Spectrum of microarchitectural bone disease in inborn errors of metabolism: a cross-sectional, observational study
Orphanet Journal of Rare Diseases volume 15, Article number: 251 (2020)
Patients diagnosed with inborn errors of metabolism (IBEM) often present with compromised bone health leading to low bone density, bone pain, fractures, and short stature. Dual-energy X-ray absorptiometry (DXA) is the current gold standard for clinical assessment of bone in the general population and has been adopted for monitoring bone density in IBEM patients. However, IBEM patients are at greater risk for scoliosis, short stature and often have orthopedic hardware at standard DXA scan sites, limiting its use in these patients. Furthermore, DXA is limited to measuring areal bone mineral density (BMD), and does not provide information on microarchitecture.
In this study, microarchitecture was investigated in IBEM patients (n = 101) using a new three-dimensional imaging technology high-resolution peripheral quantitative computed tomography (HR-pQCT) which scans at the distal radius and distal tibia. Volumetric BMD and bone microarchitecture were computed and compared amongst the different IBEMs. For IBEM patients over 16 years-old (n = 67), HR-pQCT reference data was available and Z-scores were calculated.
Cortical bone density was significantly lower in IBEMs associated with decreased bone mass when compared to lysosomal storage disorders (LSD) with no primary skeletal pathology at both the radius and tibia. Cortical thickness was also significantly lower in these disorders when compared to LSD with no primary skeletal pathology at the radius. Cortical porosity was significantly greater in hypophosphatasia when compared to all other IBEM subtypes.
We demonstrated compromised bone microarchitecture in IBEMs where there is primary involvement of the skeleton, as well as IBEMs where skeletal complications are a secondary outcome. In conclusion, our findings suggest HR-pQCT may serve as a valuable tool to monitor skeletal disease in the IBEM population, and provides insight to the greatly varying bone phenotype for this cohort that can be used for clinical monitoring and the assessment of response to therapeutic interventions.
Inborn errors of metabolism (IBEM) are a heterogeneous group of disorders caused by a defect in the synthesis, metabolism, transport, and/or storage of metabolites . Today, more than 1000 IBEMs have been identified and include amino acid disorders, lysosomal disorders, transport and mineral disorders, and mitochondrial disorders . Despite IBEMs being individually rare, the cumulative incidence of IBEMs worldwide is predicted to be 1 in 800 newborns, and IBEMs can present at any age; fetal stage to advanced age . Clinical presentations are also highly diverse, both genetically and phenotypically . Common symptoms include growth disturbances, endocrine dysfunction, neurological abnormalities, and musculoskeletal complications. Of all presenting symptoms, musculoskeletal complications inhibiting physical functioning have been mentioned to be the one of the most debilitating aspects of the disorder by parents of diagnosed children . Imaging plays an important clinical role in diagnosis and evaluation of severity and activity of skeletal disease, as well as monitoring treatment effect .
Dual-energy X-ray absorptiometry (DXA) has been adopted for monitoring bone involvement in IBEM patients, primarily for its high clinical utility, short scan times, low radiation, and well-established reference data . In the general population, DXA has been most commonly employed for the diagnosis and prognosis of osteoporosis, assessing fracture risk, and monitoring treatment effects [7, 8]. The femoral neck and lumbar spine are standard scan regions in mature adults, as fractures at these locations have been associated with high morbidity in adults . However, the use of DXA in patients with IBEMs presents a number of challenges. First, DXA is a two-dimensional analysis of complex three-dimensional structures and therefore is highly sensitive to the size and geometry of the bone . This is particularly problematic in IBEM patients who can often be of short stature, increasing the risk of underestimating BMD. Second, given that the femoral neck and lumbar spine are standard diagnostic sites for DXA and many IBEM patients are at greater risk for scoliosis and often have orthopaedic hardware implanted at these locations, there is a greater frequency of limitations in the ability to measure BMD at these sites. Third, DXA is unable to reliably detect fracture risk in pediatrics patients, as fragility fractures have been reported in children with measurements within the normal range . Lastly, DXA is unable to provide information on bone microarchitecture and geometry, which have shown to play an important role in determining whole-bone strength [12, 13]. To advance the clinical management of skeletal complications in IBEMs, alternative imaging modalities that consider bone size and geometry and explore microarchitectural properties warrant further investigation.
High-resolution peripheral quantitative computed tomography (HR-pQCT) is a non-invasive, low radiation, in vivo bone imaging modality that scans at the distal limbs and provides an assessment of volumetric bone density and bone microarchitecture in the cortical and trabecular compartment. Given that HR-pQCT is based on three-dimensional imaging of bone, it is robust for use in short stature individuals because of the avoidance of confounding effects occurring in two-dimensional techniques such as DXA. HR-pQCT is well suited to cases of patients with orthopaedic hardware and scoliosis, as scans are being captured at the peripheral skeletal sites, rather than axial, where these issues often arise. To date, single case reports and case studies on individual IBEMs have been published examining bone microarchitecture using HR-pQCT. We and others have reported impaired bone density and microarchitecture when compared to healthy controls, with the exception of osteopetrosis, where bone density and microarchitecture is significantly elevated [14,15,16,17,18,19,20,21].
