Running Head: BONE DENSITY
Testing
Bone Density Variables and the Results
Alicia
Hull
East
Tennessee State University
Abstract
This
study is researching the facts about food and bone metabolism. The affects of
vitamins and minerals have been tested and have proved that these supplements
do affect the bone density results on a densitometry scan. However, there are
underlying factors, such as food, that may also change the results of the bone
density scan. The purpose of this study is to further the knowledge of how the
bone metabolizes nutrients, and to gain more information on bone density
disorders. Since there are so many bone density abnormalities, the study would
only be using a few select disorders to test the food variables. Hopefully the
results of this study will inform not only the physicians, but also the
patients about the affects food may or may not cause on bone density. The main
questions guiding this research are:
·
Could
eating before a bone density scan affect the results?
·
How
does food affect bone density?
·
Do
certain foods affect bone density differently?
Acknowledgements
This
research study may not appear too fancy, but the results could change the
results of how patients with bone density disorders are diagnosed. Though I
have learned plenty through researching for this study, there is still more
information on these subjects that I have not learned about. In this paper I
would like to acknowledge my family and friends who have helped and pushed me
through this project. Without their support, I do not know how I would have
done this research project. Now that the semester is almost over, I am glad to
say I’ll be free of stressful classes until next fall!
Chapter I Introduction
BACKGROUND
Bone
Density
Bone density
tests are usually performed on women ages 60-65, to measure the mineral and
calcium percentage of their bones. If bones lack calcium they are more likely
to fracture. Bone density tests also test to indicate the extent of
osteoporosis. Osteoporosis is a disease that affects the bone density and
causes the bones to become more likely to break. In an article about bone
density tests. “Today, a bone density test, also called a densitometry or DEXA
scan, can determine if you have osteoporosis or are at risk for osteoporosis
before you break any bones” (Mayo Clinic, 2008, p. 1). Patients at risk for
osteoporosis are not just middle age women, but also include those with eating
disorders can also suffer from osteoporosis.
There are
many different types of machines that measure bone density on the patient. A
dual energy x-ray absorptiometry (DEXA) method is used on patients mainly when
testing the spine, hip, or entire body. The DEXA method is the most commonly
used technique. A peripheral energy x-ray absorptiometry (PDXA) tests the
peripheral bone density on a skeleton. Specifically, this tests the heel,
wrist, or finger for the bone content. A single energy x-ray absorptiometry
(SXA) is usually used to test the bone density in the patient’s wrist and heel.
The single photon absorptiometry (SPA) is used only when testing the bone
content in the wrist. The dual photon absorptiometry (DPA), like the DEXA
method, measures the bone density of the hip, spine, or the whole body.
However, the SPA and DPA are not used very frequently. A quantitative computed
tomography (QCT) can be used to measure the bone density of the entire body, or
just the spine. Unfortunately, when using the QCT the patient is exposed to a
significantly higher amount of radiation than normal. Normal radiation on a patient is about 0.005 of an entire
radiation wave. Usually the QCT method is not used repeatedly on the same
patient nor is it used on the patients of childbearing age. The radiographic
absorptiometry (RA) method is used specifically when measuring the bone density
of the entire hand. A RA uses a special x-ray technique in order to calculate
the bone density (Optum Health, 2008).
PURPOSE
Study
of Bone Density Tests
The purpose
of this study is to determine if eating before a bone density test could affect
the test’s results? For example, patients who have taken calcium pills before a
densitometry exam, the results can change. Most physicians ask the patient to
stop taking any calcium supplements 24 hours before the day of the patient’s
densitometry exam. Also, having an exam that involves ingesting barium, such as
a CT Scan prior to a bone density test can affect the results of a bone density
test. Patients undergoing procedures using barium may have to wait 10-14 days
before a bone density exam. When a person eats, part of the fat, calcium, and
other minerals are absorbed into the bones. Considering calcium pills affect
the results of a densitometry exam, why would eating not affect the outcome of
the test? Franklin Memorial Hospital requires that patients, “Please do not
take any calcium pills (including TUMS) or multivitamins for 24 hours leading
up to the time of the exam. We will not be able to do your exam if you have
taken these pills”; however the website also reads, “You can eat normally
before the exam- it will not interfere with the results” (Franklin Memorial
Hospital, n.d., p.1). These statements tend to contradict each other.
