Triglyceride-lowering LPL alleles combined with LDL-C-lowering alleles are associated with an additively improved lipoprotein profile

Mendelian randomization studies have shown that triglyceride (TG)- lowering lipoprotein lipase (LPL) alleles and low-density lipoprotein-cholesterol (LDL-C)-lowering alleles have independent beneficial associations on cardiovascular disease (CVD) risk. We aimed to provide further insight into this o...

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Veröffentlicht in:Atherosclerosis 2021-07, Vol.328, p.144-152
Hauptverfasser: Ibi, Dorina, Blauw, Lisanne L., Noordam, Raymond, Dollé, Martijn E.T., Jukema, J. Wouter, Rosendaal, Frits R., Christodoulides, Constantinos, Neville, Matt J., Koivula, Robert, Rensen, Patrick C.N., Karpe, Fredrik, van Dijk, Ko Willems
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container_issue
container_start_page 144
container_title Atherosclerosis
container_volume 328
creator Ibi, Dorina
Blauw, Lisanne L.
Noordam, Raymond
Dollé, Martijn E.T.
Jukema, J. Wouter
Rosendaal, Frits R.
Christodoulides, Constantinos
Neville, Matt J.
Koivula, Robert
Rensen, Patrick C.N.
Karpe, Fredrik
van Dijk, Ko Willems
description Mendelian randomization studies have shown that triglyceride (TG)- lowering lipoprotein lipase (LPL) alleles and low-density lipoprotein-cholesterol (LDL-C)-lowering alleles have independent beneficial associations on cardiovascular disease (CVD) risk. We aimed to provide further insight into this observation by applying Mendelian randomization analyses of genetically-influenced TG and LDL-C levels on plasma metabolomic profiles. We quantified over 100 lipoprotein metabolomic measures in the Netherlands Epidemiology of Obesity (NEO) study (N = 4838) and Oxford Biobank (OBB) (N = 6999) by nuclear magnetic resonance (NMR) spectroscopy. Weighted genetic scores for TG via five LPL alleles and LDL-C via 19 alleles were calculated and dichotomized by the median, resulting in four genotype combinations of high/low TG and high/low LDL-C. We performed linear regression analyses using a two × two design with the group with genetically-influenced high TG and LDL-C as a reference. Compared to the individual groups with genetically-influenced lower TG or lower LDL-C only, the group with combined genetically-influenced lower TG and LDL-C showed an overall independent and additive pattern of changes in metabolomic measures. Over 100 measures were different (p < 1.35 × 10−3) compared to the reference, with effect sizes and directionality being similar in NEO and OBB. Most notably, levels of all very-low density lipoprotein (VLDL) and LDL sub-particles were lower. Our findings provide evidence that TG-lowering on top of LDL-C-lowering has additive beneficial effects on the lipoprotein profile compared to TG-lowering or LDL-C-lowering only, which is in accordance with reported additive genetic effects on CVD risk reduction. [Display omitted] •The combined triglyceride (TG) and lipoprotein-cholesterol (LDL-C)-lowering resulted in the most beneficial lipoprotein profile.•The effects of TG-lowering via LPL and LDL-C-lowering were additive and independent.•Over 100 measures were different in the combination group, most notably very-low density lipoprotein (VLDLs) and low-density lipoprotein (LDLs).•Our results support the previously reported additive beneficial LPL effects on cardiovascular disease.
doi_str_mv 10.1016/j.atherosclerosis.2021.04.015
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Wouter ; Rosendaal, Frits R. ; Christodoulides, Constantinos ; Neville, Matt J. ; Koivula, Robert ; Rensen, Patrick C.N. ; Karpe, Fredrik ; van Dijk, Ko Willems</creator><creatorcontrib>Ibi, Dorina ; Blauw, Lisanne L. ; Noordam, Raymond ; Dollé, Martijn E.T. ; Jukema, J. Wouter ; Rosendaal, Frits R. ; Christodoulides, Constantinos ; Neville, Matt J. ; Koivula, Robert ; Rensen, Patrick C.N. ; Karpe, Fredrik ; van Dijk, Ko Willems</creatorcontrib><description>Mendelian randomization studies have shown that triglyceride (TG)- lowering lipoprotein lipase (LPL) alleles and low-density lipoprotein-cholesterol (LDL-C)-lowering alleles have independent beneficial associations on cardiovascular disease (CVD) risk. We aimed to provide further insight into this observation by applying Mendelian randomization analyses of genetically-influenced TG and LDL-C levels on plasma metabolomic profiles. We quantified over 100 lipoprotein metabolomic measures in the Netherlands Epidemiology of Obesity (NEO) study (N = 4838) and Oxford Biobank (OBB) (N = 6999) by nuclear magnetic resonance (NMR) spectroscopy. Weighted genetic scores for TG via five LPL alleles and LDL-C via 19 alleles were calculated and dichotomized by the median, resulting in four genotype combinations of high/low TG and high/low LDL-C. We performed linear regression analyses using a two × two design with the group with genetically-influenced high TG and LDL-C as a reference. Compared to the individual groups with genetically-influenced lower TG or lower LDL-C only, the group with combined genetically-influenced lower TG and LDL-C showed an overall independent and additive pattern of changes in metabolomic measures. Over 100 measures were different (p &lt; 1.35 × 10−3) compared to the reference, with effect sizes and directionality being similar in NEO and OBB. Most notably, levels of all very-low density lipoprotein (VLDL) and LDL sub-particles were lower. Our findings provide evidence that TG-lowering on top of LDL-C-lowering has additive beneficial effects on the lipoprotein profile compared to TG-lowering or LDL-C-lowering only, which is in accordance with reported additive genetic effects on CVD risk reduction. 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We aimed to provide further insight into this observation by applying Mendelian randomization analyses of genetically-influenced TG and LDL-C levels on plasma metabolomic profiles. We quantified over 100 lipoprotein metabolomic measures in the Netherlands Epidemiology of Obesity (NEO) study (N = 4838) and Oxford Biobank (OBB) (N = 6999) by nuclear magnetic resonance (NMR) spectroscopy. Weighted genetic scores for TG via five LPL alleles and LDL-C via 19 alleles were calculated and dichotomized by the median, resulting in four genotype combinations of high/low TG and high/low LDL-C. We performed linear regression analyses using a two × two design with the group with genetically-influenced high TG and LDL-C as a reference. Compared to the individual groups with genetically-influenced lower TG or lower LDL-C only, the group with combined genetically-influenced lower TG and LDL-C showed an overall independent and additive pattern of changes in metabolomic measures. 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subjects Cardiovascular disease
LDL-Cholesterol-lowering
Lipoprotein lipase
Mendelian randomization
Metabolomics
Triglyceride-lowering
title Triglyceride-lowering LPL alleles combined with LDL-C-lowering alleles are associated with an additively improved lipoprotein profile
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