HR-pQCT allows the possibility for prediction of bone strength by measuring failure load using finite element techniques. The finite element method is the procedure of performing in silico biomechanical strength tests, such as compressive loading, on bone scan data generated by HR-pQCT and has been validated using mechanical testing on cadaveric samples [22, 23]. The primary output of these tests is failure load – the amount of load a bone can sustain before yielding. Failure load has been shown to provide higher acuity in fracture prediction than by examining BMD or microarchitectural measurements alone [24, 25], and serves as a convenient intrinsic summary of the complex microarchitectural phenotypes that are often encountered.
The objectives of this study were to 1) examine how density, microarchitecture, and failure load varied between different IBEMs, 2) compute Z-scores in adults using an age- and sex-matched healthy-reference cohort and, 3) compare participants with and without fracture on density, microarchitecture, and failure load measurements.
Adult and pediatric patients being managed for their IBEM diagnosis at Inherited Metabolic Disorders Clinic (Alberta Children’s Hospital, Alberta, Canada) were offered participation in the study in addition to their standard clinical care. Participants were recruited between February 2007 to July 2019. All procedures were approved by University of Calgary’s Conjoint Health Research Ethics Board (REB#15-0271) and informed written paediatric or adult consent was obtained. At the time of the scan, mobility, fracture history, and other musculoskeletal comorbidities were noted, as well as any bone-altering drugs the patient was prescribed at the time of the scan. To overcome the challenge of a small sample size in each individual IBEM, IBEMs were categorized based on their underlying pathophysiology known from the historical context of the disease (Table 1).
Patients were scanned at the distal radius and distal tibia with the first-generation HR-pQCT (XtremeCT, Scanco Medical AG, Brüttisellen, Switzerland) using a standard human in vivo scanning protocol (60 kVp, 1,000 μA, 100 ms integration time). The participants’ limbs were immobilized using a carbon cast to minimize motion during the acquisition of the scan. To identify the region of interest, a two-dimensional X-ray scan was taken. Reference lines were manually placed at the mid-inclination tuberosity and at the plateau of the tibial endplate, for radius and tibia scans, respectively. Scans were then acquired at 9.5 mm (radius) and 22.5 mm (tibia) proximally to the reference line. Each HR-pQCT scan resulted in a 9.02 mm thick stack composed of 110 slices with a nominal isotropic resolution of 82 μm. The total scan time was less than 3 minutes per limb and resulted in a maximum effective dose of approximately 5 μSv per scan. All scans underwent two independent assessments for scan quality related to movement artifact and were graded on a scale of 1 (no motion) to 5 (severe blurring and discontinuities) . Scans with a score of 4 or higher were excluded from analysis. Daily quality control assessments ranged from <1% root mean squared coefficient of variance for density to 4% root mean squared coefficient of variance for microarchitecture parameters in our laboratory . Individuals analyzing the scans were blinded to the diagnosis of the patient.
Given that 82% of humans are right hand dominant , the left tibia and left radius were used for analysis. Where a previous fracture was reported on the left limb, the opposite limb was used for analysis. For density parameters, total BMD (TtBMD, mg HA/cm3), cortical BMD (CtBMD, mg HA/cm3), and trabecular BMD (TbBMD, mg HA/cm3) were measured and reported in units of mg/cm3 of hydroxyapatite (HA). Morphometric parameters of trabecular number (TbN, mm-1), trabecular thickness (TbTh, mm), trabecular separation (TbSp, mm), cortical thickness (CtTh, mm), and cortical porosity (CtPo, %) were measured.
A semi-automated contour was generated around the periosteal surface of the bone to separate it from the surrounding soft tissue. The cortical and trabecular bone were separated using a threshold-based algorithm. From standard morphologic analysis, TtBMD, TbBMD, TbTh, and TbSp were obtained . TbN was determined using ridge-extraction methods . To determine CtBMD, CtTh, and CtPo, an auto-segmentation algorithm was used [31, 32]. This auto-segmentation algorithm has been shown to be more robust and has higher reproducibility to the standard morphologic analysis for cortical analysis, especially when the cortical bone is thin .
HR-pQCT and osteopetrosis
When analyzing scans from patients diagnosed with osteopetrosis, the segmentation of cortical from trabecular compartments was difficult. An HR-pQCT image of an osteopetrosis patient and a patient with Pompe disease are shown in Fig. 1. It can be appreciated the discrimination of cortical bone from trabecular bone is markedly more difficult in the osteopetrosis patient when compared to the Pompe patient. For this reason, osteopetrosis patients were only examined for TtBMD, as cortical and trabecular-specific parameters may not be reliable.
