Current Applications and Selected Technical Details of Dual-Energy X-Ray Absorptiometry.

The application of dual-energy X-ray absorptiometry (DXA) examinations in the assessment of bone mineral density (BMD) in the lumbar spine, hip, and forearm is the basic diagnostic method for recognition of osteoporosis. The constant development of DXA technique is due to the aging of societies and the increasing importance of osteoporosis as a public health problem. In order to assess the degree of bone demineralization in patients with hyperparathyroidism, forearm DXA examination is recommended. The vertebral fracture assessment (VFA) of the thoracic and lumbar spine, performed by a highly-skilled technician, is an interesting alternative to the X-ray examination. The DXA total body examination can be useful in the evaluation of fat redistribution among patients after bariatric surgery, in patients infected with HIV and receiving antiretroviral therapy, and in patients with metabolic diseases and suspected to have sarcopenia. The assessment of visceral adipose tissue (VAT) and detection of abdominal aortic calcifications may be useful in the prediction of cardiovascular events. The positive effect of anti-resorptive therapy may affect some parameters of DXA hip structure analysis (HSA). Long-term anti-resorptive therapy, especially with the use of bisphosphonates, may result in changes in the DXA image, which may herald atypical femur fractures (AFF). Reduction of the periprosthetic BMD in the DXA measurements can be used to estimate the likelihood of loosening the prosthesis and periprosthetic fractures. The present review aims to present current applications and selected technical details of DXA.

Background

Dual-energy X-ray absorptiometry (DXA) is currently a primary radiological technique in the diagnosis of osteoporosis, used for stratifying the risk of osteoporotic fractures by assessing bone mineral density (BMD) [1,2]. The introduction of DXA scanners in 1987 to clinical practice was a milestone that allowed the precise diagnosis of osteoporosis [2,3]. According to the first publication showing the effectiveness of bisphosphonates in the treatment of bone loss [4], DXA contributed to the management of osteoporotic patients. The introduction of fan beam radiation source technology in 1993 allowed shortening the radiation exposure time while improving the quality of the images received [5]. Based on the BMD measurements, the T-score and Z-score parameters were defined. T-score is the difference between measured BMD and young adult mean BMD (specific for gender and ethnic group) in relation to the young adult population standard deviation (SD). Z-score is the difference between measured BMD and age-matched mean BMD (specific for gender and ethnic group) in relation to age-matched population SD [2]. The improvement of the quality of the obtained images enabled application of the DXA technique in the diagnosis of vertebral compression fractures using a vertebral fracture assessment (VFA) tool, and the introduction of high-resolution VFA imaging allowed for the assessment of calcifications in the abdominal aorta [6]. The development of fan-shaped beam densitometers (associated with multiple detectors), in contrast to pencil densitometers (emitting a single rectilinear highly collimated beam of X-rays associated with a single detector), allowed fast DXA body composition assessment comprising bone mineral content (BMC), fat mass, and lean mass [7]. New types of DXA examinations, such as hip structure analysis, finite element analysis, detection of atypical femur fractures, or the periprosthetic DXA, outline new directions of the DXA development and are currently under clinical trials. The present review aims to present current applications and selected technical details of the DXA examinations.

Importance of the DXA in Diagnostics of BMD

The basic function of DXA remains the assessment of BMD, used to recognize and follow up on the effects of osteoporosis treatment. Diagnosis of osteoporosis is based on the WHO criteria of osteoporosis and osteopenia [1]:

T-score equal to or higher than −1 means normal value;

T-score from −1 to −2.5 means osteopenia;

T-score equal to or less than −2.5 means osteoporosis;

T-score equal to or less than −2.5 with the presence of one or more fragility fractures means established osteoporosis.

The T-score value is not validated for premenopausal women, men under 50 years of age, and for children. For these groups of patients, the Z-score parameter is more appropriate [2]. A Z-score equal to or less than −2.0 means “low bone density for chronologic age” [8].

