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Long-Term Fenofibrate Treatment in Primary Biliary Cholangitis Improves Biochemistry but Not the UK-PBC Risk Score.
- Source :
- Digestive Diseases & Sciences; Oct2016, Vol. 61 Issue 10, p3037-3044, 8p
- Publication Year :
- 2016
-
Abstract
- <bold>Background: </bold>Fenofibrate (FF) has been suggested as a second-line agent in primary biliary cholangitis (PBC) patients who do not achieve adequate biochemical response to ursodeoxycholic acid (UDCA) monotherapy. Limited data exist on FF use beyond 12 months, and its long-term effects are unclear.<bold>Aim: </bold>To study the biochemical outcome of long-term (>12 months) FF treatment in combination with UDCA (FF + UDCA) in PBC patients and to determine the effect on predicted prognosis using the UK-PBC Risk Score.<bold>Methods: </bold>This was a retrospective cohort study of all PBC patients treated in a specialist center with FF + UDCA therapy after failure to achieve biochemical response. Liver and renal biochemical indices and the UK-PBC Risk Score at baseline and at 12, 24, 36, 48, and 60 months of FF + UDCA treatment were compared. Biochemical response was assessed using the POISE trial criteria at the end of FF + UDCA treatment.<bold>Results: </bold>Data from 23 patients treated with FF + UDCA combination were analyzed. The median dose of fenofibrate was 200 mg/day, and median treatment duration was 21 months (range 1-123 months). Six (26 %) patients discontinued FF within 1 year. In patients who completed 12 months (n = 17) and long-term therapy, significant decrease in ALP was seen at 12 (p = 0.0002), 24 (p = 0.002), and 36 (p = 0.03) months. More than 75 % patients met the POISE criteria of ALP response at all study time points. There was no significant improvement in the 5-, 10-, and 15-year UK-PBC Risk Scores after FF + UDCA treatment. No significant renal impairment or adverse events were reported.<bold>Conclusion: </bold>The long-term treatment of PBC patients with fenofibrate as an adjunct to UDCA is safe and effective in improving ALP, but the treatment did not significantly reduce the estimated probability of liver-related death or need for liver transplantation. [ABSTRACT FROM AUTHOR]
- Subjects :
- CHOLANGITIS
FENOFIBRATE
LONG-term care facilities
BIOCHEMISTRY
THERAPEUTICS
DISEASE risk factors
ANTILIPEMIC agents
GASTROINTESTINAL agents
ALKALINE phosphatase
BILIRUBIN
COMBINATION drug therapy
CLINICAL trials
CREATININE
GLOMERULAR filtration rate
CIRRHOSIS of the liver
LONGITUDINAL method
PROGNOSIS
RESEARCH funding
SERUM albumin
TIME
ALANINE aminotransferase
TREATMENT effectiveness
RETROSPECTIVE studies
Subjects
Details
- Language :
- English
- ISSN :
- 01632116
- Volume :
- 61
- Issue :
- 10
- Database :
- Complementary Index
- Journal :
- Digestive Diseases & Sciences
- Publication Type :
- Academic Journal
- Accession number :
- 118028230
- Full Text :
- https://doi.org/10.1007/s10620-016-4250-y