Marked variation in heritability estimates of left ventricular mass depending on modality of measurement

Marked variation in heritability estimates of left ventricular mass depending on modality of measurement

Left ventricular (LV) hypertrophy is a strong risk factor for heart failure and cardiovascular death. ECG measures of LV mass are estimated as heritable in twin and family-based analyses and heritability estimates of LV mass measured by echocardiography are lower. We hypothesised that CMR-derived me...

पूर्ण विवरण

ग्रंथसूची विवरण
मुख्य लेखकों:	Nethononda, R, McGurk, K, Whitworth, P, Francis, J, Mamasoula, C, Cordell, H, Neubauer, S, Keavney, B, Mayosi, B, Farrall, M, Watkins, H
स्वरूप:	Journal article
भाषा:	English
प्रकाशित:	Nature Research 2019

समान संसाधन

Electrocardiographic measures of left ventricular hypertrophy show greater heritability than echocardiographic left ventricular mass.
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Heritability and family-based GWAS analyses of the N-acyl ethanolamine and ceramide plasma lipidome
द्वारा: McGurk, KA, और अन्य
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Electrocardiographic markers of cardiac hypertrophy show greater heritability than echocardiographic left ventricular mass: A family study
द्वारा: Mayosi, B, और अन्य
प्रकाशित: (2002)

Genome-wide linkage analysis of electrocardiographic and echocardiographic left ventricular hypertrophy in families with hypertension
द्वारा: Mayosi, B, और अन्य
प्रकाशित: (2008)

Genome-wide linkage analysis of electrocardiographic and echocardiographic left ventricular hypertrophy in families with hypertension.
द्वारा: Mayosi, B, और अन्य
प्रकाशित: (2008)

ASSOCIATION BETWEEN HSD11B1 POLYMORPHISM AND LEFT VENTRICULAR MASS IN FAMILIES WITH HYPERTENSION
द्वारा: Rahman, T, और अन्य
प्रकाशित: (2009)

Common variation in the CD36 (fatty acid translocase) gene is associated with left-ventricular mass.
द्वारा: Hall, D, और अन्य
प्रकाशित: (2011)

Relationship between CMR and ECG-derived indices of left ventricular hypertrophy
द्वारा: Alder Nicola, और अन्य
प्रकाशित: (2009-01-01)

Predictors of death in hypertensive families followed up over 14 years
द्वारा: Nethononda, MR, और अन्य
प्रकाशित: (2007)

GENETIC POLYMORPHISMS LINKED TO CORONARY ARTERY DISEASE ARE NOT ASSOCIATED WITH CAROTID ARTERY INTIMA-MEDIA THICKNESS, LEFT VENTRICULAR SIZE, OR INTERMEDIATE RISK PHENOTYPES
द्वारा: Cunnington, MS, और अन्य
प्रकाशित: (2009)

Common variation at the 11-β hydroxysteroid dehydrogenase type 1 gene is associated with left ventricular mass.
द्वारा: Rahman, T, और अन्य
प्रकाशित: (2011)

Common variation neighbouring micro-RNA 22 is associated with increased left ventricular mass.
द्वारा: Andrew R Harper, और अन्य
प्रकाशित: (2013-01-01)

Measured haplotype analysis of the aldosterone synthase gene and heart size (vol 11, pg 395, 2005)
द्वारा: Mayosi, B, और अन्य
प्रकाशित: (2005)

Measured haplotype analysis of the aldosterone synthase gene and heart size.
द्वारा: Mayosi, B, और अन्य
प्रकाशित: (2003)

Measured haplotype analysis of the aldosterone synthase gene and cardiac hypertrophy
द्वारा: Mayosi, B, और अन्य
प्रकाशित: (2002)

2032 The relationship between electrocardiographic and cardiac magnetic resonance (CMR)-derived left ventricular parameters differs between physiologic and pathologic hypertrophy
द्वारा: Keavney Bernard, और अन्य
प्रकाशित: (2008-10-01)

The growth hormone inducible transmembrane gene is a novel genetic modifier of left ventricular hypertrophy in families with hypertrophic cardiomyopathy
द्वारा: Parker, M, और अन्य
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Genetic variation at the locus encompassing 11-beta hydroxylase and aldosterone synthase accounts for heritability in cortisol precursor (11-deoxycortisol) urinary metabolite excretion
द्वारा: Imrie, H, और अन्य
प्रकाशित: (2005)

