[Obesity and bone metabolism]

Hormones (2018) 17:205–217 https://doi.org/10.1007/s42000-018-0018-4 REVIEW Obesity and bone metabolism Christos Savvidis 1 & Symeon Tournis 2 & Anastasia D. Dede 2,3 Received: 21 November 2017 / Accepted: 3 March 2018 / Published online: 24 April 2018 # Hellenic Endocrine Society 2018 Abstract The interaction between obesity and bone metabolism is complex. The effects of fat on the skeleton are mediated by both mechanical and biochemical factors. Though obesity is characterized by higher bone mineral density, studies conducted on bone microarchitecture have produced conflicting results. The majority of studies indicate that obesity has a positive effect on skeletal strength, even though most likely the effects are site-dependent and, in fact, obese individuals might be at risk of certain types of fractures. Mechanical loading and higher lean mass are associated with improved outcomes, whereas systemic inflammation, observed especially with abdominal obesity, may exert negative effects. Weight loss interventions likely lead to bone loss over time. Pharmacological treatment options seem to be safe in terms of skeletal health; however, the skeletal effects of bariatric surgery are dependent on the type of surgical procedure. Malabsorptive procedures are associated with higher short-term adverse effects on bone health. In this narrative review, we discuss the effects of obesity and weight loss interventions on skeletal health. Keywords Fracture . Diabetes . Leptin . Adipose tissue . Fat . Weight Abbreviations 1 1 β - 11β-hydroxysteroid dehydrogenase type 1 HSD1 5-HT2C 5-hydroxytryptamine 2c AACE American Association of Clinical Endocrinologists AACS acetoacetyl-CoA synthetase aBMD areal bone mineral density AGB adjustable gastric band ASBMS American Society for Metabolic and Bariatric Surgery Bglap2 bone gamma-carboxyglutamate protein 2 BM bone marrow BMC bone mineral content BMI body mass index BPD-LL long limb-biliopancreatic diversion Ca calcium c-fms colony-stimulating factor * Anastasia D. Dede [email protected] 1 Department of Endocrinology, Hippokrateion General Hospital, Athens, Greece 2 Laboratory for Research of the Musculoskeletal System “Th. Garofalidis”, KAT hospital, Medical school, Athens, Greece 3 Department of Endocrinology and Diabetes, Chelsea and Westminster Hospital, 369 Fulham Road, London SW10 9NH, UK CLA Col1a1 CSA CT DXA EMA FDA FN FRAX HFD H R pQCT IGF-1 IL-6 Insr LCN2 Lepr LS LSG MC4R NFκB NTx OPG pQCT QCT RANK conjugated linoleic acid collagen Iα1 cross-sectional area computed tomography dual energy x-ray absorptiometry European Medicines Agency Food and Drug Administration femoral neck Fracture Risk Assessment Tool high-fat diet high-resolution pQCT insulin-like growth factor-1 interleukin 6 insulin receptor lipocalin 2 leptin receptor lumbar spine laparoscopic sleeve gastrectomy melanocortin 4 receptor nuclear factor kappa-light-chain-enhancer of activated B cells N-telopeptide crosslinks osteoprotegerin peripheral QCT quantitative computed tomography receptor activator of nuclear factor kappa-B 206 RANKL RD RYGB SAT T2DM TBS TNFα TOS VAT VBG vBMD β-CTX Hormones (2018) 17:205–217 RANK ligand restricted diet Roux-en-Y gastric bypass subcutaneous adipose tissue type 2 diabetes mellitus trabecular bone score tumor necrosis factor-a The Obesity Society visceral adipose tissue vertical banded gastroplasty volumetric BMD beta C-terminal telopeptide Introduction Obesity is becoming a global epidemic, with 2.8 million people estimated to die each year as a result of being overweight or obese [1]. The worldwide prevalence of obesity virtually doubled between 1980 and 2008 and the numbers are expected to increase further. In Europe, more than 20% of men and women were obese in 2008, while, alarmingly, rates of obesity and overweight are very high among children as well [2]. The interaction of obesity with bone metabolism is complex and not as yet fully elucidated. Traditionally, it was thought that obesity, as demonstrated by high body mass index (BMI), has protective effects on the skeleton [3]. BMI is incorporated in the fracture risk assessment tool (FRAX), and higher BMI is associated with lower future fracture risk. However, this notion has recently been challenged, with studies showing that obesity is associated with lower risk for certain fractures but higher risk for others [4]. Results from animal studies have also resulted in conflicting findings. Moreover, medical and surgical management of obesity can also directly affect bone metabolism. In this narrative review, we discuss the molecular mechanisms associated with the interaction between obesity and the skeleton and discuss the effects of obesity on the risk of fractures and on bone mineral density (BMD). We also review the effects of treatment interventions for obesity on skeletal health. Pathophysiology Various molecular pathways have been proposed by which adipose tissue communicates with the bone microenvironment (Fig. 1). This involves systemic factors such as vitamin D, leptin and proinflammatory cytokines, and local factors mainly associated with local changes in the bone marrow microenvironment. Leptin Leptin, a