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Effect of denosumab, a human monoclonal antibody of receptor activator of nuclear factor kappa-B ligand (RANKL), upon glycemic and metabolic parameters: Effect of denosumab on glycemic parameters

Osteoporosis is a complication of type 2 diabetes mellitus (T2DM). Blockade of receptor activator of nuclear factor kappa-B ligand (RANKL) improves osteoporosis, but might also improve glucose tolerance through reduction of hepatic insulin resistance. However, the effect of denosumab (a human monocl...

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Autores principales: Abe, Ichiro, Ochi, Kentaro, Takashi, Yuichi, Yamao, Yuka, Ohishi, Hanako, Fujii, Hideyuki, Minezaki, Midori, Sugimoto, Kaoru, Kudo, Tadachika, Abe, Makiko, Ohnishi, Yasushi, Mukoubara, Shigeaki, Kobayashi, Kunihisa
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Wolters Kluwer Health 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6882599/
https://www.ncbi.nlm.nih.gov/pubmed/31764838
http://dx.doi.org/10.1097/MD.0000000000018067
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author Abe, Ichiro
Ochi, Kentaro
Takashi, Yuichi
Yamao, Yuka
Ohishi, Hanako
Fujii, Hideyuki
Minezaki, Midori
Sugimoto, Kaoru
Kudo, Tadachika
Abe, Makiko
Ohnishi, Yasushi
Mukoubara, Shigeaki
Kobayashi, Kunihisa
author_facet Abe, Ichiro
Ochi, Kentaro
Takashi, Yuichi
Yamao, Yuka
Ohishi, Hanako
Fujii, Hideyuki
Minezaki, Midori
Sugimoto, Kaoru
Kudo, Tadachika
Abe, Makiko
Ohnishi, Yasushi
Mukoubara, Shigeaki
Kobayashi, Kunihisa
author_sort Abe, Ichiro
collection PubMed
description Osteoporosis is a complication of type 2 diabetes mellitus (T2DM). Blockade of receptor activator of nuclear factor kappa-B ligand (RANKL) improves osteoporosis, but might also improve glucose tolerance through reduction of hepatic insulin resistance. However, the effect of denosumab (a human monoclonal antibody of RANKL) upon glycemic and metabolic parameters is controversial. We revealed the effect of denosumab upon glycemic and metabolic parameters for 52 weeks. We evaluated 20 individuals diagnosed with both osteoporosis (male and female: postmenopausal) and T2DM. We measured glycemic and metabolic parameters before and 26/52 weeks after administration of denosumab (60 mg per 26 weeks) without changing any other medication each patient was taking. All patients completed the study without complications and the T-score (lumbar spine and femoral neck) improved significantly from baseline to 52 weeks after denosumab administration (P < .001, .001, respectively). None of the glycemic parameters changed significantly from baseline to 26 weeks after denosumab administration, but levels of glycated hemoglobin and homeostasis model assessment of insulin resistance improved significantly from baseline to 52 weeks after administration (P = .019, .008, respectively). The levels of liver enzymes did not change significantly from baseline to 26 weeks after denosumab administration, but levels of aspartate transaminase and alanine aminotransferase improved significantly from baseline to 52 weeks after administration (P = .014, .004, respectively). None of the markers of lipid metabolism and body mass index changed significantly from baseline to 26/52 weeks after denosumab administration. These data demonstrated that denosumab is useful for T2DM patients with osteoporosis for glycemic control via improvement of insulin resistance. Also, the effect of denosumab might be due to improvement of hepatic function.