Finite Element (FE) analysis
Laplace-Hamming filtered and segmented HR-pQCT images were used to generate homogeneous finite element models. A linear uniaxial compression was then applied to radius and tibia models with 1% strain (Poisson’s ratio = 0.3, Young’s modulus = 6,829 MPa) . The finite element models were solved using a custom large-scale finite element software (FAIM v8.0, Numerics88 Solutions, Alberta, Canada) and failure load in Newtons (N) was estimated based on the method proposed by Pistoia and colleagues, which was defined as the force required for a 2% critical volume to exceed 7000 critical μ-strain . The precision for finite element is <4% root mean squared coefficient of variance in our laboratory .
Statistical analyses were performed using IBM® SPSS® Statistics software (v26, IBM® SPSS® Inc., Chicago, Illinois, United States). Variables were checked for normality using Shapiro-Wilk tests and histograms. For variables that were not normally distributed, a log10 transformation was performed. Comparisons between IBEMs were explored using a one-way ANOVA with a Bonferroni adjustment. For participants 16 years of age and older, age- and sex-specific Z-scores were calculated from a healthy reference database .
Sub-analyses compared participants with and without a previous fracture using a Student’s t-test. Patients with osteopetrosis were excluded because these patients are predisposed to an increased risk of fractures due defective bone resorption that can lead to regional increases in BMD, whereas in other IBEMs, a high fracture risk is due to reduced BMD . A Levene’s test for equality of variances was conducted.
For all statistical tests performed, two-sided p values below 0.05 were considered significant. Potential bone-altering confounders, such as medications, were not considered in our statistical calculations; however, a secondary analysis without inclusion of bone-altering drugs was performed and the findings were not different from our primary analysis, with some exceptions, which are reported in text.
Table 1 displays baseline characteristics of the participants recruited. A total of 101 patients consented to participant, of which 58 were female. Participants ranged from the age of 4 to 81 years. Four participants were excluded due to severe motion artifacts on both radius and tibia HR-pQCT imaging sites. One participant was excluded due to HR-pQCT imaging erroneously capturing part of the growth plate for both the radius and tibia scan. Two participants were excluded because suspected diagnosis was not confirmed using genetic testing. Eighty-nine participants had acceptable radius and tibia scans (51 females, 35 males). Four participants had an acceptable tibia scan only (2 females, 2 males), and four participants had an acceptable radius scan only (4 males). Seven participants were actively on bone-alternating treatment at the time of the scan (5 on bisphosphonate, 1 on hormone replacement therapy, and 1 on both bisphosphonates and hormone replacement therapy). Fifteen participants reported previous axial and/or appendicular fracture, and of these participants 11 had reported more than one fracture.
Comparison amongst IBEM categories
The median, interquartile range, minimum and maximum of the raw data is represented graphically in Figs. 2, 3 and 4 revealing that the outcome distributions were skewed Measurements not shown in these figures are provided in Additional file 1. The 25th, 50th, and 75th percentile lines of healthy young female adults (aged 20-29 years-old) are included on the figure for reference .
At both the radius and tibia skeletal sites the bone microarchitecture was generally poor in this population. In the radius, the median TtBMD, CtBMD and TbBMD of all IBEMs, with the exception of osteopetrosis, fell below the 50th percentile reported for healthy young female adults. Additionally, CtBMD of all IBEMs fell below the 25th percentile when compared to healthy young female adults. Contrary to CtPo and TbSp measurements in the radius, which fell above the 25th percentile. The TtBMD and CtTh of bone mineralization disorders was significantly lower compared to LSD (non-skeletal; p=0.025 and p=0.009, respectively). The CtBMD of both bone mineralization disorders and HPP was significantly lower than LSD (non-skeletal) participants (p=0.009 and p=0.013, respectively). The CtPo in HPP participants was significantly higher in comparison to restricted diets and LSD (non-skeletal) participants (p=0.034 and p=0.002, respectively). However, secondary analysis with the removal of participants with bone-altering drugs revealed CtPo of HPP to be significantly higher from LSD (non-skeletal; p=0.003) participants, only. Contrary to the cortical bone compartment, no significant findings were reported in the trabecular compartment measurements in the radius. In the tibia, TtBMD, CtBMD, and TbBMD all fell below the 25th percentile compared to healthy young female adults. The CtBMD of participants with bone mineralization disorders was significantly lower when compared to LSD (non-skeletal; p=0.039). Similarly, as in the radius, no significant differences were found in the trabecular component. As expected, the absolute values of the two osteopetrosis measurements for TtBMD were largest in comparison to all other IBEM participants’ absolute values at both the radius and tibia.
Figure 3 presents the failure load of the radius and tibia across the IBEMs, and were consistent with the microarchitectural features already noted. In the radius and tibia, failure load in all IBEMs’, with the exception of osteopetrosis participants, fell below the 50th percentile for healthy young female adults, and in the tibia all IBEMs fell below the 25th percentile. In the radius, a significant difference was found between bone mineralization disorders and LSD (non-skeletal; p=0.003), as well as HPP and LSD (non-skeletal; p=0.040). In the tibia, neuromuscular disorders were significantly lower than LSD (non-skeletal) and disorders with restricted diets (p=0.047 and p=0.035, respectively).