cytokine-like hormone, is the protein product of the ob (Lep) gene. It is produced primarily by adipocytes and is involved in the regulation of appetite and energy homeostasis by inducing satiety signals in the hypothalamus (Fig. 1). Systemic levels of leptin increase with increased fat content. Leptin plays an important role in bone metabolism with both direct and indirect effects, by peripheral and central (hypothalamic) pathways, though in vivo studies have produced seemingly discrepant results, depending on the experimental design. In vitro, leptin stimulates the differentiation of stromal cells to osteoblasts [5], increases proliferation of osteoblasts, and inhibits osteoclastogenesis, without affecting mature osteoclasts [6]. Deficiency in leptin signaling, through knockout of the leptin receptor gene, decreases bone volume and BMD [7], indicating an important role of leptin in bone homeostasis. In mice, peripheral action through the administration of low doses of leptin seems to promote bone formation, without inducing anorexigenic actions of the hormone to the central nervous system [8]. In animal models, increased leptin levels caused by increased adipose tissue seem to have a protective role in / effect on bone tissue [9]. By contrast, leptin-deficient models have increased cancellous bone volume fraction [10] and increased trabecular content (volume and thickness), indicating a possible antiosteogenic role of leptin [11]. The negative effects of leptin in bone homeostasis seem to be mediated through its central hypothalamic action, as intracerebroventricular infusion of leptin in both leptindeficient and wild-type mice induces bone loss [12]. This effect seems to be mediated by activation of the sympathetic nervous system (Fig. 1) [13]. Data in humans are also conflicting, indicating either a beneficial role of leptin [14, 15] or a detrimental one [16, 17], this probably being due to limitations of association studies. Moreover, obesity is characterized by leptin tolerance, at least as concerns the hypothalamus, as administration of leptin has not proved to be an effective treatment for obesity [18]. Overall, the high levels of leptin observed in obese individuals are unlikely to have negative effects on bone metabolism. High-fat diet There are data from animal studies implying possible negative effects of obesity on bone metabolism. These effects are likely to be mediated through local alterations in the bone microenvironment or through systemic effects of obesity, mainly through inflammation. One of the most commonly used models to study the effects of adiposity on bone metabolism is obesity caused by a high-fat diet (HFD). Trabecular BMD decreased in mice that were fed with HFD [19], while obesity induced by HFD is associated with higher bone tissue quantity but worse bone quality [20]. Obesity induced by HFD causes Hormones (2018) 17:205–217 207 Fig. 1 Principal central and peripheral molecular signaling between bone, adipose tissue, and SNSLeptin action has, through the hypothalamus, direct and indirect effects on osteoblast and osteoclast activity that alters bone metabolism. IGF-1 and inflammation increase cortisol response of fat tissue and proinflammatory cytokines, such as TNF-a, and increase cortisol action on bone by increasing the expression of 11β-HSD1. Insulin promotes the differentiation of osteoblasts through the insulin receptor and also promotes the production of osteocalcin. Osteocalcin, a non-collagenous bone matrix protein, regulates energy and glucose metabolism, closing the loop of calcium and glucose metabolism. Inflammation has both systemic and local actions.SNS: sympathetic nervous system, IGF-1: insulin growth factor 1, TNF-a: tumor necrosis factor a, 11β-HSD1: 11β-hydroxysteroid dehydrogenase type 1 significant bone resorption [21] and can increase bone marrow adiposity leading to alteration of trabecular architecture. The bone marrow (BM) microenvironment in obesity seems to be associated with bone resorption; meanwhile, accumulation of adipocytes in the BM microenvironment promotes inflammation that leads to increased bone resorption by enhancing osteoclastogenesis and inhibiting osteoblast development [22]. Adiposity is associated with proinflammatory cytokines such as TNF-a and IL-6. TNF-α stimulates osteoclastogenesis via the activation of NFκB in hyperphagiainduced obesity by increasing the expression of c-fms, RANK, and RANKL [23]. Several studies have 208 demonstrated a role of TNF-α in obesity-related bone loss through its enhancement of adipogenesis and osteoclastogenesis and suppression of osteoblastogenesis [24, 25]. In addition, HFD-induced obesity, through IL-6, suppresses osteoblasts, upregulates osteoclasts, and inhibits osteoclast apoptosis [26]. Acetoacetyl-CoA synthetase (AACS) is a ketone body-utilizing enzyme that converts acetoacetate to acetoacetyl-CoA in the cytosol and consequently provides acetyl units as the precursors for lipogenesis [27]. AACS mRNA expression in the adult femur is increased in HFD, in the differentiated osteoclast cells (RAW 264), and upregulated by IL-6 only in osteoclasts. These results indicate that bone resorption is induced by HFD through bone inflammation