoto; A Yokomizo; A Takeuchi; E Kashiwagi; T Dejima; K Kiyoshima; J Inokuchi; K Tatsugami; M Eto
Journal:  Prostate Cancer Prostatic Dis       Date:  2016-02-09       Impact factor: 5.554

Review 3.  Targeting alternative sites on the androgen receptor to treat castration-resistant prostate cancer.

Authors:  Nada Lallous; Kush Dalal; Artem Cherkasov; Paul S Rennie
Journal:  Int J Mol Sci       Date:  2013-06-14       Impact factor: 5.923

  3 in total

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