The creatine kinase (CK) is a key enzyme involved in brain bioenergetics, playing a key role in brain function and the pathogenesis of neurological and psychiatric diseases, but imaging its activity noninvasively in the human brain in vivo remains a significant challenge. This study aims to advance the magnetization transfer (MT)- P magnetic resonance fingerprinting (MRF) for 3D Creatine Kinase Imaging (CKI). The method was implemented and validated on a clinical 7 Tesla MRI scanner.
View Article and Find Full Text PDFPurpose: Phosphorus Magnetic Resonance Spectroscopy (P MRS) enables non-invasive assessment of energy metabolism, yet its application is hindered by sensitivity limitations. To overcome this, often high magnetic fields are used, leading to challenges such as spatial inhomogeneity and therefore the need for accurate flip angle determination in accelerated acquisitions with short repetition times . In response to these challenges, we propose a novel short and look-up table-based Double-Angle Method for fast 3D P mapping (fDAM).
View Article and Find Full Text PDFA new and efficient magnetisation transfer P magnetic resonance fingerprinting (MT- P-MRF) approach is introduced to measure the creatine kinase metabolic rate between phosphocreatine (PCr) and adenosine triphosphate (ATP) in human brain. The MRF framework is extended to overcome challenges in conventional P measurement methods in the human brain, enabling reduced acquisition time and specific absorption rate (SAR). To address the challenge of creating and matching large multiparametric dictionaries in an MRF scheme, a nested iteration interpolation method (NIIM) is introduced.
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