New pharmacological treatment options for nonalcoholic fatty liver disease.
New pharmacological treatment options for nonalcoholic fatty liver disease.
Internist 61, 759-765 (2020)
DOI
PMC
Open Access Green möglich sobald Postprint bei der ZB eingereicht worden ist.
The prevalence of nonalcoholic fatty liver disease (NAFLD) continues to increase worldwide, presently affecting 25% of the adult population, and is associated with an elevated risk of total and liver-specific mortality. NAFLD is a chronic disease and results from a combination of genetic, environmental and predominantly lifestyle-related causes. Therefore, NAFLD, similarly to cardiovascular disease, type 2 diabetes and many different types of cancer, can be considered a noncommunicable disease. Consequently, lifestyle intervention, particularly if associated with a large amount of weight loss, is considered highly effective and safe to treat NAFLD. For patients with advanced-stage NAFLD or that cannot lose weight, metabolically-based pharmacotherapy is effective to improve liver histology and cardiometabolic risk profile. If a moderate or advanced stage of liver fibrosis is present, additional antifibrotic therapy is necessary to halt the progression of the disease.
The prevalence of nonalcoholic fatty liver disease
(NAFLD) continues to increase worldwide, presently affecting 25% of the
adult population, and is associated with an elevated risk of total and
liver-specific mortality. NAFLD is a chronic disease and results from
a combination of genetic, environmental and predominantly
lifestyle-related causes. Therefore, NAFLD, similarly to cardiovascular
disease, type 2 diabetes and many different types of cancer, can be
considered a noncommunicable disease. Consequently, lifestyle
intervention, particularly if associated with a large amount of weight
loss, is considered highly effective and safe to treat NAFLD. For
patients with advanced-stage NAFLD or that cannot lose weight,
metabolically-based pharmacotherapy is effective to improve liver
histology and cardiometabolic risk profile. If a moderate or advanced
stage of liver fibrosis is present, additional antifibrotic therapy is
necessary to halt the progression of the disease.
Impact Factor
Scopus SNIP
Web of Science
Times Cited
Scopus
Cited By
Altmetric
Publikationstyp
Artikel: Journalartikel
Dokumenttyp
Review
Typ der Hochschulschrift
Herausgeber
Schlagwörter
Nonalcoholic Steatohepatitis ; Diabetes Mellitus ; Type 2 ; Cardiovascular Diseases ; Pioglitazone ; Vitamin E; Reduces Features; Obeticholic Acid; Steatohepatitis; Fibrosis; Placebo; Weight
Keywords plus
Sprache
deutsch
Veröffentlichungsjahr
2020
Prepublished im Jahr
HGF-Berichtsjahr
2020
ISSN (print) / ISBN
0020-9554
e-ISSN
1432-1289
ISBN
Bandtitel
Konferenztitel
Konferzenzdatum
Konferenzort
Konferenzband
Quellenangaben
Band: 61,
Heft: 7,
Seiten: 759-765
Artikelnummer: ,
Supplement: ,
Reihe
Verlag
Springer
Verlagsort
Berlin ; Heidelberg
Tag d. mündl. Prüfung
0000-00-00
Betreuer
Gutachter
Prüfer
Topic
Hochschule
Hochschulort
Fakultät
Veröffentlichungsdatum
0000-00-00
Anmeldedatum
0000-00-00
Anmelder/Inhaber
weitere Inhaber
Anmeldeland
Priorität
Begutachtungsstatus
Peer reviewed
POF Topic(s)
90000 - German Center for Diabetes Research
Forschungsfeld(er)
Helmholtz Diabetes Center
PSP-Element(e)
G-502400-001
Förderungen
Copyright
Erfassungsdatum
2020-05-18