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Published in: Endocrine 1/2023

03-10-2022 | Chronic Kidney Disease | Original Article

Roxadustat improves renal osteodystrophy by dual regulation of bone remodeling

Authors: Luyao Li, Afang Li, Liangying Gan, Li Zuo

Published in: Endocrine | Issue 1/2023

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Abstract

Purpose

Renal osteodystrophy (ROD), a component of chronic kidney disease-mineral and bone disorder (CKD-MBD) can lead to bone loss increasing fracture risks in CKD patients. Therefore, it is important to prevent and treat ROD. Activation of hypoxia-inducible factor-1α (HIF-1α) signaling was reported to prevent osteoporotic bone loss. Roxadustat, which is used to treat renal anemia in the clinic, is a novel HIF stabilizer. In our study, we aimed to investigate the effects of roxadustat on ROD.

Methods

We established an adenine-induced CKD rat model. Roxadustat was administered intragastrically to normal and CKD rats for 4 weeks. Hemoglobin concentrations and serum biochemical parameters were tested, and bone histomorphometric analysis was performed.

Results

CKD rats exhibited impaired renal function with anemia, secondary hyperparathyroidism and high-turnover ROD-induced significant bone loss. Roxadustat ameliorated renal anemia and attenuated the extreme increase in intact parathyroid hormone (iPTH) and fibroblast growth factor 23 (FGF23) in CKD rats. Bone histomorphometric analysis showed that roxadustat significantly alleviated bone loss and bone microarchitecture deterioration in CKD rats by increasing osteoblast activity and inhibiting osteoclast activity. We did not find that roxadustat had significant effects on bone metabolism in normal rats.

