TY - JOUR
T1 - Testosterone replacement therapy in older male subjective memory complainers
T2 - double-blind randomized crossover placebo-controlled clinical trial of physiological assessment and safety
AU - Asih, Prita R.
AU - Wahjoepramono, Eka J.
AU - Aniwiyanti, Vilia
AU - Wijaya, Linda K.
AU - de Ruyck, Karl
AU - Taddei, Kevin
AU - Fuller, Stephanie J
AU - Sohrabi, Hamid
AU - Dhaliwal, Satvinder S.
AU - Verdile, Giuseppe
AU - Carruthers, Malcolm
AU - Martins, Ralph N.
PY - 2015
Y1 - 2015
N2 - Testosterone replacement therapy (TRT) has been investigated in older men as a preventative treatment against Alzheimer’s disease and dementia. However, previous studies have been contradictory. We assessed TRT physiological effects in 44 older men (aged 61 ± 7.7 years) with subjective memory complaints using a double blind, randomized, crossover, placebo-controlled study. Participants were randomized into 2 groups, one group received transdermal testosterone (50 mg) daily for 24 weeks, followed by a 4 week wash-out period, then 24 weeks of placebo; the other group received the reverse treatment. Blood evaluation revealed significant increases in total testosterone, free (calculated) testosterone, dihydrotestosterone, and a decrease in luteinizing hormone levels (p<0.001) following TRT. Although there were significant increases in red blood cell counts, hemoglobin and prostate specific antigen levels following TRT, they remained within normal ranges. No significant differences in plasma amyloid beta, estradiol, sex hormone binding globulin, insulin levels, body fat percentage, or body mass index were detected. This is the first carefully controlled study that has investigated the influence of TRT in Indonesian men on blood biomarkers linked to dementia risk. Our study suggests TRT is safe and well-tolerated in this Indonesian cohort, yet longitudinal studies with larger cohorts are needed to assess TRT further, and to establish whether TRT reduces dementia risk.
AB - Testosterone replacement therapy (TRT) has been investigated in older men as a preventative treatment against Alzheimer’s disease and dementia. However, previous studies have been contradictory. We assessed TRT physiological effects in 44 older men (aged 61 ± 7.7 years) with subjective memory complaints using a double blind, randomized, crossover, placebo-controlled study. Participants were randomized into 2 groups, one group received transdermal testosterone (50 mg) daily for 24 weeks, followed by a 4 week wash-out period, then 24 weeks of placebo; the other group received the reverse treatment. Blood evaluation revealed significant increases in total testosterone, free (calculated) testosterone, dihydrotestosterone, and a decrease in luteinizing hormone levels (p<0.001) following TRT. Although there were significant increases in red blood cell counts, hemoglobin and prostate specific antigen levels following TRT, they remained within normal ranges. No significant differences in plasma amyloid beta, estradiol, sex hormone binding globulin, insulin levels, body fat percentage, or body mass index were detected. This is the first carefully controlled study that has investigated the influence of TRT in Indonesian men on blood biomarkers linked to dementia risk. Our study suggests TRT is safe and well-tolerated in this Indonesian cohort, yet longitudinal studies with larger cohorts are needed to assess TRT further, and to establish whether TRT reduces dementia risk.
KW - Aging
KW - Alzheimer’s disease
KW - Dementia
KW - Luteinizing hormone
KW - Plasma
KW - Testosterone
UR - http://www.scopus.com/inward/record.url?scp=84930520226&partnerID=8YFLogxK
U2 - 10.2174/1871527314666150429112112
DO - 10.2174/1871527314666150429112112
M3 - Article
VL - 14
SP - 576
EP - 586
JO - CNS & Neurological Disorders - Drug Targets
JF - CNS & Neurological Disorders - Drug Targets
SN - 1871-5273
IS - 5
ER -