- Open Access
The impact of type 2 diabetes on bone metabolism
Diabetology & Metabolic Syndrome volume 9, Article number: 85 (2017)
Diabetes complications and osteoporotic fractures are two of the most important causes of morbidity and mortality in older patients and share many features including genetic susceptibility, molecular mechanisms, and environmental factors. Type 2 diabetes mellitus (T2DM) compromises bone microarchitecture by inducing abnormal bone cell function and matrix structure, with increased osteoblast apoptosis, diminished osteoblast differentiation, and enhanced osteoclast-mediated bone resorption. The linkage between these two chronic diseases creates a possibility that certain antidiabetic therapies may affect bone quality. Both glycemic and bone homeostasis are under control of common regulatory factors. These factors include insulin, accumulation of advanced glycation end products, peroxisome proliferator-activated receptor gamma, gastrointestinal hormones (such as the glucose-dependent insulinotropic peptide and the glucagon-like peptides 1 and 2), and bone-derived hormone osteocalcin. This background allows individual pharmacological targets for antidiabetic therapies to affect the bone quality due to their indirect effects on bone cell differentiation and bone remodeling process. Moreover, it’s important to consider the fragility fractures as another diabetes complication and discuss more deeply about the requirement for adequate screening and preventive measures. This review aims to briefly explore the impact of T2DM on bone metabolic and mechanical proprieties and fracture risk.
Type 2 diabetes mellitus (T2DM) is associated with an increased risk of fracture, although bone mineral density (BMD) is unaffected or even higher in diabetic patients . The reasons involve likely a combination of features, including the duration of disease, inadequate glycemic control, greater risk of falling as a consequence of hypoglycemia, osteopenia, impairment of bone quality, and side effects of medication, which could lead to a higher risk of bone fragility and fractures .
Unfortunately, there is little scientific knowledge approaching the impact of diabetes and of most anti-diabetic treatments on bone quality and fracture risk. Thus, this review aims to briefly explore the impact of T2DM on bone metabolic and mechanical proprieties and fracture risk. Moreover, an accompanying review about the pros and cons of the available pharmacologic treatments for T2DM on bone mineral density and risk of fractures in humans is provided in this issue of Diabetology & Metabolic Syndrome by Vianna et al. (doi:10.1186/s13098-017-0274-5).
T2DM and higher risk of bone fracture
The prevalence of T2DM has augmented with the growth in obesity epidemics, mainly because of the lifestyle changes imposed by the modern life. Patients with poorly controlled T2DM are at increased risk for diabetic complications, including macrovascular disease, retinopathy, nephropathy, and neuropathy. Recently, an increased risk of fragility fractures has been recognized as another significant diabetes complication . According to Rotterdam study, individuals with T2DM have a 69% increased risk of having fractures when compared with healthy controls. Paradoxically, T2DM subjects had greater BMD of the femoral neck and lumbar vertebrae . The discrepancy between BMD and fracture incidence observed in T2DM patients could be attributed to a frailer bone material causing failure at lower stress or to the impaired biomechanical skeletal properties . Osteoporosis is one of the most important causes of reduced bone mineral density, and it is estimated to affect 200 million women worldwide. It accounts for more than 8.9 million fractures annually in women over age 50 . T2DM and osteoporosis are both chronic diseases that may coexist and progressively increase in prevalence and are boosted by aging [6, 7].
