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A New Potential Strategy for Acute Non-Alcoholic Steatohepatitis (NASH)

Patient: Female, 38-year-old Final Diagnosis: Non-alcoholic steatohepatitis (NASH) Symptoms: Elevated liver enzymes Medication:— Clinical Procedure: — Specialty: General and Internal Medicine OBJECTIVE: Unusual or unexpected effect of treatment BACKGROUND: Non-alcoholic fatty liver disease (NAFLD) i...

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Autores principales: Sekhon, Anupamjeet Kaur, Gollapalli, Aniruddha, Kaur, Dharamjeet, Janssen, Bryan, Stevens, Mark L., Valerio, Fernando, Sierra-Hoffman, Miguel A.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: International Scientific Literature, Inc. 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8635219/
https://www.ncbi.nlm.nih.gov/pubmed/34826302
http://dx.doi.org/10.12659/AJCR.932961
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author Sekhon, Anupamjeet Kaur
Gollapalli, Aniruddha
Kaur, Dharamjeet
Janssen, Bryan
Stevens, Mark L.
Valerio, Fernando
Sierra-Hoffman, Miguel A.
author_facet Sekhon, Anupamjeet Kaur
Gollapalli, Aniruddha
Kaur, Dharamjeet
Janssen, Bryan
Stevens, Mark L.
Valerio, Fernando
Sierra-Hoffman, Miguel A.
author_sort Sekhon, Anupamjeet Kaur
collection PubMed
description Patient: Female, 38-year-old Final Diagnosis: Non-alcoholic steatohepatitis (NASH) Symptoms: Elevated liver enzymes Medication:— Clinical Procedure: — Specialty: General and Internal Medicine OBJECTIVE: Unusual or unexpected effect of treatment BACKGROUND: Non-alcoholic fatty liver disease (NAFLD) is the most common cause of chronic liver disease in the United States, and 25% of patients with NAFLD progress to non-alcoholic steatohepatitis (NASH). NAFLD is predicted to be the most common indication for liver transplantation by 2030. Despite associated high morbidity and mortality, there is currently no approved therapy for NASH. PCSK9 inhibitors are approved for reducing LDL in patients who are statin-intolerant or need further LDL reduction. Increased LDL levels are independently associated with an elevated risk of NAFLD. CASE REPORT: We present a case of a 39-year-old woman with acute NASH with familial hypercholesterolemia that was refractory to lifestyle modifications and HMG-CoA reductase inhibitors. An episode of rhabdomyolysis warranted a search for alternatives to statin therapy. Results of a liver biopsy showed microvesicular and macrovesicular steatosis with ballooning degeneration, indicating acute NASH. She was started on PCSK9 inhibitors as salvage therapy. Three monthly doses resulted in a more than an 80% reduction in ALT and AST and a 48% reduction in LDL levels. A liver biopsy done 8 months after the first biopsy showed normalization of liver histology. CONCLUSIONS: The use of PCSK9 inhibitors showed a dramatic response in this patient who failed conventional therapies, and the encouraging results seen in this case merit further research into the use of PCSK9 inhibitors as first-line therapy for the acute phase of NASH.
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spelling pubmed-86352192021-12-16 A New Potential Strategy for Acute Non-Alcoholic Steatohepatitis (NASH) Sekhon, Anupamjeet Kaur Gollapalli, Aniruddha Kaur, Dharamjeet Janssen, Bryan Stevens, Mark L. Valerio, Fernando Sierra-Hoffman, Miguel A. Am J Case Rep Articles Patient: Female, 38-year-old Final Diagnosis: Non-alcoholic steatohepatitis (NASH) Symptoms: Elevated liver enzymes Medication:— Clinical Procedure: — Specialty: General and Internal Medicine OBJECTIVE: Unusual or unexpected effect of treatment BACKGROUND: Non-alcoholic fatty liver disease (NAFLD) is the most common cause of chronic liver disease in the United States, and 25% of patients with NAFLD progress to non-alcoholic steatohepatitis (NASH). NAFLD is predicted to be the most common indication for liver transplantation by 2030. Despite associated high morbidity and mortality, there is currently no approved therapy for NASH. PCSK9 inhibitors are approved for reducing LDL in patients who are statin-intolerant or need further LDL reduction. Increased LDL levels are independently associated with an elevated risk of NAFLD. CASE REPORT: We present a case of a 39-year-old woman with acute NASH with familial hypercholesterolemia that was refractory to lifestyle modifications and HMG-CoA reductase inhibitors. An episode of rhabdomyolysis warranted a search for alternatives to statin therapy. Results of a liver biopsy showed microvesicular and macrovesicular steatosis with ballooning degeneration, indicating acute NASH. She was started on PCSK9 inhibitors as salvage therapy. Three monthly doses resulted in a more than an 80% reduction in ALT and AST and a 48% reduction in LDL levels. A liver biopsy done 8 months after the first biopsy showed normalization of liver histology. CONCLUSIONS: The use of PCSK9 inhibitors showed a dramatic response in this patient who failed conventional therapies, and the encouraging results seen in this case merit further research into the use of PCSK9 inhibitors as first-line therapy for the acute phase of NASH. International Scientific Literature, Inc. 2021-11-26 /pmc/articles/PMC8635219/ /pubmed/34826302 http://dx.doi.org/10.12659/AJCR.932961 Text en © Am J Case Rep, 2021 https://creativecommons.org/licenses/by-nc-nd/4.0/This work is licensed under Creative Common Attribution-NonCommercial-NoDerivatives 4.0 International (CC BY-NC-ND 4.0 (https://creativecommons.org/licenses/by-nc-nd/4.0/) )
spellingShingle Articles
Sekhon, Anupamjeet Kaur
Gollapalli, Aniruddha
Kaur, Dharamjeet
Janssen, Bryan
Stevens, Mark L.
Valerio, Fernando
Sierra-Hoffman, Miguel A.
A New Potential Strategy for Acute Non-Alcoholic Steatohepatitis (NASH)
title A New Potential Strategy for Acute Non-Alcoholic Steatohepatitis (NASH)
title_full A New Potential Strategy for Acute Non-Alcoholic Steatohepatitis (NASH)
title_fullStr A New Potential Strategy for Acute Non-Alcoholic Steatohepatitis (NASH)
title_full_unstemmed A New Potential Strategy for Acute Non-Alcoholic Steatohepatitis (NASH)
title_short A New Potential Strategy for Acute Non-Alcoholic Steatohepatitis (NASH)
title_sort new potential strategy for acute non-alcoholic steatohepatitis (nash)
topic Articles
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8635219/
https://www.ncbi.nlm.nih.gov/pubmed/34826302
http://dx.doi.org/10.12659/AJCR.932961
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