Diabetes and osteoporosis are both frequent disorders. By chance they may thus occur together. However, evidence suggests that osteoporosis defined by bone scans (DXA) occurs more frequent than expected in type 1 diabetes (T1D) and less frequent than expected in T2D (). The latter may be explained by differences in body size – T2D patients being more obese than the general population and bone mineral density (BMD) increases with body size (). However, as disclosed by prior studies and by the papers in this research topic, more is present than what meets the eye at first glance on the bone density measures. More fractures are present than expected both in T1D and T2D. This could point at either a diminished bone biomechanical competence or an increased risk of trauma. The latter seems less likely. Regarding bone biomechanical competence, this series of papers has shown discordances in biochemical markers of bone turnover (). This raises the question of the potential mechanisms of uncoupling of formation and resorption, and thus a potential weakening of bone microarchitecture. Besides the issue of the interactions with bone cells such as the osteoclasts, osteocytes, and osteoblasts, interactions with both the calcium matrix and thus the crystalline structure of hydroxyapatite and interactions with collagen are possible. This opens for a wide range of possible research fields within signaling [bone – adipose tissue (), bone – pancreas etc.], imaging (crystal structure), engineering (biomechanical properties) etc.
Within each of these fields, a number of questions need to be addressed. Are the measurements of biochemical markers of bone turnover reliable? One example could be if enzymatic or non-enzymatic modification of say collagen cross-links could infer with the accuracy of assays, thus measuring lower concentrations as not all of the degraded collagen is detected. Furthermore, many interactions between glucose and osteocalcin () modify the effectiveness of this as a marker of bone turnover.
The change in biochemical markers happen rather rapidly and were in one study modified by somatostatin. The rapid changes raise novel questions as bone turnover usually is a rather slow process that takes more than hours to modify substantially. However, the interaction with somatostatin raises the possibility of an interaction from gut hormones () and ghrelin. Studies of a broader range of hormonal signaling may thus be in place.
The field of biomechanical competence may call for novel imagining techniques and new methods to study crystal structure and biomechanical competence.
The study of diabetes and bone thus not only relates to classical endocrinology and bone metabolism, but also opens new concepts of bone biomechanical competence beyond traditional DXA techniques and even beyond HrpQCT and beyond classical biochemical markers of bone turnover.
Statements
Conflict of interest
The author declares that the research was conducted in the absence of any commercial or financial relationships that could be construed as a potential conflict of interest.
References
1
VestergaardP. Discrepancies in bone mineral density and fracture risk in patients with type 1 and type 2 diabetes – a meta-analysis. Osteoporos Int (2007) 18:427–44.10.1007/s00198-006-0253-4
2
De LaetCKanisJAOdénAJohansonHJohnellODelmasPet alBody mass index as a predictor of fracture risk: a meta-analysis. Osteoporosis Int (2005) 16:1330–8.10.1007/s00198-005-1863-y
3
Starup-LindeJ. Diabetes, biochemical markers of bone turnover, diabetes control, and bone. Front Endocrinol (Lausanne) (2013) 4:21.10.3389/fendo.2013.00021
4
ConfavreuxCBLevineRLKarsentyG. A paradigm of integrative physiology, the crosstalk between bone and energy metabolisms. Mol Cell Endocrinol (2009) 310(1–2):21–9.10.1016/j.mce.2009.04.004
5
LeeNKSowaHHinoiEFerronMAhnJDConfavreuxCet alEndocrine regulation of energy metabolism by the skeleton. Cell (2007) 130:456–69.10.1016/j.cell.2007.05.047
6
HenriksenDBAlexandersenPHartmannBAdrianCLByrjalsenIBoneHGet alFour-month treatment with GLP-2 significantly increases hip BMD: a randomized, placebo-controlled, dose-ranging study in postmenopausal women with low BMD. Bone (2009) 45:833–42.10.1016/j.bone.2009.07.008
Summary
Keywords
diabetes, osteoporosis, bone quality, bone, endocrinology and bone metabolism
Citation
Vestergaard P (2014) Diabetes and Osteoporosis – Cause for Concern?. Front. Endocrinol. 5:53. doi: 10.3389/fendo.2014.00053
Received
27 March 2014
Accepted
28 March 2014
Published
16 April 2014
Volume
5 - 2014
Edited and reviewed by
Jonathan H. Tobias, University of Bristol, UK
Copyright
© 2014 Vestergaard.
This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) or licensor are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.
*Correspondence: p-vest@post4.tele.dk
This article was submitted to Bone Research, a section of the journal Frontiers in Endocrinology.
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