Efficacy of Ursodeoxycholic Acid in Treating Intrahepatic Cholestasis of Pregnancy: A Meta-analysis

被引:226
作者
Bacq, Yannick [1 ]
Sentilhes, Loic [2 ]
Reyes, Humberto B. [3 ]
Glantz, Anna [4 ]
Kondrackiene, Jurate [5 ]
Binder, Tomas [6 ]
Nicastri, Pier Luigi [7 ]
Locatelli, Anna [8 ]
Floreani, Annarosa [9 ]
Hernandez, Ismael [3 ]
Di Martino, Vincent [10 ,11 ]
机构
[1] CHRU Tours, Serv Hepatogastroenterol, F-37044 Tours, France
[2] Angers Univ Hosp, Dept Obstet & Gynecol, Angers, France
[3] Univ Chile, Dept Expt Med, Santiago, Chile
[4] Sahlgrenska Univ, Dept Obstet & Gynecol, Gothenburg, Sweden
[5] Lithuanian Univ Hlth Sci, Dept Gastroenterol, Kaunas, Lithuania
[6] Charles Univ Prague, Sch Med, Dept Obstet & Gynecol, Prague, Czech Republic
[7] Univ Bari, Dept Obstet & Gynecol, Bari, Italy
[8] ISBM San Gerardo, Dept Obstet & Gynecol, Monza, Italy
[9] Univ Padua, Dept Surg & Gastroenterol Sci, Padua, Italy
[10] Univ Franche Comte, UPRES EA 4266, F-25030 Besancon, France
[11] CHRU Besancon, Serv Hepatol, Besancon, France
关键词
Liver Disease; Preterm Birth; Drug; Newborn; RANDOMIZED CONTROLLED-TRIAL; ADENOSYL-L-METHIONINE; MOLECULAR PATHOGENESIS; S-ADENOSYLMETHIONINE; PREVALENCE; MECHANISMS;
D O I
10.1053/j.gastro.2012.08.004
中图分类号
R57 [消化系及腹部疾病];
学科分类号
100201 [内科学];
摘要
BACKGROUND & AIMS: We performed a meta-analysis to evaluate the effects of ursodeoxycholic acid (UDCA) on pruritus, liver test results, and outcomes of babies born to women with intrahepatic cholestasis of pregnancy (ICP). METHODS: We performed a systematic review of 9 published, randomized controlled trials (3 double blinded) that compared the effects of UDCA to other drugs, placebo, or no specific treatment (controls) in patients with ICP. We analyzed data from 454 patients: 207 received only UDCA, 70 received only placebo, 42 received cholestyramine, 36 received dexamethasone for 1 week and then placebo for 2 weeks, 65 received S-adenosyl-methionine, and 34 received no specific treatment. To achieve consistency among end points, a standard questionnaire was sent to all corresponding authors. For each end point, we performed pooled analysis that compared the effects of UDCA with those of all controls and UDCA with those of placebos. RESULTS: In pooled analyses that compared UDCA with all controls, UDCA was associated with total resolution of pruritus (odds ratio [OR], 0.23; 95% confidence interval [CI], 0.07-0.74; P < .01), reduced pruritis (OR, 0.27; 95% CI, 0.13-0.55; P < .0001), normalization of serum levels of alanine aminotransferase (ALT) (OR, 0.23; 95% CI, 0.10-0.50; P < .001), decreased serum level of ALT (OR, 0.24; 95% CI, 0.11-0.52; P < .0001), reduced serum levels of bile acids (OR, 0.37; 95% CI, 0.19-0.75; P < .001), fewer premature births (OR, 0.44; 95% CI, 0.24-0.79; P < .01), reduced fetal distress (OR, 0.46; 95% CI, 0.25-0.86; P < .01), less frequent respiratory distress syndrome (OR, 0.30; 95% CI, 0.12-0.74; P < .01), and fewer neonates in the intensive care unit (OR, 0.49; 95% CI, 0.25-0.98; P = .046). In pooled analyses that compared the effects of UDCA with placebo, UDCA reduced pruritus (OR, 0.21; 95% CI, 0.07-0.62; P < .01), normalized (OR, 0.18; 95% CI, 0.06-0.52; P < .001) or decreased serum levels of ALT (OR, 0.12; 95% CI, 0.05-0.31; P < .0001), and reduced serum levels of bile acids (OR, 0.30; 95% CI, 0.12-0.73; P < .01). CONCLUSIONS: Based on a meta-analysis, UDCA is effective in reducing pruritus and improving liver test results in patients with ICP; UDCA therapy might also benefit fetal outcomes.
引用
收藏
页码:1492 / 1501
页数:10
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