The DXA diagnosis of osteoporosis is based on the assessment of the T-score of vertebrae L1-L4 in the lumbar spine (Figure 1), the T-score of the femoral neck and total proximal femur (Figure 2), as well as the T-score of the nondominant forearm (Figure 3) [9,10]. According to the guidelines of the National Osteoporosis Foundation, the worst result should be chosen [11].

Figure 1

DXA examination of the lumbar spine. At the bottom of the picture is visible the borderline L5/S1, at the top the last pair of ribs connected to the Th12 vertebra. The presented image of the lumbar spine is not suitable for diagnostic objectives, but it is used to identify the ROI in the lumbar spine (vertebral bodies from L1 to L4). The diagnostic result is the T-score parameter estimated for the entire examined ROI area (circled in red). If, due to degenerative changes or artifacts, all 4 lumbar vertebrae cannot be used for analysis, 3 vertebrae should be used. The result of examination is reliable if at least 2 vertebrae are suitable for analysis.

Figure 2

DXA examination of the hip. The diagnostic result is the T-score parameter estimated for the femoral neck (the upper value in the red circle) and for the total proximal femur (the lower value in the red circle). The ROI of the femoral neck (marked as green frame) should be perpendicular to the femoral neck, should not include the greater trochanter and the ischial bone, but should include soft tissues on both sides of the femoral neck. The midline (marked as green line) should cover the long axis of the femoral neck. In the blue circle is marked the FRAX for major osteoporotic fracture (upper value) and FRAX for hip fracture (lower value).

Figure 3

The DXA examination of the right forearm. The diagnostic result is the T-score parameter estimated for the 1/3 ROI of nondominant forearm (blue frame). The reference line (marked in purple) should be positioned at the distal end of the styloid process of the ulna, the radius plate should be located outside the ROI UD (green frame), and a vertical line crossing the middle of the 1/3, MID, and UD ROI (marked in red) should cut the airspace between the radius and ulna.

To correctly perform the DXA examination of the lumbar spine, the patient should be supine in the center of the device and have lower limbs bent at a right angle in the hip and knee joints, supported by a positioner. The positioner ensures maximum flattening of the lumbar lordosis and the parallel position of the long axis of the lumbar spine in relation to the table of the device. After the examination, it should be checked whether the image of the lumbar spine is centered with sufficient airspace (equal on both sides of the lumbar spine), the spine is not rotated, the software correctly marked the boundaries of the vertebral bodies (in Figure 1 these are yellow curved lines at the borders of the vertebral bodies), and correctly separated the individual vertebral bodies from each other (in Figure 1 these are yellow straight lines between the vertebral bodies). Errors of these operations made by the software must be corrected manually.

If the T-score of the adjacent vertebrae differ by a value greater than 1.0 or in the presence of aortic calcifications and foreign bodies inside the vertebrae, such as cement or metal buttons, it is recommended to exclude a vertebra with a higher T-score from the analysis. The presence of radiation-absorbing contrast from previous radiological examinations in the examined area may disturb the assessment of BMD. The interval between radiological examination with contrast and densitometry depends on the marker used and its elimination time from the body, especially from the examined area. The lumbar spine DXA examination should start at the borderline L5/S1 to provide the correct identification of individual vertebrae and repeatability of examinations in subsequent years. An important problem may be the presence of the so-called “transitional vertebra”, found on average in 14.7% of the population [12], more often in men (28.1% vs 11.1% in men vs women, respectively) [13]. Degenerative changes due to their structure, and often due to the presence of calcifications, are characterized by much higher density and overstate the average mineral density of the vertebrae and should be removed manually by a technician from the analyzed region of interest (ROI). Otherwise, an overestimated T-score for the L1–L4 vertebrae of the lumbar spine may exclude patients from anti-resorptive therapy who in fact meet the DXA criteria for osteoporosis. The lumbar spine BMD is rarely underestimated, usually in patients after neurosurgical and orthopedic spine procedures (without the use of stabilizing materials) and in the presence of lytic neoplastic lesions in the vertebral bodies [14]. The problems described above result in incorrect estimation of BMD and they are diagnostic pitfalls of the lumbar spine DXA examination.

