4.5 Article

Baseline serum PINP level is associated with the increase in hip bone mineral density seen with Romosozumab treatment in previously untreated women with osteoporosis

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OSTEOPOROSIS INTERNATIONAL
卷 34, 期 3, 页码 563-572

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SPRINGER LONDON LTD
DOI: 10.1007/s00198-022-06642-1

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Bone mineral density; Postmenopausal osteoporosis; Responder analysis; Romosozumab; Type I procollagen N-terminal propeptide

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Baseline serum PINP value is significantly and independently associated with increased bone mineral density (≥ 3%) in both total hip and femoral necks after 12 months of romosozumab treatment in treatment-naive postmenopausal osteoporosis patients.
Baseline serum PINP value was significantly and independently associated with the increased bone mineral density ( >= 3%) in both total hip and femoral necks by 12 months of romosozumab treatment in patients with treatment-naive postmenopausal osteoporosis. Purpose Some patients fail to obtain a sufficiently increased hip bone mineral density (BMD) by romosozumab (ROMO) treatment. This study aimed to investigate the prognostic factor for increased hip BMD with ROMO in patients with treatment-naive postmenopausal osteoporosis. Methods This prospective, observational, and multicenter study included patients (n = 63: mean age, 72.6 years; T-scores of the lumbar spine [LS], - 3.3; total hip [TH], - 2.6; femoral neck [FN], - 3.3; serum type I procollagen N-terminal propeptide [PINP], 68.5 mu g/L) treated by ROMO for 12 months. BMD and serum bone turnover markers were evaluated at each time point. A responder analysis was performed to assess the patient percentage, and both univariate and multivariate analyses were performed to investigate the factors associated with clinically significant increased BMD (>= 3%) in both TH and FN. Results Percentage changes of BMD from baseline in the LS, TH, and FN areas were 17.5%, 4.9%, and 4.3%, respectively. In LS, 96.8% of patients achieved >= 6% increased LS-BMD, although 57.1% could not achieve >= 3% increased BMD in either TH or FN. Multiple regression analysis revealed that only the baseline PINP value was significantly and independently associated with >= 3% increased BMD in both TH and FN (p = 0.019, 95% confidence interval = 1.006-1.054). The optimal cut-off PINP value was 53.7 mu g/L with 54.3% sensitivity and 92.3% specificity (area under the curve = 0.752). Conclusions In a real-world setting, baseline PINP value was associated with the increased BMD of TH and FN by ROMO treatment in treatment-naive patients.

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