Am. Minihane et al., Lack of association between lipaemia and central adiposity in subjects with an atherogenic lipoprotein phenotype (ALP), INT J OBES, 24(9), 2000, pp. 1097-1106
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/
m(2), 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). s
um 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 fast
ing and postprandial insulin were observed (r=0.42-0.65), Little associatio
n between glucose responses and any measures of adiposity was evident. Unex
pectedly, there were no positive associations between measures of central a
diposity (W and W/H) and fasting and postprandial TG responses, with a tren
d 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 tha
t 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 assoc
iations between insulin and TG responses were not observed (r=-0.03 to -0.3
6).
CONCLUSION: In this ALP group the expected positive association between TG
responses and a centralized distribution of body fat was not observed, part
icularly in individuals with an apoE4 genotype. Our findings are not in lin
e with the view that there is a clear causal relationship between insulin r
esistance and the lipid abnormalities associated with ALP.