DXA examination of the proximal femur, similar to the examination of the lumbar spine, is performed in the supine position, but with lower limbs straightened and turned inwards to leave the smaller trochanter just visible. The image of a correctly performed examination should show the femoral neck, ischial bone, and greater trochanter. At least 3 cm of soft tissue should be visible below the ischial bone and above the greater trochanter. Before the analysis of the result, the physician should remember these principles and also should verify that the image is centered and does not contain foreign bodies and that the software correctly identified the bone tissue boundaries, the location of the midline, and the ROI of the femoral neck (Figure 2). Otherwise, the estimation of the BMD value will be incorrect, which is an important diagnostic pitfall.

DXA examination of forearm is a useful diagnostic tool [15], especially if it is difficult to interpret results of the lumbar spine or hip examinations, most often due to bilateral endoprostheses or obesity. This examination is also recommended in assessing bone decalcification among patients with hyperparathyroidism. Modern densitometers have standardized ROI for analysis and the measurements of BMD between the middle and distal 1/3 of the radial bone, which is considered reliable and diagnostic (Figure 3) [16,17]. Before the start of forearm examination, a patient should sit on a chair next to a table. The examined limb should be bent at the elbow, wrist placed in pronation on the table, and the hand clenched into a fist. The scan should start at the distal contact point between the radius and the ulna. The scan should show centered bones of the forearm with the visible distal epiphysis of the ulna (Figure 3).

Safety Considerations Regarding Radiation Dose

The radiation effective dose (RED) depends on the DXA scan modality used and takes the lowest values for the “fast-array” scan, intermediate values for the high-definition (HD) scan, and the highest values for the “array” scan [18]. RED is defined by the following values: 17.79–32.80 μSv for DXA examination of the lumbar spine, 5.29–9.55 μSv for DXA examination of the hip, less than 60 μSv for the VFA scan in the sagittal projection of the thoracolumbar spine, and 4–5 μSv for the body composition DXA scan performed with the latest-generation densitometers [7,18]. REDs used in DXA examinations are lower compared to the conventional radiographic examinations and are comparable to the background radiation [7,18]; therefore, the only contraindication to DXA examinations is pregnancy [19]. For comparison, the effective dose of a computed tomography of head is 2 mSv, which is equivalent to 8-month exposure to background radiation [7,20].

DXA Diagnosis of Vertebral Fractures Using VFA

The VFA tool allows diagnosis of osteoporotic fractures of vertebrae from Th4 to L4 by semi-automatic or manual assessment in the sagittal plane of 3 vertebral heights (anterior, medial, and posterior) and their percentage reduction (Figure 4). Mild fracture is recognized by a 20–25% reduction in vertebral height, moderate when the reduction is 26–40%, and severe when it exceeds 40% [21]. After analyzing vertebral heights, the software assigns the degree of fracture and its type (wedge, biconcave, or crush) to the vertebrae. The obtained results are presented as quantitative and semi-quantitative assessments (Figure 5).

Figure 4

Result of the VFA examination in the thoracic and lumbar spine. The table shows individual vertebral heights in millimeters (marked in the black circle – the posterior, middle and anterior height, respectively, in order from the left) and the degree of deformation (%) of vertebral bodies (marked in the green circle – the wedge, biconcave and crush deformation, respectively, in order from the left). The red arrow indicates the position of the sacrum and the blue arrow the position of the L5 vertebra. Clear visualization of the sacrum and vertebra L5 is necessary for identification of examined vertebrae.

Figure 5

Severe wedge fracture of the Th8 vertebra (the degree of deformation (%) marked in red circle) and mild crush fracture of the L4 vertebra (the degree of deformation (%) marked in blue circle), based on the VFA examination.

The location of measurement points in a semi-automatic manner shows particular effectiveness in the assessment of healthy vertebrae and the diagnosis of benign fractures [22]. However, it is less effective for moderate and severe fractures. In this situation, the position of the measurement points must be corrected manually. It is often difficult to assess vertebrae above T7 [23] because of the projection of mediastinal structures on the vertebral bodies or the presence of calcifications in pulmonary circulation vessels. In these situations, and in the case of severe osteoarthritis and degenerative changes, VFA shows lower sensitivity and specificity compared to radiography [24]. The most important diagnostic pitfall in the VFA examination is the possibility of a false-positive or false-negative diagnosis of vertebral fracture due to the still limited resolution of VFA images and the situations described above, which impede the identification of the individual heights of vertebral bodies.

