Metabolism of oxygen via T(2) and interleaved velocity encoding: A rapid method to quantify whole-brain cerebral metabolic rate of oxygen.
Metabolism of oxygen via T(2) and interleaved velocity encoding: A rapid method to quantify whole-brain cerebral metabolic rate of oxygen.
复制标题
DOI:
10.1002/mrm.29299
复制
发表时间:
2022-09
影响因子:
3.3
通讯作者:
Wehrli, Felix W.
中科院分区:
文献类型:
--
作者:
Deshpande, Rajiv S.;Langham, Michael C.;Cheng, Cheng-Chieh;Wehrli, Felix W.
Cerebral metabolic rate of oxygen (CMRO2) is an important biomarker of brain function. Key physiological parameters required to quantify CMRO2 include blood flow rate in feeding arteries and venous oxygen saturation (SvO2) in the draining vein. Here, a pulse sequence, Metabolism of Oxygen via T2 and Interleaved Velocity Encoding (MOTIVE), was developed to measure both parameters simultaneously and enable CMRO2 quantification in a single pass. MOTIVE interleaves a phase-contrast module between a non-selective saturation and a background-suppressed T2-prepared EPI readout (BGS-EPI) to measure T2 of blood water protons and cerebral blood flow (CBF) in 20 seconds or less. MOTIVE and standalone BGS-EPI were compared against TRUST in the brain in healthy subjects (n=24). Variants of MOTIVE to enhance resolution or shorten scan time were explored. Intra- and inter-session reproducibility studies were performed. MOTIVE experiments yielded an average SvO2 of 61 ± 6% in the superior sagittal sinus of the brain and an average CBF of 56 ± 10 mL/min/100g. The bias in SvO2 of MOTIVE and BGS-EPI to TRUST was +2 ± 4% and +1 ± 3%, respectively. The bias in CBF of MOTIVE to Cartesian phase-contrast reference was +1 ± 6 mL/min/100g. MOTIVE is an advance over existing T2-based oximetric methods. It does not require a control image and simultaneously measures SvO2 and flow velocity. The measurements agree well with TRUST and reference phase-contrast sequences. This noninvasive technique enables CMRO2 quantification in under 20 seconds and is reproducible for in vivo applications.
登录
查看更多内容
影响因子:
3.3
作者:
Jiang, Dengrong;Deng, Shengwen;Franklin, Crystal G.;O'Boyle, Michael;Zhang, Wei;Heyl, Betty L.;Pan, Li;Jerabek, Paul A.;Fox, Peter T.;Lu, Hanzhang
通讯作者:
Lu, Hanzhang
影响因子:
3.3
作者:
Foltz, WD;Stainsby, JA;Wright, GA
通讯作者:
Wright, GA
影响因子:
3.3
作者:
Magland JF;Li C;Langham MC;Wehrli FW
通讯作者:
Wehrli FW
影响因子:
3.3
作者:
He, Xiang;Yablonskiy, Dmitriy A.
通讯作者:
Yablonskiy, Dmitriy A.
影响因子:
2.2
作者:
HAACKE, EM;LINDSKOG, ED;LIN, W
通讯作者:
LIN, W