Conclusion

Roxadustat can improve ROD via dual regulation of bone remodeling. The use of roxadustat may be a promising strategy to treat osteoporotic bone disorders, such as ROD.
Appendix
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Literature
1.
go back to reference KDIGO 2017, clinical practice guideline update for the diagnosis, evaluation, prevention, and treatment of chronic kidney disease-mineral and bone disorder (CKD-MBD). Kidney Int Suppl. (2011) 7(1), 1–59 (2017)CrossRef KDIGO 2017, clinical practice guideline update for the diagnosis, evaluation, prevention, and treatment of chronic kidney disease-mineral and bone disorder (CKD-MBD). Kidney Int Suppl. (2011) 7(1), 1–59 (2017)CrossRef
2.
go back to reference M. Pazianas, P.D. Miller, Osteoporosis and chronic kidney disease-mineral and bone disorder (CKD-MBD): back to basics. Am. J. Kidney Dis. 78(4), 582–589 (2021)CrossRef M. Pazianas, P.D. Miller, Osteoporosis and chronic kidney disease-mineral and bone disorder (CKD-MBD): back to basics. Am. J. Kidney Dis. 78(4), 582–589 (2021)CrossRef
3.
go back to reference C. Ginsberg, J.H. Ix, Diagnosis and management of osteoporosis in advanced kidney disease: a review. Am. J. Kidney Dis. 79(3), 427–436 (2022)CrossRef C. Ginsberg, J.H. Ix, Diagnosis and management of osteoporosis in advanced kidney disease: a review. Am. J. Kidney Dis. 79(3), 427–436 (2022)CrossRef
4.
go back to reference E. Schipani, Posttranslational modifications of collagens as targets of hypoxia and Hif-1α in endochondral bone development. Ann. N. Y Acad. Sci. 1192, 317–321 (2010)CrossRef E. Schipani, Posttranslational modifications of collagens as targets of hypoxia and Hif-1α in endochondral bone development. Ann. N. Y Acad. Sci. 1192, 317–321 (2010)CrossRef
5.
go back to reference S. Stegen, G. Carmeliet, The skeletal vascular system - breathing life into bone tissue. Bone 115, 50–58 (2018)CrossRef S. Stegen, G. Carmeliet, The skeletal vascular system - breathing life into bone tissue. Bone 115, 50–58 (2018)CrossRef
6.
go back to reference Y. Wang, C. Wan, L. Deng, X. Liu, X. Cao, S.R. Gilbert et al. The hypoxia-inducible factor α pathway couples angiogenesis to osteogenesis during skeletal development. J. Clin. Invest 117(6), 1616–1626 (2007)CrossRef Y. Wang, C. Wan, L. Deng, X. Liu, X. Cao, S.R. Gilbert et al. The hypoxia-inducible factor α pathway couples angiogenesis to osteogenesis during skeletal development. J. Clin. Invest 117(6), 1616–1626 (2007)CrossRef
7.
go back to reference L. Zhang, L. Jin, J. Guo, K. Bao, J. Hu, Y. Zhang et al. Chronic intermittent hypobaric hypoxia enhances bone fracture healing. Front Endocrinol. (Lausanne) 11, 582670 (2021)CrossRef L. Zhang, L. Jin, J. Guo, K. Bao, J. Hu, Y. Zhang et al. Chronic intermittent hypobaric hypoxia enhances bone fracture healing. Front Endocrinol. (Lausanne) 11, 582670 (2021)CrossRef
8.
go back to reference C. Wan, S.R. Gilbert, Y. Wang, X. Cao, X. Shen, G. Ramaswamy et al. Activation of the hypoxia-inducible factor-1α pathway accelerates bone regeneration. Proc. Natl. Acad. Sci. USA 105(2), 686–691 (2008)CrossRef C. Wan, S.R. Gilbert, Y. Wang, X. Cao, X. Shen, G. Ramaswamy et al. Activation of the hypoxia-inducible factor-1α pathway accelerates bone regeneration. Proc. Natl. Acad. Sci. USA 105(2), 686–691 (2008)CrossRef
9.
go back to reference C. Wu, E.B. Rankin, L. Castellini, J.F. Alcudia, E.L. LaGory, R. Andersen et al. Oxygen-sensing PHDs regulate bone homeostasis through the modulation of osteoprotegerin. Genes Dev. 29(8), 817–831 (2015)CrossRef C. Wu, E.B. Rankin, L. Castellini, J.F. Alcudia, E.L. LaGory, R. Andersen et al. Oxygen-sensing PHDs regulate bone homeostasis through the modulation of osteoprotegerin. Genes Dev. 29(8), 817–831 (2015)CrossRef
10.
