Bone Density Measurement
The Reference Was:
Bone density is measured by a scanning machine. Special types of x-ray machines can do this, and you should be sure you get tested only with the modern testing equipment.
X-ray machines are not accurate enough to measure small amounts of bone loss. The proper procedure is called dual x-ray absorptiometry. The machines which do these are rather rare, so be sure your testing place has one. Dont accept the dual photon absorptiometry which is not as good.
Figures 1 and 2 (below) are examples of images created by a central DXA system.
Figure 1.
Example of a DXA image of the hip, including femoral neck.Figure 2.
Example of a DXA image of the lumbar spine.All full-body DXA devices have the ability to measure BMD
Hologic:1-800-343-9729
www.hologic.com/newsite/Lunar Corporation: 1-800-445-8627
www.lunarcorp.comListed below are several scientific studies which utilize this type of density measurement. Read at your leisure.
Title
Ultrasound and dual X-ray absorptiometry densitometry in women with hip fracture.
Author
Mautalen C; Vega E; González D; Carrilero P; Otaño A; Silberman F
Address
Sección Osteopat57ias Médicas, Hospital de Clínicas, Buenos Aires, Argentina.
Source
Calcif Tissue Int, 57: 3, 1995 Sep, 165-8
Abstract
To assess the usefulness of the measurement of the os calcis by ultrasound, a method that
probably reflects bone quality as well as density, we have studied 54 women with hip
fracture of the proximal femur and a control group. Ultrasound evaluation of the os calcis
[broadband ultrasound attenuation (BUA), speed of the sound (SOS), and a combined index
("stiffness")], and bone mineral density (BMD) determination over the proximal
femur by dual X-ray absorptiometry (DXA) were performed. Weight, BMD, and ultrasound
values in the hip fracture patients were significantly lower than controls (P < 0.001).
The Z-scores for BUA and stiffness were not different than that for femoral neck, Ward's
triangle or trochanteric BMD (between -1.7 and -1.5). The odds ratios determined by
receiver-operating characteristics (ROC) analysis were greater at the femoral neck (25.1)
and BUA (24.4). Intermediate values were found at stiffness (16.9), Ward's triangle
(12.8), and trochanter (11.1), and lower values were obtained at SOS (4.2). In turn,
patients with trochanteric hip fractures had a significantly lower femoral neck and Ward's
triangle BMD, stiffness, and BUA than patients with cervical hip fractures. Comparing a
subgroup of 30 women with hip fractures without vertebral fractures with an age-matched
group of 87 women with osteoporotic vertebral fractures, both groups were of similar
weight and BMD but all ultrasound values were significantly lower in the hip fractures
compared with vertebral fracture patients (P < 0.05 - P < 0.01).(ABSTRACT TRUNCATED
AT 250 WORDS)
Language of Publication
English
Unique Identifier
96039173
MeSH Heading (Major)
Densitometry, X-Ray [IS/*MT]
Hip Fractures [*US]
MeSH Heading
Adult
Aged
Aged, 80 and over
Aging
Body Weight
Bone Density
Female
Human
Middle Age
Sensitivity and Specificity
Support, Non-U.S. Gov't
Publication Type
JOURNAL ARTICLE
ISSN
0171-967X
Country of Publication
UNITED STATES
Title
Comparative x-ray densitometry of bones from ovariectomized rats.
Author
Sato M
Address
Department of Endocrine Research, Lilly Research Laboratories, Indianapolis, IN 46285,
USA.
Source
Bone, 17: 4 Suppl, 1995 Oct, 157S-162S
Abstract
Comparative analysis of dual energy x-ray absorptiometry (DXA) and quantitative computed
tomography (QCT) with phantoms and rat bones showed that both are necessary to adequately
quantitate ovariectomy induced bone changes, in vivo. Precision and accuracy analysis of a
Hologic QDR 1000/W and a Stratec 960 QCT showed that the latter is a highly precise,
modestly accurate device that is more suited to the analysis of small bones. Specifically,
smaller error was achieved by threshold optimization for the QCT in the analysis of
phantoms 1.04-9.6 mm in diameter, with precision comparable to or better than DXA.
