کد مقاله | کد نشریه | سال انتشار | مقاله انگلیسی | نسخه تمام متن |
---|---|---|---|---|
6028523 | 1580920 | 2014 | 12 صفحه PDF | دانلود رایگان |
عنوان انگلیسی مقاله ISI
Visualization of intra-thalamic nuclei with optimized white-matter-nulled MPRAGE at 7Â T
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کلمات کلیدی
SNRCOMLGNMGNCNRVLPVPLVLAICCROISTH7 T - 7 TMTT - MTTThalamus - تالاموسmammillothalamic tract - دستگاه ماملیوتالاموسDelay time - زمان تاخیرinversion time - زمان معکوسUltra high field - زمین فوق العاده بالاintraclass correlation coefficient - ضریب همبستگی داخل کلاسیGray matter - ماده خاکستریwhite matter - ماده سفیدcerebro-spinal fluid - مایع مغزی نخاعیCSF - مایع مغزی نخاعیcenter of mass - مرکز جرمregion-of-interest - منطقه مورد نظرSignal-to-noise ratio - نسبت سیگنال به نویزContrast-to-noise ratio - نسبت کنتراست به نویزHabenular nucleus - هسته Habenularmediodorsal nucleus - هسته MedidorsalalThalamic nuclei - هسته تالاموسVentral posterior lateral nucleus - هسته جانبی خلفی شکمیVentral anterior nucleus - هسته قدامی شکمred nucleus - هسته قرمزlateral dorsal nucleus - هسته پشتی جانبیmedial geniculate nucleus - هسته ژنومیک محیطیlateral geniculate nucleus - هسته ژنیکول جانبی جانبیSubthalamic nucleus - هسته ی زیرهالامیکPulvinar - والیبالPul - پول
موضوعات مرتبط
علوم زیستی و بیوفناوری
علم عصب شناسی
علوم اعصاب شناختی
پیش نمایش صفحه اول مقاله
چکیده انگلیسی
Novel MR image acquisition strategies have been investigated to elicit contrast within the thalamus, but direct visualization of individual thalamic nuclei remains a challenge because of their small size and the low intrinsic contrast between adjacent nuclei. We present a step-by-step specific optimization of the 3D MPRAGE pulse sequence at 7 T to visualize the intra-thalamic nuclei. We first measured T1 values within different sub-regions of the thalamus at 7 T in 5 individuals. We used these to perform simulations and sequential experimental measurements (n = 17) to tune the parameters of the MPRAGE sequence. The optimal set of parameters was used to collect high-quality data in 6 additional volunteers. Delineation of thalamic nuclei was performed twice by one rater and MR-defined nuclei were compared to the classic Morel histological atlas. T1 values within the thalamus ranged from 1400 ms to 1800 ms for adjacent nuclei. Using these values for theoretical evaluations combined with in vivo measurements, we showed that a short inversion time (TI) close to the white matter null regime (TI = 670 ms) enhanced the contrast between the thalamus and the surrounding tissues, and best revealed intra-thalamic contrast. At this particular nulling regime, lengthening the time between successive inversion pulses (TS = 6000 ms) increased the thalamic signal and contrast and lengthening the α pulse train time (N*TR) further increased the thalamic signal. Finally, a low flip angle during the gradient echo acquisition (α = 4°) was observed to mitigate the blur induced by the evolution of the magnetization along the α pulse train. This optimized set of parameters enabled the 3D delineation of 15 substructures in all 6 individuals; these substructures corresponded well with the known anatomical structures of the thalamus based on the classic Morel atlas. The mean Euclidean distance between the centers of mass of MR- and Morel atlas-defined nuclei was 2.67 mm (± 1.02 mm). The reproducibility of the MR-defined nuclei was excellent with intraclass correlation coefficient measured at 0.997 and a mean Euclidean distance between corresponding centers of mass found at first versus second readings of 0.69 mm (± 0.38 mm). This 7 T strategy paves the way to better identification of thalamic nuclei for neurosurgical planning and investigation of regional changes in neurological disorders.
ناشر
Database: Elsevier - ScienceDirect (ساینس دایرکت)
Journal: NeuroImage - Volume 84, 1 January 2014, Pages 534-545
Journal: NeuroImage - Volume 84, 1 January 2014, Pages 534-545
نویسندگان
Thomas Tourdias, Manojkumar Saranathan, Ives R. Levesque, Jason Su, Brian K. Rutt,