Evidence map›Paper›PMID 41024693›Full record

ArticleNMR in biomedicine2025

Magnetic Resonance Spectroscopy of 2-Hydroxyglutarate and Glycine in Adult Subjects With Brainstem Gliomas.

Vivek Tiwari, Sandeep K Ganji, Zhongxu An, Marco C Pinho, Larry T Davis, Colin D McKnight, Julia D Berry, Bret C Mobley, Leo Y Luo, Alexander C Mohler and 9 more

Abstract read
In one paragraph

Article in NMR in biomedicine, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 5 papers.

0numbers the graph read from it
0cells of the map it votes in
5citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

5 citing papers in PubMed.

  1. Review
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4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

19 authors.

Vivek TiwariDepartment of Biological Sciences, Indian Institute of Science Education and Research, Behampur, Odisha, India.
Sandeep K GanjiPhilips, Cambridge, Massachusetts, USA.
Zhongxu AnAdvanced Imaging Research Center, University of Texas Southwestern Medical Center, Dallas, Texas, USA.ORCID https://orcid.org/0000-0003-3759-5645
Marco C PinhoDepartment of Radiology, University of Texas Southwestern Medical Center, Dallas, Texas, USA.
Larry T DavisDepartment of Radiology and Radiological Sciences, Vanderbilt University Medical Center, Nashville, Tennessee, USA.
Colin D McKnightDepartment of Radiology and Radiological Sciences, Vanderbilt University Medical Center, Nashville, Tennessee, USA.
Julia D BerryDepartment of Pathology, Microbiology and Immunology, Vanderbilt University Medical Center, Nashville, Tennessee, USA.
Bret C MobleyDepartment of Pathology, Microbiology and Immunology, Vanderbilt University Medical Center, Nashville, Tennessee, USA.
Leo Y LuoDepartment of Radiation Oncology, Vanderbilt University Medical Center, Nashville, Tennessee, USA.ORCID https://orcid.org/0000-0002-3061-4287
Alexander C MohlerDepartment of Neurology, Vanderbilt University Medical Center, Nashville, Tennessee, USA.
Ryan T MerrellDepartment of Neurology, Vanderbilt University Medical Center, Nashville, Tennessee, USA.
Patrick D KellyDepartment of Neurological Surgery, Vanderbilt University Medical Center, Nashville, Tennessee, USA.
Reid C ThompsonDepartment of Neurological Surgery, Vanderbilt University Medical Center, Nashville, Tennessee, USA.
Bruce E MickeyDepartment of Neurological Surgery, University of Texas Southwestern Medical Center, Dallas, Texas, USA.
Craig R MalloyAdvanced Imaging Research Center, University of Texas Southwestern Medical Center, Dallas, Texas, USA.
John C GoreDepartment of Radiology and Radiological Sciences, Vanderbilt University Medical Center, Nashville, Tennessee, USA.
Toral R PatelDepartment of Neurological Surgery, University of Texas Southwestern Medical Center, Dallas, Texas, USA.
Elizabeth A MaherDepartment of Internal Medicine, University of Texas Southwestern Medical Center, Dallas, Texas, USA.
Changho ChoiDepartment of Radiology and Radiological Sciences, Vanderbilt University Medical Center, Nashville, Tennessee, USA.

Funding

Vanderbilt Institute for Clinical and Translational Research (VICTR) -Identifying correlates of functional immunity in SARS-CoV-2 convalescent plasmaUL1TR002243 · NCATS · VANDERBILT UNIVERSITY MEDICAL CENTER · PI Paul A. Harris, Wesley H Self · 2017 to 2026
$130.7M
Vanderbilt Clinical Oncology Research Career Development ProgramK12CA090625 · NCI · VANDERBILT UNIVERSITY MEDICAL CENTER · PI Debra L. Friedman, Paula Jill Hurley · 2001 to 2026
$16.9M
UT Southwestern NORCP30DK127984 · NIDDK · UT SOUTHWESTERN MEDICAL CENTER · PI JAY D. HORTON · 2022 to 2026
$7.4M
Understanding the role of IDH in malignant gliomasR01CA154843 · NCI · UT SOUTHWESTERN MEDICAL CENTER · PI MAHER, ELIZABETH A · 2012 to 2022
$3.5M
Replacement and Upgrade of a 3T MR Scanner for ResearchS10OD021771 · OD · VANDERBILT UNIVERSITY MEDICAL CENTER · PI GORE, JOHN C · 2016 to 2016
$2.0M
Clinical development of cancer-specific MRS biomarkers in malignant gliomasR01CA184584 · NCI · UT SOUTHWESTERN MEDICAL CENTER · PI CHOI, CHANGHO · 2014 to 2018
$1.6M
Cancer Prevention and Research Institute of Texas RP130427Cancer Prevention and Research Institute of Texas RP200456NCATS NIH HHS UL1 TR002243NCI NIH HHS K12 CA090625NCI NIH HHS R01 CA154843NCI NIH HHS R01 CA184584NIDDK NIH HHS P30 DK127984NIH HHS R01CA154843NIH HHS R01CA184584NIH HHS S10 OD021771NIH HHS S10OD021771NIH HHS UL1TR002243
6 · The paper itself

Abstract

Surgical biopsy of brainstem tumors carries a risk of neurological injury. We performed magnetic resonance spectroscopy (MRS) of 2-hydroxyglutarate (2HG) and glycine in patients with brainstem tumors to assess the feasibility of detecting and quantifying 2HG in the brainstem to obviate the need for a diagnostic biopsy and to establish the clinical significance of glycine MRS in brainstem tumors in vivo. Twenty adult patients with radiographically identified presumed brainstem gliomas were prospectively enrolled in the study. Proton MRS was obtained at 3T with a protocol tailored for detection of 2HG and glycine (TE 97-ms PRESS). Spectra were fit using LCModel software and in-house basis signals of metabolites and lipids. The metabolite concentrations were quantified with reference to water and examined with respect to clinical outcomes, including postgadolinium MRI and overall survival time. MRS data from 19 patients were included in subsequent analysis, excluding suboptimal data from one patient. Tumors with elevated 2HG (> 1.9 mM, N = 8) and undetectable 2HG (< 0.3 mM, N = 11) were clearly distinguishable. Tumors with elevated glycine (> 1.5 mM, N = 4) showed rapid progression. Kaplan-Meier survival analyses with metabolite measures demonstrated that tumors with 2HG higher than 1.0 mM were significantly associated with a favorable prognosis (p = 0.01). In contrast, tumors with glycine higher than 2.5 mM showed a strong association with poor survival (p = 0.0005). The data confirm detection of 2HG in brainstem tumors at a concentration that is consistent with an IDH mutation and expected good prognosis, whereas elevated glycine in brainstem tumors portends rapid tumor progression and a worse prognosis.

Indexed as

Brain Stem NeoplasmsGliomaGlutaratesGlycineMagnetic Resonance SpectroscopyAdultAgedBiopsyBrain StemDisease ProgressionFeasibility StudiesFemaleHumansIsocitrate DehydrogenaseKaplan-Meier EstimateMalealpha-hydroxyglutarateGlutaratesGlycineIsocitrate Dehydrogenase2‐hydroxyglutarate3Tbrainstem tumorgliomasglycinemagnetic resonance spectroscopyPRESS (point‐resolved spectroscopy)

Identifiers

PMID41024693
PMCPMC12481179

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.