Primary Biliary Cirrhosis Therapeutic Advances

被引:22
作者
Czul, Frank [1 ]
Peyton, Adam [2 ]
Levy, Cynthia [2 ]
机构
[1] Univ Miami, Miller Sch Med, Dept Med, Miami, FL 33101 USA
[2] Univ Miami, Miller Sch Med, Div Hepatol, Miami, FL 33136 USA
关键词
Primary biliary cirrhosis; Therapeutics; Ursodeoxycholic acid; Fibrates; 6 alpha-Ethyl-chenodeoxycholic acid; URSODEOXYCHOLIC ACID THERAPY; LONG-TERM PROGNOSIS; BIOCHEMICAL RESPONSE; INCOMPLETE RESPONSE; LIVER-TRANSPLANTATION; ANTIMITOCHONDRIAL ANTIBODIES; CLINICAL-FEATURES; NATURAL-HISTORY; ORAL BUDESONIDE; FOLLOW-UP;
D O I
10.1016/j.cld.2012.12.003
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
Primary Biliary Cirrhosis: Therapeutic Advances Frank Czul, Adam Peyton, and Cynthia Levy Primary biliary cirrhosis (PBC) is a chronic and slowly progressive cholestatic liver disease characterized by destruction of the interlobular bile ducts, which, if untreated, leads to fibrosis, biliary cirrhosis, and liver failure. Because liver transplantation remains the only curative option for PBC, the goals of treatment are to slow the rate of progression, to alleviate related symptoms, and to prevent complications. Ursodeoxycholic acid is the only US Food and Drug Administration-approved medical treatment of PBC. Several agents are undergoing evaluation as monotherapy or as an adjuvant to ursodeoxycholic acid. This review summarizes current therapeutic advances in the care of patients with PBC.
引用
收藏
页码:229 / +
页数:15
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