Z-Score calculation from normative data
For 67 of the 94 participants that were above the age of 16 years-old, a Z-score was calculated from available reference data (Table 2). At both the radius and tibia, all IBEMs had a negative Z-score for all density and microarchitecture measurements, with the exception of CtPo and TbSp, where the majority of the IBEMs had positive Z-scores. Osteopetrosis was an exception and had a positive TtBMD Z-score at the radius, +2.39. The Z-score for HPP was significantly larger in comparison to all other IBEMs (p<0.001) at the radius, and it was significantly larger than restricted diets and LSD (non-skeletal) at the tibia (p=0.043 and p=0.012, respectively). However, a secondary analysis with the removal of participants prescribed bone-altering drugs only revealed a significantly difference between HPP and LSD (non-skeletal) at the tibia (p=0.014). For estimated bone strength, bone mineralization disorders and disorders with restricted diet had significantly lower failure load at the radius in comparison to LSD (non-skeletal; p=0.003 and p=0.032, respectively).
Fracture versus no fracture comparison
Fifteen participants reported a fracture in either the axial or appendicular skeleton prior to the acquisition of the scan. One of these participants was diagnosed with osteopetrosis and was excluded from statistical analysis. One of the participants had a radius scan, only, and another participant had a tibia scan, only. Half of these participants were under the age of 18 years-old. Table 3 presents the comparison between IBEM participants with and without a previous fracture. For both the radius and tibia, all density, microarchitecture and strength measurements were poorer in participants who suffered a fracture in comparison to participants who did not. In the radius, a significant difference was found in TtBMD, CtBMD, CtTh, and CtPo between individuals with fracture and those with no history of fracture (p<0.000, p=0.010, p=0.033, and p=0.006 respectively). A secondary analysis without inclusion of bone-altering drugs also captured significance in an additional measurement, TbBMD, between fracture (149.9±45.1 mg HA/cm3) and non-fracture (116.2±53.0 mg HA/cm3) participants at the radius (p=0.022). At the radius, TbTh was also significantly different between the fracture and no fracture group (p=0.009), however, the secondary analysis revealed no significant differences between these two groups (p=0.407). For the tibia, TtBMD was again significantly higher in the group with no fractures (p=0.012). Both density and microarchitecture in the cortical bone of the tibia, CtBMD, CtTh and CtPo, were all significantly different between the fracture and non-fracture group (p=0.011, p=0.002, and p=0.035, respectively). Though not statistically significant, failure load was 27.5% and 19.0% lower in the fracture group at the radius and tibia, respectively, compared to the non-fracture group. There was no significant difference between the mean age of the two groups.
In this study, we surveyed bone density and microarchitecture across different rare IBEMs using HR-pQCT. In addition to defining microarchitectural characteristics, bone strength was estimated by employing finite element methods and quantifying failure load from compressive loading simulations. IBEMs where HR-pQCT has been previously implemented to investigate bone quality include Gaucher disease, Pompe disease, Fabry disease, HPP, osteopetrosis, and osteogenesis imperfecta [14,15,16,17,18,19,20,21]. However, this is the first study to examine bone density and microarchitecture in a wide range of IBEMs, as well as employ finite element methods to predict bone strength. In our investigation, despite a distribution of density and microarchitecture values across the IBEMS, all disorders had impaired cortical and trabecular bone in comparison to a reference population. Significant differences were found between bone mineralization disorders and LSD (non-skeletal), as well as HPP and LSD (non-skeletal). Lastly, bone was compromised to large extent in IBEM participants who had sustained a fracture when compared to IBEM participants with no fracture history.
In both the radius and tibia, cortical and trabecular bone were largely compromised in comparison to young, healthy female adults, with the exception of osteopetrosis. Osteopetrosis density measurement were elevated in comparison to reference data. These findings are consistent with what has been previously reported in examining bone microarchitecture in sub-types of IBEMs using HR-pQCT [14,15,16,17,18,19,20,21]. Both cortical and trabecular bone play a crucial role in maintaining bone integrity and deficits in each have been shown to increase fracture risk [24, 36, 37]. Cortical density in bone mineralization disorders and HPP was significantly lower compared to LSD (non-skeletal), and total density was also significantly lower in bone mineralization disorders compared to LSD (non-skeletal). Cortical thickness was also significantly compromised in bone mineralization disorders compared to LSD (non-skeletal). Cortical porosity was significantly higher in HPP when compared to all other IBEM subtypes. Though more work is required to establish the determinants of bone loss in these IBEM subtypes, these observed differences may in part be explained by the disease pathophysiology. The IBEMs categorized into bone mineralization disorders and HPP, both have an underlying pathophysiology in which bone is directly affected by disease processes, whereas in LSD (non-skeletal), bone is often a secondary health outcome. For example, in osteogenesis imperfecta and juvenile osteoporosis, categorized under bone mineralization disorders, bone resorption is up-regulated and bone formation is down-regulated, disrupting bone remodelling processes and resulting in low bone mass [38, 39]. Whereas in Fabry disease, a LSD (non-skeletal) disorder, there is an accumulation of globotriaosylceramide that primarily affects small blood vessels, the heart, and the kidneys. Literature on bone involvement in Fabry disease is very limited and the bone involvement that has been reported is believed to be due to solid organ transplant, chronic renal failure, and steroid therapy, all factors that have been shown to influence bone health independently [40,41,42,43]. Therefore, we expected diseases with direct skeletal implications to have more compromised bone compared to those where the skeletal effects on bone is secondary.
