TY - JOUR
T1 - Real-world effectiveness of anti-osteoporosis medications for the prevention of incident hip and clinical vertebral fractures in patients on long-term glucocorticoid therapy
T2 - A nationwide health insurance claims database study in Japan
AU - Iki, Masayuki
AU - Fujimori, Kenji
AU - Nakatoh, Shinichi
AU - Tamaki, Junko
AU - Ishii, Shigeyuki
AU - Okimoto, Nobukazu
AU - Kamiya, Kuniyasu
AU - Ogawa, Sumito
N1 - Funding Information:
There was no significant decrease in hip fracture risk in patients who received any AOM compared with those who received no AOM before adjusting for baseline characteristics (Table 3). This is possibly due to confounding by indication [24], that is, physicians might have selected patients who were at increased risk of hip fracture to administer AOMs. Thus, the therapeutic effects of AOMs might have been masked. To reduce this potential confounding effect, we adopted IPW using propensity scores for receiving AOMs. As shown in Table 4, the decrease in HR of hip fracture for any AOM use in women became significant, although patients on teriparatide still had a significantly increased risk of hip and clinical vertebral fractures in both sexes. Teriparatide has been reported to reduce vertebral fracture risk compared with alendronate [26,27]. It is possible that the results of the present study were not sufficiently adjusted for confounding factors. For example, if a physician selected a patient with a four-fold higher risk of fracture based on clinical risk factors and laboratory tests for osteoporosis, a two-fold higher risk of fracture would still remain even though the use of AOMs reduced the fracture risk by half. In Japan, prescription of teriparatide is recommended for patients with very high fracture risk, as stated in the package insert under the supervision of MHLW. This recommendation is supported by a multistakeholder coalition assembled by the American Society for Bone and Mineral Research [28]. The tendency of physicians to prescribe teriparatide specifically to patients with a very high risk of fracture might be attributed to the high cost of teriparatide, and also by the Japanese GIO management guideline that recommends the use of alendronate and risedronate as first-line treatment and teriparatide as the second-line option [12]. These circumstances may have led to an increase in fracture risk by two- to three-fold, which remained in patients on teriparatide even after adjustments for baseline characteristics. Thus, confounding by indication might have also caused an underestimation of the effectiveness of other AOMs on hip and clinical vertebral fracture prevention in the present study.Financial support for the present study was provided by a 52nd Taiju Life Social Welfare Foundation Medical Research Grant 2019, a Japan Osteoporosis Foundation Grant for Bone Research 2019, and a 28th Pfizer Health Research Grant 2019. The funding bodies had no role in designing the study, collecting, analyzing, or interpreting the data, writing the manuscript, or deciding where to submit the manuscript for publication.
Funding Information:
Financial support for the present study was provided by a 52nd Taiju Life Social Welfare Foundation Medical Research Grant 2019, a Japan Osteoporosis Foundation Grant for Bone Research 2019, and a 28th Pfizer Health Research Grant 2019. The funding bodies had no role in designing the study, collecting, analyzing, or interpreting the data, writing the manuscript, or deciding where to submit the manuscript for publication.
Publisher Copyright:
© 2022
PY - 2023/1
Y1 - 2023/1
N2 - Purpose: Early initiation of anti-osteoporosis medications (AOMs) is recommended for patients on long-term glucocorticoid (GC) therapy. This study aimed to clarify the real-world effectiveness of AOMs against incident hip and vertebral fractures in patients undergoing GC therapy using the nationwide health insurance claims database of Japan (NDBJ). Methods: Patients aged ≥50 years who were prescribed GC (≥5 mg/day prednisolone or equivalent) for ≥90 days and who were followed up regarding AOM prescription and hip and clinical vertebral fracture incidences for the subsequent 1080 days between 2012 and 2018 were selected from NDBJ. Associations of AOMs prescribed within 90 days since GC therapy initiation with hip or vertebral fracture risk were evaluated by Cox proportional hazards regression using propensity score inverse probability weighting (IPW) for receiving any AOM or individual AOMs. Results: In total, 96,475 women and 98,385 men were included in the analysis; 38.0 % of women and 27.6 % of men received AOMs. Patients who received any AOM and those who received bisphosphonates or denosumab had a significantly lower risk of hip and clinical vertebral fractures than those who received no AOM in both sexes after propensity score IPW. Teriparatide was associated with an increased risk of both fractures in women and an increased risk of clinical vertebral fractures in men. Selection biases such as confounding by indication might have caused an underestimation of AOMs' protective effects. Conclusions: Bisphosphonates and denosumab were associated with a lower fracture incidence in patients on long-term GC therapy in real-world settings.
AB - Purpose: Early initiation of anti-osteoporosis medications (AOMs) is recommended for patients on long-term glucocorticoid (GC) therapy. This study aimed to clarify the real-world effectiveness of AOMs against incident hip and vertebral fractures in patients undergoing GC therapy using the nationwide health insurance claims database of Japan (NDBJ). Methods: Patients aged ≥50 years who were prescribed GC (≥5 mg/day prednisolone or equivalent) for ≥90 days and who were followed up regarding AOM prescription and hip and clinical vertebral fracture incidences for the subsequent 1080 days between 2012 and 2018 were selected from NDBJ. Associations of AOMs prescribed within 90 days since GC therapy initiation with hip or vertebral fracture risk were evaluated by Cox proportional hazards regression using propensity score inverse probability weighting (IPW) for receiving any AOM or individual AOMs. Results: In total, 96,475 women and 98,385 men were included in the analysis; 38.0 % of women and 27.6 % of men received AOMs. Patients who received any AOM and those who received bisphosphonates or denosumab had a significantly lower risk of hip and clinical vertebral fractures than those who received no AOM in both sexes after propensity score IPW. Teriparatide was associated with an increased risk of both fractures in women and an increased risk of clinical vertebral fractures in men. Selection biases such as confounding by indication might have caused an underestimation of AOMs' protective effects. Conclusions: Bisphosphonates and denosumab were associated with a lower fracture incidence in patients on long-term GC therapy in real-world settings.
KW - Anti-osteoporosis medication
KW - Glucocorticoid-induced osteoporosis
KW - Hip fracture
KW - Nation-wide health insurance claims database study
KW - Retrospective cohort study
KW - Vertebral fracture
UR - http://www.scopus.com/inward/record.url?scp=85141781896&partnerID=8YFLogxK
UR - http://www.scopus.com/inward/citedby.url?scp=85141781896&partnerID=8YFLogxK
U2 - 10.1016/j.bone.2022.116605
DO - 10.1016/j.bone.2022.116605
M3 - Article
C2 - 36347433
AN - SCOPUS:85141781896
SN - 8756-3282
VL - 166
JO - Bone
JF - Bone
M1 - 116605
ER -