Validation of dental X-ray by cytokine RANTES – comparison of X-ray findings with cytokine overexpression in jawbone
Clinical, Cosmetic and Investigational Dentistry
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Validation of dental X-ray by cytokine
RANTES – comparison of X-ray findings
with cytokine overexpression in jawbone
This article was published in the following Dove Press journal:
Clinical, Cosmetic and Investigational Dentistry
21 August 2014
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Johann Lechner
Clinic for Integrative Dentistry,
Munich, Germany
Introduction
All X-ray findings of the jawbone are obtained by means of an optical and visual assessment by the observer. The risk of subjective distortion of the assessment is large, and it
generally diminishes with the establishment of reliable criteria of a scientifically objectified procedure. Fatty degenerative osteolytic or chronically osteonecrotic changes
of jawbone (FDOJ) seem to present particular problems in dental X-ray diagnostics,
which is why they often go undetected in terms of etiology and pathogenesis.1 Undetected FDOJ might also be a problem for the long-term stability of dental implants.2
By comparing X-ray findings with the corresponding expression of proinflammatory
mediator regulated on activation, normal T-cell expressed and secreted (RANTES)/C-C
motif ligand 5 (CCL5) in the same area of jawbone, this study tries to elucidate whether
important silent inflammation in the jawbone remains undetected.
Correspondence: Johann Lechner
Clinic for Complementary Dentistry,
10A Gruenwalder St, 81547 Munich,
Germany
Tel +49 89 697 0055
Fax +49 89 692 5830
Email
Limitations of X-ray diagnostics in dentistry
The limitations of two-dimensional panoramic tomography (2D-OPG) have been sufficiently proven scientifically: apical changes cannot be reliably assessed in 2D-OPG;
and 34% of these changes are not detected. One-third to one-half of all 2D-OPG
images are therefore not sufficiently informative for dental diagnostics.3 ln dentistry,
71
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http://dx.doi.org/10.2147/CCIDE.S69807
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Introduction: There is a need to clarify the extent to which the most common diagnostic tool
in dentistry – two-dimensional panoramic tomography (2D-OPG) – is suitable for identifying
fatty degenerative osteolysis of jawbone (FDOJ).
Materials and methods: To obtain a qualitative assessment of edentulous jawbone sections,
the results from 2D-OPG with a defined X-ray density (XrDn), expression of the cytokine
RANTES (regulated on activation, normal T-cell expressed and secreted), and a transalveolar
ultrasound system for measuring jawbone density were compared.
Results: The difference in the XrDn of healthy jawbone and FDOJ are minimal, whereas
RANTES is up to 25-fold higher in FDOJ. In contrast to 2D-OPG, transalveolar ultrasound
showed coincidental findings in FDOJ areas.
Discussion: Comparisons of the data revealed a discrepancy between the XrDn of 2D-OPGs
and the medullary osteopathies in the jawbone like FDOJ.
Conclusion: The data suggest that there is a critical attitude toward the use of 2D-OPG as
a sole imaging diagnostic tool for assessing chronic inflammatory processes in the jawbone.
Specifically, 2D-OPG is objectively not suitable for depicting FDOJ.
Keywords: osteonecrotic jawbone, silent inflammation, RANTES, bone density measurement
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the structure of the jawbone is often assessed by 2D-OPG
with reliable results if there is cortical damage. However,
significant limitations in the assessment of medullary bone
must be taken into account.3–5
Imaging FDOJ with X-ray
A typical case of FDOJ shows little formation of new bone
and little sign of healing. In the area affected by FDOJ, there
are medullary cavities. The cortical bone is generally intact,
and during operation, a clear demarcation can be observed
between the cortical bone not involved and the medullary
bone eroded by the cavities. FDOJ often presents as fatty
clumps of tissue.6 Figure 1 shows one such tissue sample
where the majority of the cancellous bone has been converted
into fat. FDOJ is characterized by the absence of typical signs
of inflammation and by typical fatty erosion and cavities in
the medullary jawbone.6 FDOJ must not be confused with
classic osteomyelitis. For FDOJ, the etiology is still largely
unknown.7 Radiographic symptoms can be so subtle that they
are almost impossible to identify without extensive diagnostic
experience.8 The problem of X-ray imaging contributes to the
neglect of FDOJ as a pathological and pathogenetic change in
the jawbone. Other authors also pointed out a significant discrepancy between X-ray findings and the structural abnormality of FDOJ.9 To elucidate this problem, this study examines
the reliability of 2D-OPG and attempts to shed light on this
with the following questions: is dental 2D-OPG a reliable
parameter for identifying medullar changes in the context
of FDOJ? Or is it possible that changes in the metabolism
of the jawbone may go undetected by 2D-OPG? Is FDOJ
eventually connected with systemic diseases?
Material and methods
This study was performed as a randomized controlled trial.
As we showed in an earlier publication,6 the defining feature
of areas of FDOJ include overexpression of the proinflammatory messenger RANTES, which is in contrast to what
is seen in normal jawbone. In this study, we will compare
areas of FDOJ defined by high levels of RANTES with the
corresponding X-ray density (XrDn) in 2D-OPG. In addition, XrDn is compared with transalveolar ultrasound (TAU)
images. Research is based on data retrieved from patients
during normal dental surgery. All patients gave their written
informed consent.
Groups of patients examined
The cases examined consisted of two groups. FDOJ
was found in 31 patients. The age range of this group of
patients extended from 27–87 years, with an average age
of 57 years and a sex ratio (female/male) of 21/10. The
age range of the control group that consisted of 19 patients
w (...truncated)