Role of Genomics in the Management of Hypertension

• Autres auteurs: Mulatero, Paolo (Éditeur intellectuel), Monticone, Silvia (Éditeur intellectuel)
• Format: Électronique Chapitre de livre
• Langue: anglais
• Publié: Basel, Switzerland MDPI - Multidisciplinary Digital Publishing Institute 2020
• Sujets: Research & information: general; Biology, life sciences; atrial natriuretic peptide; T2238C variant; endothelial dysfunction; smooth muscle cells contraction; platelet aggregation; epigenetics; cardiovascular diseases; renin; low-renin; hypertension; mineralocorticoid receptor; genetics; aldosterone; essential hypertension; blood pressure; genome-wide association studies; exome microarray; next-generation sequencing; rare variants; rare-variants association testing; burden test; sequence kernel association test; hypokalemia; low renin hypertension; monogenic hypertension; Liddle syndrome; SCNN1A; SCNN1B; SCNN1G; non-coding RNA; micro RNA; primary aldosteronism; aldosterone-producing adenoma; transcriptome profiing; DNA methylation; histone modifications; vascular smooth muscle cells; endothelial cells; Kruppel-like factor 15; left ventricular hypertrophy; cardiac hypertrophy; heart failure; genetics of left ventricular hypertrophy; fibromuscular dysplasia; non atherosclerotic vascular stenosis; PHACTR1; genetic association; cervical artery dissection; spontaneous coronary arteries dissection; CRY1; CRY2; HSD3B1; HSD3B2; cardio-tonic steroids; endogenous ouabain; adducin; renal damage; African American; ARMC5; GRK4; CACNA1D; endocrine hypertension
• Accès en ligne: DOAB: download the publication; DOAB: description of the publication

Arterial hypertension affects about 1 billion people worldwide and it is the strongest modifiable risk factor for cardiovascular disease and related disability. Since the initial discovery of rare monogenic disorders with large effects, the role of genomics has evolved into large genome-wide associa...