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贝叶斯网络建模研究:确定加拿大丙型肝炎病毒感染成年患者心血管疾病风险的影响因素。

Bayesian network modelling study to identify factors influencing the risk of cardiovascular disease in Canadian adults with hepatitis C virus infection.

机构信息

Public Health Risk Sciences Division, Public Health Agency of Canada, Toronto, Ontario, Canada

Department of Nutritional Sciences, Faculty of Medicine, University of Toronto, Toronto, Ontario, Canada.

出版信息

BMJ Open. 2020 May 5;10(5):e035867. doi: 10.1136/bmjopen-2019-035867.

Abstract

OBJECTIVES

The present study evaluates the extent of association between hepatitis C virus (HCV) infection and cardiovascular disease (CVD) risk and identifies factors mediating this relationship using Bayesian network (BN) analysis.

DESIGN AND SETTING

A population-based cross-sectional survey in Canada.

PARTICIPANTS

Adults from the Canadian Health Measures Survey (=10 115) aged 30 to 74 years.

PRIMARY AND SECONDARY OUTCOME MEASURES

The 10-year risk of CVD was determined using the Framingham Risk Score in HCV-positive and HCV-negative subjects. Using BN analysis, variables were modelled to calculate the probability of CVD risk in HCV infection.

RESULTS

When the BN is compiled, and no variable has been instantiated, 73%, 17% and 11% of the subjects had low, moderate and high 10-year CVD risk, respectively. The conditional probability of high CVD risk increased to 13.9%±1.6% (p<2.2×10) when the HCV variable is instantiated to 'Present' state and decreased to 8.6%±0.2% when HCV was instantiated to 'Absent' (p<2.2×10). HCV cases had 1.6-fold higher prevalence of high-CVD risk compared with non-infected individuals (p=0.038). Analysis of the effect modification of the HCV-CVD relationship (using median Kullback-Leibler divergence; ) showed diabetes as a major effect modifier on the joint probability distribution of HCV infection and CVD risk =0.27, IQR: 0.26 to 0.27), followed by hypertension (0.24, IQR: 0.23 to 0.25), age (0.21, IQR: 0.10 to 0.38) and injection drug use (0.19, IQR: 0.06 to 0.59).

CONCLUSIONS

Exploring the relationship between HCV infection and CVD risk using BN modelling analysis revealed that the infection is associated with elevated CVD risk. A number of risk modifiers were identified to play a role in this relationship. Targeting these factors during the course of infection to reduce CVD risk should be studied further.

摘要

目的

本研究评估丙型肝炎病毒 (HCV) 感染与心血管疾病 (CVD) 风险之间的关联程度,并使用贝叶斯网络 (BN) 分析确定介导这种关系的因素。

设计和设置

加拿大的一项基于人群的横断面调查。

参与者

年龄在 30 至 74 岁的加拿大健康测量调查 (=10115) 成年人。

主要和次要结果

在 HCV 阳性和 HCV 阴性受试者中,使用 Framingham 风险评分确定 10 年 CVD 风险。使用 BN 分析,对变量进行建模,以计算 HCV 感染中 CVD 风险的概率。

结果

当 BN 被编译并且没有变量被实例化时,分别有 73%、17%和 11%的受试者具有低、中、高 10 年 CVD 风险。当 HCV 变量被实例化为“存在”状态时,高 CVD 风险的条件概率增加到 13.9%±1.6%(p<2.2×10),而当 HCV 被实例化为“不存在”时,风险降低到 8.6%±0.2%(p<2.2×10)。与未感染者相比,HCV 病例的高 CVD 风险患病率高 1.6 倍(p=0.038)。对 HCV-CVD 关系的效应修饰(使用中位数 Kullback-Leibler 分歧; )的分析表明,糖尿病是 HCV 感染和 CVD 风险联合概率分布的主要效应修饰因子(=0.27,IQR:0.26 至 0.27),其次是高血压(0.24,IQR:0.23 至 0.25)、年龄(0.21,IQR:0.10 至 0.38)和注射吸毒(0.19,IQR:0.06 至 0.59)。

结论

使用 BN 建模分析探索 HCV 感染与 CVD 风险之间的关系表明,感染与 CVD 风险升高有关。确定了一些风险修饰因子在这种关系中发挥作用。在感染过程中针对这些因素以降低 CVD 风险应进一步研究。

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