Additionally, the QCT measured significant differences between groups in proximal tibiae
when DXA could not; and measured a larger difference between sham and ovariectomized
controls which was suitable for analysis of the dose dependent effects of a
pharmacological test compound, raloxifene. This may reflect the ability of the QCT to
measure volumetric mineral density (VMD, mg/cc), compared to two dimensional analyses by
DXA. However, QCT was not able to analyze vertebrae in vivo, a site of considerable
clinical interest. Therefore, DXA is useful to analyze the axial skeleton in vivo, while
the appendicular skeleton is better analyzed in vivo by QCT. By both techniques, a similar
dose response was observed for raloxifene, with ED50 = 0.3 mg/kg for both axial and
appendicular skeleton. Comparative analysis of rat L1-4 by the Hologic QDR 1000/W and
Lunar DPXL showed 12-14% higher BMD and BMC values for the Hologic, which is the opposite
relationship between these instruments to that observed clinically for this site.
Language of Publication
English
Unique Identifier
96119186
MeSH Heading (Major)
Bone and Bones [*RA]
Densitometry, X-Ray
Ovary [*PH]
Tomography, X-Ray Computed
MeSH Heading
Analysis of Variance
Animal
Bone Density [PH]
Evaluation Studies
Female
Ovariectomy
Phantoms, Imaging
Random Allocation
Rats
Rats, Sprague-Dawley
Reproducibility of Results
Publication Type
JOURNAL ARTICLE
ISSN
8756-3282
Country of Publication
UNITED STATES
Return To The Images Version Of Viewpoint #1
Return To The Text Only Version Of Viewpoint #1
Title
Technical considerations of dual-energy X-ray absorptiometry-based bone mineral measurements for pediatric studies.
Author
Koo WW; Walters J; Bush AJ
Address
Department of Pediatrics, University of Tennessee-Memphis, USA.
Source
J Bone Miner Res, 10: 12, 1995 Dec, 1998-2004
Abstract
Dual X-ray absorptiometry (DXA) measurements have been shown to provide useful information
on bone mineral status in young pediatric subjects. The purpose of this study was to
challenge this system under various conditions to determine the clinical and experimental
parameters that may be encountered which could interfere with DXA-based bone mineral
content (BMC) and bone mineral density (BMD) measurements. Variations in data acquisition,
including the covering of step phantom (external calibration standard) with a cotton
blanket or partial exclusion of step phantom in the scan field, tissue freezing, or the
presence of small nonmetallic objects, did not significantly alter DXA BMC or BMD
measurements. By contrast, the presence of movement artifact, radiographic contrast media,
and nonmetallic orthopedic casts significantly interfered with DXA BMC and BMC
measurements. Variability in operator-dependent analysis of DXA scans occurred with
regional analysis of whole body scans for DXA BMC and BMD measurements (average
coefficient of variation was 2.9% and 1%, respectively, depending on the region analyzed)
but did not affect the total (whole body) result. A minor adjustment in the manual
delineation of the step phantom during data analysis may result in almost a 30% difference
in DXA BMC and BMD. We conclude that movement artifact, radiographic contrast media,
nonmetallic or orthopedic cast, and variations in operator-dependent data analysis may
interfere with DXA BMC and BMD measurement in young pediatric subjects. Therefore,
appropriate care should be taken to reduce or eliminate such interference.
Language of Publication
English
Unique Identifier
96192721
MeSH Heading (Major)
Bone Density [*PH]
Densitometry, X-Ray [*MT]
MeSH Heading
Analysis of Variance
Animal
Animals, Newborn
Calibration
Human
Infant
Infant, Newborn
Linear Models
Movement
Phantoms, Imaging
Reference Standards
Reproducibility of Results
Support, Non-U.S. Gov't
Support, U.S. Gov't, P.H.S.
Swine
Publication Type
JOURNAL ARTICLE
ISSN
0884-0431
Country of Publication
UNITED STATES
Title
Reliability of in vivo neutron activation analysis for measuring body composition: comparisons with tracer dilution and dual-energy x-ray absorptiometry [see comments]
Author
Ma K; Kotler DP; Wang J; Thornton JC; Ma R; Pierson RN Jr
Address
Department of Medicine, St. Lukes-Roosevelt Hospital, New York, NY 10025, USA.
