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

Citation
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
Citations number
63
Categorie Soggetti
Endocrynology, Metabolism & Nutrition","Endocrinology, Nutrition & Metabolism
Journal title
INTERNATIONAL JOURNAL OF OBESITY
ISSN journal
03070565 → ACNP
Volume
24
Issue
9
Year of publication
2000
Pages
1097 - 1106
Database
ISI
SICI code
0307-0565(200009)24:9<1097:LOABLA>2.0.ZU;2-X
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/ 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.