SIGNIFICANCE
Affects
of Food
If eating
before a bone density test does affect the results, then physicians,
technicians, and the patients need to be aware of this. Since there are other
factors, such as multivitamins, could affect the results, it makes sense that
food would also. Finding out about the affects of ingesting food before one of
these exams, would give the patients and doctors a timeline of when the patient
could and could not eat before an exam. The results of this research could
change how patients prepare for a densitometry exam. This would include not
eating for a certain time period before a densitometry exam, or only eating
certain foods before.
RESEARCH QUESTION
Affects
on Bone Density Test
A single
question guided this research: Would food affect the results of a bone density
test? The research question in simpler terms is would foods ingested in a
normal diet affect the results. If the results indicate that such foods do, a
logical follow-up question would be, what type of foods could affect the
results of a bone density test? Testing the impact of different types of foods
on densitometry results, (for example, foods with a high fat content, foods
enriched with vitamins, foods containing calcium, or foods that are considered healthy) is important to the study. Healthy foods would be fruits and
vegetables. Another question that could guide this research: Why does food not
affect the results of a bone density test? The researcher needs to take into
consideration the patient’s diet, for example, if the patient is at a healthy
weight, or if the patient is overweight.
ASSUMPTIONS
Machines
and Methods
This study
makes the following assumptions:
1. Densitometry machines used to
collect
data are working properly.
2. The correct densitometry method
is used.
LIMITATIONS
Patients
This study
is limited to patients in Tennessee and studies performed during the months of
August through December of 2008. Having a good selection of patients to
participate in the study is important since every patient is different.
Considering not all of the patients who are going to get a bone density scan
have osteoporosis, each patient will most likely be tested in different parts
of the body. For example, every patient will not have his or her heel’s bone
density tested. This also means, that there will be different methods used on
the patients. As discussed earlier, there are different methods used on
patients depending on where the technicians are examining the bone
density. It could be important
that all of the patients used in the study are around the same weight; since,
weight could be a factor in affecting the results of a bone density test.
Chapter
II Literature Review
LITERATURE
Bone
Density
Bones are
the structure of the human body, without correct formation or growth,
abnormalities or disorders can occur. Jowsey (1977) detailed, “Disease implies
pain and discomfort. In metabolic bone disorders, it implies that a fracture of
deformity of the bone has occurred to cause the subsequent pain and discomfort”
(p.161). Bone density scans are one of the many tools to detect an abnormality.
Whalen (1978) wrote, “Before abnormality of a structure can be appreciated, an
understanding of the mechanism by which bone grows is required” (p.1). Examples
of bone abnormalities or diseases would be osteoporosis, osteopetosis, and osteogenesis
imperfecta (Whalen 1978, p. 31). Forming, modeling, remodeling, absorb, are all
common terms when diagnosing a bone disorder. Simon and Krane (1983) explained
these steps as:
“Bone
is a dynamic organ continually
remodeled during life through complex process of organized cellular activity.
Remodeling is initiated by osteoclasts which resorb old bone and is followed by
deposition of new bone by osteoblasts. Resorption and formation are tightly
coupled in the normal state so that the mass old the bone does not change.
(p.108)
Jowsey (1977) wrote, “…most
metabolic bone disease is diagnosed as a result of the fracture, frequently
many years after the bone disorder has been in existence and causing bone loss”
(p.162). Some bone disorders can be treated with special diets. Most physicians
require a patient who is receiving a bone scan to stop taking minerals or
vitamins 24 hours before the exam (RadiologyInfo, n.d.), because these could
change the density of bones. Therefore, food should affect the results of a
bone density scan as well.
