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Effect of denosumab on renal function in women with osteoporosis evaluated using cystatin C

OBJECTIVES: To investigate renal function during denosumab therapy using the estimated glomerular filtration rate based on cystatin C (eGFRcys) which is more accurate than creatinine (eGFRcr) for renal function. METHODS: Bone mineral densities (BMDs) of lumbar spine and hip regions, eGFRcys, eGFRcr,...

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Autores principales: Ohishi, Tsuyoshi, Fujita, Tomotada, Nishida, Tatsuya, Hagiwara, Kazuhiro, Murai, Reina, Matsuyama, Yukihiro
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Korean Society of Osteoporosis 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9263171/
https://www.ncbi.nlm.nih.gov/pubmed/35832419
http://dx.doi.org/10.1016/j.afos.2022.05.002
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author Ohishi, Tsuyoshi
Fujita, Tomotada
Nishida, Tatsuya
Hagiwara, Kazuhiro
Murai, Reina
Matsuyama, Yukihiro
author_facet Ohishi, Tsuyoshi
Fujita, Tomotada
Nishida, Tatsuya
Hagiwara, Kazuhiro
Murai, Reina
Matsuyama, Yukihiro
author_sort Ohishi, Tsuyoshi
collection PubMed
description OBJECTIVES: To investigate renal function during denosumab therapy using the estimated glomerular filtration rate based on cystatin C (eGFRcys) which is more accurate than creatinine (eGFRcr) for renal function. METHODS: Bone mineral densities (BMDs) of lumbar spine and hip regions, eGFRcys, eGFRcr, creatinine clearance (Ccr), and serum total homocysteine (S-Hcy) were measured during 2-year denosumab therapy in 53 women with osteoporosis naïve to anti-osteoporosis drugs (new group) and 64 women who were switched from long-term bisphosphonate treatment to denosumab therapy (switch group). RESULTS: There were no significant differences in age, eGFRcr, Ccr, eGFRcys, and S-Hcy levels at baseline between the groups. BMDs in the lumbar spine, femoral neck, and total hip increased significantly after 2-year denosumab therapy in both groups. eGFRcr decreased in the switch group, and Ccr decreased in both groups; however, eGFRcys and S-Hcy levels did not change significantly in either group. To investigate the causal factors associated with the decrease in eGFRcr and Ccr, multiple regression analysis was performed in all patients. Denosumab initiation within 3 months after fracture and eGFRcr or Ccr at baseline were independent factors for the decrease in eGFRcr or Ccr during the 2-year denosumab therapy. Decline in creatinine-based renal function could be reflected by increased muscle mass during the ongoing recovery from fracture. CONCLUSIONS: Renal function was preserved in all patients, including those in the switch group during denosumab therapy. Creatinine-based renal function should be cautiously interpreted during denosumab therapy in patients with recent fractures.
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spelling pubmed-92631712022-07-12 Effect of denosumab on renal function in women with osteoporosis evaluated using cystatin C Ohishi, Tsuyoshi Fujita, Tomotada Nishida, Tatsuya Hagiwara, Kazuhiro Murai, Reina Matsuyama, Yukihiro Osteoporos Sarcopenia Original Article OBJECTIVES: To investigate renal function during denosumab therapy using the estimated glomerular filtration rate based on cystatin C (eGFRcys) which is more accurate than creatinine (eGFRcr) for renal function. METHODS: Bone mineral densities (BMDs) of lumbar spine and hip regions, eGFRcys, eGFRcr, creatinine clearance (Ccr), and serum total homocysteine (S-Hcy) were measured during 2-year denosumab therapy in 53 women with osteoporosis naïve to anti-osteoporosis drugs (new group) and 64 women who were switched from long-term bisphosphonate treatment to denosumab therapy (switch group). RESULTS: There were no significant differences in age, eGFRcr, Ccr, eGFRcys, and S-Hcy levels at baseline between the groups. BMDs in the lumbar spine, femoral neck, and total hip increased significantly after 2-year denosumab therapy in both groups. eGFRcr decreased in the switch group, and Ccr decreased in both groups; however, eGFRcys and S-Hcy levels did not change significantly in either group. To investigate the causal factors associated with the decrease in eGFRcr and Ccr, multiple regression analysis was performed in all patients. Denosumab initiation within 3 months after fracture and eGFRcr or Ccr at baseline were independent factors for the decrease in eGFRcr or Ccr during the 2-year denosumab therapy. Decline in creatinine-based renal function could be reflected by increased muscle mass during the ongoing recovery from fracture. CONCLUSIONS: Renal function was preserved in all patients, including those in the switch group during denosumab therapy. Creatinine-based renal function should be cautiously interpreted during denosumab therapy in patients with recent fractures. Korean Society of Osteoporosis 2022-06 2022-05-27 /pmc/articles/PMC9263171/ /pubmed/35832419 http://dx.doi.org/10.1016/j.afos.2022.05.002 Text en © 2022 The Korean Society of Osteoporosis. Publishing services by Elsevier B.V. https://creativecommons.org/licenses/by-nc-nd/4.0/This is an open access article under the CC BY-NC-ND license (http://creativecommons.org/licenses/by-nc-nd/4.0/).
spellingShingle Original Article
Ohishi, Tsuyoshi
Fujita, Tomotada
Nishida, Tatsuya
Hagiwara, Kazuhiro
Murai, Reina
Matsuyama, Yukihiro
Effect of denosumab on renal function in women with osteoporosis evaluated using cystatin C
title Effect of denosumab on renal function in women with osteoporosis evaluated using cystatin C
title_full Effect of denosumab on renal function in women with osteoporosis evaluated using cystatin C
title_fullStr Effect of denosumab on renal function in women with osteoporosis evaluated using cystatin C
title_full_unstemmed Effect of denosumab on renal function in women with osteoporosis evaluated using cystatin C
title_short Effect of denosumab on renal function in women with osteoporosis evaluated using cystatin C
title_sort effect of denosumab on renal function in women with osteoporosis evaluated using cystatin c
topic Original Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9263171/
https://www.ncbi.nlm.nih.gov/pubmed/35832419
http://dx.doi.org/10.1016/j.afos.2022.05.002
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