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Published online before print May 20, 2003, 10.1148/radiol.2281010683

(Radiology 2003;228:185.)

A more recent version of this article appeared on July 1, 2003
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© RSNA, 2003

Neuroradiology

Human Immmunodeficiency Virus 1–associated Minor Motor Disorders: Perfusion-weighted MR Imaging and 1H MR Spectroscopy1

Frank Wenserski, MD, Hans-Juergen von Giesen, MD, Hans-Joerg Wittsack, PhD, Albrecht Aulich, MD and Gabriele Arendt, MD

1 From the Departments of Diagnostic Radiology (F.W., H.J.W., A.A.) and Neurology (H.J.v.G., G.A.), Heinrich-Heine-University, Moorenstr 5, 40225 Duesseldorf, Germany. Received October 15, 2001; revision requested January 8, 2002; final revision received October 11; accepted October 31. Address correspondence to F.W. (e-mail: wensersk@uni-duesseldorf.de).

PURPOSE: To investigate whether advanced magnetic resonance (MR) imaging techniques such as diffusion-weighted (DW) and perfusion-weighted (PW) MR imaging and hydrogen 1 (1H) MR spectroscopy can depict functional and pathophysiologic mechanisms in patients who have minor motor deficits (MMDs) associated with human immunodeficiency virus 1 (HIV-1).

MATERIALS AND METHODS: Thirty-two patients with results seropositive for HIV-1 and different degrees of HIV-1–related MMD underwent conventional brain MR imaging, as well as DW and PW MR imaging and 1H MR spectroscopy of the basal ganglia. PW MR imaging data were computed pixel by pixel for creation of time-to-peak, relative regional cerebral blood volume, and bolus amplitude parameter maps. In addition, quantitative regional cerebral blood flow (rCBF) maps were calculated with respect to the arterial input function by using the singular value decomposition algorithm. For 1H MR spectrocopy, a stimulated echo acquisition mode 20, or STEAM 20, sequence was used. Spectra were fit for determination of the signal intensities of the different metabolites. According to psychomotor testing results, patients were divided into three groups: group 1, 10 patients with normal motor function; group 2, eight patients with psychomotor slowing for the first time; and group 3, 14 patients who had had sustained pathologic psychomotor slowing for at least 6 months before the MR imaging examination.

RESULTS: No patients had an abnormality at either conventional or DW MR imaging. PW MR imaging depicted significantly elevated rCBF in group 2 patients (P = .039, analysis of variance [ANOVA]) and significantly elevated myo-inositol–to-creatine ratio levels in group 3 patients (P = .020, ANOVA).

CONCLUSION: Quantitative PW MR imaging and 1H MR spectroscopy can depict pathologic changes in patients who have HIV-1–related MMD but normal clinical examination and conventional MR imaging findings.

© RSNA, 2003

Index terms: Acquired immunodeficiency syndrome (AIDS), 13.2068 • Brain, MR, 13.121411, 13.121412, 13.121413, 13.121416, 13.12143, 13.12144, 13.12145 • Magnetic resonance (MR), diffusion study, 13.12144 • Magnetic resonance (MR), perfusion study, 13.12144 • Magnetic resonance (MR), spectroscopy, 13.12145




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A. B. Ragin, P. Storey, B. A. Cohen, R. R. Edelman, and L. G. Epstein
Disease burden in HIV-associated cognitive impairment: A study of whole-brain imaging measures
Neurology, December 28, 2004; 63(12): 2293 - 2297.
[Abstract] [Full Text] [PDF]




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