and increased ketone utilization [28]. Hormones (2018) 17:205–217 Conjugated linoleic acids and calcium supplementation Poor calcium intake during adolescence, especially in the presence of vitamin D deficiency, might contribute to fracture risk; however, obese and overweight adolescents have increased calcium retention (as assessed by calcium intake, fecal, and urinary calcium) when compared with healthy-weight subjects of the same age, and this is correlated positively with calcium intake [35]. In animal models, co-supplementation of conjugated linoleic acids (CLA) and calcium has beneficial effects on bone and energy-related metabolic markers in tibia in obese animals fed with HFD. It prevents bone loss induced by HF feeding and increases the expression of bone formation markers, such as bone gamma-carboxyglutamate protein 2 (Bglap2) and collagen Iα1 (Col1a1) [36]. 11β-hydroxysteroid dehydrogenase type 1 Fat and bone molecular crosstalk The negative effects of glucocorticoids on bone metabolism are well recognized. 11β-hydroxysteroid dehydrogenase type 1 (11β-HSD1) is an enzyme that converts the inactive glucocorticoid cortisone to the active glucocorticoid cortisol and is expressed in both osteoblasts and adipocytes [29]. Its expression is affected by local factors and activation results in higher local exposure to active cortisol. Local activity of 11β-HSD1 is believed to determine the skeletal response to different types of glucocorticoids [30]. The local expression of 11β-HSD1 in osteoblasts is upregulated by proinflammatory cytokines (IL-1β and TNF-a) (Fig. 1) [31]. This constitutes another mechanism by which adipocyte accumulation in the bone marrow can have detrimental effects on bone metabolism. Visceral adipose tissue (VAT) is metabolically more active than subcutaneous adipose tissue (SAT), and this might be why some human studies have indicated that VAT might be associated with a less favorable skeletal phenotype, though most studies do not find a negative association between SAT and bones. Interestingly, the crosstalk between fat and bone seems to be more complicated and to also involve effects of bone metabolism on energy homeostasis. In animal models, there are data showing positive effects of calcium on energy homeostasis. Supplementation with CLAs and calcium in adult obese mice decreases body weight and body fat [37, 38]. It also modulates the expression of genes involved in energy metabolism, insulin receptor (Insr), and leptin receptor (Lepr) [36]. Osteocalcin is a bone matrix protein and is considered a marker of bone formation. Animal studies have indicated that the undercarboxylated form of osteocalcin regulates energy homeostasis by enhancing B cell proliferation, insulin secretion, and sensitivity (Fig. 1) [39]. Emerging evidence shows that there is also crosstalk between bone and adipose tissue through central signals. For example, osteoblast-derived lipocalin 2 (LCN2), a protein that was previously known as an adipokine, suppresses appetite and decreases food intake by signaling directly to melanocortin 4 receptor-expressing hypothalamic neurons [40]. Bone density and microarchitecture Vitamin D Vitamin D deficiency is very common among obese individuals and may have significant implications for skeletal health. Supplementation with vitamin D is more effective in increasing its serum levels in non-obese children and adults compared to obese, possibly due to sequestration of vitamin D in the body fat stores [32, 33]. It has been noted that vitamin D deficiency is common in morbidly obese individuals and up to 43% of those with vitamin D deficiency also suffer from secondary hyperparathyroidism [34]. Obese individuals have higher BMD than the normal weight population, though it has been postulated that this might be an artifact due to overlying soft tissue. Moreover, the coefficient of variation between repeat measurements is higher in obesity [41] and therefore longitudinal BMD monitoring in obese individuals might be challenging. BMD measurements using quantitative computed tomography (QCT) and peripheral QCT (pQCT) are not as affected by overlying soft tissue, providing a more reliable way to assess bone density in obesity. Moreover, they provide separate information about the cortical and trabecular Hormones (2018) 17:205–217 compartment of the bone. In a cross-sectional case-control study, it was demonstrated that obese women had higher volumetric BMD (vBMD) at the lumbar spine and that both obese men and women had higher vBMD at the distal radius and distal tibia when compared to normal weight individuals [42]. This suggests that the higher BMD is a true effect and not an artifact caused by overlying soft tissue. Moreover, parameters of bone microarchitecture were better in obese compared to normal weight individuals, suggesting higher skeletal strength. Lean mass, which is usually higher in obese individuals along with fat mass, correlates positively with BMD and parameters of bone microarchitecture, as measured by pQCT [43, 44]. This is especially relevant to cortical thickness and area, whereas total fat mass has a positive correlation with trabecular number and density even after adjusting for