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Ultralong TE In Vivo H-1 MR Spectroscopy of Omega-3 Fatty Acids in Subcutaneous Adipose Tissue at 7 T

The result's identifiers

  • Result code in IS VaVaI

    <a href="https://www.isvavai.cz/riv?ss=detail&h=RIV%2F00023752%3A_____%2F19%3A43920313" target="_blank" >RIV/00023752:_____/19:43920313 - isvavai.cz</a>

  • Alternative codes found

    RIV/00023001:_____/19:00078051

  • Result on the web

    <a href="https://www.researchgate.net/publication/329869555_Ultralong_TE_In_Vivo_1_H_MR_Spectroscopy_of_Omega-3_Fatty_Acids_in_Subcutaneous_Adipose_Tissue_at_7_T_Omega-3_Fatty_Acids_Detection_at_7_T" target="_blank" >https://www.researchgate.net/publication/329869555_Ultralong_TE_In_Vivo_1_H_MR_Spectroscopy_of_Omega-3_Fatty_Acids_in_Subcutaneous_Adipose_Tissue_at_7_T_Omega-3_Fatty_Acids_Detection_at_7_T</a>

  • DOI - Digital Object Identifier

    <a href="http://dx.doi.org/10.1002/jmri.26605" target="_blank" >10.1002/jmri.26605</a>

Alternative languages

  • Result language

    angličtina

  • Original language name

    Ultralong TE In Vivo H-1 MR Spectroscopy of Omega-3 Fatty Acids in Subcutaneous Adipose Tissue at 7 T

  • Original language description

    Background Omega‐3 (n‐3) fatty acids (FA) play and important role in neural development and other metabolic diseases such as obesity and diabetes. The knowledge about the in vivo content and distribution of n‐3 FA in human body tissues is not well established and the standard quantification of FA is invasive and costly. Purpose To detect omega‐3 (n‐3 CH3) and non‐omega‐3 (CH3) methyl group resonance lines with echo times up to 1200 msec, in oils, for the assessment of n‐3 FA content, and the n‐3 FA fraction in adipose tissue in vivo. Study Type Prospective technical development. Population Three oils with different n‐3 FA content and 24 healthy subjects. Field Strength/Sequence Single‐voxel MR spectroscopy (SVS) with a point‐resolved spectroscopy (PRESS) sequence with an echo time (TE) of 1000 msec at 7 T. Assessment Knowledge about the J‐coupling evolution of both CH3 resonances was used for the optimal detection of the n‐3 CH3 resonance line at a TE of 1000 msec. The accuracy of the method in oils and in vivo was validated from a biopsy sample with gas chromatography analysis. Statistical Tests SVS data were compared to gas chromatography with the Pearson correlation coefficient. Results T2 relaxation times in oils were assessed as follows: CH2, 65 ± 22 msec; CH3, 325 ± 7 msec; and n‐3 CH3, 628 ± 34 msec. The n‐3 FA fractions from oil phantom experiments (n = 3) were in agreement with chromatography analysis and the comparison of in vivo obtained data with the results of chromatography analysis (n = 5) yielded a significant correlation (P = 0.029). Data Conclusion PRESS with ultralong‐TE can detect and quantify the n‐3 CH3 signal in vivo at 7 T. Level of Evidence 1 Technical Efficacy Stage 1

  • Czech name

  • Czech description

Classification

  • Type

    J<sub>imp</sub> - Article in a specialist periodical, which is included in the Web of Science database

  • CEP classification

  • OECD FORD branch

    20602 - Medical laboratory technology (including laboratory samples analysis; diagnostic technologies) (Biomaterials to be 2.9 [physical characteristics of living material as related to medical implants, devices, sensors])

Result continuities

  • Project

  • Continuities

    V - Vyzkumna aktivita podporovana z jinych verejnych zdroju

Others

  • Publication year

    2019

  • Confidentiality

    S - Úplné a pravdivé údaje o projektu nepodléhají ochraně podle zvláštních právních předpisů

Data specific for result type

  • Name of the periodical

    Journal of Magnetic Resonance Imaging

  • ISSN

    1053-1807

  • e-ISSN

  • Volume of the periodical

    50

  • Issue of the periodical within the volume

    1

  • Country of publishing house

    US - UNITED STATES

  • Number of pages

    12

  • Pages from-to

    71-82

  • UT code for WoS article

    000471831600006

  • EID of the result in the Scopus database

    2-s2.0-85058969321