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Philips is currently developing fast quantitative Magnetic Resonance
(MR) acquisition and data-analysis techniques for molecular-imaging
applications. MRI, a non-invasive imaging method without ionizing
radiation and with excellent depiction of internal organs, offers
the required sensitivity and precision to detect targeted contrast
agents that play an important role in molecular imaging. Evaluation
of the new techniques in collaboration with luminary clinical sites
like the University Hospital Münster, Germany, the National
Institutes of Health (NIH) in Bethesda, USA, and the Washington
University in St. Louis, USA, has shown that quantitative MRI is
indeed a powerful tool for the early assessment of diseases and for
monitoring the effects of therapy in follow-up studies. Moreover, by
non-invasive measurements of drug effects, quantitative MRI can
speed up the development and approval of drugs.
A fast developing field in diagnostic imaging, molecular imaging
provides early detection of pathological processes associated with
disease at the cellular and molecular level rather than at
anatomical level as in ‘classical’ diagnostic imaging. Key to
molecular imaging is the development of targeted contrast agents
that bind selectively to specific molecules. In addition, the
quantification of molecular imaging agents is crucial for assessing
disease progression or regression after therapy. In order to detect
the small amounts of contrast agent involved, highly sensitive and
precise imaging techniques are required. In this respect, MRI, as a
non-invasive imaging method without ionizing radiation and with
excellent depiction of internal organs, is expected to play an
important role.
To further extend the role of MRI as a molecular imaging tool,
scientists at Philips Research are currently developing fast
quantitative MR acquisition and data-analysis techniques for the
determination of absolute contrast agent concentrations. With MRI,
the influence of contrast agents on the relaxation rates of the MR
signal (which provides the imaging information) is proportional to
their local concentrations. Therefore, Philips is specifically
focusing on developing tools to measure the values and changes of
these relaxation rates.
Philips has implemented fast, robust and easy-to-use fitting and
correction software tools for the generation of relaxation rate
maps. These tools correct for artifacts arising from local
variations of the main magnetic field without lengthening the
measurement time of the MR exam. These so-called ‘susceptibility
artifacts’, which can obscure the measurement of exact contrast
agent concentration, occur even with a perfectly homogeneous MR
system due to the magnetic properties of the patient’s body
introducing local field changes.
The techniques have been evaluated in collaboration with luminary
clinical sites, such as the University Hospital Münster, Germany,
the National Institutes of Health (NIH) in Bethesda, USA, and the
Washington University in St. Louis, USA, to test their effectiveness
with newly-developed targeted agents in pre-clinical trials and also
with clinically-approved contrast agents on patients. The results
strongly support the conviction that quantitative MRI offers high
potential as a tool for the improvement of diagnosis and staging of
diseases, as well as for monitoring of treatment response.
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Quantitative measurement of contrast agent concentration in
Magnetic Resonance Imaging (MRI).
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Comparison of a conventional relaxation-weighted contrast
(left) with the concentration map obtained with the
quantitative MRI methods (right) for the diagnosis and staging
of liver tumors. Data courtesy C. Bremer, W. Heindel,
University Hospital Münster.
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