201. 3Tesla post-mortem MRI quantification of anatomical brain structures.
- Author
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Arnold, Isabel, Schwendener, Nicole, Lombardo, Paolo, Jackowski, Christian, and Zech, Wolf-Dieter
- Subjects
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MAGNETIC resonance imaging of the brain , *BRAIN anatomy , *AUTOPSY , *FORENSIC sciences , *CEREBELLUM , *BRAIN physiology , *MAGNETIC resonance imaging equipment , *BRAIN , *BODY temperature , *POSTMORTEM changes , *MAGNETIC resonance imaging , *NEURORADIOLOGY - Abstract
Quantitative post-mortem magnetic resonance imaging (PMMR) allows for measurement of T1 and T2 relaxation times and proton density (PD) of brain tissue. Quantitative PMMR values may be used for advanced post-mortem neuro-imaging diagnostics such as computer aided diagnosis. So far, the quantitative T1, T2 and PD post-mortem values of regular anatomical brain structures were unknown for a 3 Tesla PMMR application. The goal of this basic research study was to evaluate the quantitative values of post-mortem brain structures for a 3 T post-mortem magnetic resonance application with regard to various corpse temperatures. In 50 forensic cases, a quantitative PMMR brain sequence was applied prior to autopsy. Measurements of T1 (in ms), T2 (in ms), and PD (in %) values of cerebrum (Group 1: frontal grey matter, frontal white matter, thalamus, caudate nucleus, globus pallidus, putamen, internal capsule) brainstem and cerebellum (Group 2: cerebral peduncle, substantia nigra, red nucleus, pons, middle cerebellar peduncle, cerebellar hemisphere, medulla oblongata) were conducted in synthetically calculated axial PMMR brain images. Assessed quantitative values were corrected for corpse temperature. Temperature dependence was observed mainly for T1 values. ANOVA testing resulted in significant differences of quantitative values between the investigated anatomical brain structures in both groups. It can be concluded that temperature corrected 3 Tesla PMMR T1, T2 and PD values are feasible for characterization and discrimination of regular anatomical brain structures. This may provide a base for future advanced diagnostics of forensically relevant brain lesions and pathology. [ABSTRACT FROM AUTHOR]
- Published
- 2021
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