lean mass [44]. It seems that fat mass is not the main contributing factor to increased bone strength, while muscle force (represented by lean mass) is associated with osteogenic adaptation [45]. Fat mass does not seem to have a positive association with BMD in obese adults [46] and adolescents [47]. A case control study has shown that excess weight or higher BMI does not have a proportional positive effect on bone strength parameters. Moreover, lean mass seems to be an important determinant of bone microarchitecture, geometry, and metabolism when compared to fat mass [48]. As VAT is metabolically active and associated with inflammation, there has been growing interest in the differential effects of VAT and SAT. In a study investigating the correlation of visceral fat with skeletal parameters in the peripheral skeleton, VAT was measured using CT scans, and skeletal bone microarchitecture parameters were measured by highresolution pQCT (HR-pQCT) at the distal radius and tibia. The investigators found that higher visceral fat was associated with higher BMD and improved microarchitecture with the exception of higher cortical porosity at the distal radius. When findings were adjusted for BMI, they were no longer significant, suggesting that the effect is mostly associated with obesity in general rather than with visceral fat [49]. In contrast, in another study examining the correlation of VAT with vBMD using data from CT scans, researchers found that VAT had an inverse correlation with vBMD at the spine and that there was an inverse correlation with low muscle attenuation (a marker of fat infiltration in the muscle) even after adjusting for age, sex, and BMI [50]. The trabecular bone score (TBS) is a dual-energy x-ray absorptiometry (DXA)-derived variable which has a good correlation with bone microarchitecture and predicts vertebral fracture risk independent of BMD [51]. However, TBS seems to be affected by overlying soft tissue [52]. TBS has been shown to have a negative correlation with body size variables, and this correlation is higher for waist circumference than for other variables and for trunk fat mass [53, 54]. However, the 209 latter finding is probably not reflective of higher fracture risk. In older men, obesity variables were positively associated with lumbar spine vBMD, but had a negative correlation with TBS, while the association between vBMD and TBS was variable and depended significantly on BMI and lean trunk mass [55]. It is therefore postulated that TBS might not predict fracture risk in individuals with high BMIs or high trunk lean mass as accurately as in normal weight subjects. It has been postulated that the effects of fat on the skeleton might differ according to age and that they might have more pronounced negative effects during growth. In a pQCT study in girls post- adolescence where girls were divided into groups according to the percentage body fat rather than their weight, the girls with higher fat content were found to have lower total CSA and cortical CSA and lower bone strength after adjusting for body weight [56]. In a longitudinal study in adolescents, VAT was inversely associated with bone strength at the tibia and radius, as measured by pQCT, in girls but not in boys, and the association was more significant for younger rather than older girls, indicating that early obesity might have more pronounced effects on bone accrual [57]. In young adults with a history of early onset severe obesity at a young age, both obese men and women had improved bone parameters as compared to normal weight controls, but after adjustment for BMI, the findings were attenuated [58]. However, obese men had lower radius cross-sectional area after adjustment for BMI. Interestingly, even though as expected, obese individuals had lower levels of physical activity, there was no correlation between bone parameters and physical activity. Overall, these findings suggest that obesity during skeletal growth might interrupt the skeletal adaptation to mechanical forces. This might either be associated with decreased physical activity in obese individuals, with direct effects of fat on bone metabolism, or come about through negative effects on the muscles. Interestingly, in young girls, researchers found a negative association between SAT and bone strength in the weight bearing tibia, and this finding was correlated with higher fat infiltration in the calf and thigh muscles [59]. Obesity is associated with low bone turnover as measured by bone turnover markers [60]. To our knowledge, there are no histomorphometric data on bone mineralization in obese humans, apart from occasional reports showing abnormal mineralization compatible with mild osteomalacia, these, however, in the context of vitamin D deficiency and secondary hyperparathyroidism [61]. Data from animal studies indicate that obesity induced by HFD, despite inducing higher bone mass probably caused by an increase in mechanical loading, leads to reduced bone formation [62]. This is associated w i t h a n i n c r e a s e i n b o n e m a r r o w a d i p o s i t y. I n histomorphometric studies, obesity has been shown to induce lower osteoblast surface, osteoid surface, and osteoid volume, indicating low osteoblastic activity, though with no change in the mineralization process [63]. 