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Effect of Atorvastatin and Niacin/LRPT on Apolipoprotein E Distribution, Metabolism and Glycation

Yifen Liu, Jonathan D Schofield, Rahul Yadav, Salam Hama, Michael France, See Kwok, Deepak Bhatnagar, Edward Hinchliffe, Gilbert Wieringa, Paul N Durringtonand Handrean Soran

In: EAS Congress2015; 22 Mar 2015-25 Mar 2015; 2015.

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Abstract

Aim: To investigate the influence of apoE genotype on the response to atorvastatin treatment in patients with Type 2 diabetes with nephropathy and the effect of niacin/laropiprant (LRPT) on apoE and glycated apoE concentration and distribution in hyperlipidaemia.Methods: ApoE genotype and the effect of 10mg/day and 80mg/day atorvastatin treatment on apoE concentration were studied in 85 patients with type 2 diabetes with nephropathy. The effect of niacin/LRPT on apoE and glycated apoE was investigated for 36 patients with hyperlipidaemia. Results: After 12 months treatment with atorvastatin, serum apoE concentration decreased significantly in the 80mg/day, but not the 10mg/day group. This decrease was observed in patients with E3 and E4 but not E2 genotype. Hyperlipidaemia did not affect total apoE, but the apoE distribution in HDL and d>1.21g/ml lipoprotein fractions was significantly lower. Glycated apoE was significantly higher in patients with hyperlipidaemia than healthy volunteers (p<0.0001). After 3 months treatment with niacin/LRPT, apoE in apoB–containing lipoproteins (VLDL+LDL) was significantly reduced, but was unchanged in apoA-containing lipoproteins (HDL) compared with treatment with placebo. Niacin/LRPT also had no effect on the elevated glycated apoE observed in patients with hyperlipidaemia.Conclusions: The effect of atorvastatin on total apoE concentration is dependent on the dose of atorvastatin and apoE genotype in patients with type 2 diabetes with nephropathy. Niacin/LRPT has no significant effect on total apoE and glycated apoE, but does influence their distribution in lipoprotein fractions in patients with hyperlipidaemia.

Bibliographic metadata

Type of resource:
Content type:
Type of conference contribution:
Publication date:
Conference title:
EAS Congress2015
Conference start date:
2015-03-22
Conference end date:
2015-03-25
Abstract:
Aim: To investigate the influence of apoE genotype on the response to atorvastatin treatment in patients with Type 2 diabetes with nephropathy and the effect of niacin/laropiprant (LRPT) on apoE and glycated apoE concentration and distribution in hyperlipidaemia.Methods: ApoE genotype and the effect of 10mg/day and 80mg/day atorvastatin treatment on apoE concentration were studied in 85 patients with type 2 diabetes with nephropathy. The effect of niacin/LRPT on apoE and glycated apoE was investigated for 36 patients with hyperlipidaemia. Results: After 12 months treatment with atorvastatin, serum apoE concentration decreased significantly in the 80mg/day, but not the 10mg/day group. This decrease was observed in patients with E3 and E4 but not E2 genotype. Hyperlipidaemia did not affect total apoE, but the apoE distribution in HDL and d>1.21g/ml lipoprotein fractions was significantly lower. Glycated apoE was significantly higher in patients with hyperlipidaemia than healthy volunteers (p<0.0001). After 3 months treatment with niacin/LRPT, apoE in apoB–containing lipoproteins (VLDL+LDL) was significantly reduced, but was unchanged in apoA-containing lipoproteins (HDL) compared with treatment with placebo. Niacin/LRPT also had no effect on the elevated glycated apoE observed in patients with hyperlipidaemia.Conclusions: The effect of atorvastatin on total apoE concentration is dependent on the dose of atorvastatin and apoE genotype in patients with type 2 diabetes with nephropathy. Niacin/LRPT has no significant effect on total apoE and glycated apoE, but does influence their distribution in lipoprotein fractions in patients with hyperlipidaemia.

Institutional metadata

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Record metadata

Manchester eScholar ID:
uk-ac-man-scw:245846
Created by:
Liu, Yifen
Created:
10th January, 2015, 16:33:01
Last modified by:
Liu, Yifen
Last modified:
20th February, 2015, 19:16:01

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