Fracture during oral bisphosphonate therapy is associated with deteriorated bone material strength index

BACKGROUND: Some patients experience fractures while receiving oral bisphosphonates (BPs) treatment. Clinical risk factors, advanced bone density loss, and microarchitecture deterioration have been associated with such fractures but bone tissue properties other than bone mineral density (BMD) have n...

ver descrição completa

Detalhes bibliográficos
Main Authors: Nogués, X, Prieto-Alhambra, D, Güerri-Fernández, R, Garcia-Giralt, N, Rodriguez-Morera, J, Cos, L, Mellibovsky, L, Pérez, A
Formato: Journal article
Idioma:English
Publicado em: Elsevier 2017
_version_ 1826283656920956928
author Nogués, X
Prieto-Alhambra, D
Güerri-Fernández, R
Garcia-Giralt, N
Rodriguez-Morera, J
Cos, L
Mellibovsky, L
Pérez, A
author_facet Nogués, X
Prieto-Alhambra, D
Güerri-Fernández, R
Garcia-Giralt, N
Rodriguez-Morera, J
Cos, L
Mellibovsky, L
Pérez, A
author_sort Nogués, X
collection OXFORD
description BACKGROUND: Some patients experience fractures while receiving oral bisphosphonates (BPs) treatment. Clinical risk factors, advanced bone density loss, and microarchitecture deterioration have been associated with such fractures but bone tissue properties other than bone mineral density (BMD) have not been assessed. METHODS: In a cross-sectional study of postmenopausal women on bisphosphonates for at least 4years with good adherence to treatment, 21 patients with incident fractures were compared with 18 treated patients without new fractures. Demographic and clinical variables, BMD, laboratory tests, and bone material strength index (BMSi) assessed by impact microindentation at the tibial diaphysis were recorded for all participants. RESULTS: Clinical and laboratory results did not differ between patients taking BPs with incident fractures and those without new fractures. However, BMSi was significantly lower (mean±SD) in those who fractured (73.76±6.49) than in no-fracture patients (81.64±6.26; p=0.001). Lumbar spine (LS) BMD was also lower in fractured patients (p=0.03). Adjusted models including age, body mass index, years on BP treatment, and LS-BMD confirmed an increase in fracture risk per BMSi standard deviation decrease: adjusted OR 23.5 [95% CI 2.16 to 255.66], p=0.01. ROC analyses showed an area under the curve of 0.82 (95% CI 0.68 to 0.95) for BMSi, higher than that for BMD at any location, which ranged from 0.64 (95% CI 0.47 to 0.82) for femoral neck (FN) BMD to 0.71 (95% CI 0.55 to 0.87) for LS-BMD. CONCLUSIONS: Patients who fracture while receiving BPs treatment have worse BMSi scores than BP-treated patients without fractures. The potential for BMSi to provide an additional osteoporosis treatment target should be explored.
first_indexed 2024-03-07T01:02:11Z
format Journal article
id oxford-uuid:8a1a4580-0e2b-4957-a3aa-94608d57432d
institution University of Oxford
language English
last_indexed 2024-03-07T01:02:11Z
publishDate 2017
publisher Elsevier
record_format dspace
spelling oxford-uuid:8a1a4580-0e2b-4957-a3aa-94608d57432d2022-03-26T22:29:14ZFracture during oral bisphosphonate therapy is associated with deteriorated bone material strength indexJournal articlehttp://purl.org/coar/resource_type/c_dcae04bcuuid:8a1a4580-0e2b-4957-a3aa-94608d57432dEnglishSymplectic Elements at OxfordElsevier2017Nogués, XPrieto-Alhambra, DGüerri-Fernández, RGarcia-Giralt, NRodriguez-Morera, JCos, LMellibovsky, LPérez, ABACKGROUND: Some patients experience fractures while receiving oral bisphosphonates (BPs) treatment. Clinical risk factors, advanced bone density loss, and microarchitecture deterioration have been associated with such fractures but bone tissue properties other than bone mineral density (BMD) have not been assessed. METHODS: In a cross-sectional study of postmenopausal women on bisphosphonates for at least 4years with good adherence to treatment, 21 patients with incident fractures were compared with 18 treated patients without new fractures. Demographic and clinical variables, BMD, laboratory tests, and bone material strength index (BMSi) assessed by impact microindentation at the tibial diaphysis were recorded for all participants. RESULTS: Clinical and laboratory results did not differ between patients taking BPs with incident fractures and those without new fractures. However, BMSi was significantly lower (mean±SD) in those who fractured (73.76±6.49) than in no-fracture patients (81.64±6.26; p=0.001). Lumbar spine (LS) BMD was also lower in fractured patients (p=0.03). Adjusted models including age, body mass index, years on BP treatment, and LS-BMD confirmed an increase in fracture risk per BMSi standard deviation decrease: adjusted OR 23.5 [95% CI 2.16 to 255.66], p=0.01. ROC analyses showed an area under the curve of 0.82 (95% CI 0.68 to 0.95) for BMSi, higher than that for BMD at any location, which ranged from 0.64 (95% CI 0.47 to 0.82) for femoral neck (FN) BMD to 0.71 (95% CI 0.55 to 0.87) for LS-BMD. CONCLUSIONS: Patients who fracture while receiving BPs treatment have worse BMSi scores than BP-treated patients without fractures. The potential for BMSi to provide an additional osteoporosis treatment target should be explored.
spellingShingle Nogués, X
Prieto-Alhambra, D
Güerri-Fernández, R
Garcia-Giralt, N
Rodriguez-Morera, J
Cos, L
Mellibovsky, L
Pérez, A
Fracture during oral bisphosphonate therapy is associated with deteriorated bone material strength index
title Fracture during oral bisphosphonate therapy is associated with deteriorated bone material strength index
title_full Fracture during oral bisphosphonate therapy is associated with deteriorated bone material strength index
title_fullStr Fracture during oral bisphosphonate therapy is associated with deteriorated bone material strength index
title_full_unstemmed Fracture during oral bisphosphonate therapy is associated with deteriorated bone material strength index
title_short Fracture during oral bisphosphonate therapy is associated with deteriorated bone material strength index
title_sort fracture during oral bisphosphonate therapy is associated with deteriorated bone material strength index
work_keys_str_mv AT noguesx fractureduringoralbisphosphonatetherapyisassociatedwithdeterioratedbonematerialstrengthindex
AT prietoalhambrad fractureduringoralbisphosphonatetherapyisassociatedwithdeterioratedbonematerialstrengthindex
AT guerrifernandezr fractureduringoralbisphosphonatetherapyisassociatedwithdeterioratedbonematerialstrengthindex
AT garciagiraltn fractureduringoralbisphosphonatetherapyisassociatedwithdeterioratedbonematerialstrengthindex
AT rodriguezmoreraj fractureduringoralbisphosphonatetherapyisassociatedwithdeterioratedbonematerialstrengthindex
AT cosl fractureduringoralbisphosphonatetherapyisassociatedwithdeterioratedbonematerialstrengthindex
AT mellibovskyl fractureduringoralbisphosphonatetherapyisassociatedwithdeterioratedbonematerialstrengthindex
AT pereza fractureduringoralbisphosphonatetherapyisassociatedwithdeterioratedbonematerialstrengthindex