Abstract

Testosterone has effects on many organs and systems. The purpose of this study was to test the hypothesis that low testosterone is associated with changes in various non-cardiovascular biomarkers in men older than 40 who were tested for possible hypogonadism. We extracted data from 9939 outpatient men who were over 40 years old (median age 56) and who also had concurrent laboratory measurements of total testosterone and one or more biomarkers of interest: estradiol, uric acid, prostate-specific antigen (PSA), sex-hormone binding globulin (SHBG), luteinizing hormone, creatinine, bone alkaline phosphatase (BAP), creatine kinase, hemoglobin A1c, and 25-hydroxy-vitamin D, and body mass index (BMI). In a smaller exploratory study of 19 otherwise healthy men presenting for evaluation of possible hypogonadism, pre-albumin (a.k.a.transthyretin, a marker of anabolism) and testosterone were measured. Men with lower levels of testosterone had significantly (p < 0.001) lower mean levels of PSA, SHBG, luteinizing hormone, and estradiol. Overall, men with low levels of testosterone also had significantly (p < 0.001) higher mean levels of LDH and BAP, but these associations varied between men who were younger or older than 56 years. There was a moderate but statistically significant positive correlation (r = 0.63, p < 0.05) between testosterone levels and pre-albumin. These results confirm our hypothesis that testosterone deficiency is associated with a broad range of systemic changes demonstrable in hormonal and non-hormonal serum assays in men over 40 years old being tested for possible hypogonadism.

Highlights

  • 1 1 Serna, Rancho Santa Margarita, CA 92688, USAA recent study has demonstrated that low plasma testosterone is associated with elevated cardiovascular disease biomarkers [1]

  • The primary purpose of the retrospective portion of this study was to test the hypothesis that low testosterone is associated with changes in noncardiovascular biomarkers that are sometimes measured as part of the routine health assessment of men over the age of 40 who are being tested for possible adult onset hypogonadism

  • [11] From Utrecht Patient Oriented Database (UPOD), we extracted data from 9939 male outpatients over 40 years old who had a laboratory measurement of total testosterone levels as well as a measurement of one or more of the following biomarkers on the same day: free testosterone, uric acid, estradiol, prostate-specific antigen (PSA), sex-hormone binding globulin (SHBG), luteinizing hormone (LH), creatinine, bone alkaline phosphatase (BAP), creatine kinase, lactate dehydrogenase (LDH), hemoglobin A1c, 25-hydroxy-vitamin D, and body mass index. These markers were selected for inclusion in this study, because they relate to organs or functions impacted by testosterone and because they were the most likely tests to be routinely ordered as part of the general medical workup of adult men who are being tested for possible hypogonadism

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Summary

Introduction

1 1 Serna, Rancho Santa Margarita, CA 92688, USAA recent study has demonstrated that low plasma testosterone is associated with elevated cardiovascular disease biomarkers [1]. There is little published information available regarding possible associations between low levels of testosterone and changes in non-cardiovascular biomarkers that measure the functions and health of the organs and systems that are influenced by testosterone or its metabolites [4, 5]. Such associations, if they could be demonstrated to exist, might provide important insights into the physiological changes that accompany low testosterone. The primary purpose of the retrospective portion of this study was to test the hypothesis that low testosterone is associated with changes in noncardiovascular biomarkers that are sometimes measured as part of the routine health assessment of men over the age of 40 who are being tested for possible adult onset hypogonadism

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