It has been observed that T2DM negatively affect bone strength regardless of BMD [1, 8]. The greater risk of fracture is demonstrated by the health, aging and body composition study, where the relative risk (RR) of fracture was 1.64 (95% CI 1.07–2.51) in those with diabetes compared to those without, even after adjustments for hip BMD and additional risk factors for fracture . Typically, T2DM patients have a normal BMD, so this increased risk is probably due to abnormalities in bone material strength and bone biomechanical quality . Some cross-sectional studies in T2DM patients using high-resolution peripheral quantitative computed tomography (HR-pQCT) and magnetic resonance imaging (MRI) revealed quality defects in both cortical and trabecular bone . Farr et al.  by assessing bone quality with HR-pQCT in 30 postmenopausal T2DM patients at the distal radius and distal tibia, found that the cortical thickness in T2DM subjects was lower than in controls. Moreover, bone microindentation testing displayed lower bone material strength (BMS) in post menopausal women with T2DM compared to those without diabetes . Patsch et al. , investigated bone microarchitecture changes in postmenopausal T2DM patients with or without fractures at radius and tibia by using dual-energy X-ray absorptiometry (DXA) and HR-pQCT. They concluded that T2DM patients with fractures had higher pore-related deficits and a greater cortical pore volume than diabetic patients without fractures. Cortical defects often accompanied the impaired mechanical properties, such as increased failure load and low bone bending strength, that led to a reduction in overall bone strength and increase in fracture risk . It seems like that bone trabecular and cortical microarchitecture are both deranged in T2DM and may contribute to bone fragility [11, 14]. Bone remodeling decreases, as demonstrated by histomorphometric analysis of bone, which is an additional contributor to the increased the risk of fragility fractures in T2DM patients [15, 16].
Patients with T2DM have an elevated risk of all clinical fractures, particularly African-American and Latino populations . Ageing, prior fracture, corticosteroid use, longer duration of diabetes and poor glycemic control are all contributory factors. Complications comorbidities and diabetic complications such as sensory neuropathy and visual impairment imply in greater risk of falling . Moreover, falling risk may also be associated, at least partially, to increased rates of hypoglycemia, postural hypotension, and vascular disease, contributing to increased risk of fragility fracture [17,18,19].
Cross-talk between glucose homeostasis and bone metabolism
Recent evidence of common regulatory control of both glycemic and bone homeostasis enables to recognize the intimate relationship between these two entities and similarly the likelihood of antidiabetic agents to impact the bone quality. The shared regulatory control includes accumulation of advanced glycation end products (AGEs), insulin, insulin-like growth factor-1 (IGF-1), peroxisome proliferator-activated receptor gamma (PPARγ), the incretin hormones like glucose-dependent insulinotropic peptide (GIP), glucagon-like peptide 1 and 2 (GLP-1 and GLP-2), the bone-derived hormone osteocalcin and sclerostin.
The impact of vitamin D levels on glycemic control and bone mineral density in postmenopausal women with T2DM have also been studied . Vitamin D [25 (OH) D3] plays a fundamental role in bone metabolism and might impact the development and control of diabetes [21, 22]. Some studies have reported an inverse relationship between HbA1c levels and serum levels of 25 (OH) D3 , while others have found that 25 (OH) D3 supplements improve glucose control in T2DM [22, 23]. Physiologically, vitamin D seems to stimulate the expression of the insulin receptor. Therefore vitamin D deficiency might be associated with insulin resistance . Recently, Perez-Diaz et al.  have attempted to evaluate the impact of vitamin D levels on glycemic control and bone metabolism. They failed to demonstrate a clear relationship between 25 (OH) D3 levels and glucose control or osteoporotic fractures, even though reported that patients with poor glycemic control had lower 25 (OH) D3 levels than controls.
Advanced glycation end products (AGEs)
The hyperglycemia affects both cellular and extracellular bone matrix. The presence of glucose induces the formation of intermediate products containing highly reactive dicarbonyls, which ultimately leads to the production of irreversible accumulation of advanced glycation end products compounds , from a non-enzymatic glycation process . The congeries of AGEs determines the formation of defective collagens and reactive oxygen species (ROS), inducing structural changes in bone through posttranslational modifications . At the organic bone matrix, these reactions may lead to impaired bone strength [28, 29]. Higher levels of circulating AGEs are reported to increase fracture risk .
AGEs bind to the receptor for AGE (RAGE), which is a member of the immunoglobulin superfamily, and it is the AGE-RAGE interaction that mediates generation of ROS, vascular inflammation, macrophage and platelet activation, and stimulates the migration of inflammatory cells . All these reactions contribute to the development and progression of diabetic macro- and microangiopathy and result in a more brittle bone with reduced strength and less ability to deform before fracturing .
