Search Results - "Hudgins, Lisa C."
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Chylomicronemia from GPIHBP1 autoantibodies
Published in Journal of lipid research (01-11-2020)“…Some cases of chylomicronemia are caused by autoantibodies against glycosylphosphatidylinositol-anchored HDL binding protein 1 (GPIHBP1), an endothelial cell…”
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A critical role for ChREBP-mediated FGF21 secretion in hepatic fructose metabolism
Published in Molecular metabolism (Germany) (01-01-2017)“…Abstract Objective Increased fructose consumption is a contributor to the burgeoning epidemic of non-alcoholic fatty liver disease (NAFLD). Recent evidence…”
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A Dual Sugar Challenge Test for Lipogenic Sensitivity to Dietary Fructose
Published in The journal of clinical endocrinology and metabolism (01-03-2011)“…An oral challenge of glucose and fructose gives a robust lipogenic response as measured from the increase in VLDL triglyceride palmitate over 4 hours. Context:…”
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Rationale and design of the familial hypercholesterolemia foundation CAscade SCreening for Awareness and DEtection of Familial Hypercholesterolemia registry
Published in The American heart journal (01-03-2014)“…Background Familial hypercholesterolemia (FH) is a hereditary condition caused by various genetic mutations that lead to significantly elevated low-density…”
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Role for Stearoyl-CoA Desaturase-1 in Leptin-Mediated Weight Loss
Published in Science (American Association for the Advancement of Science) (12-07-2002)“…Leptin elicits a metabolic response that cannot be explained by its anorectic effects alone. To examine the mechanism underlying leptin's metabolic actions, we…”
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Long-Term Safety and Efficacy of Low-Density Lipoprotein Apheresis in Childhood for Homozygous Familial Hypercholesterolemia
Published in The American journal of cardiology (01-11-2008)“…Untreated pediatric patients with homozygous familial hypercholesterolemia usually have myocardial infarctions, heart failure, or death by the teenage years…”
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LpA-II:B:C:D:E: a new immunochemically-defined acute phase lipoprotein in humans
Published in Lipids in health and disease (28-05-2018)“…Previous studies of lipoproteins in patients with sepsis have been performed on density fractions isolated by conventional ultracentrifugation that are…”
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2023 Update on European Atherosclerosis Society Consensus Statement on Homozygous Familial Hypercholesterolaemia: new treatments and clinical guidance
Published in European heart journal (01-07-2023)“…Graphical Abstract Graphical Abstract Homozygous familial hypercholesterolaemia is a rare autosomal semi-dominant disease affecting males and females equally,…”
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Atherosclerosis in Survivors of Kawasaki Disease
Published in The Journal of pediatrics (01-10-2009)“…Objectives To test the hypothesis that long-term survivors of low-risk Kawasaki disease (KD) have ongoing vascular inflammation and dysfunction and a higher…”
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A single intravenous dose of endotoxin rapidly alters serum lipoproteins and lipid transfer proteins in normal volunteers
Published in Journal of lipid research (01-08-2003)“…Endotoxemia is associated with rapid and marked declines in serum levels of LDL and HDL by unknown mechanisms. Six normal volunteers received a single, small…”
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Relationship between carbohydrate-induced hypertriglyceridemia and fatty acid synthesis in lean and obese subjects
Published in Journal of lipid research (01-04-2000)“…We previously reported that a eucaloric, low fat, liquid formula diet enriched in simple carbohydrate markedly increased the synthesis of fatty acids in lean…”
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Lipoprotein Apheresis: Utility, Outcomes, and Implementation in Clinical Practice: A Scientific Statement From the American Heart Association
Published in Arteriosclerosis, thrombosis, and vascular biology (07-10-2024)“…Despite the availability of multiple classes of lipoprotein-lowering medications, some high-risk patients have persistent hypercholesterolemia and may require…”
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Treatment Gaps in Adults With Heterozygous Familial Hypercholesterolemia in the United States
Published in Circulation. Cardiovascular genetics (01-06-2016)“…Background-Cardiovascular disease burden and treatment patterns among patients with familial hypercholesterolemia (FH) in the United States remain poorly…”
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Treatment Gaps in Adults With Heterozygous Familial Hypercholesterolemia in the United States: Data From the CASCADE-FH Registry
Published in Circulation. Cardiovascular genetics (01-06-2016)“…BACKGROUND—Cardiovascular disease burden and treatment patterns among patients with familial hypercholesterolemia (FH) in the United States remain poorly…”
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Clinical practice recommendations on lipoprotein apheresis for children with homozygous familial hypercholesterolaemia: An expert consensus statement from ERKNet and ESPN
Published in Atherosclerosis (01-05-2024)“…Homozygous familial hypercholesterolaemia is a life-threatening genetic condition, which causes extremely elevated LDL-C levels and atherosclerotic…”
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Lipoprotein lipase controls fatty acid entry into adipose tissue, but fat mass is preserved by endogenous synthesis in mice deficient in adipose tissue lipoprotein lipase
Published in Proceedings of the National Academy of Sciences - PNAS (16-09-1997)“…Lipoprotein lipase (LPL) is the rate-limiting enzyme for the import of triglyceride-derived fatty acids by muscle, for utilization, and adipose tissue (AT),…”
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Children with Heterozygous Familial Hypercholesterolemia in the United States: Data from the Cascade Screening for Awareness and Detection-FH Registry
Published in The Journal of pediatrics (01-02-2021)“…To describe enrollment characteristics of youth in the Cascade Screening for Awareness and Detection of FH Registry. This is a cross-sectional analysis of 493…”
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Why do sweets fatten our livers?
Published in The American journal of clinical nutrition (01-10-2012)Get full text
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Contemporary Homozygous Familial Hypercholesterolemia in the United States: Insights From the CASCADE FH Registry
Published in Journal of the American Heart Association (02-05-2023)“…Background Homozygous familial hypercholesterolemia (HoFH) is a rare, treatment-resistant disorder characterized by early-onset atherosclerotic and aortic…”
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Cardiovascular outcomes in patients with homozygous familial hypercholesterolaemia on lipoprotein apheresis initiated during childhood: long-term follow-up of an international cohort from two registries
Published in The lancet child & adolescent health (01-07-2024)“…Homozygous familial hypercholesterolaemia (HoFH) is a rare genetic disease characterised by extremely high plasma LDL cholesterol from birth, causing…”
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