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Research article | Open | Open Peer Review | Published:

Increased vertebral morphometric fracture in patients with postsurgical hypoparathyroidism despite normal bone mineral density

BMC Endocrine Disordersvolume 13, Article number: 1 (2013) | Download Citation

Abstract

Background

The mechanism behind parathyroid hormone (PTH) activation of bone remodeling is intimately dependent on the time of exposure of bone cells to hormone levels. Sustained high PTH levels trigger catabolism, while transitory elevations induce anabolism. The effects of hypoparathyroidism (PhPT) on bone are unknown. The objective was to study the impact of PhPT on bone mineral density (BMD), on the frequency of subclinical vertebral fracture and on mandible morphometry.

Methods

The study comprised thirty-three postmenopausal women, 17 controls (CG) and 16 with PhPT (PhPTG) matched for age, weight and height. Bone mineral density (BMD) of lumbar spine, total hip and 1/3 radius, radiographic evaluation of vertebral morphometry, panoramic radiography of the mandible, and biochemical evaluation of mineral metabolism and bone remodeling were evaluated in both groups.

Results

There were no significant differences in lumbar spine or total hip BMD between groups. There was marked heterogeneity of lumbar spine BMD in PhPTG (high = 4, normal = 9, osteopenia = 1, and osteoporosis = 2 patients). BMD was decreased in the 1/3 radius in PhPTG P < 0.005). The PhPTG group exhibited an increased frequency of morphometric vertebral fractures and decreased mandible cortical thickness.

Conclusion

The study suggests that vertebral fragility occurs in PhPT despite normal or even high BMD. The current results encourage further studies to evaluate the use of panoramic radiography in the identification of osteometabolic disorders, such as PhPT and the development of a more physiological treatment for PhPT.

Open Peer Review reports

Background

During this decade a remarkable advance has occurred in the knowledge about the molecular and cellular action of PTH on bone [1, 2], whereas little progress has been made regarding the physiological role of PTH secretion in bone mass development and homeostasis [3]. There are few lines of evidence suggesting that individuals with normal bone mass have greater PTH release in response to physiological stimuli (hyperphosphatemic diet or modest hypocalcemia) than osteoporotic patients [4, 5]. In contrast, several studies have demonstrated increased bone mass in patients with chronic postsurgical hypoparathyroidism, (PhPT) [6, 7]. However, to date no study has addressed fracture susceptibility in patients with PhPT [6, 8].

Although the risk of fracture increases significantly with decreasing BMD, large observational studies have demonstrated that osteoporotic fractures can occur across a wide spectrum of BMDs [9, 10]. Most likely, these events are related not only to bone mass quantity but also to bone quality, a component not captured by DXA measurements [10, 11]. Great efforts are being currently devoted to the determination of clinical conditions associated with a high fracture risk despite an apparent protection by normal or increased BMD. Algorithms that combine BMD with identifiable independent risk factors to estimate a 10-year absolute fracture risk are now being used to provide a more holistic evaluation of absolute fracture risk over a 10-year period [12]. Attempts to further refine the algorithms have been made by taking into account novel variables such as type 2 diabetes mellitus, cardiovascular disease, asthma and use of tricyclic antidepressants in addition to the traditional variables of fracture risk assessment (FRAX) [13]. In addition, the use of other specific bone sites which are largely assessed by radiological exams can potentially be used for the early recognition of osteoporosis [14]. Approximately 1 in 3 of all radiological examinations is made by dentists [15]. Dental panoramic radiographs provide images of the jaws and there is evidence that jaw BMD and radiomorphometric indices developed for this site can be potentially used for the preventive diagnosis of osteoporotic patients [16, 17] and of fracture susceptibility [18]. The OSTEODENT study suggested that an automatic measurement of mandible cortical bone thickness on panoramic radiographs is a valid test for the diagnosis of osteoporosis in women aged 45 to 70 years [18]. Bone mass of the mandible have never been evaluated in patients with chronic PhPT.

The present study was designed to evaluate BMD (lumbar spine, total hip, femoral neck, 1/3 radius and total body), vertebral subclinical fracture and cortical thickness in the inferior region of the mandible in a homogenous group of patients with chronic PhPT. All patients were women previously submitted to thyroidectomy due to atoxic benign multinodular goiter. Additionally, we assessed serum levels of insulin-like growth factor (IGF-I), receptor activator of nuclear factor-κB ligand (RANK-L), osteoprotegerin (OPG), 25-hydroxyvitamin D (25-OH-D), and bone remodeling markers [serum osteocalcina (OC) and urinary deoxypyridinoline (DPD)].

Subjects and methods

Subjects

The study was conducted on 33 postmenopausal women whose clinical characteristics are shown in Table 1. The study group included 16 patients with PhPT (PhPTG) followed up at the Outpatient Clinic of Osteometabolic Disorders of the University Medical Center, School of Medicine of Ribeirão Preto, University of São Paulo (FMRP-USP). The diagnosis of permanent PhPT was established by the concomitant presence of low circulatory levels of calcium and PTH after thyroidectomy, as well as by the requirement of continued calcium and vitamin D treatment to maintain serum calcium levels within the normal range.