Impairments in bone density and microarchitecture are reflected in measured failure load. Failure load at both the radius and tibia were lower in comparison to a healthy young cohort, but the radius is particularly affected. This may be explained by the protective effect of weight bearing in the tibia as weight bearing plays a major role in maintaining bone strength . In the radius, the failure load of bone mineralization disorders and HPP was significantly lower when compared to LSD (non-skeletal). This was expected due to the severe deterioration of density and microarchitecture measured in the former IBEMs compared to LSD (non-skeletal). However, an unexpected finding was that the failure load in the tibia of neuromuscular disorders was significantly lower compared to disorders with restricted diets, as well as LSD (non-skeletal). Moreover, in adults, disorders with restricted diets had significantly lower failure load compared to LSD (non-skeletal). Ambulation was not considered in our statistical analysis and 6 of the 9 participants who had mobility impairments were diagnosed with a neuromuscular disorder. This may explain why bone strength was compromised in neuromuscular disorders to larger extent. For IBEMs with restricted diets, impairments to bone density and microarchitecture may be a result of nutritional deficiencies that can accompany strict diet restrictions that require lifelong adherence. Thus, treatment strategies in these disorders should consider the implications of these diets on bone health.
A subset of the cohort (n = 67), participants aged 16 years or over, were compared to a healthy sex- and age-matched cohort and their Z-scores were calculated. With the exception of osteopetrosis, all IBEMs had negative Z-scores at both the radius and tibia for bone density, bone microarchitecture, and failure load. These findings signify the prevalence of bone disease amongst all IBEM patients, regardless of whether skeletal complications are the primary or secondary outcome of the underlying disease pathophysiology.
Participants with previous fractures had significantly lower total bone density, cortical density and cortical thickness compared to those with no previous fracture in the radius. Cortical porosity was significantly greater in those with the previous fracture in comparison to those with no previous fractures. Similar results were found in the tibia. These findings are generally consistent with the literature, but interestingly, the affected compartments are different to extensive work done by others comparing post-menopausal women with and without fracture. Generally, these women who fracture have significantly lower overall density and cortical thickness, but cortical density was not significantly different between the two groups [24, 36]. Trabecular density and microarchitecture has been also reported to be significantly different between the fracture and non-fracture groups in these investigations. Similar findings to post-menopausal women have been reported in elderly men . However, in our cohort, we primarily found significant differences in cortical bone between fracture and non-fracture groups. This suggests patterns of bone loss in IBEM participants may be different from adults with age-related bone loss, and specifically that cortical bone plays a key role in predisposing IBEM patients to fractures and should be carefully monitored, especially when a new treatment regime is initiated. The ability to measure the cortical compartment independently from the rest of the bone is well suited to HR-pQCT technology. Treatments shown to have positive effects on cortical bone include combination therapy with teriparatide and denosumab, as well as denosumab alone, whereas bisphosphonates have shown to primarily alter trabecular bone microarchitecture [45,46,47,48].
Estimated failure load was not significantly different between IBEM participants with and without a previous fracture and this is in contrast to the findings of others who showed it to be a strong and independent predictor of fracture [24, 36, 37, 49]. The trend was toward lower bone strength in our participants who suffered a previous fracture, which is consistent with the findings of others, and it may simply be that we did not have the power to detect a significant difference given the relatively small number of participants with a fracture in our cohort. However, it should be noted that most other studies are focused on the assessment of osteoporosis, where the main age-related changes to bone are dominated by compromised architecture. In our cohort, the tissue properties of bone itself may also play an important role, and a limitation of HR-pQCT is the ability to detect alterations in tissue mineralization. For example, in HPP, where bone is under-mineralized compared to healthy bone . Therefore, caution should be used for estimated failure load when tissue properties are abnormal in the bone phenotype.
Some limitations of this study include our identification of the skeletal site for scanning by using a fixed distance scanning protocol, whereas using a relative site has been suggested as an alternative for pediatric scanning . Similarly, while normative HR-pQCT data exists for children , we were unable to compare our paediatric participants to the published reference data due to differences in scan placement methodology. It is worth noting that when this study was first initiated in the 2007, there was no agreed upon paediatric approach for HR-pQCT scanning of children. Another challenge as mentioned previously is that estimated failure load assumes normal tissue constitutive properties, and this assumption is likely violated in some IBEM disorders. Our participants with previous fractures included all types of fractures pooled together (skeletal sites were not distinguished), and was a relatively small sample size. Finally, we did not measure serum vitamin D levels, and deficiency could alter bone density independently of IBEM diagnosis.
