Low bone mass in hypogonadal males. Effect of testosterone substitution therapy, a densitometric study

Sixteen (16) male patients who were suffering from hypogonadism but who were free from bone symptoms were recruited from the Andrology Clinic. Their bone mineral density (BMD) was assessed by single photon absorptiometry in the non-dominant radius, at both the distal radius (DR) (27% trabecular bone...

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Published inMaturitas Vol. 15; no. 1; pp. 17 - 23
Main Authors Devogelaer, J.P., De Cooman, S., de Deuxchaisnes, C.Nagant
Format Journal Article
LanguageEnglish
Published Shannon Elsevier Ireland Ltd 01.08.1992
Elsevier Science
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Abstract Sixteen (16) male patients who were suffering from hypogonadism but who were free from bone symptoms were recruited from the Andrology Clinic. Their bone mineral density (BMD) was assessed by single photon absorptiometry in the non-dominant radius, at both the distal radius (DR) (27% trabecular bone) and the midshaft radius (MR) (90% cortical bone). Measurements were carried out before and during testosterone substitution therapy. BMD was found to be lower in the subjects than in the controls, to a similar extent at both the DR (0.47 ± 0.02 g/cm 2, i.e. 83.1 ± 4.3% of the value in the controls, or Z score −1.42 ± 0.39; P < 0.01) and the MR (0.68 ± 0.02 g/cm 2, i.e. 87.8 ± 2.4% of the value in the controls, or Z score −1.49 ± 0.33; P < 0.01). There was no correlation between testosterone levels and BMD at either the DR or the MR at the beginning of the study. Following testosterone substitution therapy, bone mineral content (BMC) increased significantly at the DR (+5.9 ± 1.4% per year; P < 0.01) and at the MR (+1.1 ± 0.9% per year; P < 0.01). If the study is limited to the subjects who had achieved full bone age maturity before the start of therapy, the bone gain remains significant only at the DR, a site with a sizeable proportion of trabecular bone.
AbstractList Sixteen (16) male patients who were suffering from hypogonadism but who were free from bone symptoms were recruited from the Andrology Clinic. Their bone mineral density (BMD) was assessed by single photon absorptiometry in the non-dominant radius, at both the distal radius (DR) (27% trabecular bone) and the midshaft radius (MR) (90% cortical bone). Measurements were carried out before and during testosterone substitution therapy. BMD was found to be lower in the subjects than in the controls, to a similar extent at both the DR (0.47 +/- 0.02 g/cm2, i.e. 83.1 +/- 4.3% of the value in the controls, or Z score -1.42 +/- 0.39; P less than 0.01) and the MR (0.68 +/- 0.02 g/cm2, i.e. 87.8 +/- 2.4% of the value in the controls, or Z score -1.49 +/- 0.33; P less than 0.01). There was no correlation between testosterone levels and BMD at either the DR or the MR at the beginning of the study. Following testosterone substitution therapy, bone mineral content (BMC) increased significantly at the DR (+5.9 +/- 1.4% per year; P less than 0.01) and at the MR (+1.1 +/- 0.9% per year; P less than 0.01). If the study is limited to the subjects who had achieved full bone age maturity before the start of therapy, the bone gain remains significant only at the DR, a site with a sizeable proportion of trabecular bone.
Sixteen (16) male patients who were suffering from hypogonadism but who were free from bone symptoms were recruited from the Andrology Clinic. Their bone mineral density (BMD) was assessed by single photon absorptiometry in the non-dominant radius, at both the distal radius (DR) (27% trabecular bone) and the midshaft radius (MR) (90% cortical bone). Measurements were carried out before and during testosterone substitution therapy. BMD was found to be lower in the subjects than in the controls, to a similar extent at both the DR (0.47 ± 0.02 g/cm 2, i.e. 83.1 ± 4.3% of the value in the controls, or Z score −1.42 ± 0.39; P < 0.01) and the MR (0.68 ± 0.02 g/cm 2, i.e. 87.8 ± 2.4% of the value in the controls, or Z score −1.49 ± 0.33; P < 0.01). There was no correlation between testosterone levels and BMD at either the DR or the MR at the beginning of the study. Following testosterone substitution therapy, bone mineral content (BMC) increased significantly at the DR (+5.9 ± 1.4% per year; P < 0.01) and at the MR (+1.1 ± 0.9% per year; P < 0.01). If the study is limited to the subjects who had achieved full bone age maturity before the start of therapy, the bone gain remains significant only at the DR, a site with a sizeable proportion of trabecular bone.
Author Devogelaer, J.P.
De Cooman, S.
de Deuxchaisnes, C.Nagant
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Issue 1
Keywords bone mass
osteodensitometry
androgen therapy
male hypogonadism
Human
Osteoporosis
Chemotherapy
Androgen
Diseases of the osteoarticular system
Male
Sex steroid hormone
Male genital diseases
Hypogonadism
Language English
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Elsevier Science
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Snippet Sixteen (16) male patients who were suffering from hypogonadism but who were free from bone symptoms were recruited from the Andrology Clinic. Their bone...
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StartPage 17
SubjectTerms Adolescent
Adult
androgen therapy
Biological and medical sciences
Bone Density
bone mass
Delayed-Action Preparations
Drug Combinations
Gynecology. Andrology. Obstetrics
Humans
Hypogonadism - blood
Hypogonadism - complications
Hypogonadism - drug therapy
Male
Male genital diseases
male hypogonadism
Medical sciences
Middle Aged
Non tumoral diseases
osteodensitometry
Osteoporosis - diagnosis
Osteoporosis - etiology
Osteoporosis - pathology
Testosterone - analogs & derivatives
Testosterone - blood
Testosterone - therapeutic use
Title Low bone mass in hypogonadal males. Effect of testosterone substitution therapy, a densitometric study
URI https://dx.doi.org/10.1016/0378-5122(92)90057-B
https://www.ncbi.nlm.nih.gov/pubmed/1528128
https://search.proquest.com/docview/73205613
Volume 15
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