Immune cells also express RAGE and incite activation of nuclear factor kappa-light-chain-enhancer of activated B cells (NF-κB), a central transcription factor of the immune and inflammatory response . The AGE-RAGE linkage in immune cells results in upregulation of inflammatory cell adhesion molecules and chemokines, releasing, even more, RAGE ligands, and sustaining the inflammatory tissue response, modulating the response of activated macrophages to increase the damaging signals in the tissues and suppressing the repair and remodeling reactions . In a microenvironment with incremental inflammatory cytokines, AGEs may induce osteoclastogenesis and osteoblast dysfunction, which may ultimately result in the development of osteoporosis (Fig. 1) . Pentosidine, the most studied AGE in T2DM patients, accumulates in the cortical and trabecular bone and negatively impact the bone strength and probably leads to functional changes in osteoblasts and the bone mineralization process [34, 35].
The outcome of these reactions is reduced strength and impaired biomechanical properties of both trabecular and cortical bone, including disturbance in osteoblast function and attachment to collagen matrix, damaging the healthy development [30, 35,36,37].
Insulin and IGF-1
Insulin is an anabolic hormone which acts on bone tissue through its receptors (IRS-1 and IRS-2) expressed by osteoblasts, stimulating bone formation. Insulin increases osteoblast proliferation and promotes collagen synthesis. In the same way, insulin growth factor-1 (IGF-1) acts increasing osteoblast recruitment and bone matrix deposition and diminishing collagen degradation. Studies have exhibited a positive correlation between IGF-1 and BMD, and a negative correlation with hip and vertebral fracture [38, 39].
The peroxisome proliferator-activated receptor gamma (PPARγ)
The PPARγ protein is an essential regulator of lipid, glucose, and insulin metabolism. There are two isoforms in humans, PPARγ1 and PPARγ2. PPARγ1 is expressed in a variety of cell types, including osteoclasts, promoting their differentiation and bone resorption . The PPARγ2 expression restricts to cells of adipocytic lineage . In bone, PPARγ2 plays a significant role in the regulation of mesenchymal cell (MSC) differentiation toward osteoblasts and adipocytes. When this isoform is activated, cells of osteoblast lineage are converted to terminally differentiated adipocytes, disturbing the delicate balance between bone marrow adipocytes and osteoblasts (Fig. 2) .
The role of enteric hormones
The glucose-dependent insulinotropic peptide (GIP) and the glucagon-like peptides 1 and 2 (GLP-1 and GLP-2) are hormones released by gut enteroendocrine K-cells in the duodenum and proximal jejunum and from L-cells located in the distal ileum and colon, respectively . GIP and GLP-1 are secreted just after nutrient ingestion. They are already released into circulation in their active hormonal form and bind to a specific G protein-coupled receptors present in several cells and target tissues. Both hormones have their bioactivity limited by rapid degradation and inactivation by the enzyme dipeptidyl peptidase-4 (DPP-4), which is present in plasma and expressed in most tissues . The incretin hormones (GIP and GLP-1) stimulate insulin release from β-cells to inhibit glucagon production by the α-cells . Incretin receptors are also expressed in both osteoblasts and osteoclasts. These nutritional hormones are recognized to be significant in bone turnover since as soon as a meal is ingested, bone resorption is suppressed [47, 48]. In times of energy and nutrient excess, the balance is tipped for bone formation, whereas while energy and nutrient are lacking, bone resorption increases . GIP and possibly GLP-1 and GLP-2 may link nutrient ingestion to suppression of bone resorption and stimulation of bone formation . Studies indicate that GLP-2 may affect bone remodeling by disassociating bone resorption and bone formation , acting mainly as an antiresorptive hormone , while GIP can act both as an antiresorptive and anabolic hormone [49, 51].
