3D pattern of brain atrophy in HIV/AIDS visualized using tensor-based morphometry.

Neuroimage

Laboratory of Neuro Imaging, Department of Neurology, UCLA School of Medicine, 635 Charles E. Young Drive South, Suite 225E, Los Angeles, CA 90095-7332, USA.

Published: January 2007

AI Article Synopsis

  • About 35% of HIV-infected individuals experience cognitive impairment, but the exact nature of related brain damage remains unclear.
  • Researchers developed a new MRI analysis technique using tensor-based morphometry (TBM) and the Jensen-Rényi divergence (JRD) to study brain deficits in AIDS patients.
  • The study found significant brain atrophy in sensorimotor areas, correlating with cognitive issues and decreased CD4+ T-cell counts, highlighting TBM's potential to visualize AIDS-related brain changes and predict cognitive decline.

Article Abstract

Unlabelled: 35% of HIV-infected patients have cognitive impairment, but the profile of HIV-induced brain damage is still not well understood. Here we used tensor-based morphometry (TBM) to visualize brain deficits and clinical/anatomical correlations in HIV/AIDS. To perform TBM, we developed a new MRI-based analysis technique that uses fluid image warping, and a new alpha-entropy-based information-theoretic measure of image correspondence, called the Jensen-Rényi divergence (JRD).

Methods: 3D T1-weighted brain MRIs of 26 AIDS patients (CDC stage C and/or 3 without HIV-associated dementia; 47.2+/-9.8 years; 25M/1F; CD4+ T-cell count: 299.5+/-175.7/microl; log10 plasma viral load: 2.57+/- 1.28 RNA copies/ml) and 14 HIV-seronegative controls (37.6+/-12.2 years; 8M/6F) were fluidly registered by applying forces throughout each deforming image to maximize the JRD between it and a target image (from a control subject). The 3D fluid registration was regularized using the linearized Cauchy-Navier operator. Fine-scale volumetric differences between diagnostic groups were mapped. Regions were identified where brain atrophy correlated with clinical measures.

Results: Severe atrophy ( approximately 15-20% deficit) was detected bilaterally in the primary and association sensorimotor areas. Atrophy of these regions, particularly in the white matter, correlated with cognitive impairment (P = 0.033) and CD4+ T-lymphocyte depletion (P = 0.005).

Conclusion: TBM facilitates 3D visualization of AIDS neuropathology in living patients scanned with MRI. Severe atrophy in frontoparietal and striatal areas may underlie early cognitive dysfunction in AIDS patients, and may signal the imminent onset of AIDS dementia complex.

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Source
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC3197835PMC
http://dx.doi.org/10.1016/j.neuroimage.2006.08.030DOI Listing

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