DISORDERS
Bone
Abnormalities
Whalen
(1978) described one of the bone abnormalities as, “Osteopetrosis is a disease
of universal failure of modeling” (p.31). This bone abnormality can be detected
through bone scans. Depending on where the bone issue is depends on the type of
scan used to read the bones. Bone density scans measure bone loss
(RadiologyInfo, n.d.). Another reason for bone loss is called age related. Age
related bone loss is not a disease, but it is still considered an abnormality.
As people get older, the bones in the human body deteriorate. Abnormalities are
detected with an x-ray machine with different levels of ionizing radiation.
A
common abnormality in bone density is osteoporosis (Johnston, 1983, p.317) and
Mohan (1983) agreed with this statement, “Osteoporosis, which affects one
fourth of North American postmenopausal women, is characterized by accelerated
net loss of bone mass which results in increased susceptibility to fractures”
(p.173). Siegelman (1987) provided further information on osteoporosis with, “Osteoporosis
is a common skeletal
condition characterized dynamically
by a significant period in which bone resorption exceeds bone production; physically
by a reduction of calcified
bone mass per unit volume of bone…” (p.153). Gallagher (1983) tested, “Two
major studies have reported that a large proportion of patients with
osteoporosis have impaired calcium absorption. In about one third of patients
the absorption problem is so marked that the fecal calcium exceeds the calcium
intake” (p.364). There are different levels of osteoporosis, such as,
osteoporosis, juvenile osteoporosis, post-menopausal osteoporosis, and severe
osteoporosis. Each level of osteoporosis has different effects on the body.
When Siegleman (1978) wrote, “Severe osteoporosis produces compression
deformities of the spine, but there is a phase of the disorder characterized by
alterations without deformity (p.154-155), he meant that there are cases of
osteoporosis when the patient’s spine does not curve. In concerning the mineral
content due to osteoporosis, Reeve (1983) study read, “We have recently shown
that in osteoporosis, calculated rates of whole body bone formation correlated
significantly with calcium balance data when corrected for ‘long-term’ exchange
but not when calculated without this correlation” (p.100). The correlation that
Reeve mentioned was about the tetracycline labeled osteoid surfaces and
unlabeled osteoid. Mohan (1983) also referred to another correlation:
We have proposed
that the failure of bone
formation to balance bone resorption in osteoporosis {thus resulting in net
bone loss} may be due to a progressive defect in coupling – a regulatory
mechanism by which bone formation is stimulated in proportion to bone
resorption (p.173).
BONE
DENSITY
Test
Methods
Measuring
bone density is done with a few different methods, depending on where in the
body the physicians are testing. Examples of different methods are single
energy x-ray transmission method, dual energy transmission method (DEXA),
computed tomography (CT or QCT), and scattered photon techniques (Joseph, 1978,
p.177-179). Joseph (1978) applied
his knowledge about bone density testing with, “It has become apparent that a
method for accurately measuring the mineral content of bodes in vivo is of
crucial importance for diagnosing and managing many types of metabolic bone
diseases” (p.175). Compared
between QCT and DEXA, “The potential advantage of QCT over dual photon
absorptiometry is its capability for precise 3-dimensional anatomic
localization and for spatial separation of highly responsive cancellous bone
from less responsive cortical bone” (Genant, 1983, p.40) described only one of
the differences among all of the bone density scans. The DEXA method is non
invasive and explained by a, “Measurement of bone mineral of the lumbar spine
by dual photon absorptiometry is a routine clinical test as well as a research
tool” (Wahner, 1983, p.34). Along with the different measuring methods, only
certain methods can measure specific bones.
