Abstract
This study investigates associations of the lifelong genetic inhibition of PCSK9 with plasma liver enzymes and nonalcoholic fatty liver disease by using the loss-of-function variant PCSK9-p.Arg46Leu as a genetic instrument.
Publication types
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Research Support, Non-U.S. Gov't
MeSH terms
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Alanine Transaminase / blood
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Aspartate Aminotransferases / blood
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Genetic Association Studies
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Humans
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Loss of Function Mutation
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Non-alcoholic Fatty Liver Disease
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PCSK9 Inhibitors*
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Proprotein Convertase 9 / genetics*
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gamma-Glutamyltransferase / blood
Substances
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PCSK9 Inhibitors
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gamma-Glutamyltransferase
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Aspartate Aminotransferases
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Alanine Transaminase
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PCSK9 protein, human
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Proprotein Convertase 9