Analysis of multiple B-value diffusion-weighted imaging in pediatric acute encephalopathy

• Published in: PloS one Vol. 8; no. 6; p. e63869
• Main Authors: Tachibana, Yasuhiko, Aida, Noriko, Niwa, Tetsu, Nozawa, Kumiko, Kusagiri, Kouki, Mori, Kana, Endo, Kazuo, Obata, Takayuki, Inoue, Tomio
• Format: Journal Article
• Language: English
• Published: United States Public Library of Science 03.06.2013; Public Library of Science (PLoS)
• Subjects: Acute Disease; Aquaporins; Biology; Brain; Brain Diseases - diagnosis; Brain mapping; Brain research; Change detection; Child; Child, Preschool; Children; Cortex; Cytokines; Development and progression; Diagnosis; Diagnostic imaging; Diffusion; Diffusion coefficient; Diffusion Magnetic Resonance Imaging; Edema; Encephalopathy; Ethics; Female; Genetic aspects; Girls; Humans; Infant; Ischemia; Lesions; Magnetic resonance imaging; Male; Medicine; Neuroimaging; Neurological complications; NMR; Nuclear magnetic resonance; Patients; Pediatrics; Radiology; Signal-To-Noise Ratio; University graduates; Values; Japan
• ISSN: 1932-6203; 1932-6203
• DOI: 10.1371/journal.pone.0063869

Acute encephalopathy is a disease group more commonly seen in children. It is often severe and has neurological sequelae. Imaging is important for early diagnosis and prompt treatment to ameliorate an unfavorable outcome, but insufficient sensitivity/specificity is a problem. To overcome this, a new value (fraction of high b-pair (FH)) that could be processed from clinically acceptable MR diffusion-weighted imaging (DWI) with three different b-values was designed on the basis of a two-compartment model of water diffusion signal attenuation. The purpose of this study is to compare FH with the apparent diffusion coefficient (ADC) regarding the detectability of pediatric acute encephalopathy. We retrospectively compared the clinical DWI of 15 children (1-10 years old, mean 2.34, 8 boys, 7 girls) of acute encephalopathy with another 16 children (1-11 years old, mean 4.89, 9 boys, 7 girls) as control. A comparison was first made visually by mapping FH on the brain images, and then a second comparison was made on the basis of 10 regions of interest (ROIs) set on cortical and subcortical areas of each child. FH map visually revealed diffusely elevated FH in cortical and subcortical areas of the patients with acute encephalopathy; the changes seemed more diffuse in FH compared to DWI. The comparison based on ROI revealed elevated mean FH in the cortical and subcortical areas of the acute encephalopathy patients compared to control with significant difference (P<0.05). Similar findings were observed even in regions where the findings of DWI were slight. The reduction of mean ADC was significant in regions with severe findings in DWI, but it was not constant in the areas with slighter DWI findings. The detectability of slight changes of cortical and subcortical lesions in acute encephalopathy may be superior in FH compared to ADC.