Association of apolipoprotein E genotypes with lipid levels and coronary risk

AM Bennet, E Di Angelantonio, Z Ye, F Wensley… - Jama, 2007 - jamanetwork.com
ContextPrevious reviews of associations of apolipoprotein E (apoE) genotype and coronary
disease have been dominated by smaller studies that are liable to biases. ObjectiveTo …

[HTML][HTML] Hepatic lipase, high density lipoproteins, and hypertriglyceridemia

C Chatterjee, DL Sparks - The American journal of pathology, 2011 - Elsevier
Hepatic lipase (HL) is a lipolytic enzyme that contributes to the regulation of plasma
triglyceride (TG) levels. Elevated TG levels may increase the risk of developing coronary …

Seven lipoprotein lipase gene polymorphisms, lipid fractions, and coronary disease: a HuGE association review and meta-analysis

GS Sagoo, I Tatt, G Salanti… - American journal of …, 2008 - academic.oup.com
Lipoprotein lipase (LPL) is a key enzyme in lipoprotein metabolism and a major candidate
gene for coronary heart disease (CHD). The authors assessed associations between 7 LPL …

Exercise and hyperlipidemia

N He, H Ye - Physical exercise for human health, 2020 - Springer
Hyperlipidemia is one of the common pathological conditions of human, which occurs due to
lipid metabolism disorder in the human body, resulting in serum lipid concentration beyond …

Associations of the APOB rs693 and rs17240441 polymorphisms with plasma APOB and lipid levels: a meta-analysis

C Niu, Z Luo, L Yu, Y Yang, Y Chen, X Luo… - Lipids in health and …, 2017 - Springer
Background The associations of the apolipoprotein B gene (APOB) rs693 and rs17240441
polymorphisms with plasma levels of APOB and lipids have been widely explored, but the …

Apolipoprotein E polymorphism, age and coronary heart disease

GD Kolovou, KK Anagnostopoulou - Ageing research reviews, 2007 - Elsevier
Plasma concentrations of lipids, lipoproteins, and apolipoproteins (apo) are established risk
factors for coronary heart disease (CHD). The knowledge of lipid profile may predict the …

[HTML][HTML] A novel splicing mutation in the ABCA1 gene, causing Tangier disease and familial HDL deficiency in a large family

M Maranghi, G Truglio, A Gallo, E Grieco… - Biochemical and …, 2019 - Elsevier
Tangier disease is a rare disorder of lipoprotein metabolism that presents with extremely low
levels of HDL cholesterol and apoprotein AI. It is caused by mutations in the ATP-binding …

Apolipoprotein E gene polymorphism and gender

G Kolovou, D Damaskos… - Annals of clinical & …, 2009 - Assoc Clin Scientists
Many studies have shown that the prevalence and onset of coronary heart disease (CHD) is
sex-dependent. CHD prevalence is lower in women than in men at all ages. Furthermore …

Five polymorphisms in gene candidates for cardiovascular disease in Afro‐Brazilian individuals

T Sakuma, RDC Hirata… - Journal of clinical …, 2004 - Wiley Online Library
Associations of polymorphisms in the angiotensin I‐converting enzyme (ACE),
apolipoprotein B (APOB) and apolipoprotein E (APOE) genes with hypertension and …

Association of promoter region single nucleotide polymorphisms at positions −819C/T and −592C/A of interleukin 10 gene with ischemic heart disease

GI Yu, HC Cho, YK Cho, HS Park, HJ Yoon… - Inflammation …, 2012 - Springer
Objective Ischemic heart disease (IHD) is a disease characterized by ischemia of the heart
muscle, usually due to coronary artery disease. Interleukin-10 (IL10) is a proinflammatory …