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本帖最后由 StephenW 于 2012-5-22 23:11 编辑
Hepatitis B Surface Antigen (HBsAg) Seroclearance Rate in a Multicenter U.S. Cohort Study Mo1902
Long H. Nguyen1, 2, Pelu Tran1, Kevin T. Chaung2, Vincent G. Nguyen2, Lily H. Kim3, Huy N. Trinh2, 4, Jiayi Li5, Jian Q. Zhang6, Huy A. Nguyen4, Walid Ayoub7, Aijaz Ahmed7, Mindie H. Nguyen7
Affiliation
1School of Medicine, Stanford University, Stanford, CA; 2Pacific Health Foundation, San Jose, CA; 3Stanford University, Stanford, CA; 4San Jose Gastroenterology, San Jose, CA; 5Department of Gastroenterology, Palo Alto Medical Foundation, Mountain View, CA; 6Chinese Hospital, San Francisco, CA; 7Division of Gastroenterology and Hepatology, Stanford University Medical Center, Palo Alto, CA
Abstract:
PURPOSE: The spontaneous loss of HBsAg is thought to be a rare occurrence. Persistent HBsAg seropositivity is an important risk factor for advanced liver disease including cirrhosis and hepatocellular carcinoma (HCC), and there have been few large cohort studies of U.S. patients. HBsAg seroclearance is also a rare occurrence in patients receiving antiviral therapy, though this is generally thought of as one of the most durable and desired treatment endpoints. Our objective is to determine the annual incidence rate of HBsAg seroclearance and which clinical or laboratory characteristics predict for achieving HBsAg seroclearance.
METHODS: Using ICD-9 electronic query and chart review, 1621 patients from two community GI clinics, three community primary care clinics, one community multispecialty medical center, and one university medical center were retrospectively enrolled from 2001-2008. HBsAg seroclearance was determined by documented loss of HBsAg. Persistent HBsAg was verified directly with HBsAg serology or by proxy with positive HBeAg results or detectable HBV DNA levels.
RESULTS: HBsAg seroclearance occurred in 19 patients over the course of 4895 person-years (0.39% annual seroclearance rate, 1.2% overall). Median follow-up was 32 months and did not differ significantly between those who cleared HBsAg and those who did not. Compared to those who maintained HBsAg positivity, patients who achieved HBsAg seroclearance were older (mean 49±10 years vs. 43±13, p=0.04); however, the two groups of patients did not differ significantly on the following: proportion of males, BMI, history of treatment before or during follow-up, family history of viral hepatitis/HCC/cirrhosis, baseline HBeAg status, ALT, AFP, or HBV DNA level.
Annual incidence of HBsAg seroclearance differed significantly by age (0.28% for age ≤50 years vs. 0.73% for >50, p=0.02) and trended towards significance for baseline HBV DNA levels (0.29% for >10,000 IU/mL vs. 0.62% for ≤10,000 IU/mL, p=0.09) (Figure 1). HBsAg seroclearance rates did not differ significantly by sex, baseline HBeAg status, or by treatment history.
On multivariate Cox modeling also inclusive of sex, treatment history, and HBeAg status, older age was a significant predictor for HBsAg seroclearance (HR: 1.04, 95% CI: 1.00-1.07; p=0.03) and baseline HBV DNA≤10,000 IU/mL also trended towards significance (HR: 2.3, 95% CI: 0.86-6.2; p=0.09).
CONCLUSION:
HBsAg seroclearance rates may be lower than previously described, with or without treatment with oral antiviral agents. Increasing age was an independent predictor for seroclearance and low baseline HBV DNA revealed a trend towards significance. Further studies are needed to characterize the natural history of HBsAg seroclearance in U.S. patients who are treatment-naïve and treatment-experienced and in various age groups.
Disclosure(s):
Huy N. Trinh - Advisory Committees or Review Panels: Bristol-Myers Squibb, Bristol-Myers Squibb, Gilead Sciences Inc; Grant/Research Support: Gilead Sciences; Stock Shareholder: Gilead Sciences, Bristol-Myers Squibb
Huy A. Nguyen - Speaking and Teaching: Gilead Sciences Inc
Aijaz Ahmed - Advisory Committees or Review Panels: Salix Pharmaceuticals, Inc., Schering-Plough Corp., Vertex Pharmaceuticals , Three Rivers Pharmaceuticals, LLC; Grant/Research Support: Gilead Sciences Inc, Romark Laboratories, L.C.; Speaking and Teaching: Bristol-Myers Squibb Co. , Gilead Sciences Inc, Hoffman-LaRoche
Mindie H. Nguyen - Advisory Committees or Review Panels: Salix Pharmaceuticals, Schering-Plough, Schering-Plough, Vertex Pharmaceuticals , Three Rivers Pharmaceuticals, LLC; Grant/Research Support: Gilead Sciences, Romark Laboratories; Speaking and Teaching: Bristol-Myers Squibb, Gilead Sciences, Hoffman-LaRoche
The following people have nothing to disclose: Long H. Nguyen, Pelu Tran, Kevin T. Chaung, Vincent G. Nguyen, Lily H. Kim, Jiayi Li, Jian Q. Zhang, Walid Ayoub
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