Table 1 Clinical characteristics and biochemical evaluation of control subjects (CG) and of patients with postsurgical hypoparathyroidism (PhPTG)
Full size table

The control group (CG) consisted of 17 adult women, matched to the PhPTG for age, weight, height and body mass index (BMI) (Table 1). The general exclusion criteria established for both groups were a personal or family history of osteometabolic disorders, alcohol abuse, smoking, hepatic or renal disease, or using medications known to interfere with mineral metabolism (anabolic steroids, glucocorticoids, anticonvulsants, diuretics or medication for the treatment of osteoporosis). Additionally, no woman, in both group had premature ovarian failure. The study was approved by the Ethics Committee of the School of Medicine of Ribeirão Preto, University of São Paulo (9523/2008). All subjects gave written informed consent.

The PhPT group had been on treatment for 15.3 ± 12.4 years, with daily intake of elemental calcium, calcitriol and L-thyroxin of 1713 ± 419 mg, 0.33 ± 0.18 μg and 99.3 ± 42.1 μg, respectively. The treatment target was to maintain serum total calcium in the lower limit of normal reference values and to keep serum levels of phosphorus and TSH in the normal range. We excluded from this group all individuals with a history of hyperthyroidism and those with a diagnosis of thyroid cancer, as well as individuals with a diagnosis of pseudohypoparathyroidism and autoimmune hypoparathyroidism.

Methods

Blood and urine collections and radiographic documentation were performed on two days. On the first day, blood and second void urine were samples collected in the morning between 7:00 and 9:00 after a 10–12 hour fast and kept in an ice-chilled container until centrifugation. Serum aliquots were stored at −70°C until assessment, with all determinations being carried out in the same assay. Subsequently, the volunteers were taken to the Image Center of the University Hospital, FMRP-USP, for DXA (dual energy X-ray absorptiometry) scan in total body, lumbar spine, proximal femur and forearm and standard thoracic and lumbar spine X-rays. On the second day, the individuals went to the Radiology Service of the Dental School of Ribeirão Preto, USP, to perform digital panoramic radiography.

Serum levels of calcium, phosphorus, alkaline phosphatase and creatinine were determined with an automatic biochemical analyzer (KoneLab 6.0, Winer, Argentina) on the day of blood collection. Serum IGF-I was measured by enzyme immunoassay [intra-assay coefficient of variation (CV) = 9.5%; Immunodiagnostic Systems, Fountain Hills, AZ]. Also, serum OC (CV = 5.6%; Quidel, San Diego, CA, USA), 25-OH-D (CV = 7.2%; Immunodiagnostic System, Fountain Hills, AZ), OPG (CV = 5.6%; Quidel, San Diego, CA, USA) and RANKL (CV = 6.8%; Biomedica, Austria) and urinary DPD (CV = 6.7%; Quidel, San Diego, CA, USA), were measured by enzyme immunoassay. Serum PTH was measured by chemiluminescence (CV = 4.7%; SIEMENS, Los Angeles, CA, USA).

Bone mineral density

BMD was measured by DXA at the femoral neck, total hip, lumbar spine (L1-L4) and distal radius by a trained radiologic technician (Hologic 4500 W densitometer, Hologic Inc., Bedford, MA, USA). In vivo precision was 1.2% for L1-L4, 2.3% for femoral neck, 2.7% for total hip and 1.7% for 1/3 radius, respectively. BMD values were expressed as g/cm2 and T-Score.

Vertebral morphometry

Lateral thoracic and lumbar spine radiographs were taken for each patient and images were digitized using a Vidar DiagnosticPro scanner with a spatial resolution of 84 m and the gray scale represented by 8 bits/pixel. Six points were marked with electronic calipers on each of the 13 vertebral bodies from T4 to L4 using K-PACS Workstation software, v 1.6.0. These points were positioned on the outer edge of the upper and lower endplates. Using the six points, the anterior, middle and posterior heights were determined for each vertebral body in millimeters. Image analysis was carried out by consensus between 2 radiologists, both performed by blind assessment. A senior musculoskeletal radiologist reviewed all images in which any of the measured vertebral height ratios in a single film was <0.75 and also solved difficult cases when any doubt was present regarding the positioning of the calipers or to check if the encountered deformity was related to pathologies other than insufficiency fractures. The last analysis was also performed by blind assessment.

The criteria of vertebral deformity were: 1) more than a 20% reduction between two of the above measures and/or a 20% reduction in the relation between any one of the above measurements and the measurement of the corresponding region of the vertebral body immediately superior or inferior to each vertebral body analyzed, or 2) a reduction ≥ 4 mm in the absolute vertebral height value in relation to the other heights in the same vertebral body and in relation to the similar height in the immediate neighboring vertebral bodies.

