Hostname: page-component-78c5997874-xbtfd Total loading time: 0 Render date: 2024-11-15T01:31:00.818Z Has data issue: false hasContentIssue false

DNA methylation at LRP1 gene locus mediates the association between maternal total cholesterol changes in pregnancy and cord blood leptin levels

Published online by Cambridge University Press:  22 November 2019

Simon-Pierre Guay
Affiliation:
Department of Biochemistry, Université de Sherbrooke, Sherbrooke, QC, Canada ECOGENE-21 Biocluster, Chicoutimi, QC, Canada Department of Medicine, Université de Sherbrooke, Sherbrooke, QC, Canada
Andrée-Anne Houde
Affiliation:
Department of Biochemistry, Université de Sherbrooke, Sherbrooke, QC, Canada ECOGENE-21 Biocluster, Chicoutimi, QC, Canada
Edith Breton
Affiliation:
Department of Biochemistry, Université de Sherbrooke, Sherbrooke, QC, Canada ECOGENE-21 Biocluster, Chicoutimi, QC, Canada
Jean-Patrice Baillargeon
Affiliation:
Department of Medicine, Université de Sherbrooke, Sherbrooke, QC, Canada
Patrice Perron
Affiliation:
ECOGENE-21 Biocluster, Chicoutimi, QC, Canada Department of Medicine, Université de Sherbrooke, Sherbrooke, QC, Canada
Daniel Gaudet
Affiliation:
ECOGENE-21 Biocluster, Chicoutimi, QC, Canada Department of Medicine, Université de Montréal, Montréal, QC, Canada
Marie-France Hivert
Affiliation:
Department of Medicine, Université de Sherbrooke, Sherbrooke, QC, Canada Department of Population Medicine, Harvard Pilgrim Health Care Institute, Harvard Medical School, Boston, MA, USA Diabetes Unit, Massachusetts General Hospital, Boston, MA, USA
Diane Brisson
Affiliation:
ECOGENE-21 Biocluster, Chicoutimi, QC, Canada Department of Medicine, Université de Montréal, Montréal, QC, Canada
Luigi Bouchard*
Affiliation:
Department of Biochemistry, Université de Sherbrooke, Sherbrooke, QC, Canada ECOGENE-21 Biocluster, Chicoutimi, QC, Canada
*
Address for correspondence: Pr. Luigi Bouchard, Department of Biochemistry, Université de Sherbrooke, Chicoutimi, Québec G7H 7P2, Canada. Email: [email protected]

Abstract

Placental lipids transfer is essential for optimal fetal development, and alterations of these mechanisms could lead to a higher risk of adverse birth outcomes. Low-density lipoprotein receptor (LDLR), LDL receptor-related protein 1 (LRP1), and scavenger receptor class B type 1 (SCARB1) genes are encoding lipoprotein receptors expressed in the placenta where they participate in cholesterol exchange from maternal to fetal circulation. The aim of this study was thus to investigate the association between maternal lipid changes occurring in pregnancy, placental DNA methylation (DNAm) variations at LDLR, LRP1, and SCARB1 gene loci, and newborn’s anthropometric profile at birth. Sixty-nine normoglycemic women were followed from the first trimester of pregnancy until delivery. Placental DNAm was quantified at 43 Cytosine-phosphate-Guanines (CpGs) at LDLR, LRP1, and SCARB1 gene loci using pyrosequencing: 4 CpGs were retained for further analysis. Maternal clinical data were collected at each trimester of pregnancy. Newborns’ data were collected from medical records. Statistical models included minimally newborn sex and gestational and maternal age. Maternal total cholesterol changes during pregnancy (ΔT3-T1) were correlated with DNAm variations at LDLR (r = −0.32, p = 0.01) and LRP1 (r = 0.34, p = 0.007). DNAm at these loci was also correlated with newborns’ cord blood triglyceride and leptin levels. Mediation analysis supports a causal relationship between maternal cholesterol changes, DNAm levels at LRP1 locus, and cord blood leptin concentration (pmediation = 0.02). These results suggest that LRP1 DNAm link maternal blood cholesterol changes in pregnancy and offspring adiposity at birth, which provide support for a better follow-up of blood lipids in pregnancy.

Type
Original Article
Copyright
© Cambridge University Press and the International Society for Developmental Origins of Health and Disease 2019

Access options

Get access to the full version of this content by using one of the access options below. (Log in options will check for institutional or personal access. Content may require purchase if you do not have access.)