Bone turnover markers: focus on osteocalcin
An additional approach to evaluate the impact of diabetes on bone metabolism is to assess the serum markers of bone turnover (BTM), particularly the formation markers osteocalcin (OC) and amino-terminal propeptide of procollagen type 1 (PINP), which are decreased in these patients [52, 53]. Shu et al.  investigated structural and biochemical skeletal parameters in T2DM patients and shown that postmenopausal women with T2DM had lower levels of bone formation markers when compared to controls, while their bone structure was not modified. They found lower OC and PINP levels in diabetic subjects, and these levels correlated inversely with glucose levels and fat mass. This concept supports the idea that biochemical indices of bone formation are lower in T2DM patients than in controls. Moreover, the resorption marker CTX (serum C-terminal telopeptide from type 1 collagen) is shown by some authors to be reduced in T2DM individuals [52, 55], while other revealed no difference .
Interestingly, OC seems also to have a role in energy metabolism. In its undercarboxylated form, OC stimulates insulin secretion and enhances insulin sensitivity in both adipose and muscle tissue. An inverse association between OC and metabolic syndrome has been demonstrated, suggesting that reduced levels of osteocalcin may impact in the pathophysiology of T2DM [57, 58]. Consequently, the skeleton has been considered a new endocrine organ that participates and influences glucose homeostasis.
The Wnt/ß-catenin pathway
Sclerostin is another regulator of bone metabolism and is expressed by osteocytes. It inhibits the Wnt/ß-catenin pathway by binding to low-density lipoprotein receptor-related protein (LPR) 5 or 6 and negatively regulates bone formation . The Wnt/ß-catenin pathway induces osteoblastogenesis and thereby enhances bone formation. Canonical Wnt signaling suppresses osteoclastogenesis by inducing osteoprotegerin, and, also, suppresses bone resorption by an osteoprotegerin-independent mechanism acting directly on osteoclast precursors. The dual effect of Wnt on cells of the osteoblast and osteoclast lineage results in an increase in bone mass. So, when sclerostin bind to Wnt co-receptors, inhibition of osteoblastogenesis and bone formation occurs (Fig. 3) . Patients with T2DM have higher serum levels of sclerostin, which are associated with increased risk of vertebral fractures. Studies also show that sclerostin levels is directly related to both duration of T2DM and glycated hemoglobin, and inversely related to levels of bone turnover markers [52, 60].
The impact of vitamin D
The hyperglycemia seems to play a major role on the vitamin D-calcium axis through impairment renal calcium absorption . High glycemic levels contribute to the reduced number of 1,25(OH)2D3 (1,25-dihydroxy vitamin D) receptors on osteoblasts and limit the ability of the osteoblast to synthesize osteocalcin in response to 1,25(OH)2D3 . However, the vitamin D performance in affecting T2DM and fracture risk is currently uncertain .
As reviewed in the topics above, several direct and indirect mechanisms in T2DM may affect the bone metabolism and quality, as well the risk of fractures. Table 1 review and summarize the effects of type 2 diabetes on bone.
Patients with T2DM have an augmented risk for fragility fractures, not predictable by BMD measurements. This higher risk is probably multifactorial. Despite these features, there are no current recommendations regarding routine screening or initiation of preventative medications for osteoporosis in patients with diabetes. Adequate glycemic control prevents this risk and reduces the micro-and macrovascular complications, which consequently, can contribute to diminish the production of AGE’s, reduce the vascular damage in the bone tissue and lessen the risk of falls. As reported, bone and energy metabolism are closely related, and this connection occurs since the differentiation of adipocytes and osteoblasts from the same mesenchymal stem cells. In hyperglycemic patients, bone formation decreases and all mechanisms described so far contribute to the poorer bone formation and quality, increasing fracture risk. Currently, it is essential to consider the fragility fractures as an additional diabetes complication, recognize the diabetes bone disease as a specific pathology, and discuss more deeply about the requirement for adequate screening and preventive measures.
