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使用纤维化的间接标志物评估丙型肝炎病毒和 HIV 合并感染女性的死亡率。

Assessing mortality in women with hepatitis C virus and HIV using indirect markers of fibrosis.

机构信息

University of California San Francisco, San Francisco, California 94143-0538, USA.

出版信息

AIDS. 2012 Mar 13;26(5):599-607. doi: 10.1097/QAD.0b013e32834fa121.

DOI:10.1097/QAD.0b013e32834fa121
PMID:22156972
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC3698040/
Abstract

OBJECTIVE

Co-infection with hepatitis C virus (HCV) is a major cause of morbidity and mortality in HIV-infected individuals. However, predictors of mortality are poorly defined and most studies have focused predominantly on co-infection in men. We evaluated whether two indirect markers of hepatic fibrosis, aspartate aminotransferase-to-platelet ratio index (APRI) and FIB-4 scores, were predictive of mortality in a well defined longitudinal cohort of HCV/HIV-co-infected women on HAART.

METHODS

HCV/HIV-co-infected women on antiretroviral therapy enrolled in Women's Interagency HIV Study (WIHS), a National Institutes of Health-funded prospective, multicenter, cohort study of women with and at risk for HIV infection were included. Using Cox regression analysis, associations between APRI and FIB-4 with all-cause mortality were assessed.

RESULTS

Four hundred and fifty HCV/HIV-co-infected women, of whom 191 women died, had a median follow-up of 6.6 years and 5739 WIHS visits. Compared with women with low APRI or FIB-4 levels, severe fibrosis was significantly associated with an increased risk of all-cause mortality {APRI: hazard ratio 2.78 [95% confidence interval (CI) 1.87, 4.12]; FIB-4: hazard ratio 2.58 (95% CI 1.68, 3.95)}. Crude death rates per 1000 patient-years increased with increasing liver fibrosis: 34.8 for mild, 51.3 for moderate and 167.9 for severe fibrosis as measured by FIB-4. Importantly, both APRI and FIB-4 increased during the 5 years prior to death for all women: the slope of increase was greater for women dying a liver-related death compared with nonliver-related death.

CONCLUSION

Both APRI and FIB-4 are independently associated with all-cause mortality in HCV/HIV-co-infected women and may have clinical prognostic utility among women with HIV and HCV.

摘要

目的

丙型肝炎病毒(HCV)合并感染是 HIV 感染者发病和死亡的主要原因。然而,对于死亡率的预测因素尚未明确,且大多数研究主要集中在男性合并感染上。我们评估了两种间接肝纤维化标志物,即天门冬氨酸氨基转移酶与血小板比值指数(APRI)和 FIB-4 评分,在接受高效抗逆转录病毒治疗(HAART)的 HCV/HIV 合并感染女性的明确的纵向队列研究中,是否能预测死亡率。

方法

纳入参加妇女艾滋病研究机构(WIHS)的接受抗病毒治疗的 HCV/HIV 合并感染女性,这是一项由美国国立卫生研究院资助的前瞻性、多中心、HIV 感染和有感染风险的女性队列研究。使用 Cox 回归分析,评估 APRI 和 FIB-4 与全因死亡率之间的相关性。

结果

450 例 HCV/HIV 合并感染女性,其中 191 例死亡,中位随访 6.6 年,共进行了 5739 次 WIHS 就诊。与 APRI 或 FIB-4 水平较低的女性相比,严重纤维化与全因死亡率增加显著相关{APRI:风险比 2.78(95%置信区间 1.87,4.12);FIB-4:风险比 2.58(95%置信区间 1.68,3.95)}。按纤维化程度划分的粗死亡率(每 1000 患者年)随肝纤维化程度的增加而增加:轻度纤维化为 34.8,中度纤维化为 51.3,FIB-4 重度纤维化为 167.9。重要的是,在所有女性死亡前的 5 年内,APRI 和 FIB-4 均增加:与非肝脏相关死亡相比,死于肝脏相关死亡的女性增加幅度更大。

结论

APRI 和 FIB-4 均与 HCV/HIV 合并感染女性的全因死亡率独立相关,在 HIV 和 HCV 合并感染的女性中可能具有临床预后效用。

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