Influence of ursodeoxycholic acid on the mortality and malignancy associated with primary biliary cirrhosis: A population-based cohort study

被引:55
作者
Jackson, Hannah
Solaymani-Dodaran, Masoud
Card, Tim R.
Aithal, Guruprasad P.
Logan, Richard
West, Joe
机构
[1] Univ Nottingham, Sch Med, Queens Med Ctr, Div Epidemiol & Publ Hlth, Nottingham NG7 2RD, England
[2] Sch Med, Queens Med Ctr, Wolfson Digest Dis Ctr, Nottingham, England
关键词
D O I
10.1002/hep.21795
中图分类号
R57 [消化系及腹部疾病];
学科分类号
摘要
There is debate over the mortality and malignancy risk in people with primary biliary cirrhosis (PBC) and whether this risk is reduced by use of ursodeoxycholic acid. To investigate this issue, we identified 930 people with PBC and 9,202 control subjects from the General Practice Research Database in the United Kingdom. We categorized regular ursodeoxycholic acid as treatment with 6 or more prescriptions and nonregular treatment as less than 6. We found a 2.7-fold increase in mortality for the PBC cohort compared with the general population [adjusted hazard ratio (HR), 2.69; 95% CI, 2.35-3.09]. In those having regular ursodeoxycholic acid (43%), the mortality increase was 2.2-fold (HR, 2.19; 95% CI, 1.66-2.87) and in those not treated 2.7-fold (HR, 2.69; 95% CI, 2.18-3.33). This apparent reduction in mortality was not explained by less severe disease in the ursodeoxycholic acid-treated group. The increased risk of primary liver cancer in ursodeoxycholic acid-treated patients was 3-fold (HR, 3.17; 95% CI, 0.64-15.62), in contrast to an 8-fold increase in those not treated (HR, 7.77; 95% CI, 1.30-46.65). Conclusion: We found that people with PBC had a 3-fold mortality increase when compared with the general population, which was somewhat reduced by regular treatment with ursodeoxycholic acid. However, the observed effect of ursodeoxycholic acid was not statistically significant.
引用
收藏
页码:1131 / 1137
页数:7
相关论文
共 27 条
[1]  
Caballería L, 2001, AM J GASTROENTEROL, V96, P1160
[2]   Mortality in inflammatory bowel disease: A population-based cohort study [J].
Card, T ;
Hubbard, R ;
Logan, RFA .
GASTROENTEROLOGY, 2003, 125 (06) :1583-1590
[3]   Long-term ursodeoxycholic acid therapy for primary biliary cirrhosis: a follow-up to 12 years [J].
Chan, CW ;
Gunsar, F ;
Feudjo, M ;
Rigamonti, C ;
Vlachogiannakos, J ;
Carpenter, JR ;
Burroughs, AK .
ALIMENTARY PHARMACOLOGY & THERAPEUTICS, 2005, 21 (03) :217-226
[4]   The effect of ursodeoxycholic acid therapy on the natural course of primary biliary cirrhosis [J].
Corpechot, C ;
Carrat, F ;
Bahr, A ;
Chrétien, Y ;
Poupon, RE ;
Poupon, R .
GASTROENTEROLOGY, 2005, 128 (02) :297-303
[5]   Hepatic and extrahepatic malignancies in primary biliary cirrhosis [J].
Floreani, A ;
Baragiotta, A ;
Baldo, V ;
Menegon, T ;
Farinati, F ;
Naccarato, R .
HEPATOLOGY, 1999, 29 (05) :1425-1428
[6]  
GLUUD C, 2004, COCHRANE LIB, V3
[7]   Randomised controlled trials of ursodeoxycholic-acid therapy for primary biliary cirrhosis: a meta-analysis [J].
Goulis, J ;
Leandro, G ;
Burroughs, AK .
LANCET, 1999, 354 (9184) :1053-1060
[8]  
Hollowell J, 1997, Popul Trends, P36
[9]   Cancer risk in primary biliary cirrhosis: a study in northern England [J].
Howel, D ;
Metcalf, JV ;
Gray, J ;
Newmann, WL ;
Jones, DEJ ;
James, OFW .
GUT, 1999, 45 (05) :756-760
[10]   Adult height and cryptogenic fibrosing alveolitis: a case-control study using the UK General Practice Research Database [J].
Hubbard, R ;
Venn, A .
THORAX, 2000, 55 (10) :864-866