APOE, apolipoprotein E, 348

N. diseases: 1049; N. variants: 62
Source: ALL
Disease Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
CUI: C0020443
Disease: Hypercholesterolemia
Hypercholesterolemia
0.700 GeneticVariation disease BEFREE The aim of this study was to investigate the effects of HS and GP tea consumption on anthropometric data, fasting blood glucose (FBG), and lipid concentrations in hypercholesterolemia subjects with different genotypes of the APOE and CETP TaqIB polymorphisms. 28244718 2017
CUI: C0020443
Disease: Hypercholesterolemia
Hypercholesterolemia
0.700 GeneticVariation disease BEFREE Here, we test whether hypercholesterolemia (HC) and ApoE polymorphisms affect the risk of ICH by statin use. 24008570 2013
CUI: C0020443
Disease: Hypercholesterolemia
Hypercholesterolemia
0.700 GeneticVariation disease BEFREE We analyzed whether low birth weight and apolipoprotein E (Apo E) polymorphism participate in the onset of hypercholesterolemia in children. 18052682 2008
CUI: C0020443
Disease: Hypercholesterolemia
Hypercholesterolemia
0.700 GeneticVariation disease BEFREE APOE ε4 allele is an established risk factor for Alzheimer's disease and hypercholesterolemia. 31677348 2019
CUI: C0020443
Disease: Hypercholesterolemia
Hypercholesterolemia
0.700 GeneticVariation disease BEFREE Hypercholesterolemia with statin use was associated with less risk of ICH (OR=0.30; P=0.0008) in multivariable analysis after controlling for alcohol use, hypertension, previous stroke, first-degree relative with ICH, education level, and apolipoprotein E alleles. 15087556 2004
CUI: C0020443
Disease: Hypercholesterolemia
Hypercholesterolemia
0.700 GeneticVariation disease BEFREE To examine a long-term effect of community-based education program for hypercholesterolemia and an effect modification by apolipoprotein E polymorphism, we conducted a 1-year randomized clinical trial with 8 year-follow-up. 12119210 2002
CUI: C0020443
Disease: Hypercholesterolemia
Hypercholesterolemia
0.700 GeneticVariation disease BEFREE APOE genotypes were not associated with hypercholesterolemia. 30457419 2019
CUI: C0020443
Disease: Hypercholesterolemia
Hypercholesterolemia
0.700 GeneticVariation disease BEFREE The interaction effect between APOE genotype and hypercholesterolemia was statistically significant in both cohorts. 26495840 2016
CUI: C0020443
Disease: Hypercholesterolemia
Hypercholesterolemia
0.700 GeneticVariation disease BEFREE Effect of apolipoprotein E polymorphism on the serum lipid response to a hypolipidemic diet rich in monounsaturated fatty acids in patients with hypercholesterolemia and combined hyperlipidemia. 7825526 1995
CUI: C0020443
Disease: Hypercholesterolemia
Hypercholesterolemia
0.700 GeneticVariation disease BEFREE Increased frequency of the apolipoprotein E-4 isoform in male subjects with multifactorial hypercholesterolemia. 4006269 1985
CUI: C0020443
Disease: Hypercholesterolemia
Hypercholesterolemia
0.700 GeneticVariation disease BEFREE The apolipoprotein E (APOE) epsilon4 allele is associated with elevated cholesterol and risk of atherosclerosis. 18301447 2008
CUI: C0020443
Disease: Hypercholesterolemia
Hypercholesterolemia
0.700 GeneticVariation disease BEFREE Noncarriers of the APOE ε4 allele with severe CAA compared with those without CAA had a higher prevalence of stroke (11.1% vs 3.9%, respectively; OR = 3.8; 95% CI, 1.0-14.6) and hypercholesterolemia (50.0% vs 32.7%, respectively; OR = 2.3; 95% CI, 1.1-4.7). 24797962 2014
CUI: C0020443
Disease: Hypercholesterolemia
Hypercholesterolemia
0.700 GeneticVariation disease BEFREE The Apolipoprotein E (ApoE) gene has three major isoforms encoded by the ε2, ε3, and ε4 alleles, with the ε4 allele associated with hypercholesterolemia and the ε2 allele with the opposite effect. 22350157 2012
CUI: C0020443
Disease: Hypercholesterolemia
Hypercholesterolemia
