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(Circulation. 2003;107:3199.)
© 2003 American Heart Association, Inc.
Clinical Investigation and Reports |
From the Center of Excellence on Aging and Departments of Medicine and Aging and Drug Sciences (G.D., F.C., F.S., M.P., A.F., G.C.), University of Chieti G. DAnnunzio Schools of Medicine and Pharmacy, Chieti, Italy; Department of Medicine (S.V.), University of Palermo, Palermo, Italy; and University of Rome La Sapienza (S.B., C.P.), Rome, Italy.
Correspondence to Giovanni Davì, MD, Center of Excellence on Aging and Departments of Medicine and Aging, University of Chieti, Via Colle dellAra, 66013 Chieti, Italy. E-mail gdavi{at}unich.it
Background To investigate early events possibly related to the development of diabetic angiopathy, we examined whether 8-iso-prostaglandin F2
(8-iso-PGF2
) formation, a marker of in vivo oxidant stress, is altered in different stages of type 1 diabetes (T1DM) and whether it correlates with the rate of thromboxane (TX) A2 biosynthesis, a marker of in vivo platelet activation. We also investigated the relationship between inflammatory markers and F2-isoprostane formation in this setting.
Methods and Results A cross-sectional study was performed in 23 insulin-treated patients aged <18 years with new-onset T1DM (≤6 weeks, group A), matched for age and gender with 23 patients with stable disease (>1 year, group B). Urinary 8-iso-PGF2
and 11-dehydro-TXB2 were measured in all patients and in age- and gender-matched controls. Circulating interleukin-6 (IL-6), tumor necrosis factor-
, and C-reactive protein were also determined as markers of the inflammatory response. Fifteen of the 23 children in group A were reexamined after 12 months. Compared with either controls or group B, diabetic children in group A showed significantly higher levels of 8-iso-PGF2
, 11-dehydro-TXB2, IL-6, tumor necrosis factor-
, and C-reactive protein. Statistically significant correlations between IL-6 and both 8-iso-PGF2
(r=0.63, P<0.001) and 11-dehydro-TXB2 (r=0.51, P<0.01) were observed. The 15 patients reexamined after 1 year showed a significant reduction in lipid peroxidation and platelet activation (P<0.02 and P<0.001, respectively), consistent with reduced levels of IL-6 and tumor necrosis factor-
.
Conclusions These results demonstrate that enhanced lipid peroxidation and platelet activation represent early events in T1DM that are possibly related to an acute inflammatory response. These noninvasive indexes may help in further examining T1DM pathophysiology and monitoring pharmacological interventions to interfere with disease development and progression.
Key Words: diabetes mellitus inflammation platelets
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