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Geisinger researchers have been awarded two grants from the National Heart, Lung and Blood Institute, protein c complex generics part of the National Institutes of Health, to study risk factors associated with familial hypercholesterolemia (FH) and ways to improve screening, diagnosis and communication with patients.
FH is a common genetic disorder that causes abnormally high cholesterol levels and affects about 1 in 250 people. Left untreated, FH can lead to vascular diseases including coronary artery disease, heart attack, stroke and arterial disease. Early diagnosis and treatment can dramatically reduce the risk of arterial disease and improve health outcomes.
Matt Oetjens, Ph.D., assistant professor at Geisinger's Autism and Developmental Medicine Institute, was awarded $3.7 million for a genetic investigation of FH and its intersection with health disparities related to age, sex, race/ethnicity and rural environment. Dr. Oetjens' study will determine how to use genetics to assess risk, improve care and develop effective ways to communicate risk information to patients and providers.
"This study is an important step toward translating new genetic findings about the causes of FH into improved patient care," Dr. Oetjens said.
Laney Jones, Pharm.D., and Samuel Gidding, M.D., both of Geisinger's Genomic Medicine Institute, were awarded $3.3 million to design and conduct a clinical trial to improve the diagnosis of FH in the primary care setting. The trial will assess the effectiveness of several strategies for improving FH diagnosis, including universal screening for specific age groups using diagnostic tools like lipid panels and genetic testing, initiating early treatment and studying patient health outcomes.
"An FH diagnosis is often made too late, many times after a premature heart attack," Dr. Jones said. "Diagnosing FH in the primary care setting would optimize treatment for these people early in the course of the disease. Our long-term goal is to create an effective FH diagnosis program that is practical and sustainable in the real-world setting."
The team plans to implement the trial over a two-and-half-year period in all Geisinger primary care sites starting in February 2023.
Geisinger Health System
Posted in: Medical Research News | Medical Condition News
Tags: Autism, Blood, Cholesterol, Clinical Trial, Coronary Artery Disease, Diagnostic, Familial Hypercholesterolemia, Genetic, Genetic Disorder, Genetics, Genomic, Health Disparities, Heart, Heart Attack, High Cholesterol, Hospital, Hypercholesterolemia, Medicine, pH, Primary Care, Research, Stroke, Vascular
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