Cargando…

Role of an automated screening tool for familial hypercholesterolemia in patients with premature coronary artery disease

BACKGROUND AND AIMS: To validate an automated screening tool for patients with premature coronary artery disease (CAD) and high total cholesterol or LDL-C levels and assess if it would provide clinicians with additional support in identifying patients with Familial Hypercholesterolemia (FH). METHODS...

Descripción completa

Detalles Bibliográficos
Autores principales:	Jokiniitty, Antti, Eskola, Markku, Saarela, Tanja, Huhtala, Heini, Metso, Saara
Formato:	Online Artículo Texto
Lenguaje:	English
Publicado:	Elsevier 2022
Materias:	Full Length Article
Acceso en línea:	https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9833226/ https://www.ncbi.nlm.nih.gov/pubmed/36644564 http://dx.doi.org/10.1016/j.athplu.2022.01.001

Ejemplares similares

Genetic Analysis of Iranian Patients with Familial Hypercholesterolemia
por: Ekrami, Mahdis, et al.
Publicado: (2018)

Polygenic risk score for hypercholesterolemia in a Brazilian familial hypercholesterolemia cohort
por: Lima, Isabella Ramos, et al.
Publicado: (2022)

Subclinical atherosclerosis determined by coronary artery calcium deposition in patients with clinical familial hypercholesterolemia
por: Borg, Sanna á, et al.
Publicado: (2022)

Atherosclerosis severity in patients with familial hypercholesterolemia: The role of T and B lymphocytes
por: Fonzar, Waleria T., et al.
Publicado: (2022)

Burden of cardiovascular disease in a large contemporary cohort of patients with heterozygous familial hypercholesterolemia
por: Ferrières, Jean, et al.
Publicado: (2022)

Increased extracellular vesicles (EVs) related to T cell-mediated inflammation and vascular function in familial hypercholesterolemia
por: Nielsen, Morten Hjuler, et al.
Publicado: (2023)

Lipids, lipoproteins and prevalence of familial hypercholesterolemia in the Faroe Islands – Results from a nationwide laboratory database
por: Borg, Sanna á, et al.
Publicado: (2022)

A PCSK9 inhibitor induces a transient decrease in the neutrophil-lymphocyte ratio and monocyte-lymphocyte ratio in homozygous familial hypercholesterolemia patients
por: Li, Fangyuan, et al.
Publicado: (2022)

Young women with familial hypercholesterolemia have higher LDL-cholesterol burden than men: Novel data using repeated measurements during 12-years follow-up
por: Johansen, Anja K., et al.
Publicado: (2023)

Coronary revascularisation in stable patients after an acute coronary syndrome: a propensity analysis of early invasive versus conservative management in a register-based cohort study
por: Bugiardini, Raffaele, et al.
Publicado: (2013)

High prevalence of genetic determined familial hypercholesterolemia in premature coronary artery disease
por: Pirazzi, Carlo, et al.
Publicado: (2019)

Premature Coronary Artery Disease and Familial Hypercholesterolemia: Need for Early Diagnosis and Cascade Screening in the Indian Population
por: Setia, N., et al.
Publicado: (2012)

Reducing Premature Coronary Artery Disease in Malaysia by Early Identification of Familial Hypercholesterolemia Using the Familial Hypercholesterolemia Case Ascertainment Tool (FAMCAT): Protocol for a Mixed Methods Evaluation Study
por: Ramli, Anis Safura, et al.
Publicado: (2023)

Familial Hypercholesterolemia in Premature Acute Coronary Syndrome. Insights from CholeSTEMI Registry
por: Lorca, Rebeca, et al.
Publicado: (2020)

Prevalence of familial hypercholesterolemia in patients with confirmed premature coronary artery disease in Ranchi, Jharkhand
por: Kumar, Prakash, et al.
Publicado: (2022)

Novel CFTR Mutations in Two Iranian Families with Severe Cystic Fibrosis
por: Mohseni, Marzieh, et al.
Publicado: (2016)

The Effectiveness of Kangaroo Mother Care (KMC) on attachment of mothers with premature infants
por: Mehrpisheh, Shahrokh, et al.
Publicado: (2022)

