Bone mineralization is elevated and less heterogeneous in adults with type 2 diabetes and osteoarthritis compared to controls with osteoarthritis alone

被引:35
作者
Pritchard, J. M. [1 ]
Papaioannou, A. [2 ,3 ]
Tomowich, C. [4 ]
Giangregorio, L. M. [5 ]
Atkinson, S. A. [6 ]
Beattie, K. A. [7 ]
Adachi, J. D. [7 ]
DeBeer, J. [8 ]
Winemaker, M. [8 ]
Avram, V. [8 ]
Schwarcz, H. P. [9 ]
机构
[1] McMaster Univ, Fac Hlth Sci, Hamilton, ON L8S 4K1, Canada
[2] McMaster Univ, Dept Med, Hamilton, ON L8S 4K1, Canada
[3] McMaster Univ, Dept Clin Epidemiol & Biostat, Hamilton, ON L8S 4K1, Canada
[4] McMaster Univ, Dept Kinesiol, Hamilton, ON L8S 4K1, Canada
[5] Univ Waterloo, Dept Kinesiol, Waterloo, ON N2L 3G1, Canada
[6] McMaster Univ, Dept Pediat, Hamilton, ON L8S 4K1, Canada
[7] McMaster Univ, Charlton Med Ctr, Dept Med, Hamilton, ON L8N 1Y2, Canada
[8] McMaster Univ, Dept Surg, Hamilton, ON L8S 4K1, Canada
[9] McMaster Univ, Dept Geog & Earth Sci, Hamilton, ON L8S 4K1, Canada
基金
加拿大自然科学与工程研究理事会;
关键词
Bone mineralization density distribution (BMDD); Type; 2; diabetes; Osteoporosis; Quantitative backscattered electron imaging; Bone quality; BACKSCATTERED ELECTRON IMAGES; DENSITY DISTRIBUTION; TRABECULAR BONE; FRACTURE RISK; ILIAC CREST; OSTEOPOROTIC FRACTURES; MATRIX MINERALIZATION; MECHANICAL-PROPERTIES; BIOCHEMICAL MARKERS; CORTICAL BONE;
D O I
10.1016/j.bone.2013.01.032
中图分类号
R5 [内科学];
学科分类号
100201 [内科学];
摘要
Purpose: The purpose of this study was to determine whether trabecular bone mineralization differed in adults with type 2 diabetes compared to adults without type 2 diabetes. Methods: Proximal femur specimens were obtained following a total hip replacement procedure from men and women >= 65 years of age with and without type 2 diabetes. A scanning electron microscope was used for quantitative backscattered electron imaging (qBEI) analysis of trabecular bone samples from the femoral neck. Gray scale images (pixel size=5.6 mu m(2)) were uploaded to Image! software and gray level (GL) values were converted to calcium concentrations (weight [wt] % calcium [Ca]) using data obtained with energy dispersive X-ray spectrometry. The following bone mineralization density distribution (BMDD) outcomes were collected: the weighted mean bone calcium concentration (Ca-MEAN), the most frequently occurring bone calcium concentration (Ca-PEAK) and mineralization heterogeneity (Ca-WIDTH). Differences between groups were assessed using the Student's t-test for normally distributed data and Mann-Whitney U-test for non-normally distributed data. An alpha value of <0.05 was considered significant. Results: Thirty-five Caucasian participants were recruited (mean [standard deviation, SD] age, 75.5 [6.5] years): 14 adults with type 2 diabetes (years since type 2 diabetes diagnosis, 13.5 [7.4] years) and 21 adults without type 2 diabetes. In the adults with type 2 diabetes, bone Ca-MEAN was 4.9% greater (2036 [0.98] wt.% Ca versus 19.40 [1.07] wt.% Ca, p = 0.015) and Ca-WIDTH was 9.4% lower (median [interquartile range] 3.55 [2.99-4.12] wt.% Ca versus 3.95 [0.71] wt% Ca, p<0.001) compared to controls. There was no between-group difference in Ca-PEAK (21.12 [0.97] wt% Ca for type 2 diabetes versus 20.44 [1.30] wt.% Ca for controls, p = 0.121). Conclusion: The combination of elevated mean calcium concentration in bone and lower mineralization heterogeneity in adults with type 2 diabetes may have deleterious effects on the biomechanical properties of bone. These microscopic alterations in bone mineralization, which may be mediated by suppressed bone remodeling, further elucidate higher fracture risk in adults with type 2 diabetes. (C) 2013 Elsevier Inc. All rights reserved.
引用
收藏
页码:76 / 82
页数:7
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