Panoramic radiograph

All panoramic radiographs were obtained with an RX Veraviewepocs Digital Panoramic instrument (J. Morita Co). Digital images were examined with RADIOIMP software (Radiomemory, Brazil). In this panoramic images, the thickness of the inferior cortical region of the mandible bone were measured on both sides and in two regions (mental and goniac). The digital panoramic radiograph was inserted into the software and calibrated using magnification (30%) and resolution (300 d.p.i.) factors [19]. The projected areas of interest are used for the determination of the Mental Index and Goniac Index, as previously described [20, 21].

Statistical analysis

All statistical analyses were performed using SAS 9.0 software (SAS/STAT® User’s guide version 9.0, Cary, NC, USA: SAS Institute Inc., 2002). The Student t–test was applied using the PROC T TEST of the SAS 9.0 software to compare the results of the two groups. To determine the association of the variables of interest (BMD with hypoparathyroidism duration, IGF-I and 25-OH-D, simple linear regression models were adjusted, yielding the regression coefficients and R-square, through the REG procedure of the SAS 9.0 software. Considering the method described by Hsieh et al. [22] for determining the sample size required for the estimation of a correlation coefficient and for linear regression models, a sample of size 16 is sufficient for estimating a correlation coefficient equal to 0.65 with a level of significance of 0.05 and a power of 0.20. Thus, it was established that the sample size in each group should be at least 16. Data are expressed as mean ± SD.

Results

Table 1 shows that both groups were appropriately matched for age (range: CG = 49–70 vs PhPTG = 45–77 years), weight (range: CG = 46-94.6 vs PhPTG = 54.8–98.5 Kg) height (range: CG = 1.47–1.74 vs PhPTG = 1.47–1.69 m), BMI (range: CG = 16.9–36.1 vs PhPTG = 23.3–38.0 kg/m2). The duration of postsurgical hypoparathyroidism ranged from 2 to 44 years (mean = 15.3 ± 12.4 years). Both groups presented normal serum creatinine levels (CG = 57.96 ± 7.63 μmol/L vs PhPTG = 69.39 ± 21.35 μmol/L). All volunteers had creatinine clearance above 60 ml/min. The serum levels of TSH were normal in PhPT group (PhPTG = 2.6 ± 1.0 mIU/L).

Serum levels of total calcium (CG = 2.43 ± 0.13 vs PhPTG = 2.05 ± 0.21 mmol/L; P < 0.0001), total calcium corrected by albumin (CG = 2.39 ± 0.21 vs PhPTG = 2.01 ± 0.26 mmol/L, P < 0.005), as well as PTH (CG = 4.45 ± 1.99 vs PhPTG = 0.63 ± 0.49 pmol/L, P < 0.0001) were significantly lower in PhPTG. The control group showed significantly lower serum phosphorus levels than PhPTG (CG = 1.29 ± 0.22 vs PhPTG = 1.57 ± 0.32 mmol/L, P < 0.01). The groups showed nonsignificant differences in circulatory levels of 25-OH-D and IGF-I (Table 1).

Circulatory levels of the biochemical marker of bone formation, OC, were significantly lower in PhPTG (6.75 ± 2.36 μg/L) than in CG (9.64 ± 2.54 μg/L), P < 0.01, whereas there was no significant difference in urinary excretion of DPD (CG = 7.44 ± 3.0 vs PhTHG = 11.15 ± 13.16 nmol/mmol creatinine; p = 0.77). Both groups presented similar serum levels of RANKL (CG = 0.26 ± 0.21 vs PhPTG = 0.29 ± 0.27 pg/dl; p = 0.57) and OPG (CG = 0.094 ± 0.012 vs PhPTG = 0.1 ± 0.025 pmol/L; p = 0.44).

Total body BMD was slightly higher in PhPTG (0.923 ± 0.13 g/cm2) than in CG (0.904 ± 0.10 g/cm2). The mean values of lumbar spine BMD did not differ significantly between groups (CG = 0.970 ± 0.15 g/cm2 vs PhPTG = 1.093 ± 0.26 g/cm2). However, there was wide heterogeneity of T-score distribution within PhPTG, with 4 patients presenting a high T-score (> + 2.0 SD), 9 patients presenting a normal T-score (between +2 and −1.0 SD), 1 patient presenting a T-score compatible with osteopenia, and 2 patients presenting L1-L4 BMD compatible with osteoporosis (T-score < −2.5 SD) (Figure 1). Lumbar spine BMD was also evaluated after exclusion of the dominant vertebral body when there was a difference higher than 1 SD between two contiguous vertebral bodies. The results obtained in this second evaluation did not differ significantly from those obtained in the first evaluation (CG = 0.970 ± 0.153 vs PhPTG = 1.088 ± 0.250 g/cm2). Both groups showed similar BMD values in femoral neck (CG = 0.826 ± 0.111 vs PhPPG = 0.865 ± 0.159 g/cm2) and total hip (CG = 0.961 ± 0.145 vs PhPTG = 0.953 ± 0.162 g/cm2) (Figure 1). However, BMD values for the 1/3 radius were significantly lower in PhPTG compared to control group (CG = 0.630 ± 0.07 vs PhPTG = 0.570 ± 0.09, P < 0.05) (Figure 1).

