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Lisa de las Fuentes

Researcher at Washington University in St. Louis

Publications -  104
Citations -  5461

Lisa de las Fuentes is an academic researcher from Washington University in St. Louis. The author has contributed to research in topics: Heart failure & Genome-wide association study. The author has an hindex of 32, co-authored 104 publications receiving 4553 citations. Previous affiliations of Lisa de las Fuentes include University of Minnesota.

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Novel genetic associations for blood pressure identified via gene-alcohol interaction in up to 570K individuals across multiple ancestries

Mary F. Feitosa, +299 more
- 18 Jun 2018 - 
TL;DR: In insights into the role of alcohol consumption in the genetic architecture of hypertension, a large two-stage investigation incorporating joint testing of main genetic effects and single nucleotide variant (SNV)-alcohol consumption interactions is conducted.
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Altered myocardial fatty acid and glucose metabolism in idiopathic dilated cardiomyopathy

TL;DR: Patients with idiopathic dilated cardiomyopathy exhibit alterations in myocardial metabolism characterized by decreased fatty acid metabolism and increased myocardian glucose metabolism, a pattern similar to that shown in animal models of HF.
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Metabolic syndrome is associated with abnormal left ventricular diastolic function independent of left ventricular mass.

TL;DR: Patients with metabolic syndrome have LV diastolic dysfunction independent of LV mass, which may partially explain the increased cardiovascular morbidity and mortality associated with metabolic Syndrome.
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Myocardial fatty acid metabolism: independent predictor of left ventricular mass in hypertensive heart disease.

TL;DR: Left ventricular mass showed significant correlation with gender, diastolic and systolic blood pressure, myocardial fatty acid uptake, utilization and oxidation, myCardial blood flow, body mass index, and left ventricular ejection fraction, and myocardian fatty acid metabolism is an independent predictor of left Ventricular mass in hypertension and inleft ventricular dysfunction.