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Journal of Clinical Microbiology, August 2007, p. 2426-2433, Vol. 45, No. 8
0095-1137/07/$08.00+0     doi:10.1128/JCM.02448-06
Copyright © 2007, American Society for Microbiology. All Rights Reserved.

Factors Affecting Serum Concentrations of Hepatitis C Virus (HCV) RNA in HCV Genotype 1-Infected Patients with Chronic Hepatitis{triangledown}

John R. Ticehurst,1,2,3* Fayez M. Hamzeh,4 and David L. Thomas2,3

Johns Hopkins Bayview Medical Center Clinical Laboratories and Johns Hopkins Hospital Division of Medical Microbiology, Department of Pathology,1 Division of Infectious Diseases, Department of Medicine,2 School of Medicine, and Department of Epidemiology, Bloomberg School of Public Health,3 Johns Hopkins University, Baltimore, Maryland and Roche Laboratories, Nutley, New Jersey4

Received 6 December 2006/ Returned for modification 5 February 2007/ Accepted 17 May 2007

The serum concentration of hepatitis C virus (HCV) RNA is usually stable (4 to 8 log10 IU/ml) in untreated patients with chronic hepatitis C. While this baseline HCV RNA concentration ([HCV RNA]BL) is predictive of a sustained virologic response to treatment, its determinants are only partially identified. We therefore analyzed the baseline characteristics of 2,472 HCV genotype 1-infected patients to identify correlations with gender, age, race, weight, body mass index (BMI), HCV acquisition mode, HCV subtype, alanine aminotransferase concentration, or histopathologic changes in the liver. After separation of the data according to four [HCV RNA]BL groups (≤5.0, >5.0 to 5.6, >5.6 to 5.9, and >5.9 log10 IU/ml), we determined that increasing [HCV RNA]BL correlated (P < 0.05) with increasing proportions of patients who were male, >40 years of age, or heavier (a weight of >85 kg or a BMI of >27 kg/m2). Histologic activity index (HAI) data were available for 1,304 of these patients: increasing [HCV RNA]BL correlated with higher fibrosis and necrosis-inflammation scores. As a continuous variable, [HCV RNA]BL correlated with age, gender, weight (continuous or ≤85 versus >85 kg), BMI (continuous or ≤27 versus >27 kg/m2), subtype, fibrosis score, and necrosis-inflammation score; however, multiple-regression analysis yielded P values of <0.1 only for age, gender, BMI (≤27 versus >27 kg/m2), and fibrosis score. While our findings are suggestive of a role for these factors in maintenance of the pretreatment state of HCV infection, the multiple-regression model accounted for only ≤4.6% of the [HCV RNA]BL differences between individuals (R2 = 0.046 for 1,304 patients with HAI scores; 0.043 for all 2,472 patients).


* Corresponding author. Mailing address: Clinical Laboratories, Department of Pathology, Room A102, Johns Hopkins Bayview Medical Center, 4940 Eastern Ave., Baltimore, MD 21224. Phone: (410) 550-0648. Fax: (410) 550-2109. E-mail: jticehur{at}jhmi.edu

{triangledown} Published ahead of print on 30 May 2007.


Journal of Clinical Microbiology, August 2007, p. 2426-2433, Vol. 45, No. 8
0095-1137/07/$08.00+0     doi:10.1128/JCM.02448-06
Copyright © 2007, American Society for Microbiology. All Rights Reserved.







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