Important advantages of the VFA are quick assessment of vertebral morphology within 2 sections of the spine, the low cost of examination [25], and the ability to assess BMD in a single visit using the same device. In addition, the compatibility in the detection of vertebral fractures between traditional radiography and VFA encourages the use of VFA as a screening examination among patients with osteoporotic risk factors and for the prospective evaluation of treatment effectiveness [26]. Therefore, despite the fact that radiography is still the criterion standard for diagnosis of vertebral fractures [27], the field for the use of VFA is growing. As Korean researchers have shown [28], use of VFA as screening diagnostics of vertebral fractures [29], followed by conventional radiography, was characterized by the highest efficiency, the lowest cost, and the lowest radiation dose. However, the limitations of the VFA method should be considered, and it is important for any research center to validate the densitometer against conventional radiography of the spine [30].

Visualization of Abdominal Aortic Calcifications (AAC)

In addition to the standard VFA test, several models offer the high-definition VFA (HD VFA) examination. In addition to better resolution of images, HD VFA can be used to diagnose abdominal aortic calcifications by the AAC-8 visual scale. In addition to traditional risk factors for cardiovascular diseases, the presence of calcifications in the abdominal aorta can be associated with higher risk of myocardial infarction and stroke [31]. Predicting cardiovascular events based on AAC was demonstrated to benefit kidney transplant recipients [32]. Among patients with end-stage chronic kidney disease treated with peritoneal dialysis, the high AAC-8 calcification index is a strong predictor of mortality from any cause [33].

Evaluation of Hip Structure Analysis (HSA)

Measurements of the HSA parameters are performed automatically during the hip BMD examination. HSA involves the analysis of a number of parameters within 3 additional zones:

Narrow neck area (NN) – passing through the femoral neck at its narrowest point, perpendicular to the axis of the neck;

Intertrochanter area (IT) – connecting the smaller and the larger trochanter and at the same time constituting the bisector of the angle, formed by the axis of the neck and the axis of the femoral shaft;

Femoral shaft area (FS).

In each of these areas, the device measures analogous parameters [34]:

Outer diameter (OD), expressed in cm, is measured on both sides from the outer margins of the bone (from medial to lateral or vice versa), with correction taking into account the blur of the image;

Cross-sectional area (CSA), expressed in cm2, is the integral of linear density (cm), obtained by dividing pixel values (denoting local mineral density, expressed in g/cm2) by the average mineral density of the cortical bone in the average adult man (1053 g/cm3);

Center of mass;

Numerous derived parameters such as: centroid position, cross-sectional moment of inertia (CSMI), section modulus (SM), buckling ratio (BR), neck length (NL), and neck shaft angle (NSA).

The last 2 parameters affect the shoulder moments of bending forces in the proximal femur [35].

Studies showed the correlation between the change in the values of individual parameters of the femoral neck geometry and the treatment, with significant changes observed primarily in 2 areas: NN and IT. In contrast, the FS area is least susceptible to fractures, as well as to the effects of drugs; therefore, it is often overlooked in studies [35]. Moving to the direct interaction of individual drugs (eg, teriparatide) increases CSA and SM and reduces BR. These changes are the largest in the NN area, less expressed in IT, and practically imperceptible in the FS. Therefore, teriparatide improves resistance to bending and axial forces and increases cortical bone thickness and stability of the neck and intertrochanter region. The effect of teriparatide on femoral geometry parameters is dose-dependent [36].

After 1 year of treatment, ibandronate used once a month in men increased cortical bone thickness and CSA and reduced BR in IT and FS. Interestingly, ibandronate did not significantly affect geometric parameters in the NN area [37]. A study comparing alendronate and risedronate used once a week in women with postmenopausal osteoporosis demonstrated an overall improvement in geometric parameters in each of the 3 main areas (NN, IT, FS), showing the advantage of alendronate over risedronate [38]. Analysis of 3-year use of denosumab among Japanese women with postmenopausal osteoporosis resulted in a significant increase in cortical bone thickness, CSA, CSMI, and SM and a decrease in BR in all 3 significant regions relative to placebo [39]. Moreover, patients who started receiving denosumab instead of placebo during the study had significant improvement of femoral geometry.

