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Testosterone Replacement and Bone Mineral Density in Male Pituitary Tumor Patients

BACKGROUND: Hypopituitarism is associated with osteoporosis and osteopenia especially when hypogonadotropic hypogonadism is present. Despite hypopituitarism being an important cause of secondary osteoporosis, osteoporosis in patients receiving surgery for pituitary tumors in Korea has not been studi...

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Autores principales: Lee, Min Jeong, Ryu, Hyoung Kyu, An, So-Yeon, Jeon, Ja Young, Lee, Ji In, Chung, Yoon-Sok
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Korean Endocrine Society 2014
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3970284/
https://www.ncbi.nlm.nih.gov/pubmed/24741454
http://dx.doi.org/10.3803/EnM.2014.29.1.48
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author Lee, Min Jeong
Ryu, Hyoung Kyu
An, So-Yeon
Jeon, Ja Young
Lee, Ji In
Chung, Yoon-Sok
author_facet Lee, Min Jeong
Ryu, Hyoung Kyu
An, So-Yeon
Jeon, Ja Young
Lee, Ji In
Chung, Yoon-Sok
author_sort Lee, Min Jeong
collection PubMed
description BACKGROUND: Hypopituitarism is associated with osteoporosis and osteopenia especially when hypogonadotropic hypogonadism is present. Despite hypopituitarism being an important cause of secondary osteoporosis, osteoporosis in patients receiving surgery for pituitary tumors in Korea has not been studied. In this study, we evaluated the effects of testosterone replacement therapy (TRT) on bone mineral density (BMD) in postoperative hypogonadal patients with pituitary tumors. METHODS: To examine the effect of TRT on BMD, we performed a retrospective observational study in 21 postoperative male patients who underwent pituitary tumor surgery between 2003 and 2012 at the Ajou University Hospital. Testosterone was replaced in postoperative hypogonadal patients by regular intramuscular injection, daily oral medication, or application of transdermal gel. BMD (g/cm(2)) measurements of central skeletal sites (lumbar spine, femoral neck, and total femur) were obtained using dual-energy X-ray absorptiometry (GE Lunar). For lumbar spine BMD, L1 to L4 values were chosen for analysis. Femur neck and total femur were also analyzed. RESULTS: During the follow-up period (mean, 56 months; range, 12 to 99 months) serum testosterone levels increased with the administration of TRT (P=0.007). There was significant improvement (4.56%±9.81%) in the lumbar spine BMD compared to baseline BMD. There were no significant changes in the femur neck BMD or total femur BMD. We did not find any statistically significant relationships between changes in testosterone levels and BMD using Spearman correlation analysis. CONCLUSION: Our results indicated that TRT used in the postoperative period for hypogonadal pituitary tumor surgery patients may have beneficial effects on the BMD of the spine.
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spelling pubmed-39702842014-04-16 Testosterone Replacement and Bone Mineral Density in Male Pituitary Tumor Patients Lee, Min Jeong Ryu, Hyoung Kyu An, So-Yeon Jeon, Ja Young Lee, Ji In Chung, Yoon-Sok Endocrinol Metab (Seoul) Original Article BACKGROUND: Hypopituitarism is associated with osteoporosis and osteopenia especially when hypogonadotropic hypogonadism is present. Despite hypopituitarism being an important cause of secondary osteoporosis, osteoporosis in patients receiving surgery for pituitary tumors in Korea has not been studied. In this study, we evaluated the effects of testosterone replacement therapy (TRT) on bone mineral density (BMD) in postoperative hypogonadal patients with pituitary tumors. METHODS: To examine the effect of TRT on BMD, we performed a retrospective observational study in 21 postoperative male patients who underwent pituitary tumor surgery between 2003 and 2012 at the Ajou University Hospital. Testosterone was replaced in postoperative hypogonadal patients by regular intramuscular injection, daily oral medication, or application of transdermal gel. BMD (g/cm(2)) measurements of central skeletal sites (lumbar spine, femoral neck, and total femur) were obtained using dual-energy X-ray absorptiometry (GE Lunar). For lumbar spine BMD, L1 to L4 values were chosen for analysis. Femur neck and total femur were also analyzed. RESULTS: During the follow-up period (mean, 56 months; range, 12 to 99 months) serum testosterone levels increased with the administration of TRT (P=0.007). There was significant improvement (4.56%±9.81%) in the lumbar spine BMD compared to baseline BMD. There were no significant changes in the femur neck BMD or total femur BMD. We did not find any statistically significant relationships between changes in testosterone levels and BMD using Spearman correlation analysis. CONCLUSION: Our results indicated that TRT used in the postoperative period for hypogonadal pituitary tumor surgery patients may have beneficial effects on the BMD of the spine. Korean Endocrine Society 2014-03 2014-03-14 /pmc/articles/PMC3970284/ /pubmed/24741454 http://dx.doi.org/10.3803/EnM.2014.29.1.48 Text en Copyright © 2014 Korean Endocrine Society http://creativecommons.org/licenses/by-nc/3.0/ This is an Open Access article distributed under the terms of the Creative Commons Attribution Non-Commercial License (http://creativecommons.org/licenses/by-nc/3.0/) which permits unrestricted non-commercial use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Original Article
Lee, Min Jeong
Ryu, Hyoung Kyu
An, So-Yeon
Jeon, Ja Young
Lee, Ji In
Chung, Yoon-Sok
Testosterone Replacement and Bone Mineral Density in Male Pituitary Tumor Patients
title Testosterone Replacement and Bone Mineral Density in Male Pituitary Tumor Patients
title_full Testosterone Replacement and Bone Mineral Density in Male Pituitary Tumor Patients
title_fullStr Testosterone Replacement and Bone Mineral Density in Male Pituitary Tumor Patients
title_full_unstemmed Testosterone Replacement and Bone Mineral Density in Male Pituitary Tumor Patients
title_short Testosterone Replacement and Bone Mineral Density in Male Pituitary Tumor Patients
title_sort testosterone replacement and bone mineral density in male pituitary tumor patients
topic Original Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3970284/
https://www.ncbi.nlm.nih.gov/pubmed/24741454
http://dx.doi.org/10.3803/EnM.2014.29.1.48
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