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HEPATOLOGY, VOLUME 62, NUMBER 1 (SUPPL) AASLD ABSTRACTS 253A<br />

88<br />

Increasing Prevalence of Cirrhosis among US Adults<br />

with Chronic Hepatitis C Virus Infection: Results from<br />

NHANES 1988-1994 and 1999-2012<br />

Prowpanga Udompap, Ajitha Mannalithara, Nae-Yun Heo, Donghee<br />

Kim, W. Ray Kim; Division of Gastroenterology and Hepatology,<br />

Stanford University School of Medicine, Stanford, CA<br />

Background & Aims: Hepatitis C virus(HCV) is a major cause<br />

of end stage liver disease and hepatocellular carcinoma worldwide.<br />

While cirrhosis underlies these complications, the prevalence<br />

of HCV cirrhosis in the US remains unknown. We aim<br />

to determine the prevalence of advanced fibrosis/cirrhosis and<br />

to identify factors associated with advanced fibrosis/cirrhosis<br />

in people with chronic hepatitis C in the US population. Methods:<br />

Using the National Health and Nutrition Examination Survey(NHANES)<br />

data, we identified participants with detectable<br />

serum HCV RNA and assessed liver fibrosis using validated<br />

surrogate indicators, including APRI and FIB-4 scores. The prevalence<br />

of cirrhosis was determined for survey participants for<br />

Era 1 (1988-94), Era 2 (1999-2006) and Era 3 (2007-12).<br />

Results: Out of 52,644 participants with age ≥20, 736 (1.4%)<br />

had HCV. Based on APRI score, 6.6% (95%CI:2.2-11.0) of<br />

US adults with HCV infection in Era 1, 7.6% (95%CI:3.4-<br />

11.8) in Era 2 and 17.0% (95%CI:8.0-26.0) in Era 3 were<br />

estimated to have cirrhosis (Ishak stage 5-6). The prevalence<br />

of advanced fibrosis (Ishak stage 4-6) based on FIB-4 was<br />

8.6%, 10.1%, and 16.0% for Eras 1, 2, and 3, respectively.<br />

These data project to 370,500 Americans with cirrhosis and<br />

347,800 with advanced fibrosis in the most recent era. The<br />

higher prevalence of cirrhosis (determined by APRI) in the<br />

recent era was associated with increasing age (OR=1.04,<br />

95%CI:1.02-1.07), diabetes (OR=2.33, 95%CI:1.01-5.40)<br />

and obesity (OR=2.96, 95%CI:1.15-7.57). When FIB-4 score<br />

was used, advanced fibrosis was associated with increasing<br />

age (OR=1.08, 95%CI:1.05-1.11) and diabetes (OR=3.37,<br />

95%CI:1.24-9.5). Conclusion: Nearly one in five US adults<br />

with HCV infection have cirrhosis. The prevalence of cirrhosis<br />

is rising over time, which is in part attributable to the increasing<br />

age of the birth cohort with HCV infection. In addition, comorbidities<br />

such as diabetes and obesity accelerate liver fibrosis.<br />

These data further underscore the current recommendations<br />

for HCV screening in asymptomatic individuals and highlights<br />

the need for systematic assessment for liver fibrosis and comprehensive<br />

medical management in those with HCV infection.<br />

Characteristics of participants<br />

89<br />

Rectal Shedding of HCV in HCV/HIV Co-infected Men<br />

Andrew L. Foster 1,2 , Michael Gaisa 1 , Rosanne M. Hijdra 1,3 , Karen<br />

B. Jacobson 1 , Samuel Turner 1,2 , Tristan Morey 1,2 , Daniel S. Fierer 1 ;<br />

1 Infectious Diseases, Mount Sinai School of Medicine, New York,<br />

NY; 2 James Cook University, Cairns, QLD, Australia; 3 Amsterdam<br />

Medical Center, Amsterdam, Netherlands<br />

Introduction An epidemic of hepatitis C virus (HCV) infection<br />

is occurring among HIV-infected men who have sex with men<br />

(MSM). Epidemiological <strong>studies</strong> suggest that sexual transmission<br />

is fueling the epidemic. Blood and semen have been considered<br />

as potential mechanisms of transmission, but there are<br />

still transmission circumstances that remain unexplained. We<br />

hypothesized that HCV may be shed into rectal fluid of HCV/<br />

HIV co-infected MSM. Methods Written informed consent was<br />

obtained from 45 HIV-infected MSM with HCV infection and<br />

paired blood and rectal fluid specimens were obtained. Rectal<br />

fluid was collected using a moistened polyester-tipped swab<br />

that was gently inserted into the rectum. The swab was placed<br />

into transport medium, vortexed, and the supernatant analysed<br />

for HCV using COBAS AMPLICOR (Roche Diagnostics), lower<br />

limit of quantification 43 IU/mL, lower limit of detection 7 IU/<br />

mL. The experimentally-determined efficiency of HCV absorption<br />

to and elution from the swabs was used to calculate the<br />

rectal HCV viral load (VL). Rectal sexually-transmitted infection<br />

(STI) and blood syphilis testing were also performed. Results<br />

Visual inspection of the swabs showed no visible blood on<br />

any. HCV was detected in 20 (47%) of 43 specimens. Among<br />

those samples with HCV detected, the median rectal VL was<br />

2.92 log 10<br />

IU/mL (IQR 2.92, 4.27). Rectal HCV detection was<br />

associated with serum HCV VL >5 log 10<br />

IU/mL (p=0.011),<br />

and there was a high correlation between the magnitude of<br />

blood VL and rectal HCV VL (correlation coefficient 0.688,<br />

p

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