It is worth noting that despite the relatively low dose of radiation, measurements of femur geometry parameters are characterized by similar accuracy in both the densitometry and CT methods [40].

Diagnosis of Atypical Femur Fracture (AFF)

Atypical femur fractures are most often associated with long-term treatment with bisphosphonates; they often occur bilaterally and cause leg and groin pain [41]. The diagnosis of atypical femur fractures can be carried out during routine follow-up bone density testing [42].

Modern densitometers offer 2 technologies for AFF testing. The first is full-length femur imaging (FFI) using single-energy X-ray absorptiometry (SE). This examination has a significant advantage over the DXA technique because it guarantees an image resolution similar to X-ray and is 5 times faster than the DXA scan, lasting only 15 seconds, and covers the entire length of the shaft [43]. This is an important feature because atypical femur fractures can occur in any femoral region distal to the minor trochanter. The International Society of Clinical Densitometry indicates that it is appropriate to consider an FFI in patients with cumulative time of anti-resorptive therapy of over 3 years [44]. Radiological symptoms suggesting the possibility of atypical femoral fracture are periosteal local thickenings and cortical bumps along the lateral cortex [44]. These thickenings take the shape of a beak and are an expression of local bone formation and repair in response to cortical structure damage [45]. Another radiological symptom of atypical femoral fracture is the transverse radiopaque line, known in the literature as the “dreaded black line” [46]. Clinically, patients with AFF most often report thigh or groin pain, and these ailments precede the conversion to complete fracture by several weeks or even several months. Due to the much worse results of surgical treatment of atypical fractures [47], the diagnosis of clinical and radiological symptoms heralding the fracture may bring measurable benefits.

The second way to diagnose AFF is to extend the standard DXA scan to the entire femur. According to van de Laarschot et al [48], the positive predictive value of AFF diagnostics with DXA is 83.3%. Also, Ahlman et al [49] confirmed, despite the limitations described above, the usefulness of DXA for the diagnosis of AFF.

Evaluation of Finite Element Analysis (FEA)

A useful method of assessing bone strength and predicting fractures is finite element analysis (FEA). FEA is mathematical method describing reaction of bone structure to stress associated with loading. Several models to assess bone strength using FEA have been developed, for example:

The two-dimensional model of the assessment of femoral strength parameters was proposed by Naylor et al in 2013 [50]. An introduction to performing the FEA is conducting a standard hip DXA [51]. Then, based on the obtained image, the software divides the femur into segments and subsegments, up to individual pixels. Considering measurements of areal bone mineral density (aBMD) [52] in relation to femur length and width, the special customized software computes the thickness of femoral neck and creates a model of volumetric bone mineral density (vBMD) [53]. Using vBMD and appropriate formulas developed by Morgan et al [54], material properties are calculated. Based on these parameters and the Huber-von Misess failure criteria, stresses of individual segments up to pixels are calculated [55]. A map of stress distribution and stress characteristics for individual pixels is created. The stress ratio is the result of the von Misess stresses divided by the average value of compressive and tensile yield stresses. If the stress ratio in a given segment or group of segments is above 1, it means a high probability of damage as a result of the impact force [55]. Peak impact force is calculated based on the patient’s height and weight [56]. The point of application of force is the greater trochanter (according to the most common fall mechanism). The product of the peak impact force and the maximum value of stress ratio (caused by the peak impact force) indicates the femoral strength. If the impact force exceeds the strength, a fracture occurs. Because the maximum impact force is reduced by the protective effect of soft tissues over the trochanter (reduction by up to 1775 N) [57], a better parameter for assessing the likelihood of fracture as a result of a fall is the load-to-strength ratio (LSR). Load means the difference between the peak impact force and the suppressive strength of soft tissues. An LSR value greater than 1.0 is an equivalent of a high fracture risk [55,57] and, in combination with BMD, correlates better with this risk than BMD alone. Therefore, femoral strength assessment (and thus LSR) may be an additional useful prognostic parameter in hip fracture risk assessment.