210 In conclusion, the existing data seem to differ depending on the technique employed to estimate BMD and microarchitecture and the methods used to assess fat mass, VAT and SAT, age, and bone compartment (cortical vs trabecular). In general, obesity results in higher BMD and improved bone microarchitecture parameters, albeit it might be associated with negative effects (mostly VAT), especially during bone accrual, resulting in impaired adaptation of the skeleton to the increased weight. Fracture risk in obesity Data regarding fracture risk in obese people are somewhat contradictory (Table 1). Originally, it was thought that fracture rates in obese individuals were lower compared to normal weight individuals due to the higher areal BMD (aBMD) and local fat padding. The association of BMI with fracture risk, however, is more complex and seems to be different depending on the skeletal site [64, 65]. Data from a multisite, multiethnic cohort of 1924 women were analyzed and demonstrated that obesity is associated with increased aBMD but lower bone strength relative to load, with increased fracture hazard and increased impact forces in falls [66]. Higher applied loads from higher body weight may contribute to increased fracture risk during certain activities [67]. In a study in older men (> 65 years), it was demonstrated that overweight/obese men had a lower risk of hip, clinical vertebral, and upper limb fractures, although there was no association between BMI and the risk for proximal humerus and tibial fractures [65]. However, it should be noted that in the above study, the control group consisted of men with BMI < 25 kg/m2; therefore, men with lower BMI and thus higher fracture risk were apparently included. In a large, multinational, prospective study of postmenopausal women, obese women were shown to have a higher risk of ankle and upper leg fractures and a lower risk of wrist fractures as compared to non-obese women [4]. In a meta-analysis of 25 prospective cohorts, including 398,610 women with an average age of 63 years and a follow-up for approximately 2.26 million person-years, it was demonstrated that even though osteoporotic fractures as a whole were observed less often in obese compared to nonobese women (HR 0.85, 95% CI 0.82–0.88), upper arm fractures were observed more often, while there was no association between BMI and lower leg fractures [64]. As previously demonstrated, low BMI was associated with a higher risk of all osteoporotic fractures but was, however, protective against lower leg fractures. The differences in the effects of obesity at different skeletal sites are thought to be related to differences in the pattern of falls and the characteristics of mechanical forces induced by a fall. However, it should be noted that differences among studies might also be related to the control Hormones (2018) 17:205–217 Table 1 Fracture risk in obese individuals compared to normal weight Upper limb Lower limb Ref. ↓ ↓ 83 ↓ ↑ ↑ ↔ ↑ 4 82 86 ↑ 87 population. Including subjects with low BMI as controls might mask the increased fracture risk associated with obesity or increased risk for certain fractures. Interestingly, differences in fat distribution seem to be important for skeletal health. Two separate recent meta-analyses showed that abdominal obesity might in fact be associated with higher hip fracture rates [68, 69]. Higher waist circumference and higher waist to hip ratio conferred a higher risk of hip fracture and individuals with a waist circumference higher than 105 cm had a 55% higher risk by comparison with those with a waist circumference of less than 80 cm [68]. The differential effects of visceral fat and subcutaneous fat to systemic inflammation might be the causal factor behind this finding. Effects of weight loss interventions on bone Diet The effects of restricted diet (RD) on body composition and musculoskeletal health in middle-aged obese female rats were evaluated and show that RD after prolonged HFD has a detrimental impact on bone matrix, remodeling, and microstructure (suppressed bone formation and increased bone resorption), probably through decreased insulin-like growth factor-1 and leptin, elevated adiponectin and proinflammatory mechanisms (increased expression of TNF-α messenger RNA) [70]. Diet-induced weight loss in obese patients is accompanied by increased bone loss [71, 72]. It is also associated with an increase in markers of bone formation (serum osteocalcin) and bone resorption (serum N-telopeptide of type I collagen, pyridinoline, deoxypyridinoline) [73]. Another interesting finding is that a history of chronic dieting behavior is associated with detrimental effects on bone health, even in obese women [74]. Weight loss is associated with higher calcium intake requirements. In a study evaluating true fractional calcium absorption, women randomized to energy-restricted diet for weight loss had lower calcium absorption compared to women randomized to a weight maintenance diet [75]. Conversely, in premenopausal women, mild-to-moderate weight reduction for a period of 3 months did not seem to have