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Changes in trabecular bone microarchitecture in postmenopausal women with and without type 2 diabetes: a two year longitudinal study
被引:24
|作者:
Pritchard, Janet M.
[1
]
Giangregorio, Lora M.
[2
]
Atkinson, Stephanie A.
[3
]
Beattie, Karen A.
[4
]
Inglis, Dean
[5
]
Ioannidis, George
[4
]
Gerstein, Hertzel
[6
]
Punthakee, Zubin
[6
]
Adachi, Jonathan D.
[4
]
Papaioannou, Alexandra
[6
]
机构:
[1] McMaster Univ, Fac Hlth Sci, Hamilton, ON L8S 4K1, Canada
[2] Univ Waterloo, Dept Kinesiol, Waterloo, ON N2L 3G1, Canada
[3] McMaster Univ, Dept Pediat, Hamilton, ON L8S 4K1, Canada
[4] McMaster Univ, Dept Med, Charlton Med Ctr, Hamilton, ON L8N 1Y2, Canada
[5] McMaster Univ, Dept Civil Engn, Hamilton, ON L8S 4K1, Canada
[6] McMaster Univ, Dept Med, Hamilton, ON L8S 4K1, Canada
关键词:
IMAGE-BASED ASSESSMENT;
MINERAL DENSITY;
DISTAL RADIUS;
OXIDATIVE STRESS;
FRACTURE RISK;
VIVO;
MELLITUS;
INTERVENTION;
ADIPONECTIN;
TURNOVER;
D O I:
10.1186/1471-2474-14-114
中图分类号:
R826.8 [整形外科学];
R782.2 [口腔颌面部整形外科学];
R726.2 [小儿整形外科学];
R62 [整形外科学(修复外科学)];
学科分类号:
摘要:
Background: The risk of experiencing an osteoporotic fracture is greater for adults with type 2 diabetes despite higher than normal bone mineral density (BMD). In addition to BMD, trabecular bone microarchitecture contributes to bone strength, but is not assessed using conventional BMD measurement by dual x-ray absorptiometry (DXA). The aim of this study was to compare two year changes in trabecular bone microarchitecture in women with and without type 2 diabetes. Methods: We used a 1 Tesla magnetic resonance imaging (MRI) scanner to acquire axial images (resolution 195 mu m x 195 mu m x 1000 mu m) of the distal radius. We report the change in the number and size of trabecular bone holes, bone volume fraction (BVTV), trabecular thickness (Tb.Th), number (Tb.N) and separation (Tb.Sp), endosteal area, nodal and branch density for each group. Lumbar spine and proximal femur BMD were measured with DXA (Hologic, Discovery QDR4500A) at baseline and follow-up. Using a multivariable linear regression model, we evaluated whether the percent change in the trabecular bone microarchitecture variables differed between women with and without type 2 diabetes. Results: Of the 54 participants at baseline with valid MRI image sets, 37 participants (baseline mean [SD] age, 70.8 [4.4] years) returned for follow-up assessment after 25.4 [1.9] months. Lumbar spine BMD was greater for women with diabetes compared to without diabetes at both baseline and follow-up. After adjustment for ethnicity, women with diabetes had a higher percent increase in number of trabecular bone holes compared to controls (10[1] % versus -7 [2]%, p=0.010), however results were no longer significant after adjustment for multiple comparisons (p=0.090). There were no differences in the change in other trabecular bone microarchitecture variables between groups. Conclusion: There were no differences in percent change in trabecular bone microarchitecture variables over two years in women with type 2 diabetes compared to women without diabetes. This study provides feasibility data, which will inform future trials assessing change in trabecular bone microarchitecture in women with type 2 diabetes. Larger studies using higher resolution imaging modalities that can assess change in trabecular and cortical bone compartments in women with type 2 diabetes are needed.
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