go back to reference Q. Zhao, X. Shen, W. Zhang, G. Zhu, J. Qi, L. Deng, Mice with increased angiogenesis and osteogenesis due to conditional activation of HIF pathway in osteoblasts are protected from ovariectomy induced bone loss. Bone 50(3), 763–770 (2012)CrossRef Q. Zhao, X. Shen, W. Zhang, G. Zhu, J. Qi, L. Deng, Mice with increased angiogenesis and osteogenesis due to conditional activation of HIF pathway in osteoblasts are protected from ovariectomy induced bone loss. Bone 50(3), 763–770 (2012)CrossRef
11.
go back to reference L. Yi, Y. Ju, Y. He, X. Yin, Y. Xu, T. Weng, Intraperitoneal injection of Desferal® alleviated the age-related bone loss and senescence of bone marrow stromal cells in rats. Stem Cell Res Ther. 12(1), 45 (2021)CrossRef L. Yi, Y. Ju, Y. He, X. Yin, Y. Xu, T. Weng, Intraperitoneal injection of Desferal® alleviated the age-related bone loss and senescence of bone marrow stromal cells in rats. Stem Cell Res Ther. 12(1), 45 (2021)CrossRef
12.
go back to reference C. Guo, K. Yang, Y. Yan, D. Yan, Y. Cheng, X. Yan et al. SF-deferoxamine, a bone-seeking angiogenic drug, prevents bone loss in estrogen-deficient mice. Bone 120, 156–165 (2019)CrossRef C. Guo, K. Yang, Y. Yan, D. Yan, Y. Cheng, X. Yan et al. SF-deferoxamine, a bone-seeking angiogenic drug, prevents bone loss in estrogen-deficient mice. Bone 120, 156–165 (2019)CrossRef
13.
go back to reference X. Liu, Y. Tu, L. Zhang, J. Qi, T. Ma, L. Deng, Prolyl hydroxylase inhibitors protect from the bone loss in ovariectomy rats by increasing bone vascularity. Cell Biochem Biophys. 69(1), 141–149 (2014)CrossRef X. Liu, Y. Tu, L. Zhang, J. Qi, T. Ma, L. Deng, Prolyl hydroxylase inhibitors protect from the bone loss in ovariectomy rats by increasing bone vascularity. Cell Biochem Biophys. 69(1), 141–149 (2014)CrossRef
14.
go back to reference J. Peng, Z.G. Lai, Z.L. Fang, S. Xing, K. Hui, C. Hao et al. Dimethyloxalylglycine prevents bone loss in ovariectomized C57BL/6J mice through enhanced angiogenesis and osteogenesis. PLoS One 9(11), e112744 (2014)CrossRef J. Peng, Z.G. Lai, Z.L. Fang, S. Xing, K. Hui, C. Hao et al. Dimethyloxalylglycine prevents bone loss in ovariectomized C57BL/6J mice through enhanced angiogenesis and osteogenesis. PLoS One 9(11), e112744 (2014)CrossRef
15.
go back to reference S. Dhillon, Roxadustat: first global approval. Drugs 79(5), 563–572 (2019)CrossRef S. Dhillon, Roxadustat: first global approval. Drugs 79(5), 563–572 (2019)CrossRef
16.
go back to reference A.A. Joharapurkar, V.B. Pandya, V.J. Patel, R.C. Desai, M.R. Jain, Prolyl hydroxylase inhibitors: a breakthrough in the therapy of anemia associated with chronic diseases. J. Med Chem. 61(16), 6964–6982 (2018)CrossRef A.A. Joharapurkar, V.B. Pandya, V.J. Patel, R.C. Desai, M.R. Jain, Prolyl hydroxylase inhibitors: a breakthrough in the therapy of anemia associated with chronic diseases. J. Med Chem. 61(16), 6964–6982 (2018)CrossRef
17.
go back to reference P.A. Hulley, I. Papadimitriou-Olivgeri, H.J. Knowles, Osteoblast-osteoclast coculture amplifies inhibitory effects of FG-4592 on human osteoclastogenesis and reduces bone resorption. JBMR 4(7), e10370 (2020) P.A. Hulley, I. Papadimitriou-Olivgeri, H.J. Knowles, Osteoblast-osteoclast coculture amplifies inhibitory effects of FG-4592 on human osteoclastogenesis and reduces bone resorption. JBMR 4(7), e10370 (2020)
18.
go back to reference C. Chen, S. Yan, S. Qiu, Z. Geng, Z. Wang, HIF/Ca2+/NO/ROS is critical in roxadustat treating bone fracture by stimulating the proliferation and migration of BMSCs. Life Sci. 264, 118684 (2021)CrossRef C. Chen, S. Yan, S. Qiu, Z. Geng, Z. Wang, HIF/Ca2+/NO/ROS is critical in roxadustat treating bone fracture by stimulating the proliferation and migration of BMSCs. Life Sci. 264, 118684 (2021)CrossRef
19.
