Nonalcoholic fatty liver disease. Issue 3 (May 2015)
- Record Type:
- Journal Article
- Title:
- Nonalcoholic fatty liver disease. Issue 3 (May 2015)
- Main Title:
- Nonalcoholic fatty liver disease
- Authors:
- Hardy, Timothy
Anstee, Quentin M.
Day, Christopher P. - Abstract:
- <abstract> <title> <x xml:space="preserve">Abstract</x> </title> <sec> <title>Purpose of review</title> <p>Nonalcoholic fatty liver disease is the most common cause of liver dysfunction in the western world because of its close association with obesity, insulin resistance and dyslipidaemia. Nonalcoholic steatohepatitis (NASH) is a particular health concern due to the increased morbidity and mortality associated with progressive disease. At present, without specific targeted pharmacological therapies, the mainstay of therapy remains weight loss through dietary modification and lifestyle change; thus, the purpose of this review is to summarize the recent evidence for current and emerging therapies in NASH.</p> </sec> <sec> <title>Recent findings</title> <p>Some existing medications, including pioglitazones and angiotensin receptor antagonists, may be repurposed to help treat this condition. Vitamin E may improve histology in NASH, but safety issues limit its use. Recently, a number of novel agents specifically targeting nonalcoholic fatty liver disease pathogenesis have entered clinical trials, including the farnesoid X receptor agonist obeticholic acid, which has shown significant histological improvements in steatohepatitis and fibrosis.</p> </sec> <sec> <title>Summary</title> <p>Diet/lifestyle modification remains the mainstay of treatment. For patients with NASH and advanced fibrosis, current liver-directed pharmacotherapy with vitamin E and pioglitazone offer some<abstract> <title> <x xml:space="preserve">Abstract</x> </title> <sec> <title>Purpose of review</title> <p>Nonalcoholic fatty liver disease is the most common cause of liver dysfunction in the western world because of its close association with obesity, insulin resistance and dyslipidaemia. Nonalcoholic steatohepatitis (NASH) is a particular health concern due to the increased morbidity and mortality associated with progressive disease. At present, without specific targeted pharmacological therapies, the mainstay of therapy remains weight loss through dietary modification and lifestyle change; thus, the purpose of this review is to summarize the recent evidence for current and emerging therapies in NASH.</p> </sec> <sec> <title>Recent findings</title> <p>Some existing medications, including pioglitazones and angiotensin receptor antagonists, may be repurposed to help treat this condition. Vitamin E may improve histology in NASH, but safety issues limit its use. Recently, a number of novel agents specifically targeting nonalcoholic fatty liver disease pathogenesis have entered clinical trials, including the farnesoid X receptor agonist obeticholic acid, which has shown significant histological improvements in steatohepatitis and fibrosis.</p> </sec> <sec> <title>Summary</title> <p>Diet/lifestyle modification remains the mainstay of treatment. For patients with NASH and advanced fibrosis, current liver-directed pharmacotherapy with vitamin E and pioglitazone offer some benefits; obeticholic acid appears promising and is currently being tested. Comorbidities must be diagnosed and treated; cardiovascular disease remains a primary cause of death in these patients.</p> </sec> </abstract> … (more)
- Is Part Of:
- Current opinion in gastroenterology. Volume 31:Issue 3(2015:May)
- Journal:
- Current opinion in gastroenterology
- Issue:
- Volume 31:Issue 3(2015:May)
- Issue Display:
- Volume 31, Issue 3 (2015)
- Year:
- 2015
- Volume:
- 31
- Issue:
- 3
- Issue Sort Value:
- 2015-0031-0003-0000
- Page Start:
- Page End:
- Publication Date:
- 2015-05
- Subjects:
- Gastroenterology -- Periodicals
616.33 - Journal URLs:
- http://journals.lww.com/pages/default.aspx ↗
- DOI:
- 10.1097/MOG.0000000000000175 ↗
- Languages:
- English
- ISSNs:
- 0267-1379
- Deposit Type:
- Legaldeposit
- View Content:
- Available online (eLD content is only available in our Reading Rooms) ↗
- Physical Locations:
- British Library DSC - 3500.775000
British Library DSC - BLDSS-3PM
British Library STI - ELD Digital store - Ingest File:
- 3183.xml