Bone complications, particularly fractures, can often be the most debilitating aspect of a disorder due to the high morbidity and mortality associated with them . A high risk of fractures has been reported in IBEMs where there is primary involvement of the skeleton, such as HPP and osteogenesis imperfecta. There are important limitations of using DXA as a basis for measuring bone density, and HR-pQCT is an emerging alternate technology that provides three-dimensional assessment of bone microarchitecture and associated bone strength that is particularly useful in these complex bone phenotypes. In the IBEM population we demonstrated that there is suboptimal bone quality at both the radius and tibia, with a greater burden on cortical bone, which can help inform future treatment approaches. Models of finite element analysis show these microarchitectural changes may result in fracture as lower failure load was estimated in IBEMs. In conclusion, we suggest that HR-pQCT provides unique insight into a personalized assessment of bone microarchitecture and associated failure load.
Availability of data and materials
The datasets generated during and/or analyzed during the current study are available from the corresponding author on reasonable request.
Inborn error of metabolism
Dual-energy X-ray absorptiometry
High-resolution peripheral quantitative computed tomography
Bone mineral density
Lysosomal storage disorder
Total bone mineral density
Cortical bone mineral density
Trabecular bone mineral density
Garrod AE, Harris H. Inborn errors of metabolism. In: Harper P, editor. Landmarks in Medical Genetics. New York: Oxford University Press; 1909. p. 170–80.
Pampols T. Inherited metabolic rare disease. Adv Exp Med Biol. 2010;686:397–431.
Mak CM, Lee HC, Chan AY, Lam CW. Inborn errors of metabolism and expanded newborn screening: review and update. Crit Rev Clin Lab Sci. 2013;50(6):142–62.
Eggink H, Kuiper A, Peall KJ, Contarino MF, Bosch AM, Post B, Sival DA, Tijssen MA, de Koning TJ. Rare inborn errors of metabolism with movement disorders: a case study to evaluate the impact upon quality of life and adaptive functioning. Orphanet J Rare Dis. 2014;9(1):177.
Haugeberg G. Imaging of metabolic bone diseases. Best Pract Res Clin Rheumatol. 2008;22(6):1127–39.
Johnell O, Kanis J. Epidemiology of osteoporotic fractures. Osteoporos Int. 2005;16(2):S3–7.
Nayak S, Roberts MS, Greenspan SL. Cost-effectiveness of different screening strategies for osteoporosis in postmenopausal women. Ann Intern Med. 2011;155(11):751–61.
Blake GM, Fogelman I. The role of DXA bone density scans in the diagnosis and treatment of osteoporosis. Postgrad Med J. 2007;83(982):509–17.
El Maghraoui A, Roux C. DXA scanning in clinical practice. QJM. 2008;101(8):605–17.
Bolotin HH. DXA in vivo BMD methodology: an erroneous and misleading research and clinical gauge of bone mineral status, bone fragility, and bone remodelling. Bone. 2007;41(1):138–54.
Bishop N, Arundel P, Clark E, Dimitri P, Farr J, Jones G, Makitie O, Munns CF, Shaw N. Fracture prediction and the definition of osteoporosis in children and adolescents: the ISCD 2013 Pediatric Official Positions. J Clin Densitom. 2014;17(2):275–80.
Bouxsein ML. Bone quality: where do we go from here? Osteoporos Int. 2003;14(5):118–27.
Turner CH. Biomechanics of bone: determinants of skeletal fragility and bone quality. Osteoporos Int. 2002;13(2):97–104.
Arruda M, Coelho MC, Moraes AB, de Paula Paranhos-Neto F, Madeira M, Farias ML, Neto LV. Bone mineral density and microarchitecture in patients with autosomal dominant osteopetrosis: a report of two cases. J Bone Miner Res 2016;31(3):657-662.
Butscheidt S, Rolvien T, Kornak U, Schmidt FN, Schinke T, Amling M, Oheim R. Clinical Significance of DXA and HR-pQCT in Autosomal Dominant Osteopetrosis (ADO II). Calcif Tissue Int. 2018;102(1):41–52.
Folkestad L, Hald JD, Hansen S, Gram J, Langdahl B, Abrahamsen B, Brixen K. Bone geometry, density, and microarchitecture in the distal radius and tibia in adults with osteogenesis imperfecta type I assessed by high-resolution pQCT. J Bone Miner Res. 2012;27(6):1405–12.
Khan A, Weinstein Z, Hanley DA, et al. In vivo bone architecture in Pompe disease using high-resolution peripheral computed tomography. J Inherit Metab Dis Rep. 2013;7:81–8.
Khan A, Hanley DA, McNeil C, Boyd S. Improvement in bone mineral density and architecture in a patient with gaucher disease using teriparatide. J Inherit Metab Dis Reports. 2015;22:23–8.
