Type 1 Diabetes Is Associated With Increased Cyclooxygenase- and Cytokine-Mediated Inflammation
- Samar Basu, MSC, PHD1,
- Anders Larsson, MD, PHD2,
- Johan Vessby, MD1,
- Bengt Vessby, MD, PHD1 and
- Christian Berne, MD, PHD3
- 1Section of Geriatrics and Clinical Nutrition Research, Uppsala University, Uppsala, Sweden
- 2Section of Clinical Chemistry, Uppsala University, Uppsala, Sweden
- 3Section of Internal Medicine, Faculty of Medicine, Uppsala University, Uppsala, Sweden
- Address correspondence and reprint requests to Samar Basu, PhD, Section of Geriatrics and Clinical Nutrition Research, Faculty of Medicine, Uppsala University, P.O. Box 609, SE-751 25 Uppsala, Sweden. E-mail: samar.basu{at}pubcare.uu.se
Abstract
OBJECTIVE—The extent of involvement of cyclooxygenase (COX)-mediated inflammation in type 1 diabetes is unknown, and the association between the COX- and cytokine-mediated inflammatory responses in type 1 diabetes is not fully understood.
RESEARCH DESIGN AND METHODS—Plasma high-sensitivity C-reactive protein (CRP), 24-h urinary and plasma 15-keto-dihydro-prostaglandin F2α (a metabolite of prostaglandin F2α [PGF2α] and an indicator of COX-mediated inflammation), serum amyloid protein A (SAA), and interleukin (IL)-6 (indicators of inflammation) were measured in 38 subjects with type 1 diabetes and 41 healthy age- and sex-matched control subjects.
RESULTS—The inflammatory indicators (urinary 15-keto-dihydro-PGF2α, P < 0.01; IL-6, P < 0.04) were increased in men with diabetes. CRP and SAA did not show any significant difference between the diabetic and the control subjects. Urinary levels of 15-keto-dihydro-PGF2α correlated with the degree of glycemic control, HbA1c (r = 0.42, P < 0.0005). No correlation was found between the duration of diabetes and the inflammatory biomarkers or metabolic measurements.
CONCLUSIONS—These results suggest that an early low-grade inflammatory process reflected by elevated levels of PGF2α and IL-6 is involved in type 1 diabetes. Thus, both COX- and cytokine-mediated inflammatory pathways are significantly related to type 1 diabetes.
- COX, cyclooxygenase
- CRP, C-reactive protein
- IL, interleukin
- PGF2α, prostaglandin F2α
- SAA, serum amyloid A
Footnotes
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A table elsewhere in this issue shows conventional and Système International (SI) units and conversion factors for many substances.
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- Accepted March 3, 2005.
- Received October 28, 2004.
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