detrimental effects on bone strength, as assessed by pQCT [76], even after a 9-month weight maintenance period [77]. Moreover, during a 1-year weight loss maintenance Hormones (2018) 17:205–217 program following weight loss by restricted-energy-diet, there were no negative effects on BMD and bone mineral content (BMC) [78]. Potential strategies to avoid bone loss associated with dietinduced weight loss include higher calcium intake and exercise. Energy restriction is associated with reduced urinary calcium excretion; however, a high-protein diet rich in calcium prevents increases in bone resorption markers and minimizes bone loss when compared to a high-protein diet alone [79]. In healthy overweight premenopausal women who lost 7.2 ± 3.3% of body weight (5.5 ± 3.2 kg) after 6 months, intake of 1 g Ca/day prevented bone loss and intake 1.8 g Ca/day increased BMD [80]. Exercise during weight loss In animal models, exercise during weight loss seems to protect from bone loss. Combinations of diet and exercise appear to be of great importance for losing weight without affecting bone mass [81]. The moderate intensity exercise improved the tibia BMD of obese rats and was associated with preservation of microarchitecture parameters as compared to weight loss alone. Another study has shown that the voluntary wheel running exercise under a high-fat diet increases metaphyseal trabecular density and decreases marrow cavity, while eventually decreasing maximum flexure load in the femoral neck, this showing the complex interaction between physical activity and obesity [82]. Moderate treadmill exercise reduced the body weight of obese Zucker rats without causing significant differences in femoral or tibial bone mass [83]. In humans, the data are somewhat contradictory. A 1-year randomized, controlled trial showed that exercise training with diet-induced weight loss cannot prevent hip bone loss and the associated high bone turnover [84]. These changes persist after partial weight regain independently of continued weight-bearing aerobic exercise [85]. However, in another randomized trial, older obese individuals who lost weight with a combination of diet and exercise rather than diet alone did not exhibit increases in bone turnover, and this was associated with an attenuation of the observed hip BMD loss [86]. Even though it seems that exercise is unlikely to be enough to prevent bone loss induced by weight loss, it seems that it attenuates the effects of weight loss and should therefore be encouraged alongside weight management strategies in order to minimize bone loss. Pharmacological management of obesity Orlistat, a gastrointestinal lipase inhibitor, an agent that has been approved for the treatment of obesity for many years, had no significant effect on biomarkers of bone formation and resorption when given for 21 days to obese men [87]. A relative increase in bone resorption but no changes in bone 211 mass and density were observed when it was administered for 1 year [88]. Liraglutide is a GLP-1 analog, initially licensed for the management of T2DM, that was recently licensed both by the Food and Drug Administration (FDA) and European Medicines Agency (EMA) for the management of obesity, albeit at a different dose (3 mg daily) to that used to treat T2DM. There are some data on the effects of liraglutide on bone metabolism in both animal and human studies. In animal studies, liraglutide has been shown to exert anabolic effects on bone [89, 90]. In humans, in a randomized control trial, liraglutide (1.2 mg) was administered for 52 weeks in healthy obese women after achieving weight loss of 12% with a lowcalorie diet [91]. Administration of liraglutide resulted in preservation of BMC and increase in bone formation markers as compared to the control group that experienced loss of BMC and no change in bone formation. Both the liraglutide and control groups maintained their initial weight loss. In two different meta-analyses of RCTs conducted in patients with T2DM (and using the lower dose), the use of liraglutide was associated with either similar or lower risk of fractures compared to controls [92, 93]. Even though there are no data on skeletal effects from the weight loss studies with liraglutide, results so far are reassuring. A combination of phentermine and topiramate is licensed by the FDA for the treatment of obesity in the USA. The effects of the combination on bone metabolism have not been investigated in trials; however, its use has been associated with metabolic acidosis [94] which could potentially have negative effects on bones. This is a theoretical concern and investigations into the issue are warranted. Lorcacerin is a 5-HT2C receptor agonist approved by the FDA for the treatment of obesity. In a double-blind, randomized, placebo-controlled trial, lorcacerin had no effects on total BMC and total BMD [95]. A combination of naltrexone hydrochloride and bupropion hydrochloride is approved for obesity by the FDA and EMA. To date, there are no data on its effects on bone metabolism. Bariatric surgery Bariatric surgery leads to weight loss by restricting the capacity of the stomach (restricting procedures) or causing malabsorption of calories