Association Between ESR2 Genetic Variants and Risk of Myocardial Infarction (Lipids, Lipoproteins, And Cardiovascular Risk Factors) (Clinical Report) Association Between ESR2 Genetic Variants and Risk of Myocardial Infarction (Lipids, Lipoproteins, And Cardiovascular Risk Factors) (Clinical Report)

Association Between ESR2 Genetic Variants and Risk of Myocardial Infarction (Lipids, Lipoproteins, And Cardiovascular Risk Factors) (Clinical Report‪)‬

Clinical Chemistry 2008, July, 54, 7

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وصف الناشر

Myocardial infarction (MI) [4] and related atherosclerotic cardiovascular disease (CVD) are the leading cause of death in men and women, although women develop CVD approximately 10 years later than men (1). Multiple environmental and genetic factors contribute to the development of these complex diseases. The genes coding for the estrogen receptors (ERs), which belong to the nuclear receptor gene family of transcription factors, are ideal candidates to explain the sex differences observed. Extensive studies of the role of the ER[alpha] and ER[beta] receptors in cardiovascular disease have shown that both receptors are expressed in humans in vascular endothelial, smooth muscle, and myocardial cells (2). ER[beta] is expressed more highly in vascular smooth muscle cells in women than men, whereas ER[alpha] is present in equal quantities (3 ). In the human heart, ER[beta] is up-regulated by pressure overload, and ER[beta] mRNA levels have been observed to be increased in hearts of patients with aortic stenosis, with the greatest increases seen in women (4 ). ER[alpha] has also been associated with the development of coronary artery disease in women (5).

النوع
علم وطبيعة
تاريخ النشر
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١ يوليو
اللغة
EN
الإنجليزية
عدد الصفحات
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الناشر
American Association for Clinical Chemistry, Inc.
البائع
The Gale Group, Inc., a Delaware corporation and an affiliate of Cengage Learning, Inc.
الحجم
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ك.ب.
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C677T and AI298C Polymorphisms of the Methylenetetrahydrofolate Reductase Gene: Incidence and Effect of Combined Genotypes on Plasma Fasting and Post-Methionine Load Homocysteine in Vascular Disease (Molecular Diagnostics and Genetics) C677T and AI298C Polymorphisms of the Methylenetetrahydrofolate Reductase Gene: Incidence and Effect of Combined Genotypes on Plasma Fasting and Post-Methionine Load Homocysteine in Vascular Disease (Molecular Diagnostics and Genetics)
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Effect of Riboflavin Status on the Homocysteine-Lowering Effect of Folate in Relation to the MTHFR (C677T) Genotype (Nutrition) Effect of Riboflavin Status on the Homocysteine-Lowering Effect of Folate in Relation to the MTHFR (C677T) Genotype (Nutrition)
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