Distribution of brain sodium long and short relaxation times and concentrations: a multi-echo ultra-high fieldNa MRI study

Standard

Distribution of brain sodium long and short relaxation times and concentrations: a multi-echo ultra-high fieldNa MRI study. / Ridley, Ben; Nagel, Armin M; Bydder, Mark; Maarouf, Adil; Stellmann, Jan-Patrick; Gherib, Soraya; Verneuil, Jeremy; Viout, Patrick; Guye, Maxime; Ranjeva, Jean-Philippe; Zaaraoui, Wafaa.

in: SCI REP-UK, Jahrgang 8, Nr. 1, 12.03.2018, S. 4357.

Publikationen: SCORING: Beitrag in Fachzeitschrift/ZeitungSCORING: ZeitschriftenaufsatzForschungBegutachtung

Harvard

Ridley, B, Nagel, AM, Bydder, M, Maarouf, A, Stellmann, J-P, Gherib, S, Verneuil, J, Viout, P, Guye, M, Ranjeva, J-P & Zaaraoui, W 2018, 'Distribution of brain sodium long and short relaxation times and concentrations: a multi-echo ultra-high fieldNa MRI study', SCI REP-UK, Jg. 8, Nr. 1, S. 4357. https://doi.org/10.1038/s41598-018-22711-0

APA

Ridley, B., Nagel, A. M., Bydder, M., Maarouf, A., Stellmann, J-P., Gherib, S., Verneuil, J., Viout, P., Guye, M., Ranjeva, J-P., & Zaaraoui, W. (2018). Distribution of brain sodium long and short relaxation times and concentrations: a multi-echo ultra-high fieldNa MRI study. SCI REP-UK, 8(1), 4357. https://doi.org/10.1038/s41598-018-22711-0

Vancouver

Bibtex

@article{531da90997044b599acb9493e063cffc,
title = "Distribution of brain sodium long and short relaxation times and concentrations: a multi-echo ultra-high fieldNa MRI study",
abstract = "Sodium (23Na) MRI proffers the possibility of novel information for neurological research but also particular challenges. Uncertainty can arise in in vivo23Na estimates from signal losses given the rapidity of T2* decay due to biexponential relaxation with both short (T2*short) and long (T2*long) components. We build on previous work by characterising the decay curve directly via multi-echo imaging at 7 T in 13 controls with the requisite number, distribution and range to assess the distribution of both in vivo T2*shortand T2*longand in variation between grey and white matter, and subregions. By modelling the relationship between signal and reference concentration and applying it to in vivo23Na-MRI signal,23Na concentrations and apparent transverse relaxation times of different brain regions were measured for the first time. Relaxation components and concentrations differed substantially between regions of differing tissue composition, suggesting sensitivity of multi-echo23Na-MRI toward features of tissue composition. As such, these results raise the prospect of multi-echo23Na-MRI as an adjunct source of information on biochemical mechanisms in both physiological and pathophysiological states.",
keywords = "Journal Article",
author = "Ben Ridley and Nagel, {Armin M} and Mark Bydder and Adil Maarouf and Jan-Patrick Stellmann and Soraya Gherib and Jeremy Verneuil and Patrick Viout and Maxime Guye and Jean-Philippe Ranjeva and Wafaa Zaaraoui",
year = "2018",
month = mar,
day = "12",
doi = "10.1038/s41598-018-22711-0",
language = "English",
volume = "8",
pages = "4357",
journal = "SCI REP-UK",
issn = "2045-2322",
publisher = "NATURE PUBLISHING GROUP",
number = "1",

}

RIS

TY - JOUR

T1 - Distribution of brain sodium long and short relaxation times and concentrations: a multi-echo ultra-high fieldNa MRI study

AU - Ridley, Ben

AU - Nagel, Armin M

AU - Bydder, Mark

AU - Maarouf, Adil

AU - Stellmann, Jan-Patrick

AU - Gherib, Soraya

AU - Verneuil, Jeremy

AU - Viout, Patrick

AU - Guye, Maxime

AU - Ranjeva, Jean-Philippe

AU - Zaaraoui, Wafaa

PY - 2018/3/12

Y1 - 2018/3/12

N2 - Sodium (23Na) MRI proffers the possibility of novel information for neurological research but also particular challenges. Uncertainty can arise in in vivo23Na estimates from signal losses given the rapidity of T2* decay due to biexponential relaxation with both short (T2*short) and long (T2*long) components. We build on previous work by characterising the decay curve directly via multi-echo imaging at 7 T in 13 controls with the requisite number, distribution and range to assess the distribution of both in vivo T2*shortand T2*longand in variation between grey and white matter, and subregions. By modelling the relationship between signal and reference concentration and applying it to in vivo23Na-MRI signal,23Na concentrations and apparent transverse relaxation times of different brain regions were measured for the first time. Relaxation components and concentrations differed substantially between regions of differing tissue composition, suggesting sensitivity of multi-echo23Na-MRI toward features of tissue composition. As such, these results raise the prospect of multi-echo23Na-MRI as an adjunct source of information on biochemical mechanisms in both physiological and pathophysiological states.

AB - Sodium (23Na) MRI proffers the possibility of novel information for neurological research but also particular challenges. Uncertainty can arise in in vivo23Na estimates from signal losses given the rapidity of T2* decay due to biexponential relaxation with both short (T2*short) and long (T2*long) components. We build on previous work by characterising the decay curve directly via multi-echo imaging at 7 T in 13 controls with the requisite number, distribution and range to assess the distribution of both in vivo T2*shortand T2*longand in variation between grey and white matter, and subregions. By modelling the relationship between signal and reference concentration and applying it to in vivo23Na-MRI signal,23Na concentrations and apparent transverse relaxation times of different brain regions were measured for the first time. Relaxation components and concentrations differed substantially between regions of differing tissue composition, suggesting sensitivity of multi-echo23Na-MRI toward features of tissue composition. As such, these results raise the prospect of multi-echo23Na-MRI as an adjunct source of information on biochemical mechanisms in both physiological and pathophysiological states.

KW - Journal Article

U2 - 10.1038/s41598-018-22711-0

DO - 10.1038/s41598-018-22711-0

M3 - SCORING: Journal article

C2 - 29531255

VL - 8

SP - 4357

JO - SCI REP-UK

JF - SCI REP-UK

SN - 2045-2322

IS - 1

ER -