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European Journal of Heart Failure 2007 9(10):1044-1050; doi:10.1016/j.ejheart.2007.07.013
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© 2007 European Society of Cardiology

LV systolic impairment in patients with asymptomatic coronary heart disease and type 1 diabetes is related to coronary atherosclerosis, glycaemic control and advanced glycation endproducts

Kjetil Steinea,*, Jakob R. Larsenb, Marie Stugaarda, Tore Julsrud Berga, Magne Brekkeb and Knut Dahl-Jørgensenb

a Aker University Hospital N-0514 Oslo, Norway
b Ullevål University Hospital Oslo, Norway

* Corresponding author. Tel.: +47 22894743; fax: +47 22894008. E-mail address: kjetil.steine{at}medisin.uio.no (K. Steine).


   Abstract

Aims: To evaluate whether heart failure in type 1 diabetes is linked to poor glycaemic control, coronary atherosclerosis or advanced glycation endproducts (AGEs).

Methods: Twenty six patients with type 1 diabetes (mean duration 32±5years), and 16 age matched controls were recruited. Mean HbA1c through 18years (HbA1c18), serum levels of AGEs and coronary atherosclerotic burden (CAB) were determined by IVUS. Peak tissue velocities and strain by tissue Doppler imaging were measured in 12 LV regions as an evaluation of LV function.

Results: Systolic tissue velocity was inversely correlated to CAB (r=0.53, p<0.01), to HbA1c18 (r=0.46, p<0.05) and to the duration of diabetes (r=0.46, p<0.05). Systolic strain was inversely correlated to HbA1c18 (r=0.45, p<0.05), to duration of diabetes (r=0.41, p<0.05), and tended to correlate with AGEs (r=0.37, p=0.07). In multiple regression analyses, CAB and HbA1c18 were significant independent predictors for systolic velocity, while AGEs and duration of diabetes were significant predictors of systolic strain.

Conclusion: LV systolic function was impaired by increasing coronary atherosclerosis and worsening of glycaemic control. AGEs might be another mechanism for the increased risk of heart failure in type 1 diabetes.

Key Words: Heart failure • Diabetes type 1 • Advanced glycation endproducts • HbA1c • Coronary atherosclerosis • Tissue Doppler imaging

Received October 20, 2006; Revised April 24, 2007; Accepted July 19, 2007


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