<HashMap><database>biostudies-literature</database><scores/><additional><omics_type>Unknown</omics_type><submitter>Alcicek S</submitter><funding>Mildred-Scheel Career Center of the German Cancer Aid</funding><funding>Discovery &amp; Development Project Grant of the LOEWE Frankfurt Cancer Institute</funding><pubmed_abstract>&lt;h4>Background&lt;/h4>Glutamate and glutamine are critical metabolites in gliomas, each serving distinct roles in tumor biology. Separate quantification of these metabolites using in vivo MR spectroscopy (MRS) at clinical field strengths (≤ 3T) is hindered by their molecular similarity, resulting in overlapping, hence indistinguishable, spectral peaks.&lt;h4>Purpose&lt;/h4>To develop an MRS imaging (MRSI) protocol to map glutamate and glutamine separately at 3T within clinically feasible time, using J-modulation to enhance spectral differentiation, demonstrate its reliability/reproducibility, and quantify the metabolites in glioma subregions.&lt;h4>Study type&lt;/h4>Prospective.&lt;h4>Population&lt;/h4>Phantoms, 5 healthy subjects, and 30 patients with suspected glioma. IDH wild-type glioblastoma cases were ev</pubmed_abstract><journal>Journal of magnetic resonance imaging : JMRI</journal><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC12335340</full_dataset_link><repository>biostudies-literature</repository><pubmed_title>Optimized Long-TE &amp;lt;sup&amp;gt;1&amp;lt;/sup&amp;gt;H sLASER MR Spectroscopic Imaging at 3T for Separate Quantification of Glutamate and Glutamine in Glioma.</pubmed_title><pmcid>PMC12335340</pmcid><pubmed_authors>Ronellenfitsch MW</pubmed_authors><pubmed_authors>Weber KJ</pubmed_authors><pubmed_authors>Thomas DC</pubmed_authors><pubmed_authors>Manzhurtsev A</pubmed_authors><pubmed_authors>Pilatus U</pubmed_authors><pubmed_authors>Wenger KJ</pubmed_authors><pubmed_authors>Steinbach JP</pubmed_authors><pubmed_authors>Hattingen E</pubmed_authors><pubmed_authors>Forster MT</pubmed_authors><pubmed_authors>Alcicek S</pubmed_authors><pubmed_authors>Prinz V</pubmed_authors></additional><is_claimable>false</is_claimable><name>Optimized Long-TE &amp;lt;sup&amp;gt;1&amp;lt;/sup&amp;gt;H sLASER MR Spectroscopic Imaging at 3T for Separate Quantification of Glutamate and Glutamine in Glioma.</name><description>&lt;h4>Background&lt;/h4>Glutamate and glutamine are critical metabolites in gliomas, each serving distinct roles in tumor biology. Separate quantification of these metabolites using in vivo MR spectroscopy (MRS) at clinical field strengths (≤ 3T) is hindered by their molecular similarity, resulting in overlapping, hence indistinguishable, spectral peaks.&lt;h4>Purpose&lt;/h4>To develop an MRS imaging (MRSI) protocol to map glutamate and glutamine separately at 3T within clinically feasible time, using J-modulation to enhance spectral differentiation, demonstrate its reliability/reproducibility, and quantify the metabolites in glioma subregions.&lt;h4>Study type&lt;/h4>Prospective.&lt;h4>Population&lt;/h4>Phantoms, 5 healthy subjects, and 30 patients with suspected glioma. IDH wild-type glioblastoma cases were ev</description><dates><release>2025-01-01T00:00:00Z</release><publication>2025 Apr</publication><modification>2026-05-01T08:47:09.933Z</modification><creation>2026-04-07T16:45:27.427Z</creation></dates><accession>S-EPMC12335340</accession><cross_references><pubmed>40197808</pubmed><doi>10.1002/jmri.29787</doi></cross_references></HashMap>