(Circulation. 2001;103:2771.)
© 2001 American Heart Association, Inc.
Editorial |
From the Department of Veterans Affairs Medical Center, Dallas, and the Departments of Radiology and Internal Medicine, University of Texas Southwestern Medical Center, Dallas, Tex.
Correspondence to Craig R. Malloy, MD, Mary Nell and Ralph B. Rogers Magnetic Resonance Center, 5801 Forest Park Road, Dallas, TX 75235-9085. E-mail craig.malloy@utsouthwestern.edu
Key Words: Editorials heart failure brain spectroscopy metabolism magnetic resonance imaging
Patients with severe congestive heart failure have deranged cognition,1 2 and their ability to manage everyday problems is impaired.3 Cardiovascular reflexes, as well as autonomic and endocrine functions that may involve the central nervous system, are also profoundly disrupted. It is therefore of the utmost importance to understand the consequences of severe congestive heart failure for brain function and metabolism. In vivo proton magnetic resonance spectroscopy (1H MRS) is generating interest for 2 reasons. First, 1H MRS provides a new probe of cerebral function that measures important brain metabolites by detecting the hydrogen nuclei in these molecules. Furthermore, this examination is becoming widely available, and the patients experience is virtually identical to that with conventional MRI.
A large number of biochemical intermediates,
neurotransmitters, peptides, and structural molecules could, in
principle, be detected by MRS; however, biological factors and current
limitations on the MRS experiment limit the number of different signals
that may be observed in routine clinical examinations. For example, the
concentration of the metabolite must be high, which means that
important neurotransmitters (such as dopamine or serotonin)
and low-concentration metabolites cannot be observed. Another factor is
the molecular weight and physical environment of the compound: ideally,
the molecular weight is low and the molecule is freely diffusing in
aqueous solution. Large molecules, such as relatively immobile membrane
lipids or proteins, do not contribute discrete resonances in the
clinical1H magnetic resonance
spectrum. Another factor is the chemical structure itself.
Organic molecules contain many hydrogen nuclei in different positions
that
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