Figure 1
figure1

Distribution of bone mineral density values of lumbar spine (A), femoral neck (B), total hip (C) and 1/3 d forearm (D) of the control group (CG) and of the postsurgical hypoparathyroidism group (PhPTG).

Full size image

Table 2 shows that 10 of the 16 PhPTG patients (63%) had morphometric vertebral fractures, as opposed to only 2 CG individuals. The table also shows that morphometric vertebral fractures were not restricted to individuals with a low bone mass. Actually, 3 of the 4 patients with a BMD T-score above + 2SD had subclinical fractures in the thoracic and/or lumbar spine.

Table 2 Number of vertebral fractures, bone mineral density (T-score) and mental index in the control group (CG) and postsurgical hypoparathyroidism group (PhPTG)
Full size table

There was a significant correlation between the duration of postsurgical hypoparathyroidism and lumbar spine BMD (Figure 2). However, there was no correlation between the duration of postsurgical hypoparathyroidism and vertebral fracture. There was no correlation between BMD and serum IGF-I levels or between BMD and serum 25-OH-D levels.

Figure 2
figure2

(Right) Correlation between bone mineral density in lumbar spine and duration of postsurgical hypoparathyroidism (p = 0.03 adjusted by TSH; R2 = 0.35) and (Left) correlation between bone mineral density and cortical thickness of the mental region of the mandible (p < 0.01; R2 = 0.30).

Full size image

There was no significant difference between groups regarding inferior cortical thickness in the region of the mandible angle (goniac). Inferior cortical thickness in the mental mandible was significantly decreased in PhPTG (Table 2). There was no significant correlation between lumbar spine BMD and cortical thickness in the mental region of the mandible. However, this last index was significantly and positively correlated with 1/3 distal forearm BMD (Figure 2).

Discussion

Skeletal fracture has not been considered a potential problem in postsurgical hypoparathyroidism, especially after clinical investigation, based on surrogate parameters, have shown that BMD is preserved or even enhanced in PhPT [7, 23]. The present study demonstrated that patients with PhPT have marked heterogeneity in lumbar spine BMD, usually exhibiting high or normal bone mass, while densitometric osteoporosis is uncommon. Paradoxically, we have observed a high frequency of morphometric fracture of lumbar and thoracic vertebrae in patients with PhPT, which is not restricted to those with low bone mass. A previous nonvertebral fracture was present in one patient of the PhPT group, while no individual of the control group sustained clinical fracture. In addition, our results show that panoramic radiography of the mandible is a useful tool for the recognition of bone disorders in PhPT. These results are of great significance in the clinical setting since these data correspond to the first evidence of increased risk of fractures in postsurgical hypoparathyroidism. Therefore, these preliminary results encourage further investigation of the etiopathogenesis and prevalence of this condition and a more appropriate approach to the management of this particular group of patients.

There are studies showing a differential impact of PhPT on diverse bone sites, the increase in BMD being higher in the lumbar spine than in the proximal femur [23], whereas forearm BMD was not positively affected [24]. For Instance, Duan et al. evaluated 10 postmenopausal women harboring postsurgical hypoparathyroidism. The duration of PhPT in this group varied from 0.5 to 51 yr. These authors observed that BMD in patients with hypoparathyroidism was higher when compared with the age predicted mean at the lumbar spine and proximal femur, but not at the distal radius [25]. The present study replicates this spectrum on a different level, with BMD being only slightly increased in the lumbar spine due to wide heterogeneity among patients and being modestly decreased in the proximal femur of PhPT patients, whereas bone mass was decreased in the distal forearm. The divergences between studies are probably due to differences in the profile of the patients examined. Different from other studies, we adopted more rigid criteria for the selection of volunteers. Patients with previous diagnosis of thyroid cancer and hyperthyroidism were excluded, ultimately avoiding the inclusion of individuals affected by other disorders associated with bone loss and fracture. Another difference is that previous studies included pre- and postmenopausal women, whereas only postmenopausal women participated in the present study. Akin to other studies, our patients showed a great variability in the duration of PhPT [25]. This aspect can, at least in part, account for the large variation of BMD values in patients with PhPT. The relevance of this point is reinforced by the strong positive correlation between PhPT duration and BMD.

It should be mentioned that BMD assessment by DXA in PhPT was comparable to that described in primary hyperparathyroidism. It is well known that cortical bone is preferentially affected by primary hyperparathyroidism, and the same pattern was observed in PhPT. It should be pointed out that the control group also had distal forearm BMD within the osteopenia range, a fact possibly related to population characteristics, since the same profile was observed in normal individuals in previous studies performed in our laboratory [25]. However, PhPT patients showed significantly lower distal forearm BMD compared to control individuals. Furthermore, the panoramic radiography of the mandible was especially useful to capture the reduction in cortical thickness in another bone site.