Kocijan R, Muschitz C, Haschka J, Hans D, Nia A, Geroldinger A, Ardelt M, Wakolbinger R, Resch H. Bone structure assessed by HR-pQCT, TBS and DXL in adult patients with different types of osteogenesis imperfecta. Osteoporos Int. 2015;26(10):2431–40.
Rosa Neto NS, Bento JC, Takayama L, Caparbo VF, Pereira RM. Bone microarchitecture as measured using HR-pQCT of male Fabry disease patients and GLA gene GVUS subjects. Mol Genet Metab. 2019;126(2):S126. https://doi.org/10.1016/j.ymgme.2018.12.322.
Schmidt T, Mussawy H, Rolvien T, Hawellek T, Hubert J, Rüther W, Amling M, Barvencik F. Clinical, radiographic and biochemical characteristics of adult hypophosphatasia. Osteoporos Int. 2017;28(9):2653–62.
MacNeil JA, Boyd SK. Bone strength at the distal radius can be estimated from high-resolution peripheral quantitative computed tomography and the finite element method. Bone. 2008;42(6):1203–13.
Arias-Moreno AJ, Hosseini HS, Bevers MS, Ito K, Zysset P, van Rietbergen B. Validation of distal radius failure load predictions by homogenized-and micro-finite element analyses based on second-generation high-resolution peripheral quantitative CT images. Osteoporos Int. 2019;30(7):1433–43.
Boutroy S, Van Rietbergen B, Sornay-Rendu E, Munoz F, Bouxsein ML, Delmas PD. Finite element analysis based on in vivo HR-pQCT images of the distal radius is associated with wrist fracture in postmenopausal women. J Bone Miner Res 2008;23(3):392-399.
Nishiyama KK, Macdonald HM, Hanley DA, Boyd SK. Women with previous fragility fractures can be classified based on bone microarchitecture and finite element analysis measured with HR-pQCT. Osteoporos Int. 2013;24(5):1733–40.
Pauchard Y, Liphardt AM, Macdonald HM, Hanley DA, Boyd SK. Quality control for bone quality parameters affected by subject motion in high-resolution peripheral quantitative computed tomography. Bone. 2012;50(6):1304–10.
MacNeil JA, Boyd SK. Improved reproducibility of high-resolution peripheral quantitative computed tomography for measurement of bone quality. Med Eng Phys. 2008;30(6):792–9.
Crosby CA, Wehbé MA. Hand strength: normative values. J Hand Surg Am. 1994;19(4):665–70.
Boutroy S, Bouxsein ML, Munoz F, Delmas PD. In vivo assessment of trabecular bone microarchitecture by high-resolution peripheral quantitative computed tomography. J Clin Endocrinol Metab. 2005;90(12):6508–15.
Hildebrand T, Rüegsegger P. A new method for the model-independent assessment of thickness in three-dimensional images. J Microsc. 1997;185(1):67–75.
Buie HR, Campbell GM, Klinck RJ, MacNeil JA, Boyd SK. Automatic segmentation of cortical and trabecular compartments based on a dual threshold technique for in vivo micro-CT bone analysis. Bone. 2007;41(4):505–15.
Burghardt AJ, Buie HR, Laib A, Majumdar S, Boyd SK. Reproducibility of direct quantitative measures of cortical bone microarchitecture of the distal radius and tibia by HR-pQCT. Bone. 2010;47(3):519–28.
Pistoia W, Van Rietbergen B, Lochmüller EM, Lill CA, Eckstein F, Rüegsegger P. Estimation of distal radius failure load with micro-finite element analysis models based on three-dimensional peripheral quantitative computed tomography images. Bone. 2002;30(6):842–8.
Burt LA, Liang Z, Sajobi TT, Hanley DA, Boyd SK. Sex-and site-specific normative data curves for HR-pQCT. J Bone Miner Res. 2016;31(11):2041–7.
Tolar J, Teitelbaum SL, Orchard PJ. Osteopetrosis. N Engl J Med. 2004;351(27):2839–49.
Vilayphiou N, Boutroy S, Sornay-rendu E, Munoz F, Delmas PD, Chapurlat R. Finite element analysis performed on radius and tibia HR-pQCT images and fragility fractures at all sites in postmenopausal women. Bone. 2010;46(4):1030–7.
Vilayphiou N, Boutroy S, Szulc P, van Rietbergen B, Munoz F, Delmas PD, Chapurlat R. Finite element analysis performed on radius and tibia HR-pQCT images and fragility fractures at all sites in men. J Bone Miner Res. 2011;26(5):965–73.
Rauch F, Glorieux FH. Osteogenesis imperfecta. Lancet. 2004;363(9418):1377–85.
Rauch F, Travers R, Norman ME, Taylor A, Parfitt AM, Glorieux FH. Deficient bone formation in idiopathic juvenile osteoporosis: a histomorphometric study of cancellous iliac bone. J Bone Miner Res. 2000;15(5):957–63.
Cunningham J. Posttransplantation bone disease. Transplantation. 2005;79(6):629–34.
