Type 2 Diabetes and Bone

被引:309
作者
Leslie, William D. [1 ]
Rubin, Mishaela R. [2 ]
Schwartz, Ann V. [3 ]
Kanis, John A. [4 ]
机构
[1] Univ Manitoba, Dept Med, Winnipeg, MB, Canada
[2] Columbia Univ, Dept Med, New York, NY USA
[3] Univ Calif San Francisco, Dept Epidemiol & Biostat, San Francisco, CA 94143 USA
[4] Univ Sheffield, WHO Collaborating Ctr Metab Bone Dis, Sheffield, S Yorkshire, England
关键词
OSTEOPOROSIS; DIABETES; FRAX; FRACTURE PREDICTION; BONE MINERAL DENSITY; CLINICAL RISK-FACTORS; FRACTURE RISK; MINERAL DENSITY; OSTEOPOROTIC FRACTURES; VERTEBRAL FRACTURES; FEMORAL-NECK; POSTMENOPAUSAL WOMEN; HIP-FRACTURES; OLDER-ADULTS; BIOMECHANICAL PROPERTIES;
D O I
10.1002/jbmr.1759
中图分类号
R5 [内科学];
学科分类号
100201 [内科学];
摘要
There is a growing body of research showing that diabetes is an independent risk factor for fracture. Type 2 diabetes (T2D), which predominates in older individuals and is increasing globally as a consequence of the obesity epidemic, is associated with normal or even increased dual-energy x-ray absorptiometry (DXA)-derived areal bone mineral density (BMD). Therefore, the paradoxical increase in fracture risk has led to the hypothesis that there are diabetes-associated alterations in material and structural properties. An overly glycated collagen matrix, confounded by a low turnover state, in the setting of subtle cortical abnormalities, may lead to compromised biomechanical competence. In current clinical practice, because BMD is central to fracture prediction, a consequence of this paradox is a lack of suitable methods, including FRAX, to predict fracture risk in older adults with T2D. The option of adding diabetes to the FRAX algorithm is appealing but requires additional data from large population-based cohorts. The need for improved methods for identification of fracture in older adults with T2D is an important priority for osteoporosis research. (C) 2012 American Society for Bone and Mineral Research.
引用
收藏
页码:2231 / 2237
页数:7
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