The FEA model of distal radius microstructure was created using the quantitative computed tomography, in which researchers have shown that the strains variability in the FEA mesh depends on the aBMD, age, height, and body weight [58].

The vertebral FEA model was created using a planar DXA image of the lumbar spine. Based on the grayscale mesh of the FEA and the mechanical properties of the vertebral bone tissue (experimentally calculated using specimens of porcine vertebrae), the authors introduced a new parameter, strain index of bone, and demonstrated that the association of this parameter with BMD correlates better with fracture risk in comparison to BMD alone [59].

Evaluation of FRAX

FRAX is a validated tool for the 10-year risk assessment of hip fracture and major osteoporotic fractures (forearm, proximal humerus, thoracic and lumbar vertebrae, hip) [60]. Modern densitometers display a survey with questions necessary to calculate FRAX. The software incorporates age, gender, height, weight, and ethnicity from data routinely entered prior to starting a hip DXA scan. The survey contains a series of questions that the patient should answer in order to calculate the FRAX value, such as: history of prior fractures in adult life (spontaneous or caused by low-energy trauma that does not result in a fracture in healthy people), history of hip fractures in parents, exposure to glucocorticoid therapy, diagnosis of rheumatoid arthritis, current smoking, and alcohol drinking. FRAX can be computed using BMI, without DXA examination and using BMD, with the T-score of the femoral neck [60]. FRAX is a strong, independent, additional risk factor for osteoporosis, but intervention thresholds vary considerably depending on the country and the guidelines of professional societies. It is possible to adjust the FRAX result by another, independent risk factor for osteoporosis, the trabecular bone score (TBS).

Definition and Importance of TBS

TBS is a parameter determining the microarchitecture of the trabecular bone, based on the texture (shade of gray) of the lumbar spine DXA image in the anterior-posterior projection [61]. It takes values from 0.5 to 2.0, and a higher index value is associated with less trabecular bone weaving damage and fracture. A result above 1.35 is considered as normal, a result lower than 1.20 indicates serious damage to the microstructure of the trabecular bone, and an intermediate result indicates partial damage [62]. TBS is not a direct marker of microarchitecture, but it reflects the number of trabeculae and their connections and divisions [63]. Knowing the TBS value, a modified FRAX can be obtained using special algorithms [64]. Previous studies demonstrated that the use of anti-resorptive treatment in postmenopausal women is associated with a significant increase in BMD and TBS in comparison to untreated patients [65]. An interesting application of TBS may be the assessment of fracture risk among patients with advanced osteoarthritis of the spine because it was proved that in the L4 vertebra (where degenerative changes are most severe) BMD measurement is significantly overstated in comparison to TBS measurement [62].

Body Composition Assessment

Although the diagnostic standard for assessing muscle mass remain computed tomography (CT) and magnetic resonance imaging (MRI) [66], a very valuable diagnostic option is DXA assessment of the body composition. The total body examination provides abundant information, such as calculations of the BMC, BMD, lean mass, and fat mass for the total body and in division into individual body regions (Figures 6, 7). The T-score and Z-score parameters are also calculated for the total body, but the T-score and Z-score for the entire skeleton cannot be used as the basis for the diagnosis of osteoporosis. The modern devices also calculate fat mass and total mass in android and gynoid areas with the ratio of android fat to gynoid fat (A/G), as well as mass, area, and volume of the visceral adipose tissue (VAT). The A/G ratio is strongly and positively correlated with glycated hemoglobin (HbA1c) and triglycerides (TG) and inversely related to HDL-C level [67]. DXA measurements of VAT are characterized by a sufficient level of precision [68] and are not inferior to CT and MRI examinations [69,70]. Excessive amounts of VAT in comparison to subcutaneous adipose tissue increases total mortality risk due to all causes in men [71]. In addition, increased VAT is associated with worse lipid, glycemic, hematocrit, and kidney profiles in the elderly [72].

