Effect of Bone Resorption Inhibitors on Serum Cholesterol Level and Fracture Risk in Osteoporosis: Randomized Comparative Study Between Minodronic Acid and Raloxifene

被引:0
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作者
Hiroaki Ohta
Yukari Uemura
Teruki Sone
Shiro Tanaka
Satoshi Soen
Satoshi Mori
Hiroshi Hagino
Masao Fukunaga
Toshitaka Nakamura
Hajime Orimo
Masataka Shiraki
机构
[1] Kawasaki Medical School,Department of Obstetrics and Gynecology 2
[2] National Center for Global Health and Medicine,Biostatistics Section, Department of Data Science, Center for Clinical Sciences
[3] Kawasaki Medical School,Department of Nuclear Medicine
[4] Kyoto University,Department of Clinical Biostatistics, Graduate School of Medicine
[5] Soen Orthopaedics,Bone and Joint Surgery
[6] Osteoporosis and Rheumatology Clinic,School of Health Science
[7] Seirei Hamamatu General Hospital,Department of Internal Medicine
[8] Tottori University Faculty of Medicine,undefined
[9] Kawasaki Medical School,undefined
[10] Touto Sangenjaya Rehabilitation Hospital,undefined
[11] Japan Osteoporosis Foundation,undefined
[12] Research Institute and Practice for Involutional Diseases,undefined
来源
关键词
Cholesterol; Nitrogen-containing bisphosphonates; Selective estrogen receptor modulators; Fractures; Osteoporosis;
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摘要
The positive link between osteoporosis and hypercholesterolemia has been documented, and bone resorption inhibitors, such as nitrogen-containing bisphosphonates (N-BP) and selective estrogen receptor modulators (SERMs), are known to reduce serum cholesterol levels. However, the relationship between the baseline cholesterol level and incident fracture rate under the treatment using the bone resorption inhibitors has not been documented. We investigated the relation between vertebral fracture incident and the baseline cholesterol levels and cholesterol-lowering effect of N-BP and SERM in osteoporosis through a prospective randomized open-label study design. Patients with osteoporosis (n = 3986) were allocated into two groups based on the drug used for treatment: minodronic acid (MIN) (n = 1624) as an N-BP and raloxifene (RLX) as an SERM (n = 1623). Serum levels of cholesterol and incidence of vertebral fracture were monitored for 2 years. The vertebral fracture rates between the two groups were compared using the pre-specified stratification factors. The patients receiving MIN with baseline low-density lipoprotein (LDL)-cholesterol level of ≥ 140 mg/dL, high-density lipoprotein cholesterol level < 40 mg/dL, age group of ≥ 75 years, and T score of BMD ≥ -3 SD had significantly lower vertebral fracture rates than those receiving RLX (incidence rate ratios (IRR) 0.45 [95% confidence interval (CI) 0.30 0.75, p = 0.001], 0.25 [95% CI 0.09 0.65, p = 0.005], 0.71 [95% CI 0.56 0.91, p = 0.006], 0.47 [95% CI 0.30 0.75, p = 0.0012], respectively). The cholesterol-lowering effect was stronger in the RLX group than in the MIN group, regardless of prior statin use. These results indicated that MIN treatment was more effective in reducing fracture risk in patients with higher LDL cholesterol levels, although its cholesterol-lowering ability was lesser than the RLX treatment.
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页码:430 / 439
页数:9
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