Genetic variation at the locus encompassing 11-beta hydroxylase and aldosterone synthase accounts for heritability in cortisol precursor (11-deoxycortisol) urinary metabolite excretion.
द्वारा: Keavney, B, और अन्य
प्रकाशित: (2005)

Plasma C-reactive protein (CRP), a novel cardiovascular risk factor, shows high heritability but no association with the-174 G/C polymorphism of the interleukin-6 (IL-6) gene in human families.
द्वारा: Keavney, B, और अन्य
प्रकाशित: (2000)

Genetic variation at the CYP11B locus accounts for heritabilities of aldosterone metabolite (THAIdo) excretion and 11beta-hydroxylase activity
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प्रकाशित: (2006)

Concentric left ventricular remodeling and aortic stiffness: a comparison of obesity and hypertension.
द्वारा: Rider, O, और अन्य
प्रकाशित: (2013)

Concentric left ventricular remodeling and aortic stiffness: A comparison of obesity and hypertension
द्वारा: Rider, O, और अन्य
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Association between aldosterone production and variation in the gene encoding 11-beta hydroxylase (CYP11B1)
द्वारा: Imrie, H, और अन्य
प्रकाशित: (2007)

Association between aldosterone production and variation in the 11beta-hydroxylase (CYP11B1) gene.
द्वारा: Imrie, H, और अन्य
प्रकाशित: (2006)

Impaired left ventricular energy metabolism in hypertrophic cardiomyopathy is not due to fibrosis.
द्वारा: Petersen, SE, और अन्य
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Association between the-174G/C polymorphism of the interleukin-6 gene and carotid atherosclerosis: Family study and meta-analysis
द्वारा: Mayosi, B, और अन्य
प्रकाशित: (2005)

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द्वारा: Chien Kuo-Liong, और अन्य
प्रकाशित: (2006-08-01)

Ambulatory blood pressure is associated with polymorphic variation in P2X receptor genes.
द्वारा: Palomino-Doza, J, और अन्य
प्रकाशित: (2008)

Novel genetic variants linked to coronary artery disease by genome-wide association are not associated with carotid artery intima-media thickness or intermediate risk phenotypes.
द्वारा: Cunnington, MS, और अन्य
प्रकाशित: (2009)

The C-532T polymorphism of the angiotensinogen (AGT) gene is associated with arterial stiffness: A possible explanation for heterogeneity in genetic association studies of AGT and hypertension
द्वारा: Rahman, T, और अन्य
प्रकाशित: (2007)

The C-532T polymorphism of the angiotensinogen gene is associated with pulse pressure: a possible explanation for heterogeneity in genetic association studies of AGT and hypertension.
द्वारा: Baker, M, और अन्य
प्रकाशित: (2007)

Association between common polymorphisms of the proopiomelanocortin gene and body fat distribution: a family study.
द्वारा: Baker, M, और अन्य
प्रकाशित: (2005)

A rare variant of the leptin (LEP) gene has large effects on blood pressure (BP) and carotid intima-medial thickness (CIMT): Study of 1428 individuals in 248 families
द्वारा: Imrie, H, और अन्य
प्रकाशित: (2005)

Association between common polymorphisms of the pro-opiomelanocortin (POMC) gene and body fat distribution: A family study
द्वारा: Baker, M, और अन्य
प्रकाशित: (2005)

A rare variant of the leptin gene has large effects on blood pressure and carotid intima-medial thickness: a study of 1428 individuals in 248 families.
द्वारा: Gaukrodger, N, और अन्य
प्रकाशित: (2005)

Genotype at the -174G/C polymorphism of the interleukin-6 gene is associated with common carotid artery intimal-medial thickness: family study and meta-analysis.
द्वारा: Mayosi, B, और अन्य
प्रकाशित: (2005)

The genetic basis of variation in plasma fibrinogen and C-reactive protein levels
द्वारा: Mayosi, B, और अन्य
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Quantitative genetic study of plasma fibrinogen level and the-455 G/A polymorphism of the beta-fibrinogen gene using novel family-based association methods.
द्वारा: Mayosi, B, और अन्य
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