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. 2012;7(9):e44624.
doi: 10.1371/journal.pone.0044624. Epub 2012 Sep 10.

Reproductive status is associated with the severity of fibrosis in women with hepatitis C

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Reproductive status is associated with the severity of fibrosis in women with hepatitis C

Erica Villa et al. PLoS One. 2012.

Abstract

Introduction: Chronic hepatitis C is the main cause of death in patients with end-stage liver disease. Prognosis depends on the increase of fibrosis, whose progression is twice as rapid in men as in women. Aim of the study was to evaluate the effects of reproductive stage on fibrosis severity in women and to compare these findings with age-matched men.

Materials and methods: A retrospective study of 710 consecutive patients with biopsy-proven chronic hepatitis C was conducted, using data from a clinical database of two tertiary Italian care centers. Four age-matched groups of men served as controls. Data about demographics, biochemistry, liver biopsy and ultrasonography were analyzed. Contributing factors were assessed by multivariate logistic regression analysis.

Results: Liver fibrosis was more advanced in the early menopausal than in the fully reproductive (P<0.0001) or premenopausal (P = 0.042) group. Late menopausal women had higher liver fibrosis compared with the other groups (fully reproductive, P<0.0001; premenopausal, P = <0.0001; early menopausal, P = 0.052). Multivariate analyses showed that male sex was independently associated with more severe fibrosis in the groups corresponding to premenopausal (P = 0.048) and early menopausal (P = 0.004) but not late menopausal pairs. In women, estradiol/testosterone ratio decreased markedly in early (vs. reproductive age: P = 0.002 and vs. premenopausal: P<0.0001) and late menopause (vs. reproductive age: P = 0.001; vs. premenopausal: P<0.0001). In men age-matched with menopausal women, estradiol/testosterone ratio instead increased (reproductive age group vs. early: P = 0.002 and vs. late M: P = 0.001).

Conclusions: The severity of fibrosis in women worsens in parallel with increasing estrogen deprivation and estradiol/testosterone ratio decrease. Our data provide evidence why fibrosis progression is discontinuous in women and more linear and severe in men, in whom aging-associated estradiol/testosterone ratio increase occurs too late to noticeably influence the inflammatory process leading to fibrosis.

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Conflict of interest statement

Competing Interests: The study was supported by an unrestricted grant by Merck & Co (Whitehouse Station, NJ, USA). The funding source had no role in the design of the study; collection, analysis, and interpretation of the data; drafting of the manuscript or decision to submit the manuscript for publication. Corresponding Author is serving as Academic Editor for PLOS ONE. This does not alter the authors’ adherence to all the PLOS ONE policies on sharing data and materials.

Figures

Figure 1
Figure 1. Mean necro-inflammation and fibrosis scores in the four subgroups of female and age-matched male patients with chronic hepatitis (Women: triangles; Men: squares).
Levels of significance of the intra- and inter-group comparison are reported in the text.
Figure 2
Figure 2. Mean serum levels of anti-müllerian hormone (AMH) in women divided according to reproductive phases.
AMH levels were significantly lower in premenopausal women in comparison with women in full reproductive age (p<0.0001) and became undetectable in menopausal women (both early and late).
Figure 3
Figure 3. Estradiol and Testosterone serum levels and E2/T ratio in men and women divided according to women’s reproductive phases as described in Methods.
Values (reported as mean±SD) were compared by Mann-Whitney test. The levels of significance are reported in the text.

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