Evidence map›Paper›PMID 34482182›Full record

ArticleJournal of pharmaceutical and biomedical analysis2021

Development and validation of a LC-MS/MS method for quantitation of 3-hydroxypentanoic acid and 3-oxopentanoic acid in human plasma and its application to a clinical study of glucose transporter type I deficiency (G1D) syndrome.

Raja Reddy Kallem, Sharon Primeaux, Adrian Avila, Juan M Pascual, William C Putnam

Open access · greenAbstract read
In one paragraph

Article in Journal of pharmaceutical and biomedical analysis, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 3 papers.

0numbers the graph read from it
0cells of the map it votes in
3citing papers in PubMed
0.5field-weighted citation impact, top 37% of its field
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

3 citing papers in PubMed, 4 citations in OpenAlex.

  1. Article
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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

5 authors at 4 institutions in 1 country.

Raja Reddy KallemDepartment of Pharmacy Practice, Jerry H. Hodge School of Pharmacy, Texas Tech University Health Sciences Center, Dallas, TX 75235, USA; Clinical Pharmacology and Experimental Therapeutics Center, Jerry H. Hodge School of Pharmacy, Texas Tech University Health Sciences Center, Dallas, TX 75235, United States.
Sharon PrimeauxRare Brain Disorders Program, UT Southwestern Medical Center, Dallas, TX 75390, United States; Department of Neurology, UT Southwestern Medical Center, Dallas, TX 75390, United States.
Adrian AvilaRare Brain Disorders Program, UT Southwestern Medical Center, Dallas, TX 75390, United States; Department of Neurology, UT Southwestern Medical Center, Dallas, TX 75390, United States.
Juan M PascualRare Brain Disorders Program, UT Southwestern Medical Center, Dallas, TX 75390, United States; Department of Neurology, UT Southwestern Medical Center, Dallas, TX 75390, United States; Departments of Physiology, and Pediatrics, UT Southwestern Medical Center, Dallas, TX 75390, United States; Eugene McDermott Center for Human Growth & Development / Center for Human Genetics, UT Southwestern Medical Center, Dallas, TX 75390, United States.
William C PutnamDepartment of Pharmacy Practice, Jerry H. Hodge School of Pharmacy, Texas Tech University Health Sciences Center, Dallas, TX 75235, USA; Clinical Pharmacology and Experimental Therapeutics Center, Jerry H. Hodge School of Pharmacy, Texas Tech University Health Sciences Center, Dallas, TX 75235, United States; Department of Pharmaceutical Sciences, Jerry H. Hodge School of Pharmacy, Texas Tech University Health Sciences Center, Dallas, TX 75235, United States. Electronic address: trey.putnam@ttuhsc.edu.
Texas Tech University · USSouthwestern Medical CenterSouthwestern Medical Center · USThe University of Texas Southwestern Medical Center · US

Funding

Dietary treatment of Glut1 deficiency (G1D) - Revision - 1R01NS094257 · NINDS · UT SOUTHWESTERN MEDICAL CENTER · PI PASCUAL, JUAN M. · 2016 to 2021
$4.0M
Pyruvate dehydrogenase encephalopathy: mechanisms and therapyR01NS102588 · NINDS · UT SOUTHWESTERN MEDICAL CENTER · PI PASCUAL, JUAN M. · 2017 to 2021
$1.8M
NINDS NIH HHS R01 NS094257NINDS NIH HHS R01 NS102588
6 · The paper itself

Abstract

Interest in human and experimental animal metabolism of substrates containing an odd number of carbons capable of fueling the tricarboxylic acid cycle such as heptanoic acid has motivated us to develop and validate a selective and specific liquid chromatographytandem mass spectrometric method for the simultaneous, quantitative determination of the ketone body byproducts 3-hydroxypentanoic acid and 3-oxopentanoic acid in plasma. Human plasma samples were protein-precipitated with methanol containing 0.2% formic acid. Chromatographic resolution was achieved on a Phenomenex Luna C18 column using gradient elution with mobile phases of water containing 0.1% formic acid and methanol containing 0.1% formic acid at 0.3 mL/min flow rate. The retention times of 3-hydroxypentanoic acid, 3-oxopentanoic acid and sulbactam (internal standard) were 3.85, 4.23, and 5.11 min, respectively. Validation was conducted in accordance with United States Food and Drug Administration guidance. The validated range of 3-hydroxypentanoic acid was 0.078-5 µg/mL and 0.156-10 µg/mL for 3-oxopentanoic acid. The method was accurate and precise over this range and exhibited 10-fold dilution integrity in human plasma. Recovery> 88% was achieved for analytes and internal standard. There was no matrix effect observed in human plasma. Both 3-hydroxypentanoic acid and 3-oxopentanoic acid were stable across conditions including autosampler, benchtop and freeze-thaw, as well as demonstrated long-term stability at -80 °C. The method was applied to the measurement of 3-hydroxypentanoic acid and 3-oxopentanoic acid concentrations in plasma from subjects receiving the triglyceride triheptanoin (as a source of heptanoate) for the experimental treatment of glucose transporter type I deficiency (G1D) syndrome.

Indexed as

Organic ChemicalsTandem Mass SpectrometryAnimalsCarbohydrate Metabolism, Inborn ErrorsChromatography, LiquidGlucose Transport Proteins, FacilitativeHumansMonosaccharide Transport ProteinsReproducibility of ResultsGlucose Transport Proteins, FacilitativeMonosaccharide Transport ProteinsOrganic Chemicals3-hydroxypentanoic acid3-oxopentanoic acidBHPBKPLC-MS methodβ-hydroxy valeric acid, plasma

Identifiers

PMID34482182
PMCPMC8488017
OpenAlexW3198615176

What OpenQuestion holds

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Registered trials

None linked

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.