Footnotes

These authors contributed equally to this work.

References

Potter, JM, Nestel, PJ.The hyperlipidemia of pregnancy in normal and complicated pregnancies. Am J Obstet Gynecol. 1979; 133(2), 165170.CrossRefGoogle ScholarPubMed
Desoye, G, Gauster, M, Wadsack, C.Placental transport in pregnancy pathologies. Am J Clin Nutr. 2011; 94(6 Suppl), 1896S902S.CrossRefGoogle ScholarPubMed
Bansal, N, Cruickshank, JK, McElduff, P, Durrington, PN.Cord blood lipoproteins and prenatal influences. Curr Opin Lipidol. 2005; 16(4), 400408.CrossRefGoogle ScholarPubMed
Misra, VK, Trudeau, S.The influence of overweight and obesity on longitudinal trends in maternal serum leptin levels during pregnancy. Obesity (Silver Spring). 2011; 19(2), 416421.CrossRefGoogle ScholarPubMed
Palinski, W, Yamashita, T, Freigang, S, Napoli, C.Developmental programming: maternal hypercholesterolemia and immunity influence susceptibility to atherosclerosis. Nutr Reviews. 2007; 65(12 Pt 2), S182S187.CrossRefGoogle ScholarPubMed
Edison, RJ, Berg, K, Remaley, A, et al.Adverse birth outcome among mothers with low serum cholesterol. Pediatrics. 2007; 120(4), 723733.CrossRefGoogle ScholarPubMed
Leiva, A, Fuenzalida, B, Westermeier, F, et al.Role for tetrahydrobiopterin in the fetoplacental endothelial dysfunction in maternal supraphysiological hypercholesterolemia. Oxid Med Cell Longev. 2015; 2015, 5346327.Google ScholarPubMed
Mudd, LM, Holzman, CB, Evans, RW.Maternal mid-pregnancy lipids and birthweight. Acta Obstet Gynecol Scand. 2015; 94(8), 852860.CrossRefGoogle ScholarPubMed
Napoli, C, D’Armiento, FP, Mancini, FP, et al.Fatty streak formation occurs in human fetal aortas and is greatly enhanced by maternal hypercholesterolemia. Intimal accumulation of low density lipoprotein and its oxidation precede monocyte recruitment into early atherosclerotic lesions. J Clin Invest. 1997; 100(11), 26802690.CrossRefGoogle ScholarPubMed
Hentschke, MR, Poli-de-Figueiredo, CE, da Costa, BE, Kurlak, LO, Williams, PJ, Mistry, HD.Is the atherosclerotic phenotype of preeclamptic placentas due to altered lipoprotein concentrations and placental lipoprotein receptors? Role of a small-for-gestational-age phenotype. J Lipid Res. 2013; 54(10), 26582664.CrossRefGoogle ScholarPubMed
Wadsack, C, Tabano, S, Maier, A, et al.Intrauterine growth restriction is associated with alterations in placental lipoprotein receptors and maternal lipoprotein composition. Am J Physiol Endocrinol Metab. 2007; 292(2), E476E484.CrossRefGoogle ScholarPubMed
Ethier-Chiasson, M, Duchesne, A, Forest, JC, et al.Influence of maternal lipid profile on placental protein expression of LDLr and SR-BI. Biochem Biophys Res Commun. 2007; 359(1), 814.CrossRefGoogle ScholarPubMed
Stefulj, J, Panzenboeck, U, Becker, T, et al.Human endothelial cells of the placental barrier efficiently deliver cholesterol to the fetal circulation via ABCA1 and ABCG1. Circ Res. 2009; 104(5), 600608.CrossRefGoogle ScholarPubMed
Lillycrop, KA, Burdge, GC.Epigenetic changes in early life and future risk of obesity. Int J Obes (Lond). 2011; 35(1), 7283.CrossRefGoogle ScholarPubMed
Henikoff, S, Matzke, MA.Exploring and explaining epigenetic effects. Trends Genet. 1997; 13(8), 293295.CrossRefGoogle ScholarPubMed
Bird, A.DNA methylation patterns and epigenetic memory. Genes Dev. 2002; 16(1), 621.CrossRefGoogle ScholarPubMed
Heijmans, BT, Tobi, EW, Stein, AD, et al.Persistent epigenetic differences associated with prenatal exposure to famine in humans. Proc Natl Acad Sci USA. 2008; 105(44), 1704617049.CrossRefGoogle ScholarPubMed
