FMRI INDICES AND CSF VIRAL LOAD IN HIV-INFECTION
FMRI INDICES AND CSF VIRAL LOAD IN HIV-INFECTION
批准号:
6649820
负责人:
TERRY L. JERNIGAN
金额:
$27.47万
依托单位国家:
美国
项目类别:
财政年份:
2001
资助国家:
美国
项目状态:
已结题
起止时间:
2001-09-30 至 2006-08-31
关键词:
AIDS /HIV neuropathy behavioral /social science research tag bioimaging /biomedical imaging caudate nucleus cerebrospinal fluid diagnosis design /evaluation functional magnetic resonance imaging human immunodeficiency virus 1 human subject magnetic resonance imaging nervous system disorder diagnosis neural degeneration neuroimaging neurologic manifestations neuropsychological tests noninvasive diagnosis patient oriented research virus RNA virus replication
中文摘要
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英文摘要
DESCRIPTION (Provided by applicant): High levels of CSF HIV-1 RNA, and
associated neurobehavioral deficits, have been reported without commensurate
serum viral levels (Ellis et al., 2000; Ellis et al., 1997; McArthur et al.,
1997; Staprans et al., 1999; Wong et al., 1997). The implication is that serial
lumbar puncture, although invasive, may be the best available method for
monitoring the progression of HIV-related neurodegenerative processes.
Sensitive noninvasive methods for detecting and monitoring HIV-related CNS
effects are needed. The aim of the proposed studies is to evaluate the
application of structural (SMRI) and functional (FMRI) imaging methods for
predicting CNS viral replication. The approach is guided by previous studies
suggesting that neurodegeneration in the striatum and diffuse cerebral white
matter damage are the two most consistent structural abnormalities present in
this population (Jernigan et al., 1993; Stout et al., 1998) and psychomotor
slowing is the most prominent functional deficit. Since CSF HIV-1 RNA is
currently the best available index of CNS viral replication, this measure will
be the primary dependent variable for the proposed studies. Groups of
neurobehaviorally impaired and unimpaired seropositive individuals, and yoked
seronegative controls, will be studied with repeated sMRI/fMRI examinations at
baseline, and 6 and 12 weeks after initiation (in the seropositive subjects) of
aggressive HAART therapy aimed at reducing CSF HIV-1 RNA levels. Measures of
white matter signal change, of caudate nucleus volume, and of task-related
change in blood oxygenation in the caudate nucleus (during motor tasks) will be
correlated with levels of CSF HIV-1 RNA within the seropositive subjects. The
utility of these SMRI and FMRI measures in predicting CSF viral levels will be
compared with that of behavioral measures, and possibly with that of other
noninvasive methods (such as MR spectroscopy), in univariate and multivariate
prediction models.
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