Aims/hypothesis Glucose fluctuations may help predict diabetic complications. We evaluated the relation between glucose variability and oxidative stress in patients with type 1 diabetes. Methods Continuous glucose monitors were inserted subcutaneously in 25 patients. During the measurement, patients collected two 24 h urine samples, while 24 healthy controls collected one 24 h urine sample for determination of 15(S)-8-iso-prostaglandin F2 alpha (PGF(2 alpha)) using HPLC tandem mass spectrometry. Mean of the daily differences (MODD), mean amplitude of glycaemic excursions (MAGE) and continuous overlapping net glycaemic action calculated with n hour time-intervals (CONGA-n) were calculated as markers for glucose variability and correlation with 15(S)-8-iso-PGF2 alpha excretion was calculated. Results Median [interquartile range (IQR)] urinary 15(S)-iso-PGF(2 alpha) was higher in patients than healthy controls: 161 (140-217) pg/mg creatinine vs 118 (101-146) pg/mg creatinine (p=0.001). Median (IQR) MODD was 3.7 (3.2-5.0) mmol/l, MAGE 7.6 (6.4-9.0) mmol/l and CONGA-1 2.3 (2.1-2.8) mmol/l. Univariate regression did not reveal an association for MODD (r(2)=0.01), MAGE (0.08) or CONGA-1 ( 0.07) with 15(S)-8-iso-PGF(2 alpha) excretion, nor was an association revealed when corrected for HbA(1c), age, sex and smoking. Spearman correlation coefficients (r) between 15(S)-8-iso-PGF(2 alpha) excretion and MODD, MAGE and CONGA-1 were non-significant: -0.112, -0.381 and -0.177. Conclusions/interpretation We report that there is no relationship between glucose variability and urinary 15(S)-8-iso-PGF(2 alpha). We also confirm that patients with type 1 diabetes have higher levels of urinary 15(S)-8-iso-PGF(2 alpha) than healthy controls, suggesting that in addition to glucose variability, other factors favouring oxidative stress may exist. We did not see a relation between high glucose variability and elevated levels of oxidative stress in patients with type 1 diabetes.
机构:
Univ Montreal, Fac Med, Dept Physiol, Res Gr Auton Nervous Syst, Montreal, PQ H3C 3J7, CanadaUniv Montreal, Fac Med, Dept Physiol, Res Gr Auton Nervous Syst, Montreal, PQ H3C 3J7, Canada
El Midaoui, A
de Champlain, J
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Univ Montreal, Fac Med, Dept Physiol, Res Gr Auton Nervous Syst, Montreal, PQ H3C 3J7, CanadaUniv Montreal, Fac Med, Dept Physiol, Res Gr Auton Nervous Syst, Montreal, PQ H3C 3J7, Canada