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Dxa scanner

Manufactured by Hologic
Sourced in United States

The DXA (Dual-energy X-ray Absorptiometry) scanner is a medical imaging device used to measure bone mineral density. It employs two different X-ray energies to differentiate between bone and soft tissue, providing detailed information about the patient's bone health.

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24 protocols using dxa scanner

1

Anthropometric and Body Composition Assessment

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Height and body mass will be measured with the participants in light clothing and barefoot. Body mass index will be calculated by dividing the body mass in kilograms by the square of height in meters (kg/m2). Waist circumference will be measured to the nearest 0.1 cm at the umbilical region using an inelastic measuring tape at the end of normal expiration. DXA is used to measure percent body fat and muscle mass (Hologic QDR-4500, DXA Scanner, Hologic Inc., Waltham, MA, USA) by a recognized technologist.
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2

DXA Anthropometric Parameter Changes

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Changes in anthropometric parameters were determined using a DXA scanner (Horizon, Hologic, MA, USA).
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3

FRAX-Based Fracture Risk Assessment

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To assess the risk of fractures, FRAX is able to provide the 10-year probability of a major osteoporotic fracture and hip fracture, respectively. FRAX assessment requires the information about age, gender, height, weight, previous fracture, family history of hip fracture, current smoking, use of glucocorticoids, history of rheumatoid arthritis and secondary osteoporosis, amount of daily alcohol consumption, and femoral neck BMD (http://www.shef.ac.uk/FRAX). BMD at femoral neck was measured using a DXA scanner (Hologic Inc., Bedford, MA, USA). High risk of fracture was defined as 10-year probability of hip fracture ≥3% or a major osteoporotic fracture ≥20% (27 (link), 28 (link)).
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4

Cross-sectional Osteoporosis Study in Omaha

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The Omaha osteoporosis study (OOS) is a cross-sectional study of osteoporosis with 1,000 unrelated participants of European ancestry living in Omaha, NE, USA, and its surrounding areas. The participants were normal healthy subjects defined by a comprehensive suite of exclusion criteria, as described elsewhere (6 (link)). BFM and BLM were measured by DXA scanner (Hologic Inc., Bedford, MA, USA), following the manufacturer's protocol.
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5

Bone Mineral Density Measurement Using DXA

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The bone mineral density of each group was determined using a DXA scanner (Delphi, Hologic). Concisely, the samples were fixed in 10% formalin and washed with PBS thrice. A regional high-resolution x-ray with line spacing and point resolution of 0.0311 cm each was conducted for a scan area of 4 cm to cover the whole sample. The cross-sectional area of the cylindrical bone core was used to calculate the bone mineral density area mean in g/cm2. This was further divided by the sample's actual thickness measured using calipers to get a value of bone mineral density in units g/cm3. Each sample was scanned three times, and the average value was used in our calculation.
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6

Kansas City Osteoporosis Study

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The Kansas City osteoporosis study (KCOS) is a cross-sectional study of osteoporosis with 2,286 unrelated participants of European ancestry living in Kansas City, MO, USA, and its surrounding areas. The participants were normal healthy subjects defined by a comprehensive suite of exclusion criteria, as described elsewhere (13 (link)). BFM and BLM were measured again by DXA scanner (Hologic Inc., Bedford, MA, USA), following the manufacturer's protocol.
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7

Bone Density Mapping from Nano-CT Scans

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A 2D bone density mapping was generated for each nano‐CT VOI (n = 30) by projecting all bone voxels onto a planar FN ROI. The anatomical location, orientation, and width of the FN ROI were consistent with the Hologic DXA scanner used for the validation study. The 2D mapping was called the pseudo‐DXA image (Fig. 1C). This analysis focused exclusively on the number of bone voxels, since the X‐ray attenuation giving rise to BMC and the associated image reflects primarily the mineral component.(33) The contributions of marrow and X‐ray scattering to the pseudo‐DXA image were not assessed, as this initial study focused on the relative contributions of cortical and trabecular tissues to the DXA parameters.
The parameters calculated from the pseudo‐DXA images included the ROI area (pseudo‐DXA area), number of cortical bone voxels, number of trabecular bone voxels, total number of bone voxels (pseudo‐DXA BMC), and total number of bone voxels/area (pseudo‐DXA BMD). The numbers of cortical and trabecular bone voxels above (superior) and below (inferior) the FN ROI midline were also calculated. The average FN width and minimum FN width were measured directly from the pseudo‐DXA image. All terms preceded by pseudo‐DXA designate traits defined from the projected nano‐CT images, whereas terms preceded by DXA refer to traits determined by the DXA system.
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8

KNHANES Health Behavior and Bone Density

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The KNHANES included a self-reported health behavior questionnaire and health examinations. The health behavior questionnaire surveys demographic information, health status, and health behavior, and also includes questions related to income, marital status, smoking habits, alcohol consumption, and exercise. Subject height (m) and weight (kg) were measured. Body mass index (BMI) was calculated by dividing weight by the square of height. All data were gathered by trained staff using standardized tools. BMD was measured by using a DXA scanner (Hologic, Bedford, MA, USA). Lumbar spine (L1–4) and proximal femur BMD values were obtained. The presence of osteoporosis was defined by the mean of lumbar spines (L1–4), femoral neck, or total femur T-scores ≤−2.5 SD, according to the World Health Organization criteria. Subjects with foreign bodies in the bones, such as surgical pins or cement, or with evidence of compression fractures or degenerative changes, were excluded from the analysis.
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9

Comprehensive Assessment of Body Composition and Physical Activity

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Body mass index (BMI) was calculated as body mass in kilograms divided by height in meters squared (kg/m2). Body fat mass (kg), body muscle mass (kg), and body fat percentages (%) were estimated using DXA (Hologic QDR-4500, DXA Scanner, Hologic Inc., Newark, DE, USA) by a recognized technologist. The average systolic blood pressure (SBP) and diastolic blood pressure (DBP) of ankle and arm were measured using a non-invasive vascular screening device (BP-203RPE II device; Omron Healthcare, Kyoto, Japan).
Physical activity information was obtained using the long form of the International Physical Activity Questionnaire (IPAQ), except for when participants were attending the exercise program. Metabolic equivalent task (MET) values in minutes/week were calculated [26 (link)]. The mean weekly sunlight exposure score was calculated from sun exposure time and exposed skin area. Additional details are provided elsewhere [27 (link)]. The above indicators were determined at t1 and t2.
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10

Body Composition Measurement by DXA and InBody

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Height and body mass were assessed prior to a dual energy X-ray absorptiometry (DXA) scan (Hologic DXA Scanner, Hologic HorizonTM; Danbury, CT). One noninvasive whole-body scan, anteroposterior view of the total body lying supine was performed. Testing was completed according to the manufacturer’s instructions and specifications. Results were analyzed with APEX software, version 4.5.2.1 (Hologic Inc.). The quality analysis for the densitometer was conducted daily using a standard aluminum spine block (Hologic Phantom) provided by the manufacturer. Measurements of the phantom fell within the manufacturer’s precision standard with a coefficient of variation <0.5%. Test-retest interclass coefficient of variation (CV; %) using DXA for LM (kg) and FM (kg) was 1.1% and 0.69%, respectively. The minimum detectable difference using DXA for LM (kg) and FM (kg) were 0.27 and 0.21 respectively. Total body water (TBW) was assessed via InBody scan (In-Body 270). Participants removed their socks and had their hands and feet wiped clean prior to standing on the InBody platform and grabbing the handles. Participants stood on the testing platform while holding hand electrodes for approximately 45 seconds. The minimal detectable difference using InBody for TBW (kg) was 0.19.
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