VITAMINS
Breakdown
of Bone
Minerals,
vitamins, and hormones are needed in the bones, such as calcium, calcitonin,
cortisol, and vitamin D. Bones absorb and reabsorb minerals and vitamins that
come from the plasma. With skeletal homeostasis, Rasmussen (1983) suggested,
“For example, it is clear that the process of bone mineralization can take
place normally when the plasma calcium concentration is as low as 5 mg/dL or as
high as 15 mg/dL” (p.83). Vitamin D was mentioned as, “Traditional views of the
action of vitamin D are that this agent has two major physiological effects: it
increases mineral ion absorption in the intestine, and it increases the
resorption of mineral ions from bone” (Rasmussen, 1983, p.85). Since vitamin D
plays such a large role in resorption, it is also explained, “… vitamin D
increases bone growth, bone mass, and mineralization by some direct effect on
the formation-mineralization side of bone modeling and bone remodeling”
(Rasmussen, 1983, p.85). Calcium affects the growth with structural metabolic,
and Lanyon (1983) suggests, “’Metabolic remodeling’ is required to provide a
supply of mineral to maintain serum Ca” (p.183). An additional factor in bone
remodeling is, “Hormones are known to influence the number of remodeling sites,
and perhaps the rate of remodeling as well… The major stimulators of resorption
are parathyroid hormone and…vitamin D3, and the major inhibitor is calcitonin,
although cortisol may act as a resorption inhibitor at physiological concentrations”
(Peck, 1983, p.179).
The
formation of bones has many detailed steps, Krane (1983) described one of the
steps, “In the process of bone formation, mineral ions enter the inorganic
phase; these ions are then removed in the process of bone resorption” (p.96).
Bones have many stages to go through, and, “Remodeling has received
considerable attention because it becomes abnormal in most metabolic bone
disorders. Efforts have been directed towards measuring rates of new bone
formation and resorption, both locally in the skeleton as a whole” (Reeve, 1983,
p.99). Having bones formed with
the correct sequence is necessary, and Peck (1983) writes it best as, “Of
particular importance in the remodeling scenario are the factors that might
link resorption and formation” (p.180). Another fact about bone remodeling that
Parfitt (1983) suggested, “According to the quantum concept of bone remodeling
proposed by Frost, bone formation in the adult human normally occurs only at
sites where bone resorption has recently been completed” (p.171). Referring
to bone loss due to age, “It
is obvious that for bone loss to occur the rate of total body bone resorption
must exceed the rate of total body bone formation. In terms of the quantum
concept, this imbalance must be focal and must apply to the average remodeling
cycle on nay surface that is losing bone” (Parfitt, 1983, p.328).
Sometime
between the ages of 30 and 40 human bone mass reaches its’ peak, and after that
bone mass decreases with age (Heaney, 1983, p.333). With age related bone loss,
“The decline is particularly rapid in women in the 5-15 years following
menopause. Reduction in bone mass comes about through bone remodeling…”
(Heaney, 1983, p.333). “Osteoclasts are responsible for the following two major
functions: {1} the remodeling of bone to form the adult skeleton in conjunction
with osteoblasts, and {2} the maintenance of serum calcium under the control of
parathyroid hormone” (Jowsey, 1977, p.74).
Dietary
histories pertaining to metabolism needs to have an average for the intake of
phosphorus and calcium (Jowsey, 1977, p.87). Jowsey (1977) also writes, “… also
some evaluation of other substances that affect mineral metabolism, such as
vitamin D intake and exposure to the sun” (p.87). Dairy products and leafy vegetables
contain calcium (Jowsey, 1977, p.87), and usually these products are in a
human’s daily diet. When concerning the mineral calcium, “The recommended
calcium intake is 800 mg per day for an adult” (Jowsey, 1977, p.89). Jowsey
(1977) suggests, “Calcium balance generally reflects bone metabolism. In general,
a positive balance represents an increase in bone mass, whereas negative
balance implies a loss of bone tissue” (p.90).
