Lessons From the Testosterone Trials

Abstract The Testosterone Trials (TTrials) were a coordinated set of seven placebo-controlled, double-blind trials in 788 men with a mean age of 72 years to determine the efficacy of increasing the testosterone levels of older men with low testosterone. Testosterone treatment increased the median te...

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Veröffentlicht in:Endocrine reviews 2018-06, Vol.39 (3), p.369-386
Hauptverfasser: Snyder, Peter J, Bhasin, Shalender, Cunningham, Glenn R, Matsumoto, Alvin M, Stephens-Shields, Alisa J, Cauley, Jane A, Gill, Thomas M, Barrett-Connor, Elizabeth, Swerdloff, Ronald S, Wang, Christina, Ensrud, Kristine E, Lewis, Cora E, Farrar, John T, Cella, David, Rosen, Raymond C, Pahor, Marco, Crandall, Jill P, Molitch, Mark E, Resnick, Susan M, Budoff, Matthew, Mohler, Emile R, Wenger, Nanette K, Cohen, Harvey Jay, Schrier, Stanley, Keaveny, Tony M, Kopperdahl, David, Lee, David, Cifelli, Denise, Ellenberg, Susan S
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container_end_page 386
container_issue 3
container_start_page 369
container_title Endocrine reviews
container_volume 39
creator Snyder, Peter J
Bhasin, Shalender
Cunningham, Glenn R
Matsumoto, Alvin M
Stephens-Shields, Alisa J
Cauley, Jane A
Gill, Thomas M
Barrett-Connor, Elizabeth
Swerdloff, Ronald S
Wang, Christina
Ensrud, Kristine E
Lewis, Cora E
Farrar, John T
Cella, David
Rosen, Raymond C
Pahor, Marco
Crandall, Jill P
Molitch, Mark E
Resnick, Susan M
Budoff, Matthew
Mohler, Emile R
Wenger, Nanette K
Cohen, Harvey Jay
Schrier, Stanley
Keaveny, Tony M
Kopperdahl, David
Lee, David
Cifelli, Denise
Ellenberg, Susan S
description Abstract The Testosterone Trials (TTrials) were a coordinated set of seven placebo-controlled, double-blind trials in 788 men with a mean age of 72 years to determine the efficacy of increasing the testosterone levels of older men with low testosterone. Testosterone treatment increased the median testosterone level from unequivocally low at baseline to midnormal for young men after 3 months and maintained that level until month 12. In the Sexual Function Trial, testosterone increased sexual activity, sexual desire, and erectile function. In the Physical Function Trial, testosterone did not increase the distance walked in 6 minutes in men whose walk speed was slow; however, in all TTrial participants, testosterone did increase the distance walked. In the Vitality Trial, testosterone did not increase energy but slightly improved mood and depressive symptoms. In the Cognitive Function Trial, testosterone did not improve cognitive function. In the Anemia Trial, testosterone increased hemoglobin in both men who had anemia of a known cause and in men with unexplained anemia. In the Bone Trial, testosterone increased volumetric bone mineral density and the estimated strength of the spine and hip. In the Cardiovascular Trial, testosterone increased the coronary artery noncalcified plaque volume as assessed using computed tomographic angiography. Although testosterone was not associated with more cardiovascular or prostate adverse events than placebo, a trial of a much larger number of men for a much longer period would be necessary to determine whether testosterone increases cardiovascular or prostate risk. The Testosterone Trials were conducted to determine if testosterone treatment would benefit older men with low testosterone. This report describes the Trials' development and results and the lessons learned.
