PMID- 34349619 OWN - NLM STAT- PubMed-not-MEDLINE LR - 20240403 IS - 1662-4548 (Print) IS - 1662-453X (Electronic) IS - 1662-453X (Linking) VI - 15 DP - 2021 TI - Using Perfusion Contrast for Spatial Normalization of ASL MRI Images in a Pediatric Craniosynostosis Population. PG - 698007 LID - 10.3389/fnins.2021.698007 [doi] LID - 698007 AB - Spatial normalization is an important step for group image processing and evaluation of mean brain perfusion in anatomical regions using arterial spin labeling (ASL) MRI and is typically performed via high-resolution structural brain scans. However, structural segmentation and/or spatial normalization to standard space is complicated when gray-white matter contrast in structural images is low due to ongoing myelination in newborns and infants. This problem is of particularly clinical relevance for imaging infants with inborn or acquired disorders that impair normal brain development. We investigated whether the ASL MRI perfusion contrast is a viable alternative for spatial normalization, using a pseudo-continuous ASL acquired using a 1.5 T MRI unit (GE Healthcare). Four approaches have been compared: (1) using the structural image contrast, or perfusion contrast with (2) rigid, (3) affine, and (4) nonlinear transformations - in 16 healthy controls [median age 0.83 years, inter-quartile range (IQR) +/- 0.56] and 36 trigonocephaly patients (median age 0.50 years, IQR +/- 0.30) - a non-syndromic type of craniosynostosis. Performance was compared quantitatively using the real-valued Tanimoto coefficient (TC), visually by three blinded readers, and eventually by the impact on regional cerebral blood flow (CBF) values. For both patients and controls, nonlinear registration using perfusion contrast showed the highest TC, at 17.51 (CI 6.66-49.38) times more likely to have a higher rating and 17.45-18.88 ml/100 g/min higher CBF compared with the standard normalization. Using perfusion-based contrast improved spatial normalization compared with the use of structural images, significantly affected the regional CBF, and may open up new possibilities for future large pediatric ASL brain studies. CI - Copyright (c) 2021 de Planque, Mutsaerts, Keil, Erler, Dremmen, Mathijssen and Petr. FAU - de Planque, Catherine A AU - de Planque CA AD - Department of Plastic and Reconstructive Surgery and Hand Surgery, University Medical Center Rotterdam, Rotterdam, Netherlands. FAU - Mutsaerts, Henk J M M AU - Mutsaerts HJMM AD - Department of Radiology and Nuclear Medicine, Amsterdam Neuroscience, Amsterdam University Medical Center, Amsterdam, Netherlands. FAU - Keil, Vera C AU - Keil VC AD - Department of Radiology and Nuclear Medicine, Amsterdam Neuroscience, Amsterdam University Medical Center, Amsterdam, Netherlands. FAU - Erler, Nicole S AU - Erler NS AD - Department of Biostatistics, University Medical Center Rotterdam, Rotterdam, Netherlands. AD - Department of Epidemiology, Erasmus Medical Center, Rotterdam, Netherlands. FAU - Dremmen, Marjolein H G AU - Dremmen MHG AD - Department of Radiology and Nuclear Medicine, University Medical Center Rotterdam, Rotterdam, Netherlands. FAU - Mathijssen, Irene M J AU - Mathijssen IMJ AD - Department of Plastic and Reconstructive Surgery and Hand Surgery, University Medical Center Rotterdam, Rotterdam, Netherlands. FAU - Petr, Jan AU - Petr J AD - Department of Radiology and Nuclear Medicine, Amsterdam Neuroscience, Amsterdam University Medical Center, Amsterdam, Netherlands. AD - Helmholtz-Zentrum Dresden-Rossendorf, Institute of Radiopharmaceutical Cancer Research, Dresden, Germany. LA - eng PT - Journal Article DEP - 20210719 PL - Switzerland TA - Front Neurosci JT - Frontiers in neuroscience JID - 101478481 PMC - PMC8326566 OTO - NOTNLM OT - ASL OT - craniosynostosis OT - pediatric OT - registration OT - segmentation OT - spatial normalization COIS- The authors declare that the research was conducted in the absence of any commercial or financial relationships that could be construed as a potential conflict of interest. EDAT- 2021/08/06 06:00 MHDA- 2021/08/06 06:01 PMCR- 2021/01/01 CRDT- 2021/08/05 06:23 PHST- 2021/04/20 00:00 [received] PHST- 2021/06/04 00:00 [accepted] PHST- 2021/08/05 06:23 [entrez] PHST- 2021/08/06 06:00 [pubmed] PHST- 2021/08/06 06:01 [medline] PHST- 2021/01/01 00:00 [pmc-release] AID - 10.3389/fnins.2021.698007 [doi] PST - epublish SO - Front Neurosci. 2021 Jul 19;15:698007. doi: 10.3389/fnins.2021.698007. eCollection 2021.