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1.621000 四川绵阳,四川绵阳四〇四医院感染科
2.610044 成都,四川大学华西医院感染性疾病中心
[雷学忠;E-mail:18980601317@163.comLEI Xuezhong, E-mail: 18980601317@163.com
收稿:2022-09-13,
修回:2022-11-06,
纸质出版:2023-04-30
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文丽娟, 雷学忠, 司果, 等. HIV/AIDS患者出现肝损伤的预测模型初步建立和验证[J]. 陆军军医大学学报, 2023,45(8):817-824.
Lijuan WEN, Xuezhong LEI, Guo SI, et al. Establishment and validation of a prediction model for liver injury in HIV/AIDS patients[J]. Journal of Army Medical University, 2023, 45(8): 817-824.
文丽娟, 雷学忠, 司果, 等. HIV/AIDS患者出现肝损伤的预测模型初步建立和验证[J]. 陆军军医大学学报, 2023,45(8):817-824. DOI: 10.16016/j.2097-0927.202209114.
Lijuan WEN, Xuezhong LEI, Guo SI, et al. Establishment and validation of a prediction model for liver injury in HIV/AIDS patients[J]. Journal of Army Medical University, 2023, 45(8): 817-824. DOI: 10.16016/j.2097-0927.202209114.
目的
2
调查HIV/AIDS患者出现肝损伤发生情况,建立其预测模型并进行验证。
方法
2
选择2021年1~12月四川绵阳四○四医院接诊的290例新确诊HIV/AIDS患者,以7 ∶3分为模型组203例与验证组87例。收集可能影响HIV/AIDS患者肝损伤的因素,根据有无出现肝损伤将患者分为2组,比较2组患者性别、年龄、BMI等各因素,采用LASSO回归筛选变量后行多因素Logistic回归筛选出独立性影响因素,根据Logistic回归结果构建列线图模型。
结果
2
肝损伤组与无肝损伤组患者饮酒史、CD4
+
T淋巴细胞水平、抗真菌药物使用情况、合并结核感染、使用其他类型抗反转录病毒药物、磺胺类药物使用情况、糖尿病、心血管病、营养状况差异均具有统计学意义(
P
<
0.05)。LASSO回归模型筛选出7个潜在影响因素:饮酒史、CD4
+
T淋巴细胞水平、抗真菌药物使用情况、合并结核感染、糖尿病、心血管病、营养状况。多因素Logistic回归分析显示:饮酒史、CD4
+
T淋巴细胞水平、抗真菌药物使