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Volume 2, Issue 1, Pages 38-42 (April 2010)


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Metabolic syndrome in type 1 diabetes

Sujoy GhoshaCorresponding Author Informationemail address, Andrew Colliera, Mario Hairb, Iqbal Malika, Tarik Elhadda

Received 28 July 2009; received in revised form 14 October 2009; accepted 24 October 2009. published online 30 November 2009.

Abstract 

Objectives

The aim of this study was to assess the prevalence and effects of the presence of metabolic syndrome in patients with type 1 diabetes.

Research design and methods

Retrospective analysis of data from a one year period of patients attending annual review clinic was undertaken. Body weight, height and blood pressure were measured along with assessment of micro-/macro-vascular complications. HbA1c, urea, cholesterol, triglyceride, urinary albumin: creatinine ratios were also measured. Patients were divided into those with and those without metabolic syndrome.

Results

Data from 365 type 1 diabetic patients was analysed. Hundred and twelve had metabolic syndrome. There was no difference according to gender or smoking. Type 1 diabetic patients with metabolic syndrome had longer duration of diabetes, were significantly older, heavier, had higher blood pressure, higher triglyceride and lower HDL cholesterol levels. There were significant increases in mean BMI, urea, serum creatinine, urinary albumin: creatinine ratio, cholesterol and triglyceride in the group with metabolic syndrome even after controlling for both age and duration of diabetes. Neuropathy and macro-vascular complications were commoner in patients with metabolic syndrome. Patients with metabolic syndrome were more likely to be on statins, ACE inhibitors and angiotensin receptor blockers and had a significantly higher mean insulin dosage requirement per kg.

Conclusions

This study highlights the importance of the presence of the metabolic syndrome in patients with type 1 diabetes. It shows that metabolic syndrome is associated with a higher incidence of diabetes-related complications, a need for higher insulin doses and a more aggressive multifactorial intervention.

a Diabetes Day Centre, The Ayr Hospital, Dalmellington Road, Ayr, Scotland KA6 6DX, United Kingdom

b Department of Physical Sciences, University of the West of Scotland, United Kingdom

Corresponding Author InformationCorresponding author. Tel.: +44 1292 610555; fax: +44 1292 614538.

PII: S1877-5934(09)00057-5

doi:10.1016/j.ijdm.2009.10.005


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