HISTORY
Diagnosis
All of the
mentioned bone abnormalities are measured with some form of radiography. Also,
fractures in bone disorders usually help bring the physician’s attention to the
bone, and can also lead to diagnosing a bone disorder. Levels of minerals,
vitamins, and hormones affect the bone density by resorbtion and bone
formation. Lack of or in excess of these factors, will lead to abnormalities in
the bones. In some instances, one bone disease can lead to another, “Since the
majority of patients with rickets or osteomalacia have developed a
mineralization failure as a result of a lack of adequate levels of calcium in the
serum, stimulation of the parathyroid glands must be expected. This can occur
before, during, or after the development of osteomalacia” (Jowsey, 1977,
p.192). Bone abnormalities are not difficult to diagnose; however, the intake
of food does affect bone density as mentioned earlier, but somehow physicians
still claim it is fine to eat before a bone density scan (RadiologyInfo, n.d.).
For every
research project, there is a different method that suits the research data
best. The two main categories of research designs are qualitative and
quantitative methods. Qualitative deals mostly with groups and categories,
while quantitative covers the numerical data or ratio. Under both qualitative
and quantitative methods, there are different types of studies that a researcher
can use. Qualitative method is best explained as, “The Discovery of Grounded Theory, qualitative researchers have been
debating whether the purpose of qualitative research should be to develop new
theory, verify existing theory, or both” (Bailey, 1997 p. 134).
Chapter III Research Method
COLLECTING
DATA
Techniques
Bailey
(1997) wrote, “Sometimes the research method dictates data collection
techniques” (p. 94). Different techniques to gather data are observation,
interview, written questionnaire, record and artifact review, hardware
instrumentation, test, measures, and inventories. For some collecting data
techniques there are a qualitative and a quantitative method. Observations
could consist of, “…human subjects, videotape recordings of subjects or events,
or nonhuman items such as pieces of equipment” (Bailey, 1997 p. 94-95). When
using qualitative observations, “The researcher keeps field notes of everything
observed that might be remotely useful in the study, such as the environment,
the participants’ appearance and manner, routines, unusual events, human
groupings at specific times, and so on” (Bailey, 1997 p. 95). Bailey’s (1997)
description of record and artifact review was, “Review of written records may
be a means of data gathering in many types of research, including experimental,
ethnographic, historical, and case study designs” (p.101). Examples of some of
the written documents the researcher reviews are medical records, case
conferences, letters, speeches, articles, books, notes, newsletters, and
newspapers (Bailey, 1997 p.101). For another data collection method, hardware
instrumentation is described as, “Physical or mechanical instruments that
provide a valid and reliable measurement are usually more desirable in
experimental research than the subjective feedback given by subjects” (Bailey,
1997 p.101-102). This type of data collection would be used for experiments or
variables that cannot be measured or seen without technical support. Tests,
measures, and inventories test the “Variables that can be measured be these
written means include psychological factors, cognitive abilities, perceptual
motor skills, child development stages, prevocational skills, vocational
interests, personality factors, attitudes, and values” (Bailey, 1997 p. 102).
When collecting data, there are many different methods, but Bailey (1997)
points out, “In summarizing and interpreting the data gathered, the researcher
must use logical analysis and try to be as objective as possible” (p.101).
Collecting useful data is important for the research, and these methods are
just a few of the techniques to do so.
RESEARCH
METHOD
Qualitative
For
researching if eating before a bone density scan could affect the results, the
qualitative research design is the most appropriate. The issue with bone
density scans is there are limitations to the patient. For example, before the
patient has a bone density scan, he or she cannot take calcium pills or
vitamins, because those could affect the results of the scan. There have been
studies done that prove these pills affect the bone density results. Food
consists of some of the same ingredients in the calcium pills and vitamins. So,
in theory, food should also affect the results of a bone density scan. For this
research study, a case method research design fits the criteria. The case
method research design is, “…studying an individual person, program, or
institution” (Bailey, 1997 p. 138). The subject needs to have a bone density
disease, such as osteoporosis, in order to be useful in the study.
DATA
Validity
The
data collected from the patients needs to be precise and valid, or else the
research is useless. Two methods would be helpful with this research study such
as record artifact review and hardware instrumentation. The record artifact
review gives the medical history of the subject. Medical history is important
for the researcher to be familiar with, because the subject will need to have a
bone density disorder. Also, the researcher will need to know information about
metabolism in the bones to know what types of food can affect the bone density.