Source
J Lab Clin Med, 127: 5, 1996 May, 420-7
Abstract
In vivo neutron activation (IVNA) analysis has the capacity to measure several total body
elements in human subjects. Although it has been considered a criterion method for the
past 3 decades, the reliability of IVNA analysis has been tested only in phantom
calibrations. In 5 male weight-stable patients with AIDS, total body N, Ca, Cl, Na, P, and
C were measured three times in 16 weeks at Brookhaven National Laboratory. With tracer
dilution methods for total body water (TBW) by 3H2O and for extracellular water (ECW) by
35SO4 and NaBr, and dual-energy x-ray absorptiometry (DXA), total body calcium (TBCa) and
fat percentage were measured within 2 weeks of IVNA measurements. For comparison, tracer
dilution for TBW by D2O and ECW by NaBr, plus DXA measurements, were performed three times
in 5 weight-stable healthy volunteers. The reliability of the IVNA technique was very high
in patients with AIDS; it ranged from 0.99 for total body chloride (TBCI) to 0.84 for
total body phosphorus (TBP), and it agreed with phantom calibration results in the
literature. The reliability for measuring fat percentage and TBCa by DXA was similar in
patients with AIDS and in healthy volunteers. Tracer dilution for measuring TBW by 3H2O in
patients with AIDS and by D2O in healthy volunteers had a reliability score similar to
those found with IVNA and DXA. The reliability scores for measuring ECW in patients with
AIDS by 35SO4 and NaBr, 0.66 and 0.68, respectively, were the lowest among all
measurements, whereas the reliability score for NaBr in healthy volunteers was 0.96, as
with the other measurements.
Language of Publication
English
Unique Identifier
96209135
MeSH Heading (Major)
Body Composition
Densitometry, X-Ray
Neutron Activation Analysis [*SN]
Radioisotope Dilution Technique
MeSH Heading
Acquired Immunodeficiency Syndrome
Adult
Body Water
Bromides [AN]
Calcium [AN]
Comparative Study
Deuterium
Extracellular Space
Human
Male
Sodium Compounds [AN]
Sulfates
Sulfur Radioisotopes [DU]
Support, U.S. Gov't, P.H.S.
Tritium
Comment Citation
Comment in: J Lab Clin Med 1996 May;127(5):414-5
Publication Type
JOURNAL ARTICLE
ISSN
0022-2143
Country of Publication
UNITED STATES
CAS Registry/EC Number
0 (Bromides)
0 (Sodium Compounds)
0 (Sulfates)
0 (Sulfur Radioisotopes)
10028-17-8 (Tritium)
7440-70-2 (Calcium)
7647-15-6 (sodium bromide)
7782-39-0 (Deuterium)
Title
Osteoporosis and its relationship to oral bone loss.
Author
Loza JC; Carpio LC; Dziak R
Address
State University of New York, Buffalo, USA.
Source
Curr Opin Periodontol, 3:1996, 27-33
Abstract
Osteoporosis, an age-related condition, is classified into primary and secondary types.
Primary osteoporosis encompasses the postmenopausal and senile types; secondary
osteoporosis occurs "secondary" to endocrine and renal diseases. Subjects
affected by osteoporosis have an overall reduced bone mass and become highly susceptible
to bone fractures. Dual energy x-ray absorptiometry is the method most often used to
determine the risk for osteoporotic fractures. In the past decade, a number of studies
have suggested a possible correlation between systemic osteoporosis and alveolar bone loss
in periodontal disease pathogenesis. It appears that a clear correlation between
periodontal health and the general mineral status of the skeleton is still lacking. This
review addresses the pathogenesis of osteoporosis and emphasizes the multifactorial nature
of bone loss. The current concepts in alveolar bone loss resulting from osteoporosis and
its implications as a risk factor in periodontal disease development are also presented.
Language of Publication
English
Unique Identifier
96241517
MeSH Heading (Major)
Alveolar Bone Loss [*ET/PP]
Osteoporosis [*CO/ET/GE]
MeSH Heading
Aged
Calcitriol [PH]
Cytokines [PH]
Female
Human
Male
Middle Age
Osteoporosis, Postmenopausal [CO]
Tooth Loss [ET]
Publication Type
JOURNAL ARTICLE
REVIEW
REVIEW, TUTORIAL
ISSN
1065-626X
Country of Publication
UNITED STATES
Number Of References
42
CAS Registry/EC Number
0 (Cytokines)
32222-06-3 (Calcitriol)
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