Bone Tissue Composition in Postmenopausal Women Varies With Glycemic Control From Normal Glucose Tolerance to Type 2 Diabetes Mellitus

被引:28
|
作者
Hunt, Heather B. [1 ]
Miller, Nicholas A. [1 ]
Hemmerling, Kimberly J. [1 ]
Koga, Maho [1 ]
Lopez, Kelsie A. [1 ]
Taylor, Erik A. [2 ]
Sellmeyer, Deborah E. [3 ]
Moseley, Kendall F. [4 ]
Donnelly, Eve [1 ,5 ]
机构
[1] Cornell Univ, Dept Mat Sci & Engn, 227 Bard Hall, Ithaca, NY 14853 USA
[2] Cornell Univ, Sibley Sch Mech Engn, Ithaca, NY 14853 USA
[3] Stanford Univ, Sch Med, Palo Alto, CA 94304 USA
[4] Johns Hopkins Univ, Sch Med, Div Endocrinol Gerontol & Metab, Baltimore, MD 21224 USA
[5] Hosp Special Surg, 535 E 70th St, New York, NY 10021 USA
基金
美国国家科学基金会;
关键词
TYPE 2 DIABETES MELLITUS; FRACTURE RISK; POSTMENOPAUSAL WOMEN; BIOCHEMICAL MARKERS OF BONE TURNOVER; COLLAGEN CROSS-LINKS; ILIAC CREST BIOPSIES; FRACTURE RISK; NONENZYMATIC GLYCATION; MINERAL DENSITY; HIP FRACTURE; SPECTROSCOPIC CHARACTERIZATION; INFRARED-SPECTROSCOPY; CANCELLOUS BONE; I COLLAGEN;
D O I
10.1002/jbmr.4186
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
The risk of fragility fracture increases for people with type 2 diabetes mellitus (T2DM), even after controlling for bone mineral density, body mass index, visual impairment, and falls. We hypothesize that progressive glycemic derangement alters microscale bone tissue composition. We used Fourier-transform infrared (FTIR) imaging to analyze the composition of iliac crest biopsies from cohorts of postmenopausal women characterized by oral glucose tolerance testing: normal glucose tolerance (NGT; n = 35, age = 65 +/- 7 years, HbA1c = 5.8 +/- 0.3%), impaired glucose tolerance (IGT; n = 26, age = 64 +/- 5 years, HbA1c = 6.0 +/- 0.4%), and overt T2DM on insulin (n = 25, age = 64 +/- 6 years, HbA1c = 9.13 +/- 0.6). The distributions of cortical bone mineral content had greater mean values (+7%) and were narrower (-10%) in T2DM versus NGT groups (p < 0.05). The distributions of acid phosphate, an indicator of new mineral, were narrower in cortical T2DM versus NGT and IGT groups (-14% and -14%, respectively) and in trabecular NGT and IGT versus T2DM groups (-11% and -10%, respectively) (all p < 0.05). The distributions of crystallinity were wider in cortical NGT versus T2DM groups (+16%) and in trabecular NGT versus T2DM groups (+14%) (all p < 0.05). Additionally, bone turnover was lower in T2DM versus NGT groups (P1NP: -25%, CTx: -30%, ucOC: -24%). Serum pentosidine was similar across groups. The FTIR compositional and biochemical marker values of the IGT group typically fell between the NGT and T2DM group values, although the differences were not always statistically significant. In summary, worsening glycemic control was associated with greater mineral content and narrower distributions of acid phosphate, an indicator of new mineral, which together are consistent with observations of lower turnover; however, wider distributions of mineral crystallinity were also observed. A more mineralized, less heterogeneous tissue may affect tissue-level mechanical properties and in turn degrade macroscale skeletal integrity. In conclusion, these data are the first evidence of progressive alteration of bone tissue composition with worsening glycemic control in humans. (c) 2020 American Society for Bone and Mineral Research (ASBMR).
引用
收藏
页码:334 / 346
页数:13
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