Cortical thinning and progressive cortical porosity in female patients with systemic lupus erythematosus on long-term glucocorticoids: a 2-year case-control study
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  • 作者:T. Y. Zhu ; J. F. Griffith ; L. Qin ; V. W. Y. Hung ; T.-N. Fong…
  • 关键词:Bone microstructure ; Glucocorticoids ; HR ; pQCT ; Osteoporosis ; Systemic lupus erythematosus
  • 刊名:Osteoporosis International
  • 出版年:2015
  • 出版时间:June 2015
  • 年:2015
  • 卷:26
  • 期:6
  • 页码:1759-1771
  • 全文大小:1,007 KB
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    11.Tang XL, Qin L, Kwok AW, Zhu TY, Kun EW, Hung VW, Griffith JF, Leung PC, Li EK, Tam LS (2013) Alterations of bone geometry, density, microarchitecture, and biomechanical properties in systemic lupus erythematosus on long-term glucocorticoid: a case-control study using HR-pQCT. Osteoporos Int 24(6):1817-826. doi:10.-007/?s00198-012-2177-5 PubMed View Article
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  • 作者单位:T. Y. Zhu (1) (2)
    J. F. Griffith (3)
    L. Qin (2)
    V. W. Y. Hung (2)
    T.-N. Fong (2)
    S.-K. Au (4)
    X.-L. Tang (1)
    E. W. Kun (5)
    A. W. Kwok (4)
    P.-C. Leung (4)
    E. K. LI (1)
    L.-S. Tam (1) (6)

    1. Department of Medicine and Therapeutics, The Chinese University of Hong Kong, Shatin, Hong Kong SAR, China
    2. Bone Quality and Health Center, Department of Orthopedics and Traumatology, The Chinese University of Hong Kong, Shatin, Hong Kong SAR, China
    3. Department of Imaging and Interventional Radiology, The Chinese University of Hong Kong, Shatin, Hong Kong SAR, China
    4. The Jockey Club Centre for Osteoporosis Care and Control, The Chinese University of Hong Kong, Shatin, Hong Kong SAR, China
    5. Department of Medicine and Geriatrics, Tai Po Hospital, Tai Po, Hong Kong SAR, China
    6. Department of Medicine & Therapeutics, The Prince of Wales Hospital, 9/F Clinical Sciences Building, 30-32 Ngan Shing Street, Shatin, N.T, Hong Kong SAR, China
  • 刊物类别:Medicine
  • 刊物主题:Medicine & Public Health
    Orthopedics
    Gynecology
    Endocrinology
    Rheumatology
  • 出版者:Springer London
  • ISSN:1433-2965
文摘
Summary In this study, we characterized longitudinal changes of volumetric bone mineral density and cortical and trabecular microstructure at the distal radius using HR-pQCT in female systemic lupus erythematosus (SLE) patients on long-term glucocorticoids. Cortical thinning and increased cortical porosity are the major features of longitudinal microstructural deterioration in SLE patients. Introduction The study aims to characterize longitudinal changes of volumetric bone mineral density (vBMD) and bone microstructure at distal radius in female systemic lupus erythematosus (SLE) patients on long-term glucocorticoids. Methods This 2-year case-control study consisted of 166 premenopausal subjects (75 SLE patients and 91 controls) and 79 postmenopausal subjects (44 SLE patients and 35 controls). We obtained areal BMD (aBMD) by dual-energy X-ray absorptiometry at multiple skeletal sites and indices of vBMD and microstructure at distal radius by high-resolution peripheral quantitative computed tomography (HR-pQCT) at baseline, 12 and 24?months. Results In either premenopausal or postmenopausal subjects, changes in aBMD did not differ between patients and controls except that decrease in aBMD at total hip at 24?months in premenopausal patients was significantly higher. In premenopausal subjects, decrease in cortical area (?.51 vs. ?.06?%, p--.039) and thickness (?.63 vs. 0.02?%, p--.031) and increase in cortical porosity (21.7 vs. 7.16?%, p--.030) over study period were significantly larger in patients after adjustment of age and body mass index. Decreased in trabecular vBMD was significantly less (?.63 vs. ?.32?%, p--.001) with trabecular microstructure better maintained in patients. In postmenopausal subjects, decrease in cortical vBMD (?.66 vs. ?.56?%, p--.039) and increase in cortical porosity (41.6 vs. 16.3?%, p--.021) were significantly higher in patients, and there was no group-wise difference in change of trabecular microstructure. Conclusion Longitudinal microstructural deterioration in SLE is characterized by cortical thinning and increased cortical porosity. Cortical bone is an important source of bone loss in SLE patients on glucocorticoids.

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