Despite the BMD of the lumbar spine, 63% of patients with PhPT showed at least one morphometric fracture in the dorsal/lumbar spine, and morphometric fractures were also detected in patients showing high bone mass. No study has previously evaluated fracture susceptibility in PhPT. The results indicate deterioration of bone quality, the other component that assures bone strength. A previous study [6] detected by Fourier transform infrared imaging of transiliac biopsies that the collagen cross-link ratio was significantly higher in hypoparathyroid subjects compared to normal individuals. Based on these and other results the authors suggested that bone has low turnover rate and acquires a mature or hypermature profile in PhPTH [6]. Although, we have assessed only osteocalcin and DPD as biochemical bone markers of bone remodeling, our results support previous data obtained by bone histomorphometry. Decreased osteocalcin reflects reduced osteoblast activity in hypoparathyroidism. A reduced rate of bone remodeling which was reversed by intermittent administration of subcutaneous PTH has also been demonstrated by histomorphometric analysis in PhPT patients [7]. In support of these data we observed that osteocalcin levels were significantly lower in PhPT patients than in normal individuals. On a long-term basis, the impairment of bone renewal is implicated in inefficient repair of microdamage and ultimately in fracture susceptibility.

Other factors must be taken into account regarding impairment of bone strength in PhPT patients, especially in those with high BMD. Thickening of trabecular bone could compromise bone strength by reducing resilience [26, 27]. In normal bone, the elastic properties of trabecular bone allow the skeleton to absorb energy by deforming reversibly when loaded [28]. Although the greater mineral content in the hypoparathyroid bone might produce greater material stiffness, it may do so at the expense of the ability of the bone to deform and thus to absorb and dissipate energy. Without elastic deformation, it is possible that hypoparathyroid bone could be vulnerable to structural failure. Because the effectiveness of bone in stopping cracks is directly proportional to the stiffness ratio across its internal interfaces, a homogeneous material will be less effective in slowing or stopping cracks initiated in the bone matrix, permitting cracks to grow more quickly to critical size and ultimately increase fracture risk [29, 30].

Previous studies have shown that growth hormone deficiency impairs PTH circadian rhythm [31] and PTH action [32, 33]. In order to detect hormonal alterations in the growth hormone (GH)/IGF-I axis, in the present study we assessed serum IGF-I levels and the results showed that PhPT patients have a lightly lower circulatory IGF-I level than control individuals. However, we did not measure GH secretion or GH/IGF-I sensitivity in PhPT patients. Additionally, vitamin D sufficiency was evaluated and all patients showed normal serum 25(OH)D levels conferring a convenient substrate supply for paracrine/autocrine synthesis of 1,25(OH)2D. Endocrine levels of 1,25(OH)2D are largely dependent of PTH secretion, but all patients were taking physiological doses of calcitriol. Although, no woman of the control group was receiving calcium and vitamin D supplementation, they exhibited normal serum levels of 25-OHD. In agreement with these results, we did not observe a high frequency of hypovitaminosis D in this region of the state of São Paulo, Brazil, in previous studies [34, 35]. As vitamin D deficiency is associated with worse bone outcome, it is likely that our groups were in advantageous conditions compared to other populations with a higher incidence of vitamin D deficiency [36].

Previous studies have shown increased serum levels of RANKL and maintained OPG levels in primary hyperparathyroidism [37]. Also, it was observed that intermittent administration of PTH to glucocorticoid-treated patients increases serum levels of RANKL and decreases serum levels of OPG [38]. In the present study no difference was detected in RANKL and OPG serum level of PhPT patients in comparison to control subjects. To our knowledge, no previous study addressed serum RANKL levels in postsurgical hypoparathyroidism. Although low PTH levels might be expected to provoke decreased RANKL levels, it should be considered that 1,25(OH)2D stimulates RANKL synthesis.

The present study has some limitation; the number of patients studied was insufficient to definitively associate postsurgical hypoparathyroidism with increased fracture risk. However, these are important preliminary data for a more comprehensive study to examine the dissociation between bone fragility and bone mineral density in patients harboring postsurgical hypoparathyroidism.

Conclusions

Our results suggest that PhPT has a great impact on bone structure which is not necessarily detected by BMD density. Subclinical vertebral fracture was identified in more than 60% of PhPT patients, including those exhibiting high BMD. Panoramic radiography of the mandible should be thoroughly scrutinized to determine its place in the diagnosis or screening of osteoporosis. This site was useful to reveal cortical changes in PhPT. Panoramic radiography has the additional advantage of relying on a dentist for the screening of osteoporotic patients. The study encourages further investigation to determine the role of PTH as hormone replacement therapy in postsurgical hypoparathyroidism.