Figure 6

Result of the body composition assessment - skeletal system. ROIs are defined by lines 1–7. The line number 1 separating the head should pass directly below the chin. The line number 2 separating the spine from the chest should pass as close to the spine as possible. The line number 3 separating the upper limbs from the body should pass through the shoulder joints as close to the body as possible. A perpendicular line inside the area defined by line number 2 should separate the thoracic spine from the lumbar spine. The line number 4 separating the pelvis from the trunk should pass over the upper edge of the iliac crests. The line number 5 separating the pelvis from the lower limbs should cross the femoral necks. Line number 6 should cut the airspace between the upper and lower limbs and line number 7 the airspace between the lower limbs.

Figure 7

Result of the body composition assessment – soft tissues. The table on the left shows (parameters from the left, marked in the black circle, respectively): the mass of adipose tissue, the sum of the mass of other soft tissues and bone tissue, the total mass, and the percentage of fat tissue in individual ROIs, including the android and gynoid region (A and G in red circle, respectively). In the tables on the right are presented, among others: percentage of total body fat mass (blue circle), parameters of visceral adipose tissue (green circle), and parameters useful in the assessment of loss of muscle mass (purple circle).

Based on the assessment of the body fat mass, it was proven that higher fat mass reduces the overall risk of death in elderly women [73]. The total body examination can also be used to assess fat redistribution in patients infected with HIV and receiving antiretroviral therapy [74], as well as in patients with metabolic diseases [75] and anorexia [76]. It is a valuable tool for assessing the effectiveness of bariatric procedures [77]. The ASMM index (ASMMI), defined as appendicular skeletal muscle mass (ASMM, kg) per height squared (m2) [78] indicates low muscle mass if its value is below 7.0 kg/m2 for men and below 6.0 kg/m2 for women [79]. The result of ASMMI is available directly on the printout of the DXA examination of the body composition (Figure 7).

Evaluation of Periprosthetic DXA

DXA is the diagnostic standard in the assessment of periprosthetic BMD [80]. Current analysis approaches of periprosthetic BMD rely on the creation of ROI and calculating an average BMD value within them based on a pixel map [81,82]. The bone density analysis around the prosthesis can be carried out using 5 ROIs [83]. ROI subject to analysis should contain periprosthetic metaphyseal and diaphyseal bone around and away from the implant [84]. Validation of the current image processing techniques allowed development of a high spatial resolution tool for the assessment of periprosthetic BMD, called DXA region-free analysis [81,85]. Evaluation of the remodeled bone tissue around the prosthesis can provide useful information. The degree of BMD reduction in areas adjacent to the prosthesis can be used to estimate the likelihood of prosthesis loosening and periprosthetic fractures [86]. Distal femur BMD is about 10% lower in the leg after total knee arthroplasty and can be associated with increased periprosthetic fracture risk [87]. DXA is appropriate even for periprosthetic BMD measurement around the proximal component of total wrist arthroplasties [88].

Other Functions

Due to the low dose of radiation, DXA is also increasingly used in children; for example, to assess body fat [89]. Lumbar spine DXA examinations for infants and young children 0–5 years of age as well as total body DXA measurements for children >3 years of age have been approved by ISCD as being feasible and reproducible [84]. Based on DXA scans, it was proved that the BMD of premature newborns is lower compared to children born at term. Furthermore, the acceleration of bone mineralization in premature newborns allows achieving BMD values typical of term newborns after 6 months [90]. Based on the assessment of vitamin D serum concentration in pregnant women and neonatal BMD measurements, it was demonstrated that 25-hydroxyvitamin D deficiency in pregnancy results in reduced BMD and lower birth weight of newborns [91].

Conclusions

The basic and most important application of the DXA technique is the assessment of BMD with the calculation of the T-score, which is the only validated method of diagnosing osteoporosis. The constantly growing importance of DXA examinations and the development of new applications of this technique are associated with the increasing percentage of osteoporotic elderly people, the low radiation dose, and the possibility of performing additional DXA measurements with the assessment of BMD.