and nutrients (malabsorptive procedures), or by a combination of both. In addition, bariatric procedures often cause hormonal changes which are thought to promote weight loss. There are four major types of bariatric surgery, Roux-en-Y gastric bypass (RYGB), laparoscopic adjustable gastric banding (AGB), sleeve gastrectomy (SG), and duodenal switch with biliopancreatic diversion. These procedures lead to different results, especially as regards average excess weight loss and the improvement of obesity-related comorbidities. Bariatric surgery patients show rapid weight reduction 212 for the first 4 months following surgery. Slower weight loss is observed for the remaining follow-up of 4 years. Gastric bypass and sleeve gastrectomy are associated with greater initial weight reduction rate than gastric banding [96]. Trends in body weight post-surgically show that patients undergoing RYGB exhibit the greatest weight loss, patients undergoing SG experience less weight loss and patients undergoing AGB have the least weight loss [97]. Several studies have investigated the effects of bariatric surgery on BMD and bone turnover markers. The results are somewhat conflicting as regards investigation of bone loss after bariatric surgery, and again, there are differences among the types of procedures and methods of BMD measurement, while there are also differences associated with baseline vitamin D and parathyroid function status. Effects of bariatric surgery on bone turnover Bariatric surgery has been associated with increased bone turnover [98, 99]. RYGB in morbidly obese patients increases bone resorption 1-year postoperatively [100] and this is independent of weight loss [101]. Bone resorption can predict bone loss, a longitudinal study having demonstrated that morbidly obese patients have an increase in bone resorption markers as early as 3 months after RYGB associated with a decrease in BMD after 9 months [98]. Bone resorption is increased also after LSG, as demonstrated by a significant increase in N-telopeptide crosslinks (NTx) [102]. Marked weight loss after long limb-biliopancreatic diversion (BPDLL) increases bone turnover [103] and increases in bone turnover are associated with percentage of lost BMI in patients who underwent biliopancreatic diversion [104]. Effects of bariatric surgery on BMD A decrease in BMD occurred during weight loss in morbidly obese patients undergoing vertical banded gastroplasty (VBG). The change in BMD was evident 1 year postsurgery and was associated with the degree of weight reduction [105]. The marked weight loss after long limbbiliopancreatic diversion (BPD-LL) has been associated with decrease in BMD 1 year after surgery [103], RYGB in morbidly obese patients decreases BMC and BMD 1 year postoperatively [106] and, similarly, in a study with follow-up for a year after gastric bypass surgery there was total hip BMD decrease as well as at the lumbar spine [107]. Fewer data are available for the relatively newer sleeve gastrectomy. A longitudinal study shows that laparoscopic sleeve gastrectomy (LSG) may lead to a significant decline in BMD at the spine and proximal femur [71] and in a study comparing the effects of RYGB and SG on age- and BMI-matched morbidly obese women, BMD at the femoral neck and the lumbar spine 1 year after bariatric surgery was similar between the two groups Hormones (2018) 17:205–217 [108], suggesting that even if SG is not a typical malabsorptive procedure, it might have effects that are similar to RYGB. In contrast, in another 2-year follow-up study of patients undergoing LSG, a significant increase in BMD of the lumbar spine was demonstrated mainly during the first year post-surgery [109]. However, in this study, patients at baseline had vitamin D deficiency and secondary hyperparathyroidism which were corrected during follow-up. In a meta-analysis of studies evaluating LS and FN BMD post-bariatric surgery, it was shown that bariatric surgery was associated with lower FN but not LS BMD [110]. As DXA can be affected by overlying soft tissue, it has been suggested that weight loss can result in factitious loss of BMD. In a study comparing QCT and DXA post-RYGB, there was loss of LS BMD with both modalities, whereas at the femur, the loss of aBMD observed with DXA was not confirmed with QCT [111]. Studies in the peripheral skeleton using HR-pQCT indicate that postbariatric surgery, the cortical compartment of bone is affected and this results in decreased bone strength, which is more significant for the tibia than for the radius [112, 113]. In longer follow-up studies (2 years), even though cortical bone loss stabilized after 12 months, further deterioration in trabecular parameters was observed at 24 months [114]. Results, however, have not been unanimous, with occasional studies showing preservation of bone strength [115]. Effects of bariatric surgery on fracture risk There are some data concerning the effects of bariatric surgery on fracture risk, with most studies reporting a higher risk of fracture post-surgery [116–118]. The type of surgical procedure seems to play a very important role, malabsorptive procedures being associated with a higher risk and restrictive ones having