Abbreviations

BMD:

Bone mineral density

BMI:

Body mass index

CG:

Control group

CV:

Coefficient of variation

DPD:

Urinary deoxypyridinoline

DXA:

Dual energy X-ray absorptiometry

FMRP-USP:

School of Medicine of Ribeirão Preto, University of São Paulo

IGF-I:

Insulin-like growth factor

OPG:

Osteoprotegerin

OC:

Osteocalcin

PTH:

Parathyroid hormone

PhPT:

Hypoparathyroidism

PhPTG:

Hypoparathyroidism group

RANK-L:

Receptor activator of nuclear factor-κB ligand

25-OH-D:

25-hydroxyvitamin D.

References

  1. 1.

    Jilka RL: Molecular and cellular mechanisms of the anabolic effect of intermittent PTH. Bone. 2007, 40: 1434-1446. 10.1016/j.bone.2007.03.017.

  2. 2.

    Jilka RL, O’Brien CA, Bartell SM, Weinstein RS, Manolagas SC: Continuous elevation of PTH increases the number of osteoblasts via both osteoclast-dependent and -independent mechanisms. J Bone Miner Res. 2010, 25: 2427-2437. 10.1002/jbmr.145.

  3. 3.

    de Paula FJ, Rosen CJ: Back to the future: revisiting parathyroid hormone and calcitonin control of bone remodeling. Horm Metab Res. 2010, 42: 299-306. 10.1055/s-0030-1248255.

  4. 4.

    Pereira LC, Pereira FA, Sá MF, Foss MC, de Paula FJ: Parathyroid hormone secretion in women in late menopause submitted to EDTA-induced hypocalcemia. Maturitas. 2008, 59: 91-94. 10.1016/j.maturitas.2007.10.002.

  5. 5.

    Silverberg SJ, Shane E, de la Cruz L, Segre GV, Clemens TL, Bilezikian JP: Abnormalities in parathyroid hormone secretion and 1,25-diydroxyvitamin D3 formation in women with osteoporosis. N Engl J Med. 1989, 320: 277-281. 10.1056/NEJM198902023200503.

  6. 6.

    Rubin MR, Bilezikian JP: Hypoparathyroidism: clinical features, skeletal microstructure and parathyroid hormone replacement. Arq Bras Endocrinol Metabol. 2010, 54: 220-226. 10.1590/S0004-27302010000200019.

  7. 7.

    Rubin MR, Manavalan JS, Dempster DW, Shah J, Cremers S, Kousteni S, Zhou H, McMahon DJ, Kode A, Sliney J, Shane E, Silverberg SJ, Bilezikian JP: Parathyroid hormone stimulates circulating osteogenic cells in hypoparathyroidism. J Clin Endocrinol Metab. 2011, 96: 176-186. 10.1210/jc.2009-2682.

  8. 8.

    Laway BA, Goswami R, Singh N, Gupta N, Seith A: Pattern of bone mineral density in patients with sporadic idiopathic hypoparathyroidism. Clin Endocrinol (Oxf). 2006, 64: 405-409.

  9. 9.

    World Health Organization: Assessment of fracture risk and its application to screening for postmenopausal osteoporosis. 1994, Geneva: Switzerland

  10. 10.

    Khosla S, Melton LJ: Clinical practice. Osteopenia. N Engl J Med. 2007, 356: 2293-2300. 10.1056/NEJMcp070341.

  11. 11.

    Kanis JA, Oden A, Johnell O, Johansson H, De Laet C, Brown J, Burckhardt P, Cooper C, Christiansen C, Cummings S, Eisman JA, Fujiwara S, Glüer C, Goltzman D, Hans D, Krieg MA, La Croix A, McCloskey E, Mellstrom D, Melton LJ, Pols H, Reeve J, Sanders K, Schott AM, Silman A, Torgerson D, van Staa T, Watts NB, Yoshimura N: The use of clinical risk factors enhances the performance of BMD in the prediction of hip and osteoporotic fractures in men and women. Osteoporos Int. 2007, 18: 1033-1046. 10.1007/s00198-007-0343-y.

  12. 12.

    Seeman E, Delmas PD: Bone quality–the material and structural basis of bone strength and fragility. N Engl J Med. 2006, 354: 2250-2261. 10.1056/NEJMra053077.

  13. 13.

    Hippisley-Cox J, Coupland C: Predicting risk of osteoporotic fracture in men and women in England and Wales: prospective derivation and validation of QFracture Scores. BMJ. 2009, 339: b4229-10.1136/bmj.b4229.

  14. 14.

    Vlasiadis KZ, Damilakis J, Velegrakis GA, Skouteris CA, Fragouli I, Goumenou A, Matalliotakis J, Koumantakis EE: Relationship between BMD, dental panoramic radiographic findings and biochemical markers of bone turnover in diagnosis of osteoporosis. Maturitas. 2008, 59: 226-233. 10.1016/j.maturitas.2008.01.006.