Tobi, EW, Lumey, LH, Talens, RP, et al.DNA methylation differences after exposure to prenatal famine are common and timing- and sex-specific. Human Mol Genet. 2009; 18(21), 40464053.CrossRefGoogle ScholarPubMed
Finer, S, Mathews, C, Lowe, R, et al.Maternal gestational diabetes is associated with genome-wide DNA methylation variation in placenta and cord blood of exposed offspring. Human Mol Genet. 2015; 24(11), 30213029.CrossRefGoogle ScholarPubMed
Houde, AA, Guay, SP, Desgagne, V, et al.Adaptations of placental and cord blood ABCA1 DNA methylation profile to maternal metabolic status. Epigenetics. 2013; 8(12), 12891302.CrossRefGoogle ScholarPubMed
Houde, AA, Ruchat, SM, Allard, C, et al.LRP1B, BRD2 and CACNA1D: new candidate genes in fetal metabolic programming of newborns exposed to maternal hyperglycemia. Epigenomics. 2015; 7(7), 11111122.CrossRefGoogle ScholarPubMed
Ruchat, SM, Houde, AA, Voisin, G, et al.Gestational diabetes mellitus epigenetically affects genes predominantly involved in metabolic diseases. Epigenetics. 2013; 8(9), 935943.CrossRefGoogle ScholarPubMed
Houde, AA, St-Pierre, J, Hivert, MF, et al.Placental lipoprotein lipase DNA methylation levels are associated with gestational diabetes mellitus and maternal and cord blood lipid profiles. J Dev Origins Health Dis. 2014; 5(2), 132141.CrossRefGoogle ScholarPubMed
Ahima, RS.Digging deeper into obesity. J Clin Invest. 2011; 121(6), 20762079.CrossRefGoogle ScholarPubMed
Norgan, NG.A review of: “Anthropometric Standardization Reference Manual”. Edited by T. G. LOHMAN, A. F. ROCHE and R. MARTORELL. (Champaign, IL.: Human Kinetics Books, 1988.) [Pp. vi+ 177.] £28·00. ISBN 087322 121 4. Ergonomics. 1988; 31(10), 14931494.CrossRefGoogle Scholar
Lohman, TG, Roche, AF, Martorell, R.Anthropometric Standardization Reference Manual, 1988. Champaign, IL: Human Kinetics Books.Google Scholar
Friedewald, WT, Levy, RI, Fredrickson, DS.Estimation of the concentration of low-density lipoprotein cholesterol in plasma, without use of the preparative ultracentrifuge. Clin Chem. 1972; 18(6), 499502.CrossRefGoogle ScholarPubMed
Fenton, TR, Kim, JH.A systematic review and meta-analysis to revise the Fenton growth chart for preterm infants. BMC Pediatr. 2013; 13, 59.CrossRefGoogle ScholarPubMed
Bouchard, L, Thibault, S, Guay, SP, et al.Leptin gene epigenetic adaptation to impaired glucose metabolism during pregnancy. Diabetes Care. 2010; 33(11), 24362441.CrossRefGoogle ScholarPubMed
Cote, S, Gagne-Ouellet, V, Guay, SP, et al.PPARGC1alpha gene DNA methylation variations in human placenta mediate the link between maternal hyperglycemia and leptin levels in newborns. Clin Epigenet. 2016; 8, 72.CrossRefGoogle ScholarPubMed
Marsh, S.Pyrosequencing applications. Methods Mol Biol. 2007; 373, 1524.Google ScholarPubMed
Guay, SP, Brisson, D, Lamarche, B, et al.DNA methylation variations at CETP and LPL gene promoter loci: new molecular biomarkers associated with blood lipid profile variability. Atherosclerosis. 2013; 228(2), 413420.CrossRefGoogle ScholarPubMed
Guay, SP, Brisson, D, Lamarche, B, Gaudet, D, Bouchard, L.Epipolymorphisms within lipoprotein genes contribute independently to plasma lipid levels in familial hypercholesterolemia. Epigenetics. 2014; 9(5), 718729.CrossRefGoogle ScholarPubMed
Chatzi, L, Plana, E, Daraki, V, et al.Metabolic syndrome in early pregnancy and risk of preterm birth. American J Epidemiol. 2009; 170(7), 829836.CrossRefGoogle ScholarPubMed
