Phenotypic Differences Between Polygenic and Monogenic Hypobetalipoproteinemia.
Adult
Apolipoprotein B-100
/ genetics
Biomarkers
/ blood
Cholesterol, LDL
/ blood
Down-Regulation
Female
Genetic Predisposition to Disease
Humans
Hypobetalipoproteinemias
/ blood
Male
Multifactorial Inheritance
Mutation
Non-alcoholic Fatty Liver Disease
/ diagnostic imaging
Phenotype
Proprotein Convertase 9
/ genetics
Retrospective Studies
Risk Assessment
Risk Factors
Young Adult
apolipoproteins
cholesterol
hypobetalipoproteinemias
liver diseases
mutation
polygenic risk score
Journal
Arteriosclerosis, thrombosis, and vascular biology
ISSN: 1524-4636
Titre abrégé: Arterioscler Thromb Vasc Biol
Pays: United States
ID NLM: 9505803
Informations de publication
Date de publication:
01 2021
01 2021
Historique:
pubmed:
20
11
2020
medline:
2
2
2021
entrez:
19
11
2020
Statut:
ppublish
Résumé
Primary hypobetalipoproteinemia is characterized by LDL-C (low-density lipoprotein cholesterol) concentrations below the fifth percentile. Primary hypobetalipoproteinemia mostly results from heterozygous mutations in the This study highlights the importance of genetic diagnosis in the clinical care of primary hypobetalipoproteinemia patients. It shows for the first time that a polygenic origin of hypobetalipoproteinemia is associated with a lower risk of liver steatosis and liver injury versus monogenic hypobetalipoproteinemia. Thus, polygenic risk score is a useful tool to establish a more personalized follow-up of primary hypobetalipoproteinemia patients.
Identifiants
pubmed: 33207932
doi: 10.1161/ATVBAHA.120.315491
doi:
Substances chimiques
APOB protein, human
0
Apolipoprotein B-100
0
Biomarkers
0
Cholesterol, LDL
0
PCSK9 protein, human
EC 3.4.21.-
Proprotein Convertase 9
EC 3.4.21.-
Types de publication
Comparative Study
Journal Article
Research Support, Non-U.S. Gov't
Langues
eng
Sous-ensembles de citation
IM