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VIII 因子和 FVIII/PC 比值对肝硬化门静脉血栓形成的影响:系统评价和荟萃分析。

Effect of factor VIII and FVIII/PC ratio on portal vein thrombosis in liver cirrhosis: a systematic review and meta‑analysis.

机构信息

Department of Infectious Diseases, the Hebei Medical University Third Hospital, Shijiazhuang, 050051, China.

出版信息

BMC Gastroenterol. 2024 Sep 19;24(1):320. doi: 10.1186/s12876-024-03399-1.

DOI:10.1186/s12876-024-03399-1
PMID:39300356
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC11411769/
Abstract

BACKGROUND

To date, there is an ongoing debate regarding the ability to predict PVT development using markers of FVIII or FVIII/PC ratio. This study presents evidence-based medical findings on the influence of FVIII activity levels and FVIII/PC values in the formation of PVT in cirrhosis.

METHODS

The search for original studies on risk factors for portal vein thrombosis (PVT) associated with cirrhosis was conducted, which primarily focused on comparing circulating FVIII activity levels or FVIII/PC ratio in cirrhotic patients with and without PVT. The quality of evidence from each study was assessed using the Newcastle-Ottawa Scale.

RESULTS

The meta-analysis included a total of 10 original studies. In total, 2250 cirrhotic patients were included, with 414 having PVT and 1836 without PVT. The pooled analysis using a random-effects model showed no significant difference in standardized mean difference (SMD) for FVIII activity levels in cirrhotic patients with or without PVT (SMD = 0.12, 95% CI=-0.46 to 0.70, P = 0.68), but there was significant heterogeneity (I = 95.52%, P = 0.00). Meta-regression analysis indicated that differences in mean FVIII activity levels in the PVT group, the number of cases in the non-PVT group, and the study design methods partially contributed to the heterogeneity (P < 0.05). However, compared to the non-PVT group, the PVT group had higher FVIII/PC ratio with a statistically significant difference (SMD = 0.39, 95% CI: 0.15 to 0.63, P = 0.00), and there was no significant heterogeneity (I = 28.62%).

CONCLUSION

In conclusion, the FVIII/PC ratio not only reflects the severity of liver disease, but also can be used as one of the predictors of PVT development.

摘要

背景

迄今为止,关于使用 FVIII 或 FVIII/PC 比值的标志物预测 PVT 发展的能力,仍存在争议。本研究提供了循证医学证据,证明 FVIII 活性水平和 FVIII/PC 值在肝硬化形成 PVT 中的影响。

方法

对与肝硬化相关的门静脉血栓形成(PVT)危险因素的原始研究进行了检索,主要侧重于比较肝硬化伴或不伴 PVT 的患者循环 FVIII 活性水平或 FVIII/PC 比值。使用纽卡斯尔-渥太华量表评估每个研究的证据质量。

结果

荟萃分析共纳入 10 项原始研究。共纳入 2250 例肝硬化患者,其中 414 例有 PVT,1836 例无 PVT。使用随机效应模型的汇总分析显示,肝硬化患者伴或不伴 PVT 的 FVIII 活性水平标准化均数差(SMD)无显著差异(SMD=0.12,95%CI=-0.46 至 0.70,P=0.68),但存在显著异质性(I=95.52%,P=0.00)。Meta 回归分析表明,PVT 组平均 FVIII 活性水平差异、非 PVT 组病例数以及研究设计方法部分导致了异质性(P<0.05)。然而,与非 PVT 组相比,PVT 组的 FVIII/PC 比值更高,差异具有统计学意义(SMD=0.39,95%CI:0.15 至 0.63,P=0.00),且无显著异质性(I=28.62%)。

结论

综上所述,FVIII/PC 比值不仅反映了肝脏疾病的严重程度,还可作为 PVT 发展的预测因子之一。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b2a3/11411769/6860c909bb26/12876_2024_3399_Fig5_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b2a3/11411769/2b47a59b26cf/12876_2024_3399_Fig1_HTML.jpg
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https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b2a3/11411769/6860c909bb26/12876_2024_3399_Fig5_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b2a3/11411769/2b47a59b26cf/12876_2024_3399_Fig1_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b2a3/11411769/5270061896de/12876_2024_3399_Fig2_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b2a3/11411769/1e07fff16437/12876_2024_3399_Fig3_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b2a3/11411769/7c4a9752e033/12876_2024_3399_Fig4_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b2a3/11411769/6860c909bb26/12876_2024_3399_Fig5_HTML.jpg

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本文引用的文献

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Thromb Haemost. 2023 Jul;123(7):714-722. doi: 10.1055/a-2052-9381. Epub 2023 Mar 13.
2
Potential utility of a multi-component coagulation factor panel to calculate MELD scores and assess the risk of portal vein thrombosis in chronic liver disease.多组分凝血因子检测对计算 MELD 评分及评估慢性肝病门静脉血栓形成风险的潜在应用。
BMC Gastroenterol. 2023 Mar 9;23(1):65. doi: 10.1186/s12876-023-02695-6.
3
Haemostasis in cirrhosis: Understanding destabilising factors during acute decompensation.
肝硬化中的止血:了解急性失代偿期间的不稳定因素。
J Hepatol. 2023 May;78(5):1037-1047. doi: 10.1016/j.jhep.2023.01.010. Epub 2023 Jan 25.
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Incidence and factors predictive of recurrent thrombosis in people with non-cirrhotic portal vein thrombosis.非肝硬化性门静脉血栓形成患者复发性血栓形成的发生率及预测因素。
J Hepatol. 2023 Jan;78(1):114-122. doi: 10.1016/j.jhep.2022.08.023. Epub 2022 Sep 2.
5
ADAMTS-13/von Willebrand factor ratio: A prognostic biomarker for portal vein thrombosis in compensated cirrhosis. A prospective observational study.ADAMTS-13/血管性血友病因子比率:代偿性肝硬化门静脉血栓形成的预后生物标志物。一项前瞻性观察研究。
Dig Liver Dis. 2022 Dec;54(12):1672-1680. doi: 10.1016/j.dld.2022.06.004. Epub 2022 Jun 29.
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