TY - JOUR
T1 - Effect of zoledronic acid with or without methylprednisolone on 3D bone area and bone shape in patients with symptomatic knee osteoarthritis
T2 - A post-hoc analysis of the ZAP2 trial
AU - Cai, Guoqi
AU - Laslett, Laura L.
AU - Bowes, Michael A.
AU - Conaghan, Philip G.
AU - Cicuttini, Flavia
AU - Wluka, Anita E.
AU - March, Lyn
AU - Hill, Catherine
AU - Winzenberg, Tania
AU - Jones, Graeme
AU - Aitken, Dawn
N1 - Funding Information:
The preparation of this work was partly supported by the National Natural Science Foundation of China (No. 82103933 ). The ZAP2 study was funded by a project grant from the National Health and Medical Research Council of Australia (NHMRC, APP1045415 ). Voltarra Pharmaceuticals provided part funding for the VOLT01 sub-study. DA is a recipient of a NHMRC/MRFF Career Development Fellowship (Level 1). LLL is a recipient of an NHMRC Early Career Fellowship. AEW is a recipient of the RACP Fellows Career Development Fellowship. GJ is a recipient of a NHMRC Practitioner Fellowship. PGC is supported in part by the UK National Institute for Health and Care Research (NIHR) Leeds Biomedical Research Centre. The views expressed are those of the authors and not necessarily those of the NHS, the NIHR or the Department of Health.
Funding Information:
LLL reports personal fees from Amgen Pty Ltd, outside the submitted work. MB is an employee of Imorphics Ltd, a company providing measurement of imaging biomarkers, which is wholly owned by Stryker Corp, and MB has share options in that company. PGC has done consultancies or speakers bureaus for AbbVie, Amgen, AstraZeneca, Eli Lilly, Galapagos, Gilead, GlaxoSmithKline, Novartis, Pfizer, Stryker and UCB. LM has received funding unrelated to this study with grants from Janssen and speaker fees from Pfizer, Abbvie, Lilly. TW reports personal fees from AMGEN, outside the submitted work. GJ reports personal fees from BMS, Roche, AbbVie, Amgen, Lilly, Novartis, Jannsen, and grants from Covance, outside the submitted work. Other authors declare that they have no other conflict of interests.
Publisher Copyright:
© 2022
PY - 2022/10
Y1 - 2022/10
N2 - Objective: To evaluate the effect of annual infusions of zoledronic acid (ZA) with or without a single injection of methylprednisolone, compared to placebo, on quantitative magnetic resonance imaging 3-D bone area and bone shape in participants with symptomatic knee osteoarthritis (OA). Methods: This was a post-hoc analysis of the ZAP2 trial. Active appearance modelling was used to assess bone area (mm2) and femur bone shape (B-score) in 262 participants (mean 61.8 ± 8.0 years, 51% female) at baseline, 6, and 24 months. Radiographic joint space narrowing (JSN) was measured at baseline. An ‘OA shape’ was defined as a B-score of >1.96. Results: At baseline 65% of participants demonstrated an OA shape. Treatment with ZA plus methylprednisolone but not ZA alone, compared to placebo, was associated with significantly slower expansion in bone area at the medial femoral (-33.9 mm2, 95% confidence interval [CI] -61.8 to -6.0) and lateral femoral (-22.0 mm2, 95%CI -40.7 to -3.4) compartments over 24 months. B-score increased in all groups, with no significant between-group differences. There were significant interactions of JSN (grade 0 vs grade 1–2) and B-score (≤1.96 vs >1.96) with treatment effect on bone area (p < 0.05), such that ZA plus methylprednisolone slowed the expansion of medial and lateral femoral bone area over 24 months in participants with JSN grade 1–2 or a B-score of >1.96. Conclusions: ZA plus methylprednisolone may retard expansion of bone area over 24 months, but ZA alone may not. Neither ZA with or without methylprednisolone slowed progression of bone shape over 6 or 24 months.
AB - Objective: To evaluate the effect of annual infusions of zoledronic acid (ZA) with or without a single injection of methylprednisolone, compared to placebo, on quantitative magnetic resonance imaging 3-D bone area and bone shape in participants with symptomatic knee osteoarthritis (OA). Methods: This was a post-hoc analysis of the ZAP2 trial. Active appearance modelling was used to assess bone area (mm2) and femur bone shape (B-score) in 262 participants (mean 61.8 ± 8.0 years, 51% female) at baseline, 6, and 24 months. Radiographic joint space narrowing (JSN) was measured at baseline. An ‘OA shape’ was defined as a B-score of >1.96. Results: At baseline 65% of participants demonstrated an OA shape. Treatment with ZA plus methylprednisolone but not ZA alone, compared to placebo, was associated with significantly slower expansion in bone area at the medial femoral (-33.9 mm2, 95% confidence interval [CI] -61.8 to -6.0) and lateral femoral (-22.0 mm2, 95%CI -40.7 to -3.4) compartments over 24 months. B-score increased in all groups, with no significant between-group differences. There were significant interactions of JSN (grade 0 vs grade 1–2) and B-score (≤1.96 vs >1.96) with treatment effect on bone area (p < 0.05), such that ZA plus methylprednisolone slowed the expansion of medial and lateral femoral bone area over 24 months in participants with JSN grade 1–2 or a B-score of >1.96. Conclusions: ZA plus methylprednisolone may retard expansion of bone area over 24 months, but ZA alone may not. Neither ZA with or without methylprednisolone slowed progression of bone shape over 6 or 24 months.
KW - Bone area
KW - Bone shape
KW - Methylprednisolone
KW - Osteoarthritis
KW - Zoledronic acid
UR - https://www.scopus.com/pages/publications/85133231331
U2 - 10.1016/j.semarthrit.2022.152054
DO - 10.1016/j.semarthrit.2022.152054
M3 - Article
AN - SCOPUS:85133231331
SN - 0049-0172
VL - 56
JO - Seminars in Arthritis and Rheumatism
JF - Seminars in Arthritis and Rheumatism
M1 - 152054
ER -