Reid IR, Heap SW. Determinants of vertebral mineral density in patients receiving long-term glucocorticoid therapy. Arch Intern Med. 1990;150(12):2545–8.
Rix M, Andreassen H, Eskildsen P, Langdahl B, Olgaard K. Bone mineral density and biochemical markers of bone turnover in patients with predialysis chronic renal failure. Kidney Int. 1999;56(3):1084–93.
Sacre K, Lidove O, Leprieur BG, Ouali N, Laganier J, Caillaud C, Papo T. Bone and joint involvement in Fabry disease. Scand J Rheumatol. 2010;39(2):171–4.
Kazakia GJ, Tjong W, Nirody JA, Burghardt AJ, Carballido-Gamio J, Patsch JM, Link T, Feeley BT, Ma CB. The influence of disuse on bone microstructure and mechanics assessed by HR-pQCT. Bone. 2014;63:132–40.
Burghardt AJ, Kazakia GJ, Sode M, de Papp AE, Link TM, Majumdar S. A longitudinal HR-pQCT study of alendronate treatment in postmenopausal women with low bone density: relations among density, cortical and trabecular microarchitecture, biomechanics, and bone turnover. J Bone Miner Res. 2010;25(12):2558–71.
Hansen S, Hauge EM, Beck Jensen JE, Brixen K. Differing effects of PTH 1–34, PTH 1–84, and zoledronic acid on bone microarchitecture and estimated strength in postmenopausal women with osteoporosis: An 18-month open-labeled observational study using HR-pQCT. J Bone Miner Res. 2013;28(4):736–45.
Tsai JN, Uihlein AV, Burnett-Bowie SA, Neer RM, Zhu Y, Derrico N, Lee H, Bouxsein ML, Leder BZ. Comparative effects of teriparatide, denosumab, and combination therapy on peripheral compartmental bone density, microarchitecture, and estimated strength: the DATA-HRpQCT Study. J Bone Miner Res. 2015;30(1):39–45.
Tsai JN, Uihlein AV, Burnett-Bowie SM, Neer RM, Derrico NP, Lee H, Bouxsein ML, Leder BZ. Effects of two years of teriparatide, denosumab, or both on bone microarchitecture and strength (DATA-HRpQCT study). J Clin Endocrinol Metab. 2016;101(5):2023–30.
Samelson EJ, Broe KE, Xu H, Yang L, Boyd S, Biver E, Szulc P, Adachi J, Amin S, Atkinson E, Berger C. Cortical and trabecular bone microarchitecture as an independent predictor of incident fracture risk in older women and men in the Bone Microarchitecture International Consortium (BoMIC): a prospective study. Lancet Diabetes Endocrinol. 2019;7(1):34–43.
Barvencik F, Beil FT, Gebauer M, Busse B, Koehne T, Seitz S, Zustin J, Pogoda P, Schinke T, Amling M. Skeletal mineralization defects in adult hypophosphatasia—a clinical and histological analysis. Osteoporos Int. 2011;22(10):2667–75.
Gabel L, Macdonald HM, McKay HA. Sex differences and growth-related adaptations in bone microarchitecture, geometry, density, and strength from childhood to early adulthood: a mixed longitudinal HR-pQCT study. J Bone Miner Res. 2017;32(2):250–63.
Hallberg I, Rosenqvist AM, Kartous L, Löfman O, Wahlström O, Toss G. Health-related quality of life after osteoporotic fractures. Osteoporos Int. 2004;15(10):834–41.
The authors wish to thank all IBEM patients who participated in this study, as well as the staff of Alberta Children’s Hospital and McCaig Institute for Bone and Joint Health for booking appointments and collecting the imaging data.
Ethics approval and consent to participate
This study was carried out in accordance with the ethical standard of the responsible committee on human experimentation, The Code of Ethics of the World Medical Association (Declaration of Helsinki). The University of Calgary’s Conjoint Health Research Ethics Board (CHREB) approved this study (REB#15-0271).
Consent for publication
AK is on the medical advisory board and has received consultant fees from Alexion®. SKB is a co-founder of Numerics88 Solutions Inc. KS, BA, and LAB have declared no conflict of interest.
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Additional HR-pQCT measurements plotted. Radius and tibia analysis shown as box-and-whisker plot for HR-pQCT measured microarchitecture. Red lines, from top-to-bottom, represent 75th, 50th, and 25th percentile in a reference population of young female adults aged 20-29 years-old . Open square bracket with an asterisk (*) represents significant difference between two groups at an alpha value of 0.05.
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Sidhu, K., Ali, B., Burt, L.A. et al. Spectrum of microarchitectural bone disease in inborn errors of metabolism: a cross-sectional, observational study. Orphanet J Rare Dis 15, 251 (2020). https://doi.org/10.1186/s13023-020-01521-6
- Inherited metabolic disease
- Rare disease
- Lysosomal storage disorders
- High-resolution peripheral quantitative compute tomography
- Finite element analysis
- Bone density