Trabecular bone histomorphometry in humans with Type 1 Diabetes Mellitus.
Trabecular bone histomorphometry in humans with Type 1 Diabetes Mellitus.
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DOI:
10.1016/j.bone.2011.09.055
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发表时间:
2012-01
期刊:
影响因子:
4.1
通讯作者:
Recker, Robert R.
中科院分区:
文献类型:
--
作者:
Armas, Laura A. G.;Akhter, Mohammed P.;Drincic, Andjela;Recker, Robert R.
Patients with Type 1 Diabetes Mellitus (DM) have markedly increased risk of fracture, but little is known about abnormalities in bone micro-architecture or remodeling properties that might give insight into the pathogenesis of skeletal fragility in these patients. We report here a case-control study comparing bone histomorphometric and micro-CT results from iliac biopsies in 18 otherwise healthy subjects with Type 1 Diabetes Mellitus with those from healthy age- and sex- matched non-diabetic control subjects. Five of the diabetics had histories of low-trauma fracture. Transilial bone biopsies were obtained after tetracycline labeling. The biopsy specimens were fixed, embedded, and scanned using a desktop μCT at 16 micron resolution. They were then sectioned and quantitative histomorphometry was performed as previously described by Recker et al. 1988. Two sections, >250 μm apart, were read from the central part of each biopsy. Overall there were no significant differences between diabetics and controls in histomorphometric or micro-CT measurements. However, fracturing diabetics had structural and dynamic trends different from nonfracturing diabetics by both methods of analysis. In conclusion, Type 1 Diabetes Mellitus does not result in abnormalities in bone histomorphometric or micro-CT variables in the absence of manifest complications from the diabetes. However, diabetics suffering fractures may have defects in their skeletal microarchitecture that may underlie the presence of excess skeletal fragility.
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DOI:
10.1359/jbmr.080713
发表时间:
2008-12
期刊:
Journal of bone and mineral research : the official journal of the American Society for Bone and Mineral Research
影响因子:
--
作者:
Moyer-Mileur LJ;Slater H;Jordan KC;Murray MA
通讯作者:
Murray MA
影响因子:
16.2
作者:
American Diabetes Association
通讯作者:
American Diabetes Association
影响因子:
15.9
作者:
ISLEY, WL;UNDERWOOD, LE;CLEMMONS, DR
通讯作者:
CLEMMONS, DR
影响因子:
8.2
作者:
Forsén, L;Meyer, HE;Edna, TH
通讯作者:
Edna, TH
影响因子:
3.8
作者:
Bridges, MJ;Moochhala, SH;Kelly, CA
通讯作者:
Kelly, CA