What is Osteoporosis?
Osteoporosis is the end result of bone loss. Bone loss is a natural, age
related process. Bone mass peaks by age 30 and then starts a gradual decline.
When enough bone mineral is lost so that the remaining bone will not support
normal loads, the bone collapses. Low bone density as measured by SXA, DEXA, QCT,
or ultrasound is a strong risk predictor for the occurrence of the non-traumatic
bone fractures, which are characteristic of osteoporosis.
Who is at risk to develop Osteoporosis?
Postmenopausal women over 60 who have had limited or no estrogen replacement
therapy at menopause are the major high-risk group. Asthmatics or other lung
patients, or rheumatoid arthritis patients treated with high-dose
corticosteroids, lose trabecular bone and experience fractures, as do patients
with Cushing's Syndrome. Other disorders including renal failure and certain
types of cancer cause bone loss, along with chronic use of drugs such as
anticonvulsants, anticoagulants, excess alcohol, and too much thyroid medication.
Young women who experience amenorrhea due to athletic activity, weight loss,
stress, or the nutritional deficiency of bulimia or anorexia nervosa lose bone;
so do young women who have an early natural or surgical menopause and are not
given estrogen replacement therapy. Not all of the patients in all of these
groups will develop osteoporosis; however, they will all lose bone more rapidly
than otherwise and be at increased risk for the development of osteoporosis over
the long run.
Why do we measure bone density?
Over seventy percent of people at risk for development of osteoporosis and it's
associated fractures have a low bone density as measured quantitatively using
SXA, DEXA, QCT, or ultrasound. The other factors contributing to bone strength
are varied, including the internal structure of bone, level of physical activity,
neuromuscular coordination, and lifestyle factors that are difficult to quantify.
Because of this, bone density is the single most useful measurement in
estimating an individual patient's relative risk for osteoporosis and associated
fractures. Identifying patients with low bone density early, before fractures
develop enables your physician to prescribe treatments that will stop and
reverse the process of bone loss.
How do we measure bone density?
All commercially available methods for bone density measurement pass a
low-intensity beam of X-rays or gamma-rays through a patient, and a radiation
detector on the other side measures how much of the beam is absorbed. Part of
the beam is absorbed by the bone and part by the surrounding soft tissue, and
each technique measures these differently. Quantitative Computed Tomography (QCT)
provides a cross-sectional or 3-dimensional image from which the bone is
measured directly, independent of the surrounding soft tissue. Dual energy X-ray
absorptiometry (DEXA) measures the bone by computing the difference in
absorption of low-energy photons and high-energy photons by the mixture of soft
tissue and bone in the path of the beam, and can generate a 2-dimensional image
for localization of the bone. Single energy X-ray absorptiometry (SXA) computes
bone mineral from the increased absorption of the beam as it passes from a
constant thickness of soft tissue or water bag into the bone. Localization for
SXA is normally done using external landmarks without an image. Radiographic
absorptiometry (RA) measures bone density in the fingers relative to an
aluminium calibration wedge on the film. Non-absorptiometric methods such as
ultrasound of bone do not measure bone density directly, but give alternative
information about properties of bone such as the speed of sound that are related
to bone density and structure.
What is quantitative computed tomography (QCT)?
QCT refers to a class of techniques in which the CT numbers, or X-ray
attenuation of a tissue is properly referenced to a calibration standard and
then used to quantify some property of the tissue. Techniques were developed and
published from 1978 to 1982 for bone mineral density, lung nodule calcification,
liver and brain tumor volumes, body fat measurement, muscle mass, liver iron
measurement, kidney stone composition, and tissue blood flow. Of these, bone
mineral density, lung nodule calcification, and tissue blood flow have been
commercialized.
How does 3-D QCT compare to DEXA or SXA?
QCT is the only commercially available technique that is 3-dimensional, meaning
it can be used to measure 100% isolated trabecular bone. All other techniques
measure a mixture of both trabecular bone and the overlying compact bone. There
are two bone compartments; trabecular bone is located deeper inside the bone is
the more metabolically active bone compartment. Compact bone is the bone near
the surface of the bone. In the spine, trabecular bone makes up 30 to 35% of the
total, in the ultradistal radius (wrist) it is 35 to 50%. Bone mineral loss
affects the trabecular bone first and that is why the trabecular bone in the
spine is considered the most reliable indicator of overall bone health. By
focusing only on the trabecular bone compartment, 3-D QCT takes the best picture
of bone health.
It is also important to consider the precision of any measurement of bone
density. QCT is the most accurate tool to measure bone density. In terms of the
ability to pick up bone disease, 3-D QCT is 2-3 times more sensitive than DEXA
and 5 times more sensitive than SXA for detecting bone disease.
How do we interpret QCT results?
Bone densitometry results are reported in standard deviation (SD) as
T-scores and Z-scores, both of which determine the difference between an
individual’s bone mineral density (BMD) with a population mean. The T-score
references a young healthy population of the same sex whereas the Z-score
population standard is adjusted to match the patient age. A low T-score is a
measure of future fracture risk, since this risk is due to absolute bone loss. A
low Z-score indicates that the patient’s BMD is worse than others of the same
age. If so, an evaluation for a secondary cause of osteoporosis may be
indicated.
The World Health Organization has defined the following categories based on bone
density in white women:
Normal bone: T-score better than -1.
Osteopenia: T-score between -1 and -2.5
Osteoporosis: T-score less than -2.5
Established (severe) osteoporosis includes the presence of a non-traumatic
fracture.
The WHO committee did not have enough data to create definitions for men or
other ethnic groups.
QCT, like any bone density measurement, is used to compare an individual's bone
to an absolute reference value, and to measure any change in the individual's
bone density over time. Medical researchers have established a fracture
threshold level for all bone density methods; people whose bone density is above
this threshold level rarely develop osteoporotic fractures, while below it the
prevalence of fractures rises. This level is about 100-110 mg/cm3 for QCT. As
the value decreases below this the fracture prevalence increases, so that below
50 mg/cm3 most people already have spinal fractures. Your QCT value, when added
to other diagnostic information, is used by your physician to determine you
treatment. Serial QCT measurements can establish the rate of change of bone
mineral density in both treated and untreated patients. In most cases, a decline
of 8-10 mg/cm3 is considered significant and several serial
measurements all changing the same direction improve our confidence in the
result. Women within 1-3 years after menopause average 7 mg/cm3/yr
loss, so yearly measurements can be helpful. Bone loss may be slower in older
individuals. The frequency for each patient will depend on other diagnostic and
treatment factors, and it is important that your doctor interpret your bone
density results within the context of your clinical status.
Last updated:
06-06-2006 Copyright 2006 © Dziednieciba Ltd All rights reserved |