go back to reference P.G. Reeves, F.H. Nielsen, G.C. Fahey Jr, AIN-93 purified diets for laboratory rodents: final report of the American Institute of Nutrition ad hoc writing committee on the reformulation of the AIN-76A rodent diet. J. Nutr. 123(11), 1939–1951 (1993)CrossRef P.G. Reeves, F.H. Nielsen, G.C. Fahey Jr, AIN-93 purified diets for laboratory rodents: final report of the American Institute of Nutrition ad hoc writing committee on the reformulation of the AIN-76A rodent diet. J. Nutr. 123(11), 1939–1951 (1993)CrossRef
20.
go back to reference M.L. Bouxsein, S.K. Boyd, B.A. Christiansen, R.E. Guldberg, K.J. Jepsen, R. Müller, Guidelines for assessment of bone microstructure in rodents using micro-computed tomography. J. Bone Min. Res 25(7), 1468–1486 (2010)CrossRef M.L. Bouxsein, S.K. Boyd, B.A. Christiansen, R.E. Guldberg, K.J. Jepsen, R. Müller, Guidelines for assessment of bone microstructure in rodents using micro-computed tomography. J. Bone Min. Res 25(7), 1468–1486 (2010)CrossRef
21.
go back to reference D.W. Dempster, J.E. Compston, M.K. Drezner, F.H. Glorieux, J.A. Kanis, H. Malluche et al. Standardized nomenclature, symbols, and units for bone histomorphometry: a 2012 update of the report of the ASBMR Histomorphometry Nomenclature Committee. J. Bone Min. Res 28(1), 2–17 (2013)CrossRef D.W. Dempster, J.E. Compston, M.K. Drezner, F.H. Glorieux, J.A. Kanis, H. Malluche et al. Standardized nomenclature, symbols, and units for bone histomorphometry: a 2012 update of the report of the ASBMR Histomorphometry Nomenclature Committee. J. Bone Min. Res 28(1), 2–17 (2013)CrossRef
22.
go back to reference A.C. Ferreira, P. Cotovio, I. Aires, M. Mendes, D. Navarro, C. Silva et al. The role of bone volume, FGF23 and sclerostin in calcifications and mortality; a cohort study in CKD stage 5 patients. Calcif. Tissue Int. 110(2), 215–224 (2022)CrossRef A.C. Ferreira, P. Cotovio, I. Aires, M. Mendes, D. Navarro, C. Silva et al. The role of bone volume, FGF23 and sclerostin in calcifications and mortality; a cohort study in CKD stage 5 patients. Calcif. Tissue Int. 110(2), 215–224 (2022)CrossRef
23.
go back to reference X. Lu, M.C. Hu, Klotho/FGF23 axis in chronic kidney disease and cardiovascular disease. Kidney Dis. (Basel) 3(1), 15–23 (2017)CrossRef X. Lu, M.C. Hu, Klotho/FGF23 axis in chronic kidney disease and cardiovascular disease. Kidney Dis. (Basel) 3(1), 15–23 (2017)CrossRef
24.
go back to reference S. Singh, A. Grabner, C. Yanucil, K. Schramm, B. Czaya, S. Krick et al. Fibroblast growth factor 23 directly targets hepatocytes to promote inflammation in chronic kidney disease. Kidney Int 90(5), 985–996 (2016)CrossRef S. Singh, A. Grabner, C. Yanucil, K. Schramm, B. Czaya, S. Krick et al. Fibroblast growth factor 23 directly targets hepatocytes to promote inflammation in chronic kidney disease. Kidney Int 90(5), 985–996 (2016)CrossRef
25.
go back to reference M.L. Noonan, E.L. Clinkenbeard, P. Ni, E.A. Swallow, S.P. Tippen, R. Agoro et al. Erythropoietin and a hypoxia-inducible factor prolyl hydroxylase inhibitor (HIF-PHDi) lowers FGF23 in a model of chronic kidney disease (CKD). Physiol. Rep. 8(11), e14434 (2020)CrossRef M.L. Noonan, E.L. Clinkenbeard, P. Ni, E.A. Swallow, S.P. Tippen, R. Agoro et al. Erythropoietin and a hypoxia-inducible factor prolyl hydroxylase inhibitor (HIF-PHDi) lowers FGF23 in a model of chronic kidney disease (CKD). Physiol. Rep. 8(11), e14434 (2020)CrossRef
26.
go back to reference E. Patino, O. Akchurin, Erythropoiesis-independent effects of iron in chronic kidney disease. Pediatr. Nephrol. 37(4), 777–788 (2022)CrossRef E. Patino, O. Akchurin, Erythropoiesis-independent effects of iron in chronic kidney disease. Pediatr. Nephrol. 37(4), 777–788 (2022)CrossRef
27.
