Published July 2013 | Version v1
Journal article

Quantitative MRI shows cerebral microstructural damage in hemolytic-uremic syndrome patients with severe neurological symptoms but no changes in conventional MRI

  • 1. Hannover Medical School, Clinic for Neurology, Hannover (Germany)
  • 2. Hannover Medical School, Institute of Diagnostic and Interventional Neuroradiology, Hannover (Germany)
  • 3. Hannover Medical School, Clinic for Nephrology and Hypertension, Hannover (Germany)

Description

Severe neurological symptoms in Shiga toxin-producing Escherichia coli infection associated hemolytic-uremic syndrome (STEC-HUS) are often accompanied by none or only mild alterations of cerebral magnetic resonance imaging (MRI). This study aims to analyze if quantitative MRI is able to reveal cerebral pathological alterations invisible for conventional MRI. In nine patients with STEC-HUS associated severe neurological symptoms but inconspicuous cerebral MRI findings maps of the parameters T2 relaxation time, relative proton density (PD), apparent diffusion coefficient (ADC), and fractional anisotropy (FA) were generated. Quantitative values of these parameters were measured at the basal ganglia, thalamus, and white matter of the frontal and parietal lobe and compared to those of nine age- and sex-matched controls. Significant T2 prolongation (p < 0.01) was found in the basal ganglia of all patients compared to controls. PD and ADC were not significantly altered. A significant reduction of FA in patients was seen at caput nuclei caudati (p < 0.01). Prolonged T2 relaxation time indicates cerebral microstructural damages in these patients despite their inconspicuous MRI findings. T2 relaxometry could be used as a complementary tool for the assessment of metabolic-toxic brain syndromes. (orig.)

Availability note (English)

Available from: http://dx.doi.org/10.1007/s00234-013-1176-3

Additional details

Identifiers

Publishing Information

Journal Title
Neuroradiology
Journal Volume
55
Journal Issue
7
Journal Page Range
p. 819-825
ISSN
0028-3940
CODEN
NRDYAB