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Serum adiponectin concentration is a positive predictor of all-cause and cardiovascular mortality in type 1 diabetes

Authors :
Per-Henrik Groop
Jan Frystyk
Daniel Gordin
Carol Forsblom
Allan Flyvbjerg
Lena M. Thorn
John Moran
Markku Saraheimo
Johan Wadén
Merlin C. Thomas
Source :
Journal of Internal Medicine. 270:346-355
Publication Year :
2011
Publisher :
Wiley, 2011.

Abstract

Forsblom C, Thomas MC, Moran J, Saraheimo M, Thorn L, Waden J, Gordin D, Frystyk J, Flyvbjerg A, Groop P-H, on behalf of the FinnDiane Study Group (Folkhalsan Institute of Genetics, Helsinki; Department of Medicine Helsinki University Central Hospital, Helsinki, Finland; The Baker IDI Heart and Diabetes Institute, Melbourne, Vic.; The Queen Elizabeth Hospital, Woodville, SA, Australia; and Aarhus University Hospital, Aarhus C., Denmark). Serum adiponectin concentration is a positive predictor of all-cause and cardiovascular mortality in type 1 diabetes. J Intern Med 2011; 270: 346–355. Background. Adiponectin is widely regarded as an anti-atherogenic, antioxidant and anti-inflammatory molecule. However, adiponectin concentration is paradoxically increased in individuals with type 1 diabetes, in whom it is positively associated with adverse clinical outcomes. Objective. To explore the association between serum adiponectin concentration and mortality outcomes in adults with type 1 diabetes. Design. Multicentre prospective cohort study. Setting. Primary and tertiary care. Subjects. Finnish adults with type 1 diabetes (n = 2034). Main outcome measures. All-cause and cardiovascular mortality. Independent predictors of mortality were determined using the Cox and the Fine and Gray competing risks proportional hazards models. Results. During a median of 11 years of follow-up, there were 173 deaths (8.5%, 1.0 per hundred person-years). Adiponectin was linearly associated with all-cause mortality [Cox model: hazard ratio (HR) 1.02, 95% confidence interval (CI) 1.01–1.03, P

Details

ISSN :
09546820
Volume :
270
Database :
OpenAIRE
Journal :
Journal of Internal Medicine
Accession number :
edsair.doi...........569d107faa50fd59a93a0f5381e3aff4
Full Text :
https://doi.org/10.1111/j.1365-2796.2011.02406.x