Academic Journal

Atorvastatin for patients with cirrhosis:A randomized, placebo-controlled trial

التفاصيل البيبلوغرافية
العنوان: Atorvastatin for patients with cirrhosis:A randomized, placebo-controlled trial
المؤلفون: Kronborg, Thit M, Schierwagen, Robert, Trošt, Kajetan, Gao, Qian, Moritz, Thomas, Bendtsen, Flemming, Gantzel, Rasmus H, Andersen, Mette L, Teisner, Ane S, Grønbæk, Henning, Hobolth, Lise, Møller, Søren, Trebicka, Jonel, Kimer, Nina
المصدر: Kronborg , T M , Schierwagen , R , Trošt , K , Gao , Q , Moritz , T , Bendtsen , F , Gantzel , R H , Andersen , M L , Teisner , A S , Grønbæk , H , Hobolth , L , Møller , S , Trebicka , J & Kimer , N 2023 , ' Atorvastatin for patients with cirrhosis : A randomized, placebo-controlled trial ' , Hepatology Communications , vol. 7 , no. 12 , e0332 . https://doi.org/10.1097/HC9.0000000000000332
سنة النشر: 2023
المجموعة: Aarhus University: Research
الوصف: BACKGROUND: Patients with cirrhosis and portal hypertension face a high risk of complications. Besides their anti-inflammatory and antifibrotic effects, statins may reduce portal pressure and thus the risk of complications and mortality. We aimed to investigate the effects of atorvastatin on hospital admissions, mortality, inflammation, and lipidomics in cirrhosis with portal hypertension. METHODS: We performed a double-blinded, randomized, placebo-controlled clinical trial among patients with cirrhosis and portal hypertension. Atorvastatin (10-20 mg/d) was administered for 6 months. We measured splanchnic hemodynamics, analyzed inflammatory markers, and performed lipidomics at baseline and after 6 months. RESULTS: Seventy-eight patients were randomized, with 38 patients allocated to atorvastatin and 40 patients to placebo. Fifty-nine patients completed 6 months of intervention. Comparisons between changes in each group were calculated. Liver-related complications and mortality were similar between the groups. The HVPG and Model for End-stage Liver Disease score did not change between groups (p=0.95 and 0.87, respectively). Atorvastatin decreased 3 of 42 inflammatory markers, CD62-L-selectin, matrix metalloproteinases-2, and TNF-α (p-values: 0.005, 0.011, and 0.023, respectively), while lipidomics was not significantly changed. CONCLUSIONS: In patients with cirrhosis, atorvastatin was safe to use, but did not reduce mortality, the risk of liver-related complications, or the HVPG. Atorvastatin induced minor anti-inflammatory effects and minor effects on lipids during a 6-month treatment period.
نوع الوثيقة: article in journal/newspaper
اللغة: English
DOI: 10.1097/HC9.0000000000000332
الاتاحة: https://pure.au.dk/portal/en/publications/6bdbc55b-30f6-4e5a-abec-cb681e12f8b8
https://doi.org/10.1097/HC9.0000000000000332
http://www.scopus.com/inward/record.url?scp=85186752478&partnerID=8YFLogxK
Rights: info:eu-repo/semantics/openAccess
رقم الانضمام: edsbas.E7E4B1F0
قاعدة البيانات: BASE
الوصف
DOI:10.1097/HC9.0000000000000332