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接受 generic risedronate 治疗的泰国绝经后骨质疏松症女性的骨转换标志物和骨密度变化。

Changes of bone turnover markers and bone mineral density among postmenopausal Thai women with osteoporosis receiving generic risedronate.

机构信息

Division of Gender, Sexual, and Climacteric Medicine, Department of Obstetrics and Gynecology, Faculty of Medicine, Chulalongkorn University, Bangkok, Thailand.

Center of Excellence in Transgender Health (CETH), Faculty of Medicine, Chulalongkorn University, Bangkok, Thailand.

出版信息

BMC Womens Health. 2024 Oct 26;24(1):572. doi: 10.1186/s12905-024-03404-5.

Abstract

BACKGROUND

Osteoporosis has been recognized as a significant health issue in Thailand. Pharmacological interventions are important way to prevent fracture. However, one of the main challenges in selecting a medication is high cost, particularly for brand-name drugs. Data on generic bisphosphonate use in Thai are still lacking. Therefore, our study aimed to assess the efficacy and safety of generic risedronate in postmenopausal Thai women with osteoporosis.

METHODS

This prospective study was conducted at King Chulalongkorn Memorial Hospital, Bangkok, Thailand, from December 2022 to January 2024. Serum C-terminal cross-linking telopeptide of type I collagen (CTX) and procollagen type I N-propeptide (P1NP) were measured at baseline. All participants subsequently received 35 milligrams of oral risedronate once weekly for 52 weeks. Serum CTX and P1NP were remeasured at different time points. BMD was reevaluated at 52 weeks after risedronate treatment initiation.

RESULTS

A total of 80 participants were included. The mean age was 65.2 ± 6.6 years. The mean body mass index (BMI) was 23.45 ± 3.49 kg/m. The median (IQR) serum CTX level at 12 weeks was significantly lower than that at baseline (0.28 (0.16-0.46) ng/mL versus 0.44 (0.26-0.64) ng/mL, respectively; p value < 0.01). The suppression of serum CTX was confirmed at 52 weeks after treatment initiation. Compared with those at baseline, the serum P1NP levels were significantly lower at 24 weeks after treatment initiation (30.33 (19.19-39.58) ng/mL versus 41.90 (30.33-68.67) ng/mL, respectively; p value < 0.01). In terms of the BMD assessment at 52 weeks, significant improvements were observed in both areal BMD (g/cm) and T scores at all measured sites compared with baseline. The lumbar spine, femoral neck, and total hip BMD increased from baseline by 4.76%, 3.84% and 4.54%, respectively.

CONCLUSION

Postmenopausal women with osteoporosis who were treated with generic risedronate demonstrated significant suppression of the bone remodelling process at 3, 6, and 12 months after treatment initiation. Additionally, significant improvements in the lumbar spine, femoral neck, and total hip BMD were observed at 12 months of therapy. These findings suggest that generic risedronate could be considered a reasonable and interesting option for treating postmenopausal women with osteoporosis in Thailand.

摘要

背景

骨质疏松症已被认为是泰国的一个重大健康问题。药物干预是预防骨折的重要手段。然而,选择药物的主要挑战之一是成本高,特别是对于品牌药物。关于泰国使用通用双膦酸盐的数据仍然缺乏。因此,我们的研究旨在评估绝经后泰国妇女使用通用利塞膦酸钠的疗效和安全性。

方法

本前瞻性研究于 2022 年 12 月至 2024 年 1 月在泰国曼谷的朱拉隆功国王纪念医院进行。在基线时测量血清 I 型胶原 C 端交联肽(CTX)和前胶原 I N 端肽(P1NP)。所有参与者随后接受每周一次口服利塞膦酸钠 35 毫克,共 52 周。在不同时间点重新测量血清 CTX 和 P1NP。在利塞膦酸钠治疗开始后 52 周重新评估骨密度。

结果

共纳入 80 名参与者。平均年龄为 65.2±6.6 岁。平均体重指数(BMI)为 23.45±3.49 kg/m。12 周时血清 CTX 水平的中位数(IQR)明显低于基线水平(0.28(0.16-0.46)ng/mL 与 0.44(0.26-0.64)ng/mL,p 值<0.01)。治疗开始后 52 周时确认了血清 CTX 的抑制作用。与基线相比,治疗开始后 24 周时血清 P1NP 水平明显降低(30.33(19.19-39.58)ng/mL 与 41.90(30.33-68.67)ng/mL,p 值<0.01)。在治疗 52 周时的骨密度评估中,与基线相比,所有测量部位的面积骨密度(g/cm)和 T 评分均有显著改善。腰椎、股骨颈和全髋骨密度分别增加了 4.76%、3.84%和 4.54%。

结论

接受通用利塞膦酸钠治疗的绝经后骨质疏松症妇女在治疗开始后 3、6 和 12 个月时骨重建过程明显受到抑制。此外,治疗 12 个月时腰椎、股骨颈和全髋骨密度均有显著改善。这些发现表明,通用利塞膦酸钠可作为治疗泰国绝经后骨质疏松症妇女的一种合理且有趣的选择。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2c54/11515129/18cd3e1ace88/12905_2024_3404_Fig1_HTML.jpg

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