doi_str_mv 10.1210/er.2017-00234
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Testosterone treatment increased the median testosterone level from unequivocally low at baseline to midnormal for young men after 3 months and maintained that level until month 12. In the Sexual Function Trial, testosterone increased sexual activity, sexual desire, and erectile function. In the Physical Function Trial, testosterone did not increase the distance walked in 6 minutes in men whose walk speed was slow; however, in all TTrial participants, testosterone did increase the distance walked. In the Vitality Trial, testosterone did not increase energy but slightly improved mood and depressive symptoms. In the Cognitive Function Trial, testosterone did not improve cognitive function. In the Anemia Trial, testosterone increased hemoglobin in both men who had anemia of a known cause and in men with unexplained anemia. In the Bone Trial, testosterone increased volumetric bone mineral density and the estimated strength of the spine and hip. 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Testosterone treatment increased the median testosterone level from unequivocally low at baseline to midnormal for young men after 3 months and maintained that level until month 12. In the Sexual Function Trial, testosterone increased sexual activity, sexual desire, and erectile function. In the Physical Function Trial, testosterone did not increase the distance walked in 6 minutes in men whose walk speed was slow; however, in all TTrial participants, testosterone did increase the distance walked. In the Vitality Trial, testosterone did not increase energy but slightly improved mood and depressive symptoms. In the Cognitive Function Trial, testosterone did not improve cognitive function. In the Anemia Trial, testosterone increased hemoglobin in both men who had anemia of a known cause and in men with unexplained anemia. In the Bone Trial, testosterone increased volumetric bone mineral density and the estimated strength of the spine and hip. In the Cardiovascular Trial, testosterone increased the coronary artery noncalcified plaque volume as assessed using computed tomographic angiography. Although testosterone was not associated with more cardiovascular or prostate adverse events than placebo, a trial of a much larger number of men for a much longer period would be necessary to determine whether testosterone increases cardiovascular or prostate risk. The Testosterone Trials were conducted to determine if testosterone treatment would benefit older men with low testosterone. This report describes the Trials' development and results and the lessons learned.</description><subject>Aged</subject><subject>Aging - blood</subject><subject>Androgens - administration &amp; dosage</subject><subject>Androgens - adverse effects</subject><subject>Androgens - pharmacology</subject><subject>Anemia</subject><subject>Angiography</subject><subject>Bone mineral density</subject><subject>Bones</subject><subject>Cardiovascular diseases</subject><subject>Cognitive ability</subject><subject>Computed tomography</subject><subject>Controlled Clinical Trials as Topic</subject><subject>Coronary artery</subject><subject>Density</subject><subject>Editor's Choice</subject><subject>Health risks</subject><subject>Hemoglobin</subject><subject>Hip</subject><subject>Hormone Replacement Therapy</subject><subject>Humans</subject><subject>Male</subject><subject>Men</subject><subject>Mental depression</subject><subject>Mood</subject><subject>Outcome Assessment, Health Care</subject><subject>Pharmaceutical industry</subject><subject>Prostate</subject><subject>Reviews</subject><subject>Sexual disorders</subject><subject>Spine</subject><subject>Testosterone</subject><subject>Testosterone - administration &amp; dosage</subject><subject>Testosterone - adverse effects</subject><subject>Testosterone - blood</subject><subject>Testosterone - pharmacology</subject><issn>0163-769X</issn><issn>1945-7189</issn><issn>1945-7189</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2018</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><sourceid>BENPR</sourceid><recordid>eNp9kkFP3DAQha2qqCy0x16rldoDF2_HTuLYl0oIlRZpJS5U6s1ynAkbmsSLnYD67zvbXSggiizZGvubZ888M_ZewEJIAZ8xLiSIkgPILH_FZsLkBS-FNq_ZDITKeKnMz312kNIVAOSgzRu2L00hJWg9Y5-WmFIY0vw0hn4-rnB-gWkMacQYBgpi67r0lu01tOC73XrIfpx-vTj5zpfn385OjpfcK5A5N1i5wklvlDCq1HXpJQ0noXK6qX1ljASJmZcKFWBd5tpVdZUXxkAtClNkh-zLVnc9VT3WHocxus6uY9u7-NsG19rHJ0O7spfhxiqpS6kFCRztBGK4nqgQ27fJY9e5AcOULHVKGiFybQj9-AS9ClMcqDyiCtAZTQ-oS9ehbYcm0L1-I2qPldFGZAQStXiGolFj33rqY9PS_qMEvk3wMaQUsbmvUYDd2Goxbh5b2r-2Ev_hYWPu6TsfCRBb4DZ0ZF361U23JLFC142rp6L8TjR_IYc-C2RkDacMDYoivtlS_3ocpvX_nr274Q8gLsZ4</recordid><startdate>201806</startdate><enddate>201806</enddate><creator>Snyder, Peter J</creator><creator>Bhasin, Shalender</creator><creator>Cunningham, Glenn R</creator><creator>Matsumoto, Alvin M</creator><creator>Stephens-Shields, Alisa J</creator><creator>Cauley, Jane A</creator><creator>Gill, Thomas M</creator><creator>Barrett-Connor, Elizabeth</creator><creator>Swerdloff, Ronald S</creator><creator>Wang, Christina</creator><creator>Ensrud, Kristine