Low serum LDL cholesterol in patients with type 2 diabetes: An analysis on two different patient populations
Introduction
Patients with type 2 diabetes (T2DM) are at a two- to threefold increased risk of cardiovascular disease [1], and cardiovascular disease is the primary cause of death in these patients [2]. The identification and treatment of cardiovascular risk factors among diabetic patients therefore are of paramount importance.
Clinically, T2DM is defined through an elevation of glucose levels [3]. However, also alterations in the lipid profile are characteristic for patients with T2DM: Typically, these patients have high triglycerides, low HDL cholesterol (HDL-C), and a small LDL particle diameter [4]. This pattern of lipid abnormalities strongly increases the risk of vascular events in diabetic patients [5] and is referred to as the atherogenic lipid triad.
Also LDL cholesterol (LDL-C) is an important risk factor in patients with T2DM [6]. Statin treatment (which primarily decreases LDL) significantly reduces vascular events by about 20% in diabetic patients, in particular in the very high-risk subgroup of diabetic patients with coronary artery disease [7]. Still, the majority of vascular events are not prevented through statin treatment in patients with T2DM. Whatsoever, LDL-C is the primary target for lipid intervention in current guidelines [8].
Given the central role of LDL in current lipid management, this atherogenic lipoprotein fraction in diabetic patients deserves particular attention. However, no previous investigation has focused on whether LDL-C levels in diabetic patients from current clinical practice differ from those of non-diabetic subjects. In the present study we therefore aimed at investigating the association of diabetes with serum LDL-C in two different large patient cohorts.
Section snippets
Patients
For the present analysis, data from two cohorts were obtained: i) from a consecutive series of patients undergoing coronary angiography for the evaluation of coronary artery disease (n = 756), and ii) from a large sample of outpatients with arterial hypertension (n = 5949).
Details on our population of angiographied coronary patients have been published previously [5], [9]. In short, we recruited 756 Caucasian patients from November 1999 through October 2000 who were referred to coronary angiography
Results
Our cohort of angiographied coronary patients was characteristic for patients undergoing coronary angiography for the evaluation of CAD, with a mean age of 63 ±10 years, a preponderance of male gender (67.9%), and a high prevalence of T2DM (21.9%), hypertension (52.0%), and smoking (58.1%). Coronary angiography in 82.0% of our patients revealed CAD, and 60.8% had significant coronary stenoses at angiography.
Table 1 summarizes characteristics of the angiographied coronary patients with respect to
Discussion
From our data we conclude that in addition to the high triglyceride/low HDL-C pattern of dyslipidemia, patients with T2DM both among angiographied coronary patients and among hypertensive outpatients have significantly lower LDL-C than non-diabetic individuals.
Our data are derived from two large patient cohorts from current clinical practice. Because statin treatment is a cornerstone in today's management of cardiovascular risk in diabetic patients, a considerable proportion of our diabetic
Contributors
The LIIFE in LIFE study board (H. Drexel, Feldkirch, Austria; B. Eber, Wels, Austria; F. Hoppichler, Salzburg, Austria; K. Huber, Vienna, Austria; W. Lang, Vienna; Austria; B. Ludvik, Vienna; Austria; G. Mayer, Innsbruck, Austria; KP. Pfeiffer, Innsbruck, Austria; M. Pichler, Salzburg, Austria; E. Rebhandl, Vienna, Austria; A. Rieder, Vienna, Austria; K. Silberbauer, Eisenstadt, Austria; J. Slany, Vienna, Austria; G. Stark, Deutschlandsberg, Austria; K. Stoschitzky, Graz, Austria; O. Traindl,
Acknowledgements
The VIVIT Institute thanks Dr. Egmond Frommelt and the Innovationsstiftung of the Liechtenstein Global Trust (LGT) Bank (Bendern, Liechtenstein), Dr. Karl Josef Hier and the Peter Goop Stiftung (Vaduz, Liechtenstein), the Fachhochschule Dornbirn (Dornbirn, Austria), and the Institute for Clinical Chemistry at the Academic Teaching Hospital Feldkirch (Feldkirch, Austria) for providing us with generous research grants. We are grateful to Franz Rauch and the Vorarlberger Industriellenvereinigung
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