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2
Screening rates and prevalence of osteoporosis in a real-world, Australian systemic sclerosis cohort.澳大利亚硬皮病真实世界队列中骨质疏松症的筛查率和流行率。
Int J Rheum Dis. 2022 Feb;25(2):175-181. doi: 10.1111/1756-185X.14254. Epub 2021 Dec 2.
3
Guidelines for the prevention and treatment of glucocorticoid-induced osteoporosis: an update of Brazilian Society of Rheumatology (2020).糖皮质激素性骨质疏松症防治指南:巴西风湿病学会2020年更新版
Arch Osteoporos. 2021 Mar 1;16(1):49. doi: 10.1007/s11657-021-00902-z.
4
Complex assessment of bone mineral density, fracture risk, vitamin D status, and bone metabolism in Hungarian systemic sclerosis patients.对匈牙利系统性硬化症患者的骨矿物质密度、骨折风险、维生素 D 状况和骨代谢进行综合评估。
Arthritis Res Ther. 2019 Dec 10;21(1):274. doi: 10.1186/s13075-019-2072-y.
5
Is there today a place for corticosteroids in the treatment of scleroderma?如今皮质类固醇在硬皮病的治疗中有一席之地吗?
Autoimmun Rev. 2019 Dec;18(12):102403. doi: 10.1016/j.autrev.2019.102403. Epub 2019 Oct 19.
6
Distal radius and tibia bone microarchitecture impairment in female patients with diffuse systemic sclerosis.弥漫性系统性硬化症女性患者的桡骨远端和胫骨骨微结构损伤。
Osteoporos Int. 2019 Aug;30(8):1679-1691. doi: 10.1007/s00198-019-04965-0. Epub 2019 Apr 27.
7
Paradoxical side effects of bisphosphonates on the skeleton: What do we know and what can we do?双膦酸盐对骨骼的矛盾副作用:我们了解什么,我们能做什么?
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8
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Arch Osteoporos. 2017 Dec;12(1):43. doi: 10.1007/s11657-017-0324-5. Epub 2017 Apr 19.
9
Systemic sclerosis.系统性硬化症。
Lancet. 2017 Oct 7;390(10103):1685-1699. doi: 10.1016/S0140-6736(17)30933-9. Epub 2017 Apr 13.
10
Low vitamin D serum levels in diffuse systemic sclerosis: a correlation with worst quality of life and severe capillaroscopic findings.弥漫性系统性硬化症患者血清维生素D水平低:与最差生活质量及严重毛细血管镜检查结果的相关性
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系统性硬化症中的症状性骨折:一项病例对照研究。

Symptomatic fractures in systemic sclerosis: A case-control study.

作者信息

Sampaio-Barros Marília M, Bortoluzzo Adriana B, da Silva Henrique Carriço, Luppino-Assad Ana Paula, Pereira Rosa Maria R, Sampaio-Barros Percival D

机构信息

Disciplina de Reumatologia, Hospital das Clinicas HCFMUSP, Faculdade de Medicina, Universidade de São Paulo, Sao Paulo, Brazil.

Insper-Instituto de Educação e Pesquisa, Sao Paulo, Brazil.

出版信息

J Scleroderma Relat Disord. 2023 Feb;8(1):79-84. doi: 10.1177/23971983221141271. Epub 2022 Dec 8.

DOI:10.1177/23971983221141271
PMID:36743808
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC9896198/
Abstract

This case-control study analyzed risk factors for symptomatic fractures in a group of 52 patients with systemic sclerosis compared with a group of 104 patients without fractures, matched for sex and age, who were attended at a single systemic sclerosis outpatient clinic from 2010 to 2020. Fractures affected predominantly vertebral (65.4%), rib (13.5%), and hip (7.7%) joints, while the mean age of fracture was 55.3 ± 9.5 years. Age at disease onset, age at diagnosis, disease duration, age at menarche, and age at menopause were similar in both groups, and 58.9% of the patients were menopausal at the time of the fracture. The presence of fractures had a significant association with densitometric osteoporosis (p < 0.001), lower weight (p = 0.032), and bone mineral index (p = 0.044), anti-RNA polymerase III (p = 0.040), use of corticosteroids (p = 0.019), and bisphosphonates (p < 0.001), as well as with densitometric T-scores of lumbar spine (p < 0.001), femoral neck (p = 0.025), and total hip (p = 0.013). Multivariate analysis showed that the variables significantly associated with fractures were high doses of corticosteroids (odds ratio = 4.10; 95% confidence interval = 1.290-13.090; p = 0.017), bisphosphonates (odds ratio = 3.91; 95% confidence interval = 1.699-8.984; p = 0.001), negative anti-Scl70 (OR = 0.34; 95% confidence interval = 0.124-0.943; p = 0.038), and lumbar T-score (odds ratio = 0.39; 95% confidence interval = 0.034-0.460; p = 0.010). In conclusion, symptomatic fractures were associated predominantly with lower bone mineral density of lumbar spine and use of high doses of corticosteroids and bisphosphonates in this cohort.

摘要

本病例对照研究分析了52例系统性硬化症患者发生症状性骨折的危险因素,并与104例未发生骨折的患者进行比较,后者与前者性别和年龄相匹配,均于2010年至2020年在一家系统性硬化症门诊就诊。骨折主要累及椎体(65.4%)、肋骨(13.5%)和髋关节(7.7%),骨折的平均年龄为55.3±9.5岁。两组患者的发病年龄、诊断年龄、病程、初潮年龄和绝经年龄相似,58.9%的患者在骨折时已绝经。骨折的发生与骨密度测定的骨质疏松症(p<0.001)、体重较低(p=0.032)、骨矿物质指数(p=0.044)、抗RNA聚合酶III(p=0.040)、使用皮质类固醇(p=0.019)和双膦酸盐(p<0.001)以及腰椎(p<0.001)、股骨颈(p=0.025)和全髋关节(p=0.013)的骨密度T值显著相关。多变量分析显示,与骨折显著相关的变量为高剂量皮质类固醇(比值比=4.10;95%置信区间=1.290-13.090;p=0.017)、双膦酸盐(比值比=3.91;95%置信区间=1.699-8.984;p=0.001)、抗Scl70阴性(OR=0.34;95%置信区间=0.124-0.943;p=0.038)和腰椎T值(比值比=0.39;95%置信区间=0.034-0.460;p=0.010)。总之,在该队列中,症状性骨折主要与腰椎骨密度较低以及高剂量皮质类固醇和双膦酸盐的使用有关。