The hardware instrumentation is necessary in order to do the DEXA exam. Since
there are a few different exams to perform on each part of the skeleton
depending on where there is low density, will depend on what type of exam is
used.
ANALYZING
Organizing
the data
The
next step after testing and collecting the data is analyzing the information
gathered. Bailey (1997) explains, “These types of studies often generate large
amounts of descriptive, nonquantifiable data that need to be organized and
synthesized in a useful manner” (p. 158). The types of studies Bailey is
referring to are the methods used for collecting data in qualitative research,
and “The style of qualitative research and data analysis method you choose will
depend on whether your ultimate goal is to inform policy, describe situations
in a novel manner, or generate theory” (Bailey, 1997 p. 159). There is a
process to analyze the data collected. First the researcher must organize and
describe the data. Bailey (1997) gives tips for the researcher organize the
data:
First organize
the data by reading
through and making sure that they are all present, filling in any gaps by
returning to the field, if necessary. Get a feel for how much data there are,
including transcriptions of interviews, field notes from observations, memos to
yourself, formal documents, descriptions of artifacts, and son on. (p.159)
Reading the documents several
times will help with indexing the data completely (Bailey, 1997 p.160). Reading
all of the data collected after testing the bone density on patients, the data
will be clearer and will make analyzing the data easier. The documents that
need to be reviewed are the field notes from observation and the subject’s medical
history. Bailey (1997) mentions that instead of writing notes in the margins of
the documents that the researcher can also write on index cards. (p. 160) The
descriptions of the index cards is:
The back of
each index card should be
coded in multiple ways: the source of the information (e.g., interview
transcription, treatment plan, observation notes) by page and paragraph number;
the particular episode during which the information was collected (e.g.,
interview with rehabilitation director, team meeting); the type of respondent
(e.g., staff person, administrator); the site where the information was
gathered (e.g., school classroom, rehabilitation clinic, supervisor’s office).
(Bailey, 1997 p. 160).
After organizing and coding
the information from the data collection, the index cards must be categorized
into different sets of information. (Bailey, 1997 p. 160) Another method for
gathering the data collected is a data display, and Bailey (1997) quotes Miles
and Huberman (1994), “Data display is an organized compressed assembly of
information that permits conclusion drawing and action… Looking at displays
helps us to understand what is happening and to do something- either analyze
further or take action- based on that understanding” (p.168). Using displays to
graph the difference, if any, between eating and not eating before a bone
density scan, will be easy to read and draw a conclusion from. Along with
drawing a conclusion from the data collected, the conclusion must be verified,
and “Verification may be as brief as a quick recheck of the data to confirm a
current idea, or as lengthy as a thorough review of data among colleagues or an
attempt to replicate a finding in another data set” (Bailey, 1997 p.169).
Verifying the data for this research project would include going over the
documents to make sure nothing was missed or misinterpreted. All of these steps
will conclude in finding answers to the research if eating before a bone
density scan affects the results.
References
Bailey, Diana M. (1997).
Research for the Health Professional A Practical Guide. In Lynn
Borders Caldwell (Ed.), Analyze
Qualitative Data (pp. 158- 179). Philadelphia,
PA: F. A. Davis Company.
Bailey, Diana M. (1997).
Research for the Health Professional A Practical Guide. In Lynn
Borders Caldwell (Ed.), Data Collection
Techniques (pp. 94- 111). Philadelphia,
PA: F. A. Davis Company.
Bailey, Diana M. (1997).
Research for the Health Professional A Practical Guide. In Lynn
Borders Caldwell (Ed.), Qualitative
Research Designs (pp. 134- 152). Philadelphia,
PA: F. A. Davis Company
Franklin Memorial Hospital
(n.d.). DEXA. Retrieved February 22,
2009 from http://www.fchn.org/fmh/advanced-technology/dexa.
