Female sex is a protective factor for the progression of fibrosis in patients with chronic hepatitis C virus (HCV) infection. Experimental data suggest that estrogens may have an antifibrotic effect. The objective of this study was to evaluate the influence of past pregnancies, oral contraceptives,
Progression of liver fibrosis in women infected with hepatitis C: Long-term benefit of estrogen exposure
β Scribed by Mical Campbell; Yu-Xiao Yang; K. Rajender Reddy
- Publisher
- John Wiley and Sons
- Year
- 2005
- Tongue
- English
- Weight
- 149 KB
- Volume
- 41
- Category
- Article
- ISSN
- 0270-9139
No coin nor oath required. For personal study only.
β¦ Synopsis
We read with interest the paper by Di Martino et al. published in the December 2004 issue of HEPATOLOGY 1 that examines estrogen-related effects on hepatitis C fibrosis. Specifically, progression of hepatitis C fibrosis was correlated with prior pregnancies, menopausal status, past use of oral contraceptives, and hormone replacement therapy. Hepatitis C-infected women who completed a survey and had previously undergone liver biopsy were eligible for the study. The investigators calculated a rate of progression of fibrosis, dividing fibrosis stage (in Metavir units) by years of hepatitis C infection. This approach has been used previously in a selfdescribed cross-sectional study. 2 The present study is labeled a "retrospective cohort study," although it would be better characterized as a cross-sectional study. Information from a single survey was correlated with results from a single liver biopsy. Patients were not followed by repeated biopsies or repeated surveys over time.
The distinction between cohort and cross-sectional is not merely semantic in this case. Figures 3 and4 are Kaplan-Meier curves for the development of significant fibrosis in "cohorts" of hepatitis C patients. Kaplan-Meier curves depend on the precise knowledge of when a patient in a cohort develops significant fibrosis. For example, a patient with a biopsy showing stage 4 fibrosis and 20 years of disease duration would be plotted on a Kaplan-Meier curve as having developed significant fibrosis (stage 2) after 20 years' disease duration. Without a prior biopsy, it is not known at what time the patient actually developed stage 2 fibrosis. To address the impossibility of accurate censoring, the authors could have back-extrapolated to estimate time to development of stage 2 fibrosis, assuming linear progression of fibrosis. The problem with that approach is that it involves using a calculated result to generate primary data-for re-analysis.
In short, even though the investigators describe a rate of progression of fibrosis, the data do not truly describe a cohort. Statistical methods generally reserved for cohort studies cannot be applied easily to cross-sectional data.
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