TY - JOUR
T1 - Real-world data from a national survey on management of CKD-associated osteoporosis among Italian nephrologists
AU - An initiative and on behalf of the CKD-MBD working group the European Renal Association and the Committee of Scientific Advisors and National Societies of the IOF
AU - Fusaro, Maria
AU - Cossettini, Althea
AU - Re Sartò, Giulia Vanessa
AU - Aghi, Andrea
AU - Mereu, Maria Cristina
AU - Gallieni, Maurizio
AU - Cosmai, Laura
AU - Bellasi, Antonio
AU - Alfieri, Carlo Maria
AU - Cejka, Daniel
AU - McCloskey, Eugene
AU - Cavalier, Etienne
AU - Harvey, Nicholas C.
AU - Nickolas, Thomas L.
AU - Brandi, Maria Luisa
AU - Ferrari, Serge
AU - Marino, Carmela
AU - Giannini, Sandro
AU - Sella, Stefania
AU - Arcidiacono, Gaetano Paride
AU - Simioni, Paolo
AU - Plebani, Mario
AU - Zaninotto, Martina
AU - De Nicola, Luca
AU - Marcantoni, Carmelita
AU - de Borst, Martin H.
AU - Ravera, Maura
AU - Frediani, Bruno
AU - Bover, Jordi
AU - Lafage-Proust, Marie Helene
AU - Reginster, Jean Yves
AU - Bertoldo, Francesco
AU - Tripepi, Giovanni
AU - Haarhaus, Mathias
N1 - Publisher Copyright:
© The Author(s), under exclusive licence to the International Osteoporosis Foundation and the Bone Health and Osteoporosis Foundation 2025.
PY - 2025/12
Y1 - 2025/12
N2 - Summary : Chronic kidney disease (CKD)-associated osteoporosis increases fracture risk, yet clinical guidance remains unclear. A survey of 89 Italian nephrologists revealed heterogeneous biomarker availability and varied treatment approaches. Denosumab was the preferred antiresorptive agent, while anabolic drugs were rarely used. Findings highlight progress in CKD-related bone health management despite existing uncertainties. CKD-associated osteoporosis comprises the skeletal effects of a complex mineral and bone disorder causing increased risks of fragility fractures (FF), cardiovascular events, and mortality. Existing clinical guidance about CKD-associated osteoporosis is vague, leading us to hypothesize that a treatment gap exists and that clinical practice is dependent on local availability of diagnostic tools. Purpose and methods: The aim of the current survey was to determine current attitudes and practices among Italian nephrologists regarding the evaluation and management of CKD-associated osteoporosis. An online survey was designed, consisting of 9 thematic groups with a set of 16 closed questions regarding the availability of biomarkers and BTMs at reference laboratories and their use for the diagnosis and treatment of CKD-associated osteoporosis in patients with different stages of CKD, including CKD stages G4-5 and dialysis patients. Results were compared to a previous survey on the use of BTMs from 2022. Results: Eighty-nine Italian nephrologists participated in the survey, reporting that parathyroid hormone (PTH), alkaline phosphatase, and 25-hydroxy-vitamin D measurements were available in 92–100% of their reference laboratories. Measurements for fibroblast growth factor-23, Klotho, Matrix Gla protein, procollagen type 1 N-terminal propeptide, and tartrate-resistant acid phosphatase 5b were available in 64–74% of cases. Regarding PTH cut-off values, 47.2% followed KDOQI and 43.8% followed KDIGO recommendations. Vitamin D was widely used across CKD stages (cholecalciferol 27–37.1%, calcifediol 9–12.4%, calcitriol 47.2–53.9%, and paricalcitol 21.3–30.3). Denosumab was the preferred antiresorptive agent in all CKD stages (22.5%–28.1%), while the use of bisphosphonates was uncommon in advanced CKD. Anabolic drugs were rarely prescribed. Conclusions: The availability of bone biomarkers is heterogeneous, and an uncertainty still exists regarding the clinical use of biomarkers in CKD-associated osteoporosis. Nonetheless, our findings indicate that Italian nephrologists are increasingly taking proactive steps to prevent and treat bone fragility in CKD patients.
AB - Summary : Chronic kidney disease (CKD)-associated osteoporosis increases fracture risk, yet clinical guidance remains unclear. A survey of 89 Italian nephrologists revealed heterogeneous biomarker availability and varied treatment approaches. Denosumab was the preferred antiresorptive agent, while anabolic drugs were rarely used. Findings highlight progress in CKD-related bone health management despite existing uncertainties. CKD-associated osteoporosis comprises the skeletal effects of a complex mineral and bone disorder causing increased risks of fragility fractures (FF), cardiovascular events, and mortality. Existing clinical guidance about CKD-associated osteoporosis is vague, leading us to hypothesize that a treatment gap exists and that clinical practice is dependent on local availability of diagnostic tools. Purpose and methods: The aim of the current survey was to determine current attitudes and practices among Italian nephrologists regarding the evaluation and management of CKD-associated osteoporosis. An online survey was designed, consisting of 9 thematic groups with a set of 16 closed questions regarding the availability of biomarkers and BTMs at reference laboratories and their use for the diagnosis and treatment of CKD-associated osteoporosis in patients with different stages of CKD, including CKD stages G4-5 and dialysis patients. Results were compared to a previous survey on the use of BTMs from 2022. Results: Eighty-nine Italian nephrologists participated in the survey, reporting that parathyroid hormone (PTH), alkaline phosphatase, and 25-hydroxy-vitamin D measurements were available in 92–100% of their reference laboratories. Measurements for fibroblast growth factor-23, Klotho, Matrix Gla protein, procollagen type 1 N-terminal propeptide, and tartrate-resistant acid phosphatase 5b were available in 64–74% of cases. Regarding PTH cut-off values, 47.2% followed KDOQI and 43.8% followed KDIGO recommendations. Vitamin D was widely used across CKD stages (cholecalciferol 27–37.1%, calcifediol 9–12.4%, calcitriol 47.2–53.9%, and paricalcitol 21.3–30.3). Denosumab was the preferred antiresorptive agent in all CKD stages (22.5%–28.1%), while the use of bisphosphonates was uncommon in advanced CKD. Anabolic drugs were rarely prescribed. Conclusions: The availability of bone biomarkers is heterogeneous, and an uncertainty still exists regarding the clinical use of biomarkers in CKD-associated osteoporosis. Nonetheless, our findings indicate that Italian nephrologists are increasingly taking proactive steps to prevent and treat bone fragility in CKD patients.
KW - Bone fracture
KW - Bone turnover markers
KW - CKD-MBD
KW - Vascular calcification
UR - https://www.scopus.com/pages/publications/105011773983
U2 - 10.1007/s11657-025-01570-z
DO - 10.1007/s11657-025-01570-z
M3 - Article
C2 - 40668510
AN - SCOPUS:105011773983
SN - 1862-3522
VL - 20
JO - Archives of Osteoporosis
JF - Archives of Osteoporosis
IS - 1
M1 - 96
ER -