4.7 Article

A multi-center 1H MRS study of the AIDS dementia complex:: validation and preliminary analysis

期刊

JOURNAL OF MAGNETIC RESONANCE IMAGING
卷 17, 期 6, 页码 625-633

出版社

WILEY
DOI: 10.1002/jmri.10295

关键词

AIDS dementia complex (ADC); MRS; HIV infection; spectroscopy; neuroimaging

资金

  1. NCRR NIH HHS [R01RR13213] Funding Source: Medline
  2. NIAID NIH HHS [AI38855] Funding Source: Medline
  3. NINDS NIH HHS [R01 NS36524, R01NS34626] Funding Source: Medline

向作者/读者索取更多资源

Purpose: To demonstrate the technical feasibility and reliability of a multi-center study characterizing regional levels of the brain metabolite ratios choline (Cho)/creatine (Cr) and myoinositol (MI)/Cr, markers of glial cell activity, and N-acetyl aspartate (NAA)/Cr, a marker of mature neurons, in subjects with AIDS dementia complex (ADC). Materials and Methods: Using an automated protocol (GE PROBE-P). short echo time spectra (TE = 35 msec) were obtained at eight sites from uniformly prepared phantoms and from three brain regions (frontal white matter, basal ganglia. and parietal cortex) of normal volunteers and ADC and HIV-negative subjects. Results: A random-effects model of the phantom and volunteer data showed no significant inter-site differences. Feasibility of a multi-center study was further validated by detection of significant differences between the metabolite ratios of ADC subjects and HIV-negative controls. ADC subjects exhibited significantly higher Cho/Cr and MI/Cr in the basal ganglia and significantly reduced NAA/Cr and significantly higher MI/Cr in the frontal white matter. These results are consistent with the predominantly subcortical distribution of the pathologic abnormalities associated with ADC. Conclusion: This is the first study to ascertain and validate the reliability and reproducibility of a short echo time H-1-MRS acquisition sequence from multiple brain regions in a multi-center setting. It should now be possible to examine the regional effects of HIV infection in the brain in a large number of subjects and to study the metabolic effects of new therapies for the treatment of ADC in a clinical trial setting.

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