Detection and Outcome of Endocervical Atypia in Cytology in Primary HPV Screening Programme
por: Pulkkinen, Johanna, et al.
Publicado: (2021)

Prevalence of familial hypercholesterolemia in patients with premature myocardial infarction
por: Cui, Yuxia, et al.
Publicado: (2019)

Premature Valvular Heart Disease in Homozygous Familial Hypercholesterolemia
por: Fahed, Akl C., et al.
Publicado: (2017)

HOTAIR Induces the Downregulation of miR-200 Family Members in Gastric Cancer Cell Lines
por: Bossaghzadeh, Fatemeh, et al.
Publicado: (2022)

Detecting premature departure in online text-based counseling using logic-based pattern matching
por: Xu, Yucan, et al.
Publicado: (2021)

Premature T cell aging in major depression: A double hit by the state of disease and cytomegalovirus infection
por: Simon, Maria S., et al.
Publicado: (2023)

Homozygosity Mapping and Targeted Sanger Sequencing Identifies Three Novel CRB1 (Crumbs homologue 1) Mutations in Iranian Retinal Degeneration Families
por: Ghofrani, Mohammad, et al.
Publicado: (2017)

The efficacy of automated feedback after internet-based depression screening: Study protocol of the German, three-armed, randomised controlled trial DISCOVER
por: Sikorski, Franziska, et al.
Publicado: (2021)

Premature Coronary Artery Disease due to Homozygous Familial Hypercholesterolemia in a 12-Year-Old Girl
por: Ekici, Filiz, et al.
Publicado: (2018)

Evaluation of a new automated immunoassay for the quantification of anti-Müllerian hormone
por: Lotierzo, Manuela, et al.
Publicado: (2021)

Supporting parents of premature infants transitioning from the NICU to home: A pilot randomized control trial of a smartphone application
por: Garfield, Craig F., et al.
Publicado: (2016)

Polg mtDNA mutator mice reveal limited involvement of vertebral bone loss in premature aging-related thoracolumbar hyperkyphosis
por: Roessinger, Olivier, et al.
Publicado: (2022)

Serum 25-hydroxyvitamin D measurement: Comparative evaluation of three automated immunoassays
por: Trimboli, Francesca, et al.
Publicado: (2021)

Convolutional neural network for automated classification of osteonecrosis and related mandibular trabecular patterns
por: Baseri Saadi, Soroush, et al.
Publicado: (2022)

Assessing the Diagnostic Value of Plasma-Free DNA in Prostate Cancer Screening
por: Seyedolmohadessin, Seyedeh Maryam, et al.
Publicado: (2018)

Usefulness of SYNTAX score II in complex percutaneous coronary interventions in the setting of acute coronary syndrome
por: Salvatore, Azzarelli, et al.
Publicado: (2016)

Development of a DNA Aptamer for Screening Neisseria meningitidis Serogroup B by Cell SELEX
por: Mirzakhani, Kimia, et al.
Publicado: (2018)

In silico Screening and Evaluation of the Anticonvulsant Activity of Docosahexaenoic Acid-Like Molecules in Experimental Models of Seizures
por: Loron, Ali Gharibi, et al.
Publicado: (2017)

Screening of Alginate Lyase-Producing Bacteria and Optimization of Media Compositions for Extracellular Alginate Lyase Production
por: Tavafi, Hadis, et al.
Publicado: (2017)

Effects of familial hypercholesterolemia-associated genes on the phenotype of premature myocardial infarction
por: Lee, Chongyou, et al.
Publicado: (2019)

Serum C-reactive protein in adolescence and risk of schizophrenia in adulthood: A prospective birth cohort study
por: Metcalf, Stephen A., et al.
Publicado: (2017)

Cancer as a tool for preclinical psychoneuroimmunology
por: Borniger, Jeremy C.
Publicado: (2021)

Usability of two brief questions as a screening tool for domestic violence and effect of #MeToo on prevalence of self-reported violence
por: Kero, Katja Maria, et al.
Publicado: (2020)

Cannot write session to /tmp/vufind_sessions/sess_c1d0hc7a7kuk21fdmajtt1l7h4