阿巴巴拉肽增加绝经后骨质疏松妇女格鲁恩区1、2、6和7相应区域的骨矿物质密度

IF 1.7 4区 医学 Q4 ENDOCRINOLOGY & METABOLISM Journal of Clinical Densitometry Pub Date : 2023-07-01 DOI:10.1016/j.jocd.2023.101397
Neil P. Sheth MD (Contributing Author) , Renaud Winzenrieth PhD (Contributing Author) , Ludovic Humbert PhD (Contributing Author) , Paul J. Kostenuik PhD (Contributing Author) , Yamei Wang PhD (Contributing Author) , John I. Boxberger PhD (Primary Author) , Mathias P. Bostrom MD (Contributing Author)
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引用次数: 0

摘要

目的/目的:我们假设,在髋关节置换术中影响股骨干固定和稳定性的Gruen区对应的髋关节区域,与安慰剂相比,阿巴巴拉肽治疗6个月和18个月后,可以观察到骨矿物质密度(BMD)的局部改善。理由/背景:全髋关节置换术(THA)时的低骨密度增加了植入物稳定性受损和骨整合延迟的风险(1)。Abaloparatide是一种PTHrP的合成类似物(1-34),已被FDA批准用于治疗男性和绝经后女性骨质疏松症。阿巴巴拉肽增加脊柱和髋部骨密度,降低椎体和非椎体骨折的风险(2)。方法从ACTIVE试验(2)中随机选择500名绝经后骨质疏松症妇女接受阿巴巴拉肽或安慰剂治疗(n=250/组)。治疗6个月和18个月后获得的髋关节DXA扫描通过3D- shaper软件进行3D建模(3),并在每次3D-DXA扫描中对虚拟Stryker (Mahwah, NJ) Accolade II髋关节进行最佳尺寸和定位。评估格鲁恩区1、2、6和7对应的假体周围区域的体积骨密度(vBMD)(整体、皮质、小梁)和皮质厚度(区3、4和5超出感兴趣的DXA区域)。采用重复测量的混合效应模型得出的P值进行治疗比较。结果在6个月和18个月时,与安慰剂相比,阿巴巴拉肽显著增加了Gruen区1、2、6和7的整体vBMD (P<所有区域均为0.01)(表1)。区域1和7的百分比增幅最大。鲍巴肽在18个月时增加了所有4个分析区的皮质vBMD (P<0.01), 6月和18月时1区和7区骨小梁vBMD增加(P<0.0001), 6个月时1区、6区和7区皮质厚度增加(P<0.01),所有区域在18个月时(P<0.001)。横断面组vBMD平均变化的彩色图显示,与安慰剂相比,阿巴巴拉肽可显著增加虚拟格林区1、2、6和7的vBMD和皮质厚度。阿巴巴拉肽可能是一种有效的药物,通过诱导骨科重要的局部骨密度增加,在THA之前优化骨骼健康。术前增强和术后治疗的进一步研究是必要的。引用:1。Aro HT等人。骨科学报2012;83;107-14;2. Miller PD等。《美国医学会杂志》2017;317:442;3. Winzenrieth等人。骨质疏松症;2021;32:575-83。
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Abaloparatide Increases Bone Mineral Density in Regions Corresponding to Gruen Zones 1, 2, 6, and 7 in Postmenopausal Women With Osteoporosis

Purpose/Aims

We hypothesized that local improvements in bone mineral density (BMD) would be observed following 6 and 18 mo of abaloparatide versus placebo in hip regions corresponding to femoral Gruen zones that influence the fixation and stability of femoral stems in hip arthroplasty.

Rationale/Background

Low BMD at the time of total hip arthroplasty (THA) increases the risk of compromised implant stability and delayed osseointegration (1). Abaloparatide, a synthetic analog to PTHrP(1-34), is FDA approved for the treatment of men and postmenopausal women with osteoporosis. Abaloparatide increases spine and hip BMD and reduces the risk of vertebral and nonvertebral fractures (2).

Methods

A subset of 500 postmenopausal women with osteoporosis from the ACTIVE trial (2) who received abaloparatide or placebo (n=250/group) were randomly selected. Hip DXA scans obtained after 6 and 18 mo of treatment underwent 3D modeling via 3D-Shaper software (3), and a virtual Stryker (Mahwah, NJ) Accolade II hip stem was optimally sized and positioned within each 3D-DXA scan. Periprosthetic regions corresponding to Gruen zones 1, 2, 6, and 7 were assessed for volumetric BMD (vBMD) (integral, cortical, trabecular) and cortical thickness (zones 3, 4, and 5 were beyond the DXA region of interest). Treatment comparisons were made with P values derived from a mixed-effect model for repeated measures.

Results

Abaloparatide significantly increased integral vBMD compared with placebo in Gruen zones 1, 2, 6, and 7 at 6 and 18 mo (P< 0.01 for all) (Table 1). The largest percent increases were in zones 1 and 7. Abaloparatide increased cortical vBMD at 18 mo in all 4 analyzed zones (P< 0.01), increased trabecular vBMD at 6 and 18 mo in zones 1 and 7 (P< 0.0001), and increased cortical thickness at 6 months in zones 1, 6, and 7 (P< 0.01) and in all zones at 18 months (P< 0.001). Color maps of cross-sectional group mean change in vBMD demonstrates more robust BMD accrual with abaloparatide (Figure 1).

Implications

Abaloparatide significantly increased vBMD and cortical thickness in virtual Gruen zones 1, 2, 6, and 7 compared with placebo. Abaloparatide may represent an effective agent for bone health optimization prior to THA by inducing orthopedically important localized gains in BMD. Additional research into preoperative augmentation and postoperative treatment is warranted. References: 1. Aro HT et al. Acta Orthop 2012;83;107-14; 2. Miller PD et al. JAMA 2017;317:442; 3. Winzenrieth R et al. Osteoporos Int 2021;32:575–83.

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来源期刊
Journal of Clinical Densitometry
Journal of Clinical Densitometry 医学-内分泌学与代谢
CiteScore
4.90
自引率
8.00%
发文量
92
审稿时长
90 days
期刊介绍: The Journal is committed to serving ISCD''s mission - the education of heterogenous physician specialties and technologists who are involved in the clinical assessment of skeletal health. The focus of JCD is bone mass measurement, including epidemiology of bone mass, how drugs and diseases alter bone mass, new techniques and quality assurance in bone mass imaging technologies, and bone mass health/economics. Combining high quality research and review articles with sound, practice-oriented advice, JCD meets the diverse diagnostic and management needs of radiologists, endocrinologists, nephrologists, rheumatologists, gynecologists, family physicians, internists, and technologists whose patients require diagnostic clinical densitometry for therapeutic management.
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