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

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 i...

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Detalles Bibliográficos
Autores principales: Gajdošík, Martin, Hingerl, Lukas, Škoch, Antonín, Freudenthaler, Angelika, Krumpolec, Patrik, Ukropec, Jozef, Ukropcová, Barbara, Šedivý, Petr, Hájek, Milan, Itariu, Bianca K., Maier, Bernhard, Baumgartner‐Parzer, Sabina, Krebs, Michael, Trattnig, Siegfried, Krššák, Martin
Formato: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley & Sons, Inc. 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6618283/
https://www.ncbi.nlm.nih.gov/pubmed/30578581
http://dx.doi.org/10.1002/jmri.26605
Descripción
Sumario: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 CH(3)) and non‐omega‐3 (CH(3)) 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 CH(3) resonances was used for the optimal detection of the n‐3 CH(3) 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: T(2) relaxation times in oils were assessed as follows: CH(2), 65 ± 22 msec; CH(3), 325 ± 7 msec; and n‐3 CH(3), 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 CH(3) signal in vivo at 7 T. Level of Evidence: 1 Technical Efficacy: Stage 1 J. Magn. Reson. Imaging 2019;50:71–82.