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Glutathione metabolism in type 2 diabetes and its relationship with microvascular complications and glycemia.

Authors :
Lutchmansingh, Fallon K.
Hsu, Jean W.
Bennett, Franklyn I.
Badaloo, Asha V.
McFarlane-Anderson, Norma
Gordon-Strachan, Georgiana M.
Wright-Pascoe, Rosemarie A.
Jahoor, Farook
Boyne, Michael S.
Source :
PLoS ONE; 6/7/2018, Vol. 13 Issue 6, p1-12, 12p
Publication Year :
2018

Abstract

Aims/Hypotheses: We hypothesized that there is decreased synthesis of glutathione (GSH) in type 2 diabetes (T2DM) especially in the presence of microvascular complications, and this is dependent on the degree of hyperglycemia. Methods: In this case-control study, we recruited 16 patients with T2DM (7 without and 9 with microvascular complications), and 8 age- and sex-matched non-diabetic controls. We measured GSH synthesis rate using an infusion of [<superscript>2</superscript>H<subscript>2</subscript>]-glycine as isotopic tracer and collection of blood samples for liquid chromatography mass spectrometric analysis. Results: Compared to the controls, T2DM patients had lower erythrocyte GSH concentrations (0.90 ± 0.42 vs. 0.35 ± 0.30 mmol/L; P = 0.001) and absolute synthesis rates (1.03 ± 0.55 vs. 0.50 ± 0.69 mmol/L/day; P = 0.01), but not fractional synthesis rates (114 ± 45 vs. 143 ± 82%/day; P = 0.07). The magnitudes of changes in patients with complications were greater for both GSH concentrations and absolute synthesis rates (P-values ≤ 0.01) compared to controls. There were no differences in GSH concentrations and synthesis rates between T2DM patients with and without complications (P-values > 0.1). Fasting glucose and HbA1c did not correlate with GSH concentration or synthesis rates (P-values > 0.17). Conclusions: Compared to non-diabetic controls, patients with T2DM have glutathione deficiency, especially if they have microvascular complications. This is probably due to reduced synthesis and increased irreversible utilization by non-glycemic mechanisms. [ABSTRACT FROM AUTHOR]

Details

Language :
English
ISSN :
19326203
Volume :
13
Issue :
6
Database :
Complementary Index
Journal :
PLoS ONE
Publication Type :
Academic Journal
Accession number :
130008510
Full Text :
https://doi.org/10.1371/journal.pone.0198626