April 2007
MSI Newsletter
Volume 2 - Issue 4
 

Featured Abstracts


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waistThe "hypertriglyceridaemic waist" phenotype as a significant marker of premature coronary artery disease
in patients with glucose intolerance and type 2 diabetes

To test whether the “hypertriglyceridaemic waist” phenotype (waist girth >90 cm in men and >85 cm in women along with a plasma triglyceride concentration of =2.0 mmol/L) predicts early coronary artery disease (CAD) in patients with abnormal glucose metabolism, oral glucose tolerance testing was performed in 1190 men and women using the American Diabetes Association criteria.
> Read entire abstract


blood pressure in childrenSystolic blood pressure in childhood as a predictor of hypertension and metabolic syndrome in later life

To assess the association between hypertension and metabolic syndrome in adulthood and blood pressures in childhood, serial data for 240 men and 253 women from the Fels Longitudinal Study were analyzed, age- and gender-specific childhood blood pressures that predicted hypertension and the metabolic syndrome were derived, and these criterion values were then validated in a larger sample.
> Read entire abstract


brainA defect in brain glucose sensing may play a role in the aetiology of the metabolic syndrome

In humans, de novo synthesis of fatty acids is performed primarily by the liver. Increased hepatic production of very low-density lipoprotein (VLDL) is a critical feature of the metabolic syndrome.
> Read entire abstract

 
Featured Expert Opinion

APOLIPOPROTEIN B/APOLIPOPROTEIN AI RATIO: SHOULD WE START USING IT?
Justo Sierra-Johnson, M.D., M.S.
Virend K. Somers, M.D., Ph.D.
Francisco Lopez- Jimenez, M.D., M.S.

Mayo Clinic, Division of Cardiovascular Diseases, 200 First Street SW, Rochester MN 55905
E-mail: sierrajohnson.justo@mayo.edu, somers.virend@mayo.edu, lopez@mayo.edu

ApoB/ApoAI Ratio

Apolipoproteins are important structural and functional proteins in lipoprotein particles, which transport lipids. Recent reports suggest that measurements of apolipoprotein B/apolipoprotein AI (apoB/apoAI) ratio may improve the prediction of risk for cardiovascular disease [1-4]. ApoB/apoAI ratio may represent the balance between pro-atherogenic and anti-atherogenic lipoproteins [5]. In several clinical studies, serum ApoB concentrations and the apoB/ApoA-I ratio have been reported to predict cardiovascular risk better than any of the cholesterol indices [6].

Metabolic Syndrome

The metabolic syndrome represents the clustering of coronary heart disease (CHD) risk factors that are often associated with insulin resistance [7-9]. Individuals with the metabolic syndrome have an increased risk of cardiovascular morbidity and mortality in most studies. While this risk may be due to the sum of the effects of the component risk factors, the disease mechanisms through which the metabolic syndrome increases CHD risk have not been elucidated.

Our Study

Our recent study [10] aimed to assess whether the metabolic syndrome was associated with a high apoB/AI ratio in a representative sample of the U.S. population, such as NHANES III. For this we analyzed data from 2,964 subjects, mean age 48 years; 1,516 men and 1,448 women.

We compared the mean values of the apoB/apoAI ratio in subjects with and without the metabolic syndrome. We reported that overall, median distribution of the apoB/apoAI ratio was significantly higher (p < 0.0001) in subjects with the ATP-III metabolic syndrome (0.90) than without (0.69). ApoB/apoAI ratio was associated significantly with each of the metabolic syndrome components in descending order of magnitude: low HDL-cholesterol (OR 5.7), high triglycerides (OR 4.7), high waist circumference (OR 2.6), high fasting glucose (OR 1.9), and high blood pressure (OR 1.5). The apoB/apoAI ratio was also different between subjects with and without the metabolic syndrome. Mean values of apoB/apoAI increased significantly as the numbers of metabolic syndrome components increased in both men (p < 0.0001) and women (p < 0.0001). After excluding HDL-cholesterol and triglycerides as criteria for metabolic syndrome, the association between means persisted (ANOVA p < 0.0001) in both men and women. ApoB/apoAI was significantly associated with the presence of the metabolic syndrome (OR 5.1, p < 0.0001). We concluded that apoB/apoAI ratio was strongly associated with the presence of individual metabolic syndrome components and with the metabolic syndrome itself.

Practical Implications

An elevated apoB/apoAI ratio may constitute an important feature of the metabolic syndrome, and is an additional mechanism to explain the increased cardiovascular risk in subjects with this syndrome.

References

  1. Meisinger C, Loewel H, Mraz W, Koenig W. Prognostic value of apolipoprotein B and A-I in the prediction of myocardial infarction in middle-aged men and women: results from the MONICA/KORA Augsburg cohort study. Eur Heart J 2005;26:271-78.