0.700 GeneticVariation disease BEFREE A total of 100 unrelated children (6 +/-3 years old, 43 boys, 57 girls) with type IIa HC (LDLC >130 mg/dL) and complete genetic testing (at loci for genes for LDLR, apolipoprotein B, proprotein convertase subtilisin-like kesin type 9, and apolipoprotein E) were selected for score elaboration. 19330934 2009
CUI: C0020443
Disease: Hypercholesterolemia
Hypercholesterolemia
0.700 GeneticVariation disease BEFREE An APOE variant was identified in three patients with isolated severe hypercholesterolemia giving a frequency of 1.3% in the cohort. 26802169 2016
CUI: C0020443
Disease: Hypercholesterolemia
Hypercholesterolemia
0.700 GeneticVariation disease BEFREE We recruited 49 nonfamilial hypercholesterolemia genetic hypercholesterolemia families (294 participants) and calculated cholesterol gene scores, derived from single nucleotide variants in SORT1, APOB, ABCG8, APOE and LDLR and lipoprotein(a) plasma concentration. 28919240 2018
CUI: C0020443
Disease: Hypercholesterolemia
Hypercholesterolemia
0.700 GeneticVariation disease BEFREE The apolipoprotein E gene (apoE) has three major isoforms encoded by the ε2, ε3, and ε4 alleles, with the ε4 allele associated with hypercholesterolemia and the ε2 allele with the opposite effect. 20861397 2010
CUI: C0020443
Disease: Hypercholesterolemia
Hypercholesterolemia
0.700 GeneticVariation disease BEFREE In the present study, we examined the levels of plasma lipids and apolipoproteins in patients with non-insulin dependent diabetes mellitus (NIDDM) with hypercholesterolemia in different apolipoprotein E (apo E) phenotypes. 8344125 1993
CUI: C0020443
Disease: Hypercholesterolemia
Hypercholesterolemia
0.700 GeneticVariation disease BEFREE In the ADH group, nine subjects (3.1%) were carriers of the APOE c.500_502delTCC, p.Leu167del mutation, cosegregating with hypercholesterolemia in studied families. 27014949 2016
CUI: C0020443
Disease: Hypercholesterolemia
Hypercholesterolemia
0.700 GeneticVariation disease BEFREE Family studies failed to demonstrate cosegregation between the new mutations and severe hyperlipoproteinemia, although a number of carriers for the APOE*3(Cys112-->Arg; Arg251-->Gly) allele and the APOE*1(Arg158-->Cys; Leu252-->Glu) allele expressed hypertriglyceridemia and/or hypercholesterolemia. 8488843 1993
CUI: C0020443
Disease: Hypercholesterolemia
Hypercholesterolemia
0.700 GeneticVariation disease BEFREE Apolipoprotein E gene polymorphisms in Lebanese with hypercholesterolemia. 23537987 2013
CUI: C0020443
Disease: Hypercholesterolemia
Hypercholesterolemia
0.700 GeneticVariation disease BEFREE Effects of ezetimibe on lipids and lipoproteins in patients with hypercholesterolemia and different apolipoprotein E genotypes. 17559752 2007
CUI: C0020443
Disease: Hypercholesterolemia
Hypercholesterolemia
0.700 GeneticVariation disease BEFREE This study shows the relevance of polymorphisms in APOB (odds ratio (OR), 1.17; 95% confidence interval (95% CI), 0.74-1.85), APOC3 (OR, 1.33; 95% CI, 0.82-2.17) and APOE (OR, 1.75; 95% CI, 1.09-2.80), as genetic risk markers for hypercholesterolemia; polymorphisms in ACE (OR, 1.68; 95% CI, 0.32-8.77) and AGT (OR, 1.74; 95% CI, 0.97-3.14) for hypertension; and in APOE*3/*4 (OR, 2.06; 95% CI, 1.70-2.51) and APOE*4/*4 (OR, 3.08; 95% CI, 1.85-5.12) as unambiguous markers of dementia. 29081697 2017
CUI: C0020443
Disease: Hypercholesterolemia
Hypercholesterolemia
0.700 GeneticVariation disease BEFREE We performed genetic analysis in 55 patients with clinical features of possible type IIa hypercholesterolemia and 76 normolipemic healthy subjects for mutations and polymorphisms in the low-density lipoprotein (LDL) receptor (LDLR), apolipoprotein B-100 (APOB), apolipoprotein E (APOE), and hepatic lipase (LIPC) genes to elucidate the important genetic factors that can influence cholesterol levels in our population. 18022922 2007
CUI: C0020443
Disease: Hypercholesterolemia
Hypercholesterolemia
0.700 GeneticVariation disease BEFREE Demographic and vascular risk factors were measured at baseline (obesity, smoking, diabetes, prehypertension, hypertension, and hypercholesterolemia) as well as presence of the APOE ε4 genotype. 28783817 2017