E</creator><creator>Lewis, Cora E</creator><creator>Farrar, John T</creator><creator>Cella, David</creator><creator>Rosen, Raymond C</creator><creator>Pahor, Marco</creator><creator>Crandall, Jill P</creator><creator>Molitch, Mark E</creator><creator>Resnick, Susan M</creator><creator>Budoff, Matthew</creator><creator>Mohler, Emile R</creator><creator>Wenger, Nanette K</creator><creator>Cohen, Harvey Jay</creator><creator>Schrier, Stanley</creator><creator>Keaveny, Tony M</creator><creator>Kopperdahl, David</creator><creator>Lee, David</creator><creator>Cifelli, Denise</creator><creator>Ellenberg, Susan S</creator><general>Endocrine Society</general><general>Copyright Oxford University Press</general><general>Oxford University Press</general><scope>CGR</scope><scope>CUY</scope><scope>CVF</scope><scope>ECM</scope><scope>EIF</scope><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>3V.</scope><scope>7QG</scope><scope>7QL</scope><scope>7QP</scope><scope>7T5</scope><scope>7TK</scope><scope>7TM</scope><scope>7X7</scope><scope>7XB</scope><scope>88E</scope><scope>8FD</scope><scope>8FI</scope><scope>8FJ</scope><scope>8FK</scope><scope>ABUWG</scope><scope>AFKRA</scope><scope>BENPR</scope><scope>C1K</scope><scope>CCPQU</scope><scope>FR3</scope><scope>FYUFA</scope><scope>GHDGH</scope><scope>H94</scope><scope>K9.</scope><scope>M0S</scope><scope>M1P</scope><scope>P64</scope><scope>PQEST</scope><scope>PQQKQ</scope><scope>PQUKI</scope><scope>PRINS</scope><scope>RC3</scope><scope>7X8</scope><scope>5PM</scope></search><sort><creationdate>201806</creationdate><title>Lessons From the Testosterone Trials</title><author>Snyder, Peter J ; Bhasin, Shalender ; Cunningham, Glenn R ; Matsumoto, Alvin M ; Stephens-Shields, Alisa J ; Cauley, Jane A ; Gill, Thomas M ; Barrett-Connor, Elizabeth ; Swerdloff, Ronald S ; Wang, Christina ; Ensrud, Kristine E ; Lewis, Cora E ; Farrar, John T ; Cella, David ; Rosen, Raymond C ; Pahor, Marco ; Crandall, Jill P ; Molitch, Mark E ; Resnick, Susan M ; Budoff, Matthew ; Mohler, Emile R ; Wenger, Nanette K ; Cohen, Harvey Jay ; Schrier, Stanley ; Keaveny, Tony M ; Kopperdahl, David ; Lee, David ; Cifelli, Denise ; Ellenberg, Susan S</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c6024-9eba5a2c9619678d7c2c2ca20ba8fdcb99202e3c26e60ed748abdb45990d15953</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2018</creationdate><topic>Aged</topic><topic>Aging - blood</topic><topic>Androgens - administration &amp; dosage</topic><topic>Androgens - adverse effects</topic><topic>Androgens - pharmacology</topic><topic>Anemia</topic><topic>Angiography</topic><topic>Bone mineral density</topic><topic>Bones</topic><topic>Cardiovascular diseases</topic><topic>Cognitive ability</topic><topic>Computed tomography</topic><topic>Controlled Clinical Trials as Topic</topic><topic>Coronary artery</topic><topic>Density</topic><topic>Editor's Choice</topic><topic>Health risks</topic><topic>Hemoglobin</topic><topic>Hip</topic><topic>Hormone Replacement Therapy</topic><topic>Humans</topic><topic>Male</topic><topic>Men</topic><topic>Mental depression</topic><topic>Mood</topic><topic>Outcome Assessment, Health Care</topic><topic>Pharmaceutical industry</topic><topic>Prostate</topic><topic>Reviews</topic><topic>Sexual disorders</topic><topic>Spine</topic><topic>Testosterone</topic><topic>Testosterone - administration &amp; 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In the Cardiovascular Trial, testosterone increased the coronary artery noncalcified plaque volume as assessed using computed tomographic angiography. Although testosterone was not associated with more cardiovascular or prostate adverse events than placebo, a trial of a much larger number of men for a much longer period would be necessary to determine whether testosterone increases cardiovascular or prostate risk. The Testosterone Trials were conducted to determine if testosterone treatment would benefit older men with low testosterone. This report describes the Trials' development and results and the lessons learned.</abstract><cop>Washington, DC</cop><pub>Endocrine Society</pub><pmid>29522088</pmid><doi>10.1210/er.2017-00234</doi><tpages>18</tpages><oa>free_for_read</oa></addata></record>
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source Oxford University Press Journals All Titles (1996-Current); MEDLINE; EZB-FREE-00999 freely available EZB journals; Alma/SFX Local Collection; Journals@Ovid Complete; ProQuest Central
subjects Aged
Aging - blood
Androgens - administration & dosage
Androgens - adverse effects
Androgens - pharmacology
Anemia
Angiography
Bone mineral density
Bones
Cardiovascular diseases
Cognitive ability
Computed tomography
Controlled Clinical Trials as Topic
Coronary artery
Density
Editor's Choice
Health risks
Hemoglobin
Hip
Hormone Replacement Therapy
Humans
Male
Men
Mental depression
Mood
Outcome Assessment, Health Care
Pharmaceutical industry
Prostate
Reviews
Sexual disorders
Spine
Testosterone
Testosterone - administration & dosage
Testosterone - adverse effects
Testosterone - blood
Testosterone - pharmacology
title Lessons From the Testosterone Trials
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