go back to reference V. Jeney, Clinical impact and cellular mechanisms of iron overload-associated bone loss. Front Pharm. 8, 77 (2017)CrossRef V. Jeney, Clinical impact and cellular mechanisms of iron overload-associated bone loss. Front Pharm. 8, 77 (2017)CrossRef
28.
go back to reference E. Balogh, G. Paragh, V. Jeney, Influence of iron on bone homeostasis. Pharm. (Basel) 11(4), 107 (2018)CrossRef E. Balogh, G. Paragh, V. Jeney, Influence of iron on bone homeostasis. Pharm. (Basel) 11(4), 107 (2018)CrossRef
29.
go back to reference Z. Liu, K. Yang, X. Yan, T. Wang, T. Jiang, Q. Zhou et al. The effects of tranylcypromine on osteoclastogenesis in vitro and in vivo. FASEB J. 33(9), 9828–9841 (2019)CrossRef Z. Liu, K. Yang, X. Yan, T. Wang, T. Jiang, Q. Zhou et al. The effects of tranylcypromine on osteoclastogenesis in vitro and in vivo. FASEB J. 33(9), 9828–9841 (2019)CrossRef
30.
go back to reference Y.M. Zhou, Y.Y. Yang, Y.X. Jing, T.J. Yuan, L.H. Sun, B. Tao et al. BMP9 reduces bone loss in ovariectomized mice by dual regulation of bone remodeling. J. Bone Min. Res 35(5), 978–993 (2020)CrossRef Y.M. Zhou, Y.Y. Yang, Y.X. Jing, T.J. Yuan, L.H. Sun, B. Tao et al. BMP9 reduces bone loss in ovariectomized mice by dual regulation of bone remodeling. J. Bone Min. Res 35(5), 978–993 (2020)CrossRef
31.
go back to reference N. Chen, C. Hao, B.C. Liu, H. Lin, C. Wang, C. Xing et al. Roxadustat treatment for anemia in patients undergoing long-term dialysis. N. Engl. J. Med 381(11), 1011–1022 (2019)CrossRef N. Chen, C. Hao, B.C. Liu, H. Lin, C. Wang, C. Xing et al. Roxadustat treatment for anemia in patients undergoing long-term dialysis. N. Engl. J. Med 381(11), 1011–1022 (2019)CrossRef
32.
go back to reference S. Fishbane, M.A. El-Shahawy, R. Pecoits-Filho, B.P. Van, M.T. Houser, L. Frison et al. Roxadustat for treating anemia in patients with CKD not on dialysis: results from a randomized phase 3 study. J. Am. Soc. Nephrol. 32(3), 737–755 (2021)CrossRef S. Fishbane, M.A. El-Shahawy, R. Pecoits-Filho, B.P. Van, M.T. Houser, L. Frison et al. Roxadustat for treating anemia in patients with CKD not on dialysis: results from a randomized phase 3 study. J. Am. Soc. Nephrol. 32(3), 737–755 (2021)CrossRef
33.
go back to reference R. Provenzano, A. Besarab, C.H. Sun, S.A. Diamond, J.H. Durham, J.L. Cangiano et al. Oral hypoxia-inducible factor prolyl hydroxylase inhibitor roxadustat (FG-4592) for the treatment of anemia in patients with CKD. Clin. J. Am. Soc. Nephrol. 11(6), 982–991 (2016)CrossRef R. Provenzano, A. Besarab, C.H. Sun, S.A. Diamond, J.H. Durham, J.L. Cangiano et al. Oral hypoxia-inducible factor prolyl hydroxylase inhibitor roxadustat (FG-4592) for the treatment of anemia in patients with CKD. Clin. J. Am. Soc. Nephrol. 11(6), 982–991 (2016)CrossRef
34.
go back to reference R. Provenzano, L. Szczech, R. Leong, K.G. Saikali, M. Zhong, T.T. Lee et al. Efficacy and cardiovascular safety of roxadustat for treatment of anemia in patients with non-dialysis-dependent CKD: pooled results of three randomized clinical trials. Clin. J. Am. Soc. Nephrol. 16(8), 1190–1200 (2021)CrossRef R. Provenzano, L. Szczech, R. Leong, K.G. Saikali, M. Zhong, T.T. Lee et al. Efficacy and cardiovascular safety of roxadustat for treatment of anemia in patients with non-dialysis-dependent CKD: pooled results of three randomized clinical trials. Clin. J. Am. Soc. Nephrol. 16(8), 1190–1200 (2021)CrossRef
Metadata
Title
Roxadustat improves renal osteodystrophy by dual regulation of bone remodeling
Authors
Luyao Li
Afang Li
Liangying Gan
Li Zuo
Publication date
03-10-2022
Publisher
Springer US
Published in
Endocrine / Issue 1/2023
Print ISSN: 1355-008X
Electronic ISSN: 1559-0100
DOI
https://doi.org/10.1007/s12020-022-03199-1

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