LPA, lipoprotein(a), 4018

N. diseases: 340; N. variants: 49
Source: ALL
Disease Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
CUI: C0027051
Disease: Myocardial Infarction
Myocardial Infarction
0.200 GeneticVariation disease BEFREE APO(a) variants and lipoprotein(a) in men with or without myocardial infarction. 12127051 2002
CUI: C0027051
Disease: Myocardial Infarction
Myocardial Infarction
0.200 Biomarker disease BEFREE APOE ε2 is a strong genetic determinant of low lipoprotein(a) concentrations but does not modify the causal association of lipoprotein(a) with myocardial infarction or aortic valve stenosis. 28651346 2017
CUI: C0027051
Disease: Myocardial Infarction
Myocardial Infarction
0.200 AlteredExpression disease BEFREE Elevated levels of lipoprotein(a) were not causally associated with increased low-grade inflammation as measured through CRP despite a causal association with increased risk of aortic valve stenosis and MI. 25938632 2015
CUI: C0027051
Disease: Myocardial Infarction
Myocardial Infarction
0.200 AlteredExpression disease BEFREE As some incorrect reclassification of individuals with no events occurred, addition of lipoprotein(a) levels ≥80th percentile overall yielded net reclassification indices of +16% (95% confidence interval: 8% to 24%) and +3% (-1% to 8%) for MI and CHD, respectively. 23375930 2013
CUI: C0027051
Disease: Myocardial Infarction
Myocardial Infarction
0.200 Biomarker disease BEFREE Alirocumab significantly reduced other lipid/lipoproteins (including lipoprotein[a]) similarly in patients with/without MI/ischemic stroke. 31076261 2020
CUI: C0027051
Disease: Myocardial Infarction
Myocardial Infarction
0.200 GeneticVariation disease BEFREE Establishing age and sex dependent upper reference limits for the plasma lipoprotein (a) in a Chinese health check-up population and according to its relative risk of primary myocardial infarction. 29883631 2018
CUI: C0027051
Disease: Myocardial Infarction
Myocardial Infarction
0.200 GeneticVariation disease BEFREE The aim of the present study was to analyze, on a double-blind basis, the relationships between the apolipoprotein(a) (apo(a)) gene and protein size polymorphisms in healthy volunteers (n = 99) and patients with premature myocardial infarction (n = 91). 14580163 2003
CUI: C0027051
Disease: Myocardial Infarction
Myocardial Infarction
0.200 GeneticVariation disease BEFREE We tested the hypotheses that high lipoprotein(a) cholesterol and LPA risk genotypes are a possible cause of clinical familial hypercholesterolaemia, and that individuals with both high lipoprotein(a) concentrations and clinical familial hypercholesterolaemia have the highest risk of myocardial infarction. 27185354 2016
CUI: C0027051
Disease: Myocardial Infarction
Myocardial Infarction
0.200 GeneticVariation disease BEFREE We found that individuals with HDL-C ≤1.25 mmol/L, GRS >20.9 and lipoprotein (a) > 0.09 g/L had a higher risk of MI than those who at the lowest risk group (OR: 5.89, 95% CI: 3.99-8.69). 29258680 2017
CUI: C0027051
Disease: Myocardial Infarction
Myocardial Infarction
0.200 Biomarker disease BEFREE Lipoprotein(a) concentration does not differ between sexes in healthy offspring of patients with premature myocardial infarction. 21519277 2011
CUI: C0027051
Disease: Myocardial Infarction
Myocardial Infarction
0.200 AlteredExpression disease BEFREE To compare lipoprotein(a) levels in diabetic patients and normoglycemic relatives in familial NIDDM and to assess whether Lp(a) is a risk factor for myocardial infarction in this population. 8495614 1993
CUI: C0027051
Disease: Myocardial Infarction
Myocardial Infarction
0.200 GeneticVariation disease GWASCAT A comprehensive 1,000 Genomes-based genome-wide association meta-analysis of coronary artery disease. 26343387 2015
CUI: C0027051
Disease: Myocardial Infarction
Myocardial Infarction