Genant, Harry K. M.D.,
Christopher K. Cann, Douglas P. Boyd, Felix O. Kolb, Bruce Ettinger,
Gilbert S. Gordan (1983). Quantitative Computed Tomography for Vertebral
Mineral Determination. In Boy Frame & John T. Potts Jr. (Eds.), Clinical Disorders of Bone and Mineral
Metabolism (p.40-47). BC, Amsterdam: Elsevier
Science Publishers.
Gonter, Neil MD. (2007,
November 14). OsteoporosisConnection.com. The
Problem with the
Bone Density Test: DEXA Scans, Bone Density, and Fracture Risk. Retrieved February
22, 2009 from http://www.healthcentral.com/osteoporosis/c/73/16405/problem-bone- density-test-dxa-scans.
Heaney, Robert P. (1983).
Determinants of Age-Related Bone Loss. In Boy Frame & John
T. Potts Jr. (Eds.), Clinical Disorders
of Bone and Mineral Metabolism (p.333-336).
BC, Amsterdam: Elsevier Science Publishers.
Jowsey, Jenifer, D. Phil.
(1977). Bone Morphology: Bone Cells. In Clement B. Sledge, M.D.
(Ed.), Metabolic Diseases of Bone: Vol. 1
Saunders Monographs in Clinical Orthopaedics
(p. 58-77). Philadelphia, PA: W. B. Saunders Company.
Jowsey, Jenifer, D. Phil.
(1977). Calcium Balance. In Clement B. Sledge, M.D. (Ed.), Metabolic Diseases of Bone: Vol. 1 Saunders
Monographs in Clinical Orthopaedics
(p.87-95). Philadelphia, PA: W. B. Saunders Company.
Jowsey, Jenifer, D. Phil.
(1977). Metabolic Bone Disease. In Clement B. Sledge, M.D. (Ed.),
Metabolic Diseases of Bone: Vol. 1
Saunders Monographs in Clinical Orthopaedics
(p.161-162). Philadelphia, PA: W. B. Saunders Company. Krane, Stephen
M. (1983). Assessment of Mineral and Matrix Turnover. In Boy Frame & John
T. Potts Jr. (Eds.), Clinical Disorders
of Bone and Mineral Metabolism (p.95-98).
BC, Amsterdam: Elsevier Science Publishers.
Lanyon, Lance E., Clinton T.
Rubin (1983). Functional Load Bearing as a Determinant for
Bone Remodelling. In Boy Frame & John T. Potts Jr. (Eds.), Clinical Disorders
of Bone and Mineral Metabolism (p.183-186). BC, Amsterdam: Elsevier
Science Publishers.
Mayo Clinic Staff (2008, July
1). Osteoporosis. Bone Density Test.
Retrieved February 22,
2009 from http://www.mayoclinic.com/health/bone-density- test/MY00304.
Mohan, Subburaman, John R.
Farley, Thomas A. Linkhart, Lee A. Murphy, David J. Baylink
(1983). Studies on Human Skeletal Growth Factor: Interaction with Known
Mitogens and Calcium Regulating Hormones. In Boy Frame & John T. Potts
Jr. (Eds.), Clinical Disorders of Bone
and Mineral Metabolism (p. 173-178).
BC, Amsterdam: Elsevier Science Publishers.
Optum Health (2008, July 11).
MyOptumHealth.com. Bone Mineral Density. Retrieved February
22, 2009 from http://www.myoptumhealth.com/portal/Information/item/Bone+Mineral+Density ?archiveChannel=Home%2FArticle&clicked=true.
Parfitt, A. M. (1983). Recent
Developments in Bone Physiology- Introduction. In Boy Frame
& John T. Potts Jr. (Eds.), Clinical
Disorders of Bone and Mineral Metabolism
(p.171-172). BC, Amsterdam: Elsevier Science Publishers.
Parfitt, A. M., C. H. E.
Mathews, A. R. Villanueva, D. S. Rao, M. Rogers, M.Kleerekoper,
B. Frame (1983). Microstructural and Cellular Basis of Age Related
Bone Loss and Osteoporosis. In Boy Frame & John T. Potts Jr. (Eds.), Clinical Disorders of Bone and Mineral
Metabolism (p. 328-332). BC, Amsterdam:
Elsevier Science Publishers.