Clausen, T, Burski, TK, Oyen, N, Godang, K, Bollerslev, J, Henriksen, T.Maternal anthropometric and metabolic factors in the first half of pregnancy and risk of neonatal macrosomia in term pregnancies. A prospective study. Eur J Endocrinol. 2005; 153(6), 887894.CrossRefGoogle ScholarPubMed
Ramsay, JE, Ferrell, WR, Crawford, L, Wallace, AM, Greer, IA, Sattar, N.Divergent metabolic and vascular phenotypes in pre-eclampsia and intrauterine growth restriction: relevance of adiposity. J Hypertens. 2004; 22(11). 21772183.CrossRefGoogle ScholarPubMed
Tyrrell, J, Richmond, RC, Palmer, TM, et al.Genetic evidence for causal relationships between maternal obesity-related traits and birth weight. JAMA. 2016; 315(11), 11291140.CrossRefGoogle ScholarPubMed
Clausen, TD, Mathiesen, ER, Hansen, T, et al.Overweight and the metabolic syndrome in adult offspring of women with diet-treated gestational diabetes mellitus or type 1 diabetes. J Clin Endocrinol Metab. 2009; 94(7), 24642470.CrossRefGoogle ScholarPubMed
Van der Graaf, A, Vissers, MN, Gaudet, D, et al.Dyslipidemia of mothers with familial hypercholesterolemia deteriorates lipids in adults offspring. Arteriosclerosis Thromb Vasc Biol. 2010; 30(12), 26732677.CrossRefGoogle ScholarPubMed
Sitras, V, Fenton, C, Paulssen, R, Vartun, A, Acharya, G.Differences in gene expression between first and third trimester human placenta: a microarray study. PLoS One. 2012; 7(3), e33294.CrossRefGoogle ScholarPubMed
Rakyan, VK, Down, TA, Balding, DJ, Beck, S.Epigenome-wide association studies for common human diseases. Nat Rev Genet. 2011; 12(8), 529541.CrossRefGoogle ScholarPubMed
Toperoff, G, Aran, D, Kark, JD, et al.Genome-wide survey reveals predisposing diabetes type 2-related DNA methylation variations in human peripheral blood. Human Mol Genet. 2012; 21(2), 371383.CrossRefGoogle ScholarPubMed
Stepan, H, Faber, R, Walther, T.Expression of low density lipoprotein receptor messenger ribonucleic acid in placentas from pregnancies with intrauterine growth retardation. Br J Obstet Gynaecol. 1999; 106(11), 12211222.CrossRefGoogle ScholarPubMed
Frantz, E, Menezes, HS, Lange, KC, et al.The effect of maternal hypercholesterolemia on the placenta and fetal arteries in rabbits. Acta Cir Bras. 2012; 27(1), 712.CrossRefGoogle ScholarPubMed
Hussain, MM, Strickland, DK, Bakillah, A.The mammalian low-density lipoprotein receptor family. Annu Rev Nutr. 1999; 19, 141172.CrossRefGoogle ScholarPubMed
May, P, Rohlmann, A, Bock, HH, et al.Neuronal LRP1 functionally associates with postsynaptic proteins and is required for normal motor function in mice. Mol Cell Biol. 2004; 24(20), 88728883.CrossRefGoogle ScholarPubMed
Liu, Q, Zhang, J, Zerbinatti, C, et al.Lipoprotein receptor LRP1 regulates leptin signaling and energy homeostasis in the adult central nervous system. PLoS Biol. 2011; 9(1), e1000575.CrossRefGoogle ScholarPubMed
Hofmann, SM, Zhou, L, Perez-Tilve, D, et al.Adipocyte LDL receptor-related protein-1 expression modulates postprandial lipid transport and glucose homeostasis in mice. J Clin Invest. 2007; 117(11), 32713282.CrossRefGoogle ScholarPubMed
Cardenas, A, Koestler, DC, Houseman, EA, et al.Differential DNA methylation in umbilical cord blood of infants exposed to mercury and arsenic in utero. Epigenetics. 2015; 10(6), 508515.CrossRefGoogle ScholarPubMed
Banik, A, Kandilya, D, Ramya, S, Stunkel, W, Chong, YS, Dheen, ST.Maternal factors that induced epigenetic changes contribute to neurological disorders in offspring. Genes. 2017; 8(6), E150.CrossRefGoogle Scholar
Supplementary material: File

Guay et al. supplementary material

Guay et al. supplementary material

Download Guay et al. supplementary material(File)
File 445.8 KB