  15. 15.

    Tanner R, Wall BF, Shrimpton PC, Hart D, Bungay DR: Frequency of medical and dental x-ray examination in the UK. 2000,  -NRPB-R320

  16. 16.

    Devlin H, Allen P, Graham J, Jacobs R, Nicopoulou-Karayianni K, Lindh C, Marjanovic E, Adams J, Pavitt S, van der Stelt P, Horner K: The role of the dental surgeon in detecting osteoporosis: the OSTEODENT study. Br Dent J. 2008, 204: E16-10.1038/sj.bdj.2008.317. discussion 560–561

  17. 17.

    Watanabe PC, Farman A, Watanabe MG, Issa JP: Radiographic signals detection of systemic disease. Orthopantomographic Radiography. Int J Morphol. 2008, 26: 915-926.

  18. 18.

    Horner K, Allen P, Graham J, Jacobs R, Boonen S, Pavitt S, Nackaerts O, Marjanovic E, Adams JE, Karayianni K, Lindh C, van der Stelt P, Devlin H: The relationship between the OSTEODENT index and hip fracture risk assessment using FRAX. Oral Surg Oral Med Oral Pathol Oral Radiol Endod. 2010, 110: 243-249. 10.1016/j.tripleo.2010.03.035.

  19. 19.

    Bras J, van Ooij CP, Abraham-Inpijn K, Kusen GJ, Wilmink JM: Interpretation of the mandibular angular cortex: a diagnostic tool in metabolic bone loss. Part I. Normal state and postmenopausal osteoporosis. Oral Surg. 1982, 53: 541-545. 10.1016/0030-4220(82)90473-X.

  20. 20.

    Ledgerton D, Horner K, Devlin H, Worthington H: Panoramic mandibular index as a radiomorphometric tool: an assessment of precision. Dentomaxillofac Radiol. 1997, 26: 95-100. 10.1038/sj.dmfr.4600215.

  21. 21.

    Taguchi A, Suei Y, Ohtsuka M, Otani K, Tanimoto K, Ohtaki M: Usefulness of panoramic radiography in the diagnosis of postmenopausal osteoporosis in women. Width and morphology of inferior cortex of the mandible. Dentomaxillofac Radiol. 1996, 25: 263-267.

  22. 22.

    Hsieh FY, Bloch DA, Larsen MD: A simple method of sample size calculation for linear and logistic regression. Stat Med. 1998, 17: 1623-1634. 10.1002/(SICI)1097-0258(19980730)17:14<1623::AID-SIM871>3.0.CO;2-S.

  23. 23.

    Chan FK, Tiu SC, Choi KL, Choi CH, Kong AP, Shek CC: Increased bone mineral density in patients with chronic hypoparathyroidism. J Clin Endocrinol Metab. 2003, 88: 3155-3159. 10.1210/jc.2002-021388.

  24. 24.

    Rubin MR, Dempster DW, Zhou H, Shane E, Nickolas T, Sliney J, Silverberg SJ, Bilezikian JP: Dynamic and structural properties of the skeleton in hypoparathyroidism. J Bone Miner Res. 2008, 23: 2018-2024. 10.1359/jbmr.080803.

  25. 25.

    Duan Y, De Luca V, Seeman E: Parathyroid hormone deficiency and excess: similar effects on trabecular bone but differing effects on cortical bone. J Clin Endocrinol Metab. 1999, 84: 718-722. 10.1210/jc.84.2.718.

  26. 26.

    Currey J: Structural heterogeneity in bone: good or bad?. J Musculoskelet Neuronal Interact. 2005, 5: 317-

  27. 27.

    Rubin MR, Dempster DW, Kohler T, Stauber M, Zhou H, Shane E, Nickolas T, Stein E, Sliney J, Silverberg SJ, Bilezikian JP, Müller R: Three dimensional cancellous bone structure in hypoparathyroidism. Bone. 2010, 46: 190-195. 10.1016/j.bone.2009.09.020.

  28. 28.

    Lanyon LE, Baggott DG: Mechanical function as an influence on the structure and form of bone. J Bone Joint Surg Br. 1976, 58-B: 436-443.

  29. 29.

    Turner CH: Bone strength: current concepts. Ann N Y Acad Sci. 2006, 1068: 429-446. 10.1196/annals.1346.039.

  30. 30.

    Shane E, Burr D, Ebeling PR, Abrahamsen B, Adler RA, Brown TD, Cheung AM, Cosman F, Curtis JR, Dell R, Dempster D, Einhorn TA, Genant HK, Geusens P, Klaushofer K, Koval K, Lane JM, McKiernan F, McKinney R, Ng A, Nieves J, O’Keefe R, Papapoulos S, Sen HT, van der Meulen MC, Weinstein RS, Whyte M, American Society for Bone and Mineral Research: Atypical subtrochanteric and diaphyseal femoral fractures: report of a task force of the American Society for Bone and Mineral Research. J Bone Miner Res. 2010, 25: 2267-2294. 10.1002/jbmr.253.

