Lack of association between lipaemia and central adiposity in subjects with an atherogenic lipoprotein phenotype (ALP)

Int J Obes Relat Metab Disord. 2000 Sep;24(9):1097-106. doi: 10.1038/sj.ijo.0801372.

Abstract

Objective: To investigate the associations between indices of adiposity and cardiovascular risk factors in individuals with an atherogenic lipoprotein phenotype (ALP).

Subjects: Fifty-five men, aged 34-69 y, body mass index (BMI) 22-35 kg/m2, with an ALP lipid profile (triglycerides (TG) 1.5-4.0 mmol/l, HDL<1.1 mmol/l; %LDL-3>40% total LDL).

Design: Each participant provided a fasting blood sample and underwent an 8 h postprandial assessment and had anthropometric measurements taken.

Outcome measures: BMI, waist circumference (W), waist-to-hip ratio (W/H), sum of skinfolds (SSK), fasting and postprandial concentrations of glucose, insulin and plasma lipids, post-heparin lipase activity, and apoE genotype.

Results: The expected positive associations between BMI, W and SSK and fasting and postprandial insulin were observed (r=0.42-0.65). Little association between glucose responses and any measures of adiposity was evident. Unexpectedly, there were no positive associations between measures of central adiposity (W and W/H) and fasting and postprandial TG responses, with a trend towards negative associations in this study group (TG AUC vs W, r=-0.23, P=0.097; TG IAUC vs W/H, r=-0.26, P=0.068). Subgroup analysis indicated that lack of a positive association between central adiposity and postprandial TG values was more evident in those with one E4 allele (r=-0.42, P=0.077) relative to non-E4 carriers (r=-0.16, P=0.430). The expected positive associations between insulin and TG responses were not observed (r=-0.03 to -0.36).

Conclusion: In this ALP group the expected positive association between TG responses and a centralized distribution of body fat was not observed, particularly in individuals with an apoE4 genotype. Our findings are not in line with the view that there is a clear causal relationship between insulin resistance and the lipid abnormalities associated with ALP.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Abdomen
  • Adult
  • Aged
  • Analysis of Variance
  • Apolipoprotein E4
  • Apolipoproteins E / genetics*
  • Area Under Curve
  • Blood Glucose / metabolism
  • Body Mass Index
  • England
  • Fatty Acids, Nonesterified / metabolism
  • Humans
  • Hyperlipidemias / blood
  • Hyperlipidemias / genetics*
  • Insulin / blood
  • Male
  • Middle Aged
  • Obesity / blood
  • Obesity / genetics*
  • Phenotype
  • Risk Factors
  • Triglycerides / blood
  • White People / genetics

Substances

  • Apolipoprotein E4
  • Apolipoproteins E
  • Blood Glucose
  • Fatty Acids, Nonesterified
  • Insulin
  • Triglycerides