minimal, if any, effect on the risk of fracture [116, 118]. In a historical cohort of patients who had undergone bariatric surgery (mostly gastric bypass, a malabsorptive procedure), a 2.3-fold risk of any fracture was demonstrated after a median follow-up of 7.7 years [117]. Interestingly, there was no correlation between the pre-operative history of fracture and fracture risk post-surgery, indicating that the higher risk was not due to a higher baseline risk but rather to the effect of the bariatric procedure itself. A study with a mean follow-up of 4.8 years, in which most patients had undergone a restrictive procedure, a 1.21-fold risk of any fracture was observed post-surgery, while there was a trend towards more fractures around 1 to 2 years after the procedure [116]. Another study showed a change in the pattern of fractures post-bariatric surgery, shifting from a pattern typically associated with obesity with a high risk of distal lower limb fractures and lower risk of upper limb fractures to a pattern associated with osteoporosis and more fractures of the upper limb, vertebral pelvic, hip, and femur [118]. A single study did not demonstrate any Hormones (2018) 17:205–217 difference in the rates of fracture between patients who had undergone bariatric surgery and controls; however, in this study, mean follow-up was only 2.2 years [119]. Moreover, the most common procedure was AGB (60% of patients). Patients who had undergone RYGB exhibited a 43% higher risk of non-vertebral fractures compared to patients who had undergone AGB, and the higher risk was observed at least 2 years post-surgery [120]. Mechanisms of skeletal effects of bariatric surgery and prevention strategies Possible explanations for the bone loss post-bariatric surgery include unloading, malabsorption of calcium and vitamin D with secondary hyperparathyroidism, malabsorption of other nutrients, and alteration in the gut hormone profile. Bone loss after surgery for morbid obesity could be an adaptation of the skeleton to the reduction of mechanical loading [121], and this is why in studies evaluating the peripheral skeleton the effects of bariatric surgery are more pronounced in the weight bearing tibia. This is probably the mechanism underlying the changes seen after purely restrictive procedures. However, in malabsorptive procedures, nutrient deficiency and secondary hyperparathyroidism probably play a significant role. Low serum 25OHD levels and poor absorption of calcium seem to be related to secondary hyperparathyroidism observed in women who had undergone RYGB [122], and there is association between changes in the cortical bone parameters and changes in PTH post-surgery [112]. A 6-month prospective clinical trial in obese patients who underwent RYGB showed a decrease in Ca absorption without alteration of the Ca-PTH axis, suggesting the implication of other regulating hormones [123]. Early studies have shown that jejunoileal bypass (end-toside jejunoileostomy) for the management of morbid obesity increases the possibility of 25OHD deficiency, with vitamin D supplementation restoring it to normal levels [124], while others observed that vitamin D levels returned to postoperative levels without the need for supplementation, possibly due to much higher mobilization of fat stores [125]. Serum OPG levels negatively correlated with the bone remodeling markers osteocalcin, β-CTX, and P1NP, suggesting a possible role of the OPG/RANKL system in bone metabolism after biliopancreatic diversion or laparoscopic RYGB [126]. Sclerostin, an endogenous inhibitor of the Wnt pathway which plays an important role in bone formation and remodeling, is correlated with the ongoing loss of BMD and this is independent of the type of bariatric surgery (RYGB or SG) [127]. The increase in the sclerostin levels could in theory be due to unloading from weight loss; however, interestingly, marked increases were observed from the first month postsurgery and were independent of weight loss. 213 Lifelong adequate supplementation with calcium and vitamin D after malabsorptive procedures is extremely important. Also, as with diet-induced weight loss, there have been some attempts to attenuate bone loss with physical exercise. In a 24month, randomized, controlled study evaluating the effects of an intervention including a combination of high vitamin D and calcium supplementation with exercise post-bariatric surgery, the intervention group had attenuated increase in bone turnover markers and less pronounced bone loss as compared with the non-intervention group [128]. In another study, a weightbearing and aerobic exercise intervention program postbariatric surgery resulted in less pronounced bone loss which was associated with preservation of muscle mass [129]. The American Association of Clinical Endocrinologists (AACE), The Obesity Society (TOS), and the American Society for Metabolic and Bariatric Surgery (ASBMS) guidelines recommend supplementation with vitamin D, at least 3000 IU per day. Preoperative determination of calcium is preferred and supplementation with 1200–1500 mg of essential, dietary, or citrate, calcium is also recommended [130]. 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