  31. 31.

    Ahmad AM, Hopkins MT, Fraser WD, Ooi CG, Durham BH, Vora JP: Parathyroid hormone secretory pattern, circulating activity, and effect on bone turnover in adult growth hormone deficiency. Bone. 2003, 32: 170-179. 10.1016/S8756-3282(02)00952-3.

  32. 32.

    Ahmad AM, Thomas J, Clewes A, Hopkins MT, Guzder R, Ibrahim H, Durham BH, Vora JP, Fraser WD: Effects of growth hormone replacement on parathyroid hormone sensitivity and bone mineral metabolism. J Clin Endocrinol Metab. 2003, 88: 2860-2868. 10.1210/jc.2002-021787.

  33. 33.

    White HD, Ahmad AM, Durham BH, Patwala A, Whittingham P, Fraser WD, Vora JP: Growth hormone replacement is important for the restoration of parathyroid hormone sensitivity and improvement in bone metabolism in older adult growth hormone-deficient patients. J Clin Endocrinol Metab. 2005, 90: 3371-3380. 10.1210/jc.2004-1650.

  34. 34.

    Ribeiro FB, Pereira Fde A, Muller E, Foss NT, de Paula FJ: Evaluation of bone and mineral metabolism in patients recently diagnosed with leprosy. Am J Med Sci. 2007, 334: 322-326. 10.1097/MAJ.0b013e318142bafb.

  35. 35.

    Pereira FA, de Castro JA, dos Santos JE, Foss MC, Paula FJ: Impact of marked weight loss induced by bariatric surgery on bone mineral density and remodeling. Braz J Med Biol Res. 2007, 40: 509-517. 10.1590/S0100-879X2006005000074.

  36. 36.

    de Paula FJ, Rosen CJ: Vitamin D safety and requirements. Arch Biochem Biophys. 2012, 523: 64-72. 10.1016/j.abb.2011.12.002.

  37. 37.

    Nakchbandi IA, Lang R, Kinder B, Insogna KL: The role of the receptor activator of nuclear factor-kappaB ligand/osteoprotegerin cytokine system in primary hyperparathyroidism. J Clin Endocrinol Metab. 2008, 93: 967-973.

  38. 38.

    Buxton EC, Yao W, Lane NE: Changes in serum receptor activator of nuclear factor-κB ligand, osteoprotegerin, and interleukin-6 levels in patients with glucocorticoid-induced osteoporosis treated with human parathyroid hormone (1–34). J Clin Endocrinol Metab. 2004, 89: 3332-3336. 10.1210/jc.2003-032066.

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Acknowledgments

M.L.M. received financial support from Coordenação de Aperfeiçoamento de Pessoal de Nível Superior (CAPES) and FJAP receive financial support from CNPq (306027/2011-9). This study received financial support from Fundação de Apoio ao Ensino Pesquisa e Assistência (FAEPA). We thank Sebastião Brandão Filho and Marta T. Nakao for technical assistance and Prof. Dr. Edson Z. Martinez for expert contribution on the statistical analysis.

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Affiliations

  1. Department of Internal Medicine, School of Medicine of Ribeirão Preto, University of São Paulo, São Paulo, Brazil

    • Maira L Mendonça
    • , Francisco A Pereira
    • , Marcello H Nogueira-Barbosa
    • , Lucas M Monsignore
    • , Sara R Teixeira
    • , Lea MZ Maciel
    •  & Francisco JA de Paula

  2. Department of Radiology, School of Dentistry of Ribeirão Preto, University of São Paulo, São Paulo, Brazil

    • Plauto CA Watanabe

  3. Department of Internal Medicine, School of Medicine of Ribeirão Preto, University of São Paulo, Av. Bandeirantes 3900, Ribeirão Preto, SP, 14049-900, Brazil

    • Francisco JA de Paula

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Correspondence to Francisco JA de Paula.

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The authors declare no conflict of interests.

Authors’ contributions

MLM participated in patient selection/sample collections, laboratory measurements and data analysis. FAP participated in sample collections, laboratory and bone mass measurerements. MHN-B participated in the study design and in the supervision of vertebral morphometry evaluation. LMM performed radiographic exams and the first blind evaluation of vertebral morphometry. SRT performed radiographic exams and the second blind evaluation of vertebral morphometry. PCAW performed radiographic exams of mandible and the correspondent evaluations. LMZM participated in patient selection, study design and laboratory evaluations. FJAdP participated in study design and laboratory measurements, supervised data collection and analysis and wrote the manuscript. All authors revised the manuscript. All authors read and approved the final manuscript.

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Keywords

  • Postsurgical hypoparathyroidism
  • Osteoporosis
  • Morphometric fracture
  • Parathyroid hormone
  • Panoramic radiography

BMC Endocrine Disorders

ISSN: 1472-6823

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