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spelling pubmed-68825992020-01-22 Effect of denosumab, a human monoclonal antibody of receptor activator of nuclear factor kappa-B ligand (RANKL), upon glycemic and metabolic parameters: Effect of denosumab on glycemic parameters Abe, Ichiro Ochi, Kentaro Takashi, Yuichi Yamao, Yuka Ohishi, Hanako Fujii, Hideyuki Minezaki, Midori Sugimoto, Kaoru Kudo, Tadachika Abe, Makiko Ohnishi, Yasushi Mukoubara, Shigeaki Kobayashi, Kunihisa Medicine (Baltimore) 4300 Osteoporosis is a complication of type 2 diabetes mellitus (T2DM). Blockade of receptor activator of nuclear factor kappa-B ligand (RANKL) improves osteoporosis, but might also improve glucose tolerance through reduction of hepatic insulin resistance. However, the effect of denosumab (a human monoclonal antibody of RANKL) upon glycemic and metabolic parameters is controversial. We revealed the effect of denosumab upon glycemic and metabolic parameters for 52 weeks. We evaluated 20 individuals diagnosed with both osteoporosis (male and female: postmenopausal) and T2DM. We measured glycemic and metabolic parameters before and 26/52 weeks after administration of denosumab (60 mg per 26 weeks) without changing any other medication each patient was taking. All patients completed the study without complications and the T-score (lumbar spine and femoral neck) improved significantly from baseline to 52 weeks after denosumab administration (P < .001, .001, respectively). None of the glycemic parameters changed significantly from baseline to 26 weeks after denosumab administration, but levels of glycated hemoglobin and homeostasis model assessment of insulin resistance improved significantly from baseline to 52 weeks after administration (P = .019, .008, respectively). The levels of liver enzymes did not change significantly from baseline to 26 weeks after denosumab administration, but levels of aspartate transaminase and alanine aminotransferase improved significantly from baseline to 52 weeks after administration (P = .014, .004, respectively). None of the markers of lipid metabolism and body mass index changed significantly from baseline to 26/52 weeks after denosumab administration. These data demonstrated that denosumab is useful for T2DM patients with osteoporosis for glycemic control via improvement of insulin resistance. Also, the effect of denosumab might be due to improvement of hepatic function. Wolters Kluwer Health 2019-11-22 /pmc/articles/PMC6882599/ /pubmed/31764838 http://dx.doi.org/10.1097/MD.0000000000018067 Text en Copyright © 2019 the Author(s). Published by Wolters Kluwer Health, Inc. http://creativecommons.org/licenses/by/4.0 This is an open access article distributed under the Creative Commons Attribution License 4.0 (CCBY), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited. http://creativecommons.org/licenses/by/4.0
spellingShingle 4300
Abe, Ichiro
Ochi, Kentaro
Takashi, Yuichi
Yamao, Yuka
Ohishi, Hanako
Fujii, Hideyuki
Minezaki, Midori
Sugimoto, Kaoru
Kudo, Tadachika
Abe, Makiko
Ohnishi, Yasushi
Mukoubara, Shigeaki
Kobayashi, Kunihisa
Effect of denosumab, a human monoclonal antibody of receptor activator of nuclear factor kappa-B ligand (RANKL), upon glycemic and metabolic parameters: Effect of denosumab on glycemic parameters
title Effect of denosumab, a human monoclonal antibody of receptor activator of nuclear factor kappa-B ligand (RANKL), upon glycemic and metabolic parameters: Effect of denosumab on glycemic parameters
title_full Effect of denosumab, a human monoclonal antibody of receptor activator of nuclear factor kappa-B ligand (RANKL), upon glycemic and metabolic parameters: Effect of denosumab on glycemic parameters
title_fullStr Effect of denosumab, a human monoclonal antibody of receptor activator of nuclear factor kappa-B ligand (RANKL), upon glycemic and metabolic parameters: Effect of denosumab on glycemic parameters
title_full_unstemmed Effect of denosumab, a human monoclonal antibody of receptor activator of nuclear factor kappa-B ligand (RANKL), upon glycemic and metabolic parameters: Effect of denosumab on glycemic parameters
title_short Effect of denosumab, a human monoclonal antibody of receptor activator of nuclear factor kappa-B ligand (RANKL), upon glycemic and metabolic parameters: Effect of denosumab on glycemic parameters
title_sort effect of denosumab, a human monoclonal antibody of receptor activator of nuclear factor kappa-b ligand (rankl), upon glycemic and metabolic parameters: effect of denosumab on glycemic parameters
topic 4300
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6882599/
https://www.ncbi.nlm.nih.gov/pubmed/31764838
http://dx.doi.org/10.1097/MD.0000000000018067
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