Literature DB >> 18058937

Imaging cadavers: cold FLAIR and noninvasive brain thermometry using CSF diffusion.

Paul S Tofts1, Jonathan S Jackson, Daniel J Tozer, Mara Cercignani, Geoffrey Keir, David G MacManus, Gerard R Ridgway, Basil H Ridha, Klaus Schmierer, Durre Siddique, John S Thornton, Stephen J Wroe, Nick C Fox.   

Abstract

There is increasing interest in imaging cadavers for noninvasive autopsies for research purposes. However, the temperature is well below that of in vivo imaging, and a variety of interesting 'cold brain' effects are observed. At lower temperatures conventional FLAIR sequences no longer produce dark cerebrospinal fluid (CSF); T(1) is reduced from about 4.0 sec in vivo to 1.7 sec at 1 degrees C. The diffusion coefficient (DC) of CSF is much reduced (from 3.1 10(-9) m(2)s(-1) in vivo to 1.1 at 1 degrees C). DC values therefore provide a noninvasive thermometer to measure brain core temperature to within 1.0 degrees C. In three cadavers DC values were 1.1-1.5 10(-9) m(2)s(-1), indicating brain core temperatures of 1-10 degrees C, consistent with external thermocouple measurements. An improved inversion time (TI(0)) can then be found for FLAIR. At 10 degrees C this Cold FLAIR sequence (TI(0) = 1.5 sec) gave black CSF. Expressions for CSF DC and T(1) as a function of temperature were produced. A measurement of CSF DC could be converted directly to temperature and the required TI(0) found. In vitro values of CSF DC were about 1% lower than that of water. Thus, FLAIR imaging can be optimized for cadaveric brains at low and unknown temperatures, thereby improving value for autopsy purposes and facilitating comparisons with in vivo imaging. 2007 Wiley-Liss, Inc

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Year:  2008        PMID: 18058937      PMCID: PMC2478723          DOI: 10.1002/mrm.21456

Source DB:  PubMed          Journal:  Magn Reson Med        ISSN: 0740-3194            Impact factor:   4.668


  12 in total

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Authors:  P S Tofts; D Lloyd; C A Clark; G J Barker; G J Parker; P McConville; C Baldock; J M Pope
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