Peck, W. A., Victor Shen,
Leonard Rifas (1983). Locally Elaborated Factors in the Coordination
of Bone Cell Activity. In Boy Frame & John T. Potts Jr. (Eds.), Clinical Disorders of Bone and Mineral
Metabolism (p.179-182). BC, Amsterdam:
Elsevier Science Publishers.
Peter, Joseph M. Ph.D.
(1978). Bone Mineral Determinations: Methods and Techniques
to Date. In Frieda Feldman M.D. (Ed.), Radiology,
Pathology, and Immunology
of Bones and Joints: A Review of Current Concepts (p.175- 182). New
York, NY: Appleton-Century-Crofts.
Prick, Marcelle OB/GYN NP.
(2009, February 19). Bone Health. Bone
Mineral Testing and
Bone Scan Results. Retrieved February 22, 2009 from http://womentowomen.com/bonehealth/bonemineraldensitytests.aspx.
RadiologyInfo the radiology
information resource for patients. (2008). Bone
Density Scan.
Retrieved March 5, 2009, from http://www.radiologyinfo.org/en/info.cfm?pg=DEXA.
Rasmussen, Howard (1983). The
Role of 1.25(OH)2D3 in the Pathogenesis of Osteomalacia.
In Boy Frame & John T. Potts Jr. (Eds.), Clinical Disorders of Bone
and Mineral Metabolism (p.82-89). BC, Amsterdam: Elsevier Science Publishers.
Reeve, Jonathan, Monique
Arlot, Richard Hesp, Marisol Tellez, Pierre J. Meunier (1983). Tracer
Measurements of Bone Remodelling and their Significance in Involutional Osteoporosis.
In Boy Frame & John T. Potts Jr. (Eds.), Clinical Disorders of Bone and
Mineral Metabolism (p.99-104). BC, Amsterdam: Elsevier Science Publishers.
St. Joseph’s Healthcare
System (n.d.). St. Joseph’s Healthcare System. DEXA. Retrieved February
22, 2009 from http://stjosephshealth.org/index.php/index.pehp?option=com_content&view=article&idmid=2928.
Siegelman, Stanley S. M.D.
(1978). Osteoporosis, Osteomalacia, and Hyperparathyroidism.
In Frieda Feldman M.D. (Ed.), Radiology,
Pathology, and
Immunology of Bones and Joints: A Review of Current Concepts (p.153-169).
New York, NY: Appleton-Century-Crofts.
Simon, Lee S., Stephen M.
Krane (1983). Procollagen Extension Peptides as Makers of
Collagen Synthesis. In Boy Frame & John T. Potts Jr. (Eds.),
Clinical Disorders
of Bone and Mineral Metabolism (p. 108-111). BC, Amsterdam: Elsevier
Science Publishers.
Wahner, Heinz W., William L.
Dunn, Kenneth P. Offord, B. Lawrence Riggs (1983). Dual
Photon Absorptiometry: Clinical Considerations. In Boy Frame & John
T. Potts
Jr. (Eds.), Clinical Disorders of Bone
and Mineral Metabolism (p.34- 39). BC,
Amsterdam: Elsevier Science Publishers.
Whalen, Joseph P. M.D.
(1978). Abnormal Structure, Modeling, and Density of Bone. In
Frieda Feldman M.D. (Ed.), Radiology, Pathology,
and Immunology of Bones and
Joints: A Review of Current Concepts (p.1-6). New York, NY: Appleton-Century-Crofts.
Whalen, Joseph P. M.D.
(1978). Skeletal Dysplasias: Osteogenesis Imperfetca, Osteopetrosis,
Hyperphosphatasemia. In Frieda Feldman M.D. (Ed.), Radiology, Pathology, and Immunology of
Bones and Joints: A Review of Current
Concepts (p. 31-32). New York, NY: Appleton-Century-Crofts.