Posez n’importe quelle question sur les cours, conférences, exercices, recherches, actualités, etc. de l’EPFL ou essayez les exemples de questions ci-dessous.
AVERTISSEMENT : Le chatbot Graph n'est pas programmé pour fournir des réponses explicites ou catégoriques à vos questions. Il transforme plutôt vos questions en demandes API qui sont distribuées aux différents services informatiques officiellement administrés par l'EPFL. Son but est uniquement de collecter et de recommander des références pertinentes à des contenus que vous pouvez explorer pour vous aider à répondre à vos questions.
Functional magnetic resonance imaging (fMRI) measures activation-induced signal changes by means of the blood-oxygenation-level-depended (BOLD) contrast. Since signal changes are typically only 1-3%, the method is intrinsically sensitive to all signal instabilities including physiological noise from respiratory and cardiac cycles. Respiration induces a periodic B0-shift [1-3], leading mainly to sub-voxel shifts in phase- encoding direction in single-shot EPI acquisitions. The observed B0-fluctuation scales with the magnetic field and - in particular at fields ≥3T – may severely degrade the accuracy of the fMRI analysis. In this work, we propose a simple pulse sequence adaptation that enables a reliable and continuous monitoring of the respiration cycle sampling at ~10Hz. The respiration-induced B0-shift is traced by monitoring the phase of the FID signal. After introduction of a slice-wise normalization, the method turns out to be thoroughly compatible with multi-slice acquisitions potentially substituting an often used respiration belt. The dynamic frequency information can be used to correct image position errors and to correct for residual respiration-induced fluctuations in subsequent post-processing steps.
Dimitri Nestor Alice Van De Ville, Nawal Noëlle Kinany, Ilaria Ricchi