0.200 GeneticVariation disease BEFREE Sequence polymorphisms in the apolipoprotein(a) gene and their association with lipoprotein(a) levels and myocardial infarction. The ECTIM Study. 10407493 1999
CUI: C0027051
Disease: Myocardial Infarction
Myocardial Infarction
0.200 GeneticVariation disease BEFREE Lipoprotein(a) [Lp(a)] levels predict the risk of myocardial infarction (MI) in populations of European ancestry; however, few data are available for other ethnic groups. 30667276 2019
CUI: C0027051
Disease: Myocardial Infarction
Myocardial Infarction
0.200 Biomarker disease BEFREE Apolipoprotein (a) [Lp(a)] phenotypes of 69 myocardial infarction survivor and 56 stroke patients were reported and compared to those of 190 healthy Chinese. 8194380 1994
CUI: C0027051
Disease: Myocardial Infarction
Myocardial Infarction
0.200 Biomarker disease BEFREE Further, in 108,602 individuals from the Copenhagen General Population Study in random nonfasting samples, the highest versus the lowest quartile of triglycerides, total cholesterol, LDL cholesterol, remnant cholesterol, non-HDL cholesterol, lipoprotein(a), and apolipoprotein B were all associated with higher risk of both ischaemic heart disease and myocardial infarction. 30522787 2019
CUI: C0027051
Disease: Myocardial Infarction
Myocardial Infarction
0.200 GeneticVariation disease BEFREE Lipoprotein(a) (Lp(a)) is an important causal cardiovascular risk factor, with serum Lp(a) levels predicting atherosclerotic heart disease and genetic determinants of Lp(a) levels showing association with myocardial infarction. 21283670 2011
CUI: C0027051
Disease: Myocardial Infarction
Myocardial Infarction
0.200 GeneticVariation disease BEFREE Lp(a) and LPA kringle IV type 2 tertiles also associated with the risk of myocardial infarction in general population studies (trend: P<0.001 to 0.003). 22516069 2012
CUI: C0027051
Disease: Myocardial Infarction
Myocardial Infarction
0.200 GeneticVariation disease BEFREE Association of polymorphisms of the apolipoprotein(a) gene with lipoprotein(a) levels and myocardial infarction. 12578871 2003
CUI: C0027051
Disease: Myocardial Infarction
Myocardial Infarction
0.200 GeneticVariation disease BEFREE Elevated lipoprotein(a) levels represent a genetically determined risk factor for myocardial infarction (MI) and aortic valve stenosis (AVS). 26656145 2016
CUI: C0027051
Disease: Myocardial Infarction
Myocardial Infarction
0.200 Biomarker disease BEFREE Lipoprotein(a) [Lp(a)] is the strongest independent genetic risk factor for both myocardial infarction and aortic stenosis. 28059953 2017
CUI: C0027051
Disease: Myocardial Infarction
Myocardial Infarction
0.200 GeneticVariation disease BEFREE Finally, we tested these 24 SNPs in a third study (475 cases and 619 controls) and found that 5 SNPs in 4 genes (ENO1, FXN (2 SNPs), HLA-DPB2, and LPA) were associated with MI in the third study (1-sided P<0.05), and had the same risk alleles in all three studies. 18682748 2008
CUI: C0027051
Disease: Myocardial Infarction
Myocardial Infarction
0.200 GeneticVariation disease BEFREE Lipoprotein Lp(a). A risk factor for myocardial infarction. 2969235 1988
CUI: C0027051
Disease: Myocardial Infarction
Myocardial Infarction
0.200 Biomarker disease BEFREE Lipoprotein(a) and Risk of Myocardial Infarction and Death in Chronic Kidney Disease: Findings From the CRIC Study (Chronic Renal Insufficiency Cohort). 28838919 2017
CUI: C0027051
Disease: Myocardial Infarction
Myocardial Infarction
0.200 GeneticVariation disease BEFREE The CD14 CC genotype was associated with incidence of new coronary occlusion (P=0.026); TNF-alpha AA genotype with history of myocardial infarction (MI, P=0.04), and A allele with total occlusions at baseline (P=0.027), and systolic blood pressure (P=0.046); and IL-6-174 CC genotype with baseline minimum lumen diameter (P=0.043) and reduction in lipoprotein(a) with fluvastatin (P=0.03). 11199329 2000