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Functional Localization of the Human Auditory and Visual Thalamus Using a Thalamic Localizer Functional Magnetic Resonance Imaging Task

John C. Williams,Philip N. Tubiolo, Zu Jie Zheng, Eilon B. Silver-Frankel, Dathy T. Pham, Natalka K. Haubold,Sameera K. Abeykoon,Anissa Abi-Dargham,Guillermo Horga,Jared X. Van Snellenberg

biorxiv(2024)

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摘要
Functional magnetic resonance imaging (fMRI) of the auditory and visual sensory systems of the human brain is an active area of investigation in the study of human health and disease. The medial geniculate nucleus (MGN) and lateral geniculate nucleus (LGN) are key thalamic nuclei involved in the processing and relay of auditory and visual information, respectively, and are the subject of blood-oxygen-level-dependent (BOLD) fMRI studies of neural activation and functional connectivity in human participants. However, localization of BOLD fMRI signal originating from neural activity in MGN and LGN remains a technical challenge, due in part to the poor definition of boundaries of these thalamic nuclei in standard T1-weighted and T2-weighted magnetic resonance imaging sequences. Here, we report the development and evaluation of an auditory and visual sensory thalamic localizer (TL) fMRI task that produces participant-specific functionally-defined regions of interest (fROIs) of both MGN and LGN, using 3 Tesla multiband fMRI and a clustered-sparse temporal acquisition sequence, in less than 16 minutes of scan time. We demonstrate the use of MGN and LGN fROIs obtained from the TL fMRI task in standard resting-state functional connectivity (RSFC) fMRI analyses in the same participants. In RSFC analyses, we validated the specificity of MGN and LGN fROIs for signals obtained from primary auditory and visual cortex, respectively, and benchmark their performance against alternative atlas- and segmentation-based localization methods. The TL fMRI task and analysis code (written in Presentation and MATLAB, respectively) have been made freely available to the wider research community. ### Competing Interest Statement Anissa Abi-Dargham received consulting fees and/or honoraria from Sunovion Pharmaceuticals Inc., Otsuka Pharmaceutical Co., Ltd., Merck & Co., Inc., Neurocrine Biosciences, Inc., F. Hoffmann-La Roche AG, and C.H. Boehringer Sohn AG & Co. KG. Anissa Abi-Dargham holds stock options in Herophilus, Inc. and in Terran Biosciences, Inc. All other authors declare that they have no known competing financial interests or personal relationships that could have influenced or appear to have influenced the work reported in this paper.
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