  2. Vaessen SF, Schaap FG, Kuivenhoven JA, et al. Apolipoprotein A-V, triglycerides and risk of coronary artery disease: the prospective Epic-Norfolk Population Study. J Lipid Res 2006;47(9):2064-70.

  3. Dunder K, Lind L, Zethelius B, Berglund L, Lithell H. Evaluation of a scoring scheme, including proinsulin and the apolipoprotein B/apolipo-protein AI ratio, for the risk of acute coronary events in middle-aged men: Uppsala Longitudinal Study of Adult Men (ULSAM). Am Heart J 2004;148:596-601.

  4. Jiang R, Schulze MB, Li T, et al. Non-HDL cholesterol and apolipoprotein B predict cardiovascular disease events among men with type 2 diabetes. Diabetes Care 2004;27:1991-97.

  5. Walldius G, Jungner I. The apoB/apoA-I ratio: a strong, new risk factor for cardiovascular disease and a target for lipid-lowering therapy--a review of the evidence. J Intern Med. 2006;259(5):493-519.

  6. Walldius G, Jungner I, Aastveit AH, Holme I, Furberg CD, Sniderman AD. The apoB/apoA-I ratio is better than the cholesterol ratios to estimate the balance between plasma proatherogenic and antiatherogenic lipoproteins and to predict coronary risk. Clin Chem Lab Med 2004;42:1355-63.

  7. Executive Summary of The Third Report of The National Cholesterol Education Program (NCEP) Expert Panel on Detection, Evaluation, And Treatment of High Blood Cholesterol In Adults (Adult Treatment Panel III). JAMA 2001;285:2486-97.

  8. Federation ID. The IDF consensus worldwide definition of the metabolic syndrome. Available here. Accessed January 18, 2007.

  9. Grundy SM, Cleeman JI, Daniels SR, et al. Diagnosis and management of the metabolic syndrome: an American Heart Association/National Heart, Lung, and Blood Institute Scientific Statement. Circulation 2005;112:2735-52.

  10. Sierra-Johnson J, Somers VK, Kuniyoshi FSH, et al. Comparison of apolipoprotein B/apolipoprotein AI in subjects with - vs - without the metabolic syndrome. Am J Cardiol 2006;15;98(10):1369-73.
 
Featured Upcoming Congresses

Framingham Risk Assessment Tool
Estimates 10-year risk of developing hard CHD
> View Tool

Procam Risk Calculator
Estimates your risk of a heart attack (myocardial infarction) within the next 10 years based upon data of the PROCAM Study
> View Calculator

SCORE (European High Risk Chart)
Estimates 10 year risk of fatal CVD in high risk regions of Europe by gender, age, systolic blood pressure, total cholesterol and smoking status.
> View Chart

UKPDS Risk Engine
The UKPDS Risk Engine is a type 2 diabetes specific risk calculator based on 53,000 patients years of data from the UK Prospective Diabetes Study, which also provides an approximate 'margin of error' for each estimate.
> View Risk Engine

 
Mission of the Metabolic
Syndrome Institute

Created in 2003, the Metabolic Syndrome Institute is an independent and not for profit association. Its members are international experts in lipid metabolism, diabetes, heart disease, endocrinology obesity, genetics, epidemiology, basic research and health economics. Being the first association totally devoted to the dissemination of knowledge about the metabolic syndrome, the Metabolic Syndrome Institute will provide an international multidisciplinary approach to a worldwide public health problem.

 
Contact Metabolic Syndrome Institute
15, rue du Marquis de Coriolis
92563 Rueil-Malmaison Cedex
FRANCE
Phone: (33) 1 41 42 20 35
Fax: (33) 1 41 42 20 01
Email:

contact@metabolic-syndrome-institute.org
Website:
http://www.metabolic- syndrome-institute.org
 
2007 - Metabolic Syndrome Institute Awards Application Deadline: June 1, 2007


"Fighting the Metabolic Syndrome:
Original Contributions"

Click here to view additional information about the
Metabolic Syndrome Institute Awards

Objective:
To promote new talents and research themes around the MetS concept

Definition:
Three awards per year

Applicants:
Young researchers / clinicians

Topics:
Any original contributions to the fight against MetS

Resources:

Jury: the Scientific Committee of the Metabolic Syndrome Institute

Reward:
$10,000 (USD) per award

Output:
- Manuscripts for peer-reviewed journals with MSI grant mentioned in acknowledgements
- Communication campaign: MSI website, press releases, press conferences

Application file:
Download application

Rules & Regulations:


 

Coordinated by Dr. Scott Grundy, President of the IAS