Sophia Swago, Neil E Wilson, Mark A Elliott, Ravi Prakash Reddy Nanga, Ravinder Reddy, Walter R Witschey
{"title":"Quantification of NAD<sup>+</sup> T<sub>1</sub> and T<sub>2</sub> Relaxation Times Using Downfield <sup>1</sup>H MRS at 7 T in Human Brain In Vivo.","authors":"Sophia Swago, Neil E Wilson, Mark A Elliott, Ravi Prakash Reddy Nanga, Ravinder Reddy, Walter R Witschey","doi":"10.1002/nbm.5324","DOIUrl":null,"url":null,"abstract":"<p><p>The purpose of this study was to measure T<sub>1</sub> and T<sub>2</sub> relaxation times of NAD<sup>+</sup> proton resonances in the downfield <sup>1</sup>H MRS spectrum in human brain at 7 T in vivo and to assess the propagation of relaxation time uncertainty in NAD<sup>+</sup> quantification. Downfield spectra from eight healthy volunteers were acquired at multiple echo times to measure T<sub>2</sub> relaxation times, and saturation recovery data were acquired to measure T<sub>1</sub> relaxation times. The downfield acquisition used a spectrally selective 90° sinc pulse for excitation centered at 9.1 ppm with a bandwidth of 2 ppm, followed by a 180° spatially selective Shinnar-Le Roux refocusing pulse for localization. Uncertainty propagation analysis on metabolite quantification was performed analytically and with Monte Carlo simulation. [NAD<sup>+</sup>] was quantified in five participants. The mean ± standard deviation of T<sub>1</sub> relaxation times of the H2, H6, and H4 NAD<sup>+</sup> protons were 205.6 ± 25.7, 211.6 ± 33.5, and 237.3 ± 42.4 ms, respectively. The mean ± standard deviation of T<sub>2</sub> relaxation times of the H2, H6, and H4 protons were 33.6 ± 7.4, 29.1 ± 4.7, and 42.3 ± 11.6 ms, respectively. The relative uncertainty in NAD<sup>+</sup> concentration due to relaxation time uncertainty was 8.4%-11.4%, and measured brain [NAD<sup>+</sup>] (N = 5) was 0.324 ± 0.050 mM. Using downfield spectrally selective spectroscopy with single-slice localization, we found T<sub>1</sub> and T<sub>2</sub> relaxation times averaged across all NAD<sup>+</sup> resonances to be approximately 218 and 35 ms, respectively, in the human brain in vivo at 7 T.</p>","PeriodicalId":19309,"journal":{"name":"NMR in Biomedicine","volume":"38 3","pages":"e5324"},"PeriodicalIF":2.7000,"publicationDate":"2025-03-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"NMR in Biomedicine","FirstCategoryId":"3","ListUrlMain":"https://doi.org/10.1002/nbm.5324","RegionNum":4,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q2","JCRName":"BIOPHYSICS","Score":null,"Total":0}
引用次数: 0
Abstract
The purpose of this study was to measure T1 and T2 relaxation times of NAD+ proton resonances in the downfield 1H MRS spectrum in human brain at 7 T in vivo and to assess the propagation of relaxation time uncertainty in NAD+ quantification. Downfield spectra from eight healthy volunteers were acquired at multiple echo times to measure T2 relaxation times, and saturation recovery data were acquired to measure T1 relaxation times. The downfield acquisition used a spectrally selective 90° sinc pulse for excitation centered at 9.1 ppm with a bandwidth of 2 ppm, followed by a 180° spatially selective Shinnar-Le Roux refocusing pulse for localization. Uncertainty propagation analysis on metabolite quantification was performed analytically and with Monte Carlo simulation. [NAD+] was quantified in five participants. The mean ± standard deviation of T1 relaxation times of the H2, H6, and H4 NAD+ protons were 205.6 ± 25.7, 211.6 ± 33.5, and 237.3 ± 42.4 ms, respectively. The mean ± standard deviation of T2 relaxation times of the H2, H6, and H4 protons were 33.6 ± 7.4, 29.1 ± 4.7, and 42.3 ± 11.6 ms, respectively. The relative uncertainty in NAD+ concentration due to relaxation time uncertainty was 8.4%-11.4%, and measured brain [NAD+] (N = 5) was 0.324 ± 0.050 mM. Using downfield spectrally selective spectroscopy with single-slice localization, we found T1 and T2 relaxation times averaged across all NAD+ resonances to be approximately 218 and 35 ms, respectively, in the human brain in vivo at 7 T.
期刊介绍:
NMR in Biomedicine is a journal devoted to the publication of original full-length papers, rapid communications and review articles describing the development of magnetic resonance spectroscopy or imaging methods or their use to investigate physiological, biochemical, biophysical or medical problems. Topics for submitted papers should be in one of the following general categories: (a) development of methods and instrumentation for MR of biological systems; (b) studies of normal or diseased organs, tissues or cells; (c) diagnosis or treatment of disease. Reports may cover work on patients or healthy human subjects, in vivo animal experiments, studies of isolated organs or cultured cells, analysis of tissue extracts, NMR theory, experimental techniques, or instrumentation.