advanced glycation end products
bone mineral density
bone material strength
bone turnover markers
C-terminal telopeptide of type 1 collagen
dual-energy X-ray absorptiometry
glucose-dependent insulinotropic peptide
glucagon-like peptide 1
glucagon-like peptide 2
- HR- pQCT:
high-resolution peripheral quantitative computed tomography
insulin-like growth factor-1
insulin receptor substrate-1
insulin receptor substrate-2
low-density lipoprotein receptor-related protein
magnetic resonance imaging
nuclear factor kappa-light-chain-enhancer of activated B cells (NF-κB)
amino-terminal propeptide of procollagen type 1
peroxisome proliferator-activated receptor gamma
reactive oxygen species
type 2 diabetes mellitus
1,25-dihydroxy vitamin D
Jackuliak P, Payer J. Osteoporosis, fractures, and diabetes. Int J Endocrinol. 2014;2014:820615. doi:10.1155/2014/820615.
Oei L, Rivadeneira F, Zillikens MC, Oei EHG. Diabetes, diabetic complications, and fracture risk. Curr Osteoporos Rep. 2015;13(2):106–15. doi:10.1007/s11914-015-0260-5.
De Liefde II, Van der Klift M, De Laet CEDH, Van Daele PLA, Hofman A, Pols HAP. Bone mineral density and fracture risk in type-2 diabetes mellitus: the rotterdam study. Osteoporos Int. 2005;16:1713–20. doi:10.1007/s00198-005-1909-1.
Oei L, Zillikens MC, et al. High bone mineral density and fracture risk in type 2 diabetes as skeletal complications of inadequate glucose control. The rotterdam study. Diabetes Care. 2013;36:1619–28. doi:10.2337/dc12-1188.
International osteoporosis foundation. The global burden of osteoporosis: a factsheet. Accessed at https://www.iofbonehealth.org. Accessed 18 Sept 2017.
Paschou SA, Dede AD, et al. Type 2 diabetes and osteoporosis: a guide to optimal management. J Clin Endocrinol Metab. 2017;102(10):3621–34. doi:10.1210/jc.2017-00042.
World Health Organization. Global report on diabetes. 2016. ISBN: 978 92 4 156525 7.
Liao C-C, Lin C-S, Shih C-C, et al. Increased risk of fracture and postfracture adverse events in patients with diabetes: two nationwide population-based retrospective cohort studies. Diabetes Care. 2014;37:2246–52. doi:10.2337/dc13-2957.
Strotmeyer ES, Cauley JA, Schwartz AV, et al. Nontraumatic fracture risk with diabetes mellitus and impaired fasting glucose in older white and black adults. Arch Intern Med. 2005;165:1612–7.
Farr JN, Khosla S. Determinants of bone strength and quality in diabetes mellitus in humans. Bone. 2016;82:28–34. doi:10.1016/j.bone.2015.07.027.
Farr JN, Drake MT, Amin S, Melton LJ, McCready LK, Khosla S. In vivo assessment of bone quality in postmenopausal women with type 2 diabetes. J Bone Miner Res. 2014;29(4):787–95. doi:10.1002/jbmr.2106.
Patsch JM, Burghardt AJ, Yap SP, et al. Increased cortical porosity in type 2 diabetic postmenopausal women with fragility fractures. J Bone Miner Res. 2013;28(2):313–24. doi:10.1002/jbmr.1763.
Wongdee K, Charoenphandhu N. Update on type 2 diabetes-related osteoporosis. World J Diabetes. 2015;6(5):673–8. doi:10.4239/wjd.v6.i5.673.
Leslie WD, Aubry-Rozier B, Lamy O, Hans D. TBS (trabecular bone score) and diabetes-related fracture risk. J Clin Endocrinol Metab. 2013;98(2):602–9. doi:10.1210/jc.2012-3118.
Moreira CA, Dempster DW. Bone histomorphometry in diabetes mellitus. Osteoporos Int. 2015;26(11):2559–60. doi:10.1007/s00198-015-3258-z.
Moreira CA, Barreto FC, Dempster DW. New insights on diabetes and bone metabolism. J Bras Nefrol. 2015;37(4):490–5. doi:10.5935/0101-2800.20150077.
Schwartz AV, Hillier TA, Sellmeyer DE, et al. Older women with diabetes have a higher risk of falls: a prospective study. Diabetes Care. 2002;25(10):1749–54. doi:10.2337/diacare.25.10.1749.
Melton LJ III, Leibson CL, Achenbach SJ, Therneau TM, Khosla S. Fracture risk in type 2 diabetes: update of a population-based study. J Bone Miner Res. 2008;23(8):1334–42. doi:10.1359/jbmr.080323.
Gilbert MP, Pratley RE. The impact of diabetes and diabetes medications on bone health. Endocr Ver. 2015;36(2):194–213. doi:10.1210/er.2012-1042.
Diaz P, Barajas GS, Hernandez-Flores ZG, et al. The impact of vitamin D levels on glycemic control and bone mineral density in postmenopausal women with type 2 diabetes. J Endocrinol Invest. 2015;38(12):1365–72. doi:10.1007/s40618-015-0394-4.
Chiu KC, Chu A, Go VLW, Saad MF. Hypovitaminosis D is associated with insulin resistance and β cell dysfunction. Am J Clin Nutr. 2004;79:820–5.
Kostoglou-Athanassiou I, Athanassiou P, Gkountouvas A, Kaldrymides P. Vitamin D and glycemic control in diabetes mellitus type 2. Ther Adv Endocrinol Metab. 2013;4:122–8. doi:10.1177/2042018813501189.
Mitri J, Muraru MD, Pittas AG. Vitamin D and type 2 diabetes: a systematic review. Eur J Clin Nutr. 2011;65:1005–15. doi:10.1038/ejcn.2011.118.
Mathieu C, Gysemans C, Giulietti A, Bouillon R. Vitamin D and diabetes. Diabetologia. 2006;48:1247–57. doi:10.1007/s00125-005-0047-9.
Singh R, Barden A, Mori T, Beilin L. Advanced glycation end-products: a review. Diabetologia. 2001;44(2):129–46. doi:10.1007/s001250051591.
Napoli N, Strollo R, Paladini A, Briganti SI, Pozzilli P, Epstein S. The alliance of mesenchymal stem cells, bone, and diabetes. Int J Endocrinol. 2014;2014:690783. doi:10.1155/2014/690783.
Strollo R, Rizzo P, Spoletini M, Landy R, Hughes C, Ponchel F, Napoli N, Palermo A, Buzzetti R, Pozzilli P, Nissim A. HLA-dependent autoantibodies against post-translationally modified collagen type II in type 1 diabetes mellitus. Diabetologia. 2013;56(3):563–72. doi:10.1007/s00125-012-2780-1.
Hernandez CJ, Tang SY, Baumbach BM, et al. Trabecular microfracture and the influence of pyridinium and non-enzymatic glycation-mediated collagen cross-links. Bone. 2005;37(6):825–32. doi:10.1016/j.bone.2005.07.019.
Ahmed N. Advanced glycation endproducts—role in pathology of diabetic complications. Diabetes Res Clin Pract. 2005;67(1):3–21. doi:10.1016/j.diabres.2004.09.004.
Epstein S, Defeudis G, Manfrini S, Napoli N, Pozzilli P. Diabetes and disordered bone metabolism (diabetic osteodystrophy): time for recognition. Osteoporos Int. 2016;27:1931–51. doi:10.1007/s00198-015-3454-x.
Manigrasso MB, Juranek J, Ramasamy R, Schmidt AM. Unlocking the biology of RAGE in diabetic microvascular complications. Trends Endocrinol Metab. 2013;25(1):15–22. doi:10.1016/j.tem.2013.08.002.
Huebschmann AG, Regensteiner JG, Vlassara H, Reusch JEB. Diabetes and advanced glycoxidation end products. Diabetes Care. 2006;29(6):1420–32. doi:10.2337/dc05-2096.
Sanguineti R, Puddu A, Mach F, Montecucco F, Viviani GL. Advanced glycation end products play adverse proinflammatory activities in osteoporosis. Mediators Inflamm. 2014;2014:975872. doi:10.1155/2014/975872.
Saito M, Fujii K, Soshi S, Tanaka T. Reductions in degree of mineralization and enzymatic collagen cross-links and increases in glycation-induced pentosidine in the femoral neck cortex in cases of femoral neck fracture. Osteoporos Int. 2006;17(7):986–95. doi:10.1007/s00198-006-0087-0.
Sanguineti R, Storace D, Monacelli F, Federici A, Odetti P. Pentosidine effects on human osteoblasts in vitro. Ann NY Acad Sci. 2008;1126:166–72. doi:10.1196/annals.1433.044.
McCarthy AD, Uemura T, Etcheverry SB, Cortizo AM. Advanced glycation endproducts interfere with integrin-mediated osteoblastic attachment to a type-I collagen matrix. Int J Biochem Cell Biol. 2004;36(5):840–8. doi:10.1016/j.biocel.2003.09.006.
Kume S, Kato S, Yamagishi S, Inagaki Y, Ueda S, Arima N, Okawa T, Kojiro M, Nagata K. Advanced glycation endproducts attenuate human mesenchymal stem cells and prevent cognate differentiation into adipose tissue, cartilage, and bone. J Bone Miner Res. 2005;20(9):1647–58. doi:10.1359/JBMR.050514.
Niu T, Rosen CJ. The insulin-like growth factor-I gene and osteoporosis: a critical appraisal. Gene. 2005;361(1–2):38–56. doi:10.1016/j.gene.2005.07.016.
Garnero P, Sornay-Rendu E, Delmas P. Low serum IGF-1 and occurrence of osteoporotic fractures in postmenopausal women. Lancet. 2000;355:898–9.
Wan Y, Chong L-W, Evans RM. PPAR-gamma regulates osteoclastogenesis in mice. Nat Med. 2007;13(12):1496–503. doi:10.1038/nm1672.
Ren D, Collingwood TN, Rebar EJ, Wolffe AP, Camp HS. PPAR gamma knockdown by engineered transcription factors: exogenous PPAR gamma 2 but not PPAR gamma 1 reactivates adipogenesis. Genes Dev. 2002;16(734):27–32. doi:10.1101/gad.953802.GENES.
Lecka-Czernik B. Safety of antidiabetic therapies on bone. Clin Rev Bone Min Metab. 2013;11(1):49–58. doi:10.1007/s12018-012-9129-7.
Kawai M, Sousa KM, MacDougald OA, Rosen CJ. The many facets of PPARγ: novel insights for the skeleton. Am J Physiol Endocrinol Metab. 2010;299(1):E3–9. doi:10.1152/ajpendo.00157.2010.
Mortensen K, Christensen LL, Holst JJ, Orskov C. GLP-1 and GIP are colocalized in a subset of endocrine cells in the small intestine. Regul Pept. 2003;114:189–96. doi:10.1016/S0167-0115(03)00125-3.
Deacon CF. Circulation and degradation of GIP and GLP-1. Horm Metab Res. 2004;36(11–12):761–5. doi:10.1055/s-2004-826160.
Drucker DJ. The role of gut hormones in glucose homeostasis. J Clin Invest. 2007;117(1):24–32. doi:10.1172/JCI30076.
Clowes JA, Khosla S, Eastell R. Potential role of pancreatic and enteric hormones in regulating bone turnover. J Bone Miner Res. 2005;20(9):1497–506. doi:10.1359/JBMR.050524.
Reid IR, Cornish J, Baldock PA. Nutrition-related peptides and bone homeostasis. J Bone Miner Res. 2005;21(4):495–500. doi:10.1359/jbmr.051105.
Xie D, Zhong Q, Ding K-H, et al. Glucose-dependent insulinotropic peptide-overexpressing transgenic mice have increased bone mass. Bone. 2007;40(5):1352–60. doi:10.1016/j.bone.2007.01.007.
Henriksen DB, Alexandersen P, Hartmann B, et al. Disassociation of bone resorption and formation by GLP-2: a 14-day study in healthy postmenopausal women. Bone. 2007;40(3):723–9. doi:10.1016/j.bone.2006.09.025.
Zhong Q, Itokawa T, Sridhar S, et al. Effects of glucose-dependent insulinotropic peptide on osteoclast function. Am J Physiol Endocrinol Metab. 2007;292(2):E543–8. doi:10.1152/ajpendo.00364.2006.
Rubin MR. Bone cells and bone turnover in diabetes mellitus. Curr Osteoporos Rep. 2015;13(3):186–91. doi:10.1007/s11914-015-0265-0.
Rosen CJ, Chesnut CH, Mallinak NJ. The predictive value of biochemical markers of bone turnover for bone mineral density in early postmenopausal women treated with hormone replacement or calcium supplementation. J Clin Endocrinol Metab. 1997;82(6):1904–10. doi:10.1210/jcem.82.6.4004.
Shu A, Yin MT, Stein E, et al. Bone structure and turnover in type 2 diabetes mellitus. Osteoporos Int. 2012;23(2):635–41. doi:10.1007/s00198-011-1595-0.
Oz SG, Guven GS, Kilicarslan A, Calik N, Beyazit Y, Sozen T. Evaluation of bone metabolism and bone mass in patients with type-2 diabetes mellitus. J Natl Med Assoc. 2006;98(10):1598–604.
Achemlal L, Tellal S, Rkiouak F, et al. Bone metabolism in male patients with type 2 diabetes. Clin Rheumatol. 2005;24(5):493–6. doi:10.1007/s10067-004-1070-9.
Zanatta LC, Boguszewski CL, Borba VZ, Kulak CA. Osteocalcin, energy and glucose metabolism. Arq Bras Endocrinol Metab. 2014;58(5):444–51. doi:10.1590/0004-2730000003333.
Pittas AG, Harris SS, Eliades M, Stark P, Dawson-Hughes B. Association between serum osteocalcin and markers of metabolic phenotype. J Clin Endocrinol Metab. 2009;94(3):827–32. doi:10.1210/jc.2008-1422.
Canalis E. Wnt signalling in osteoporosis: mechanisms and novel therapeutic approaches. Nat Rev Endocrinol. 2013;9(10):575–83. doi:10.1038/nrendo.2013.154.
García-Martín A, Rozas-Moreno P, Reyes-García R, et al. Circulating levels of sclerostin are increased in patients with type 2 diabetes mellitus. J Clin Endocrinol Metab. 2012;97(1):234–41. doi:10.1210/jc.2011-2186.
Chaiban JT, Nicolas KG. Diabetes and bone: still a lot to learn. Clin Rev Bone Miner Metab. 2015;13(1):20–35. doi:10.1007/s12018-015-9178-9.
AV and CS performed the bibliographic review, analysis of data and were major contributors in the manuscript preparation. FB was an important contributor in the statistical analysis and critical review of the manuscript. All authors read and approved the final manuscript.
The authors would like to thank all the team of the Clinical Research Department of the Curitiba Diabetes Center and the Health Sciences post-graduation program of the Pontifical Catholic University of Parana, Brazil.
The authors declare that they have no competing interests.
Availability of data and materials
Consent for publication
Ethics approval and consent to participate
Springer Nature remains neutral with regard to jurisdictional claims in published maps and institutional affiliations.
About this article
Cite this article
Sanches, C.P., Vianna, A.G.D. & Barreto, F.d. The impact of type 2 diabetes on bone metabolism. Diabetol Metab Syndr 9, 85 (2017) doi:10.1186/s13098-017-0278-1
- Type 2 diabetes
- Bone metabolism
- Bone mineral density