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  • Diagnosing impaired glucose tolerance using direct infusion mass spectrometry of blood plasma.

Diagnosing impaired glucose tolerance using direct infusion mass spectrometry of blood plasma.

PloS one (2014-09-10)
Petr G Lokhov, Oxana P Trifonova, Dmitry L Maslov, Elena E Balashova, Alexander I Archakov, Ekaterina A Shestakova, Marina V Shestakova, Ivan I Dedov
ABSTRACT

The goal of this study was to evaluate the capacity for mass spectrometry of blood plasma to diagnose impaired glucose tolerance (IGT). For this study, blood plasma samples from control subjects (n = 30) and patients with IGT (n = 20) were treated with methanol and low molecular weight fraction were then analyzed by direct infusion mass spectrometry. A total of 51 metabolite ions strongly associated with IGT were detected. The area under a receiver operating characteristic (ROC) curve (AUC) for diagnosing IGT that was based on an analysis of all these metabolites was 0.93 (accuracy 90%, specificity 90%, and sensitivity 90%). The associated reproducibility was 85%. The metabolites identified were also consistent with risk factors previously associated with the development of diabetes. Thus, direct infusion mass spectrometry of blood plasma metabolites represents a rapid, single-step, and reproducible method for the analysis of metabolites. Moreover, this method has the potential to serve as a prototype for clinical analyses that could replace the currently used glucose tolerance test with a more patient-friendly assay.

MATERIALS
Product Number
Brand
Product Description

Supelco
Methanol, analytical standard
Sigma-Aldrich
Methanol, anhydrous, 99.8%
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Methanol, purification grade, 99.8%
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Methanol, suitable for HPLC, gradient grade, ≥99.9%
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Supelco
Methanol, Pharmaceutical Secondary Standard; Certified Reference Material
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Methanol, puriss., meets analytical specification of Ph Eur, ≥99.7% (GC)
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Methanol, puriss. p.a., ACS reagent, reag. ISO, reag. Ph. Eur., ≥99.8% (GC)
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Methanol, ACS spectrophotometric grade, ≥99.9%
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Methanol, ACS reagent, ≥99.8%
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Methanol, suitable for HPLC, ≥99.9%
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Methanol, suitable for HPLC, gradient grade, suitable as ACS-grade LC reagent, ≥99.9%
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Methanol solution, contains 0.50 % (v/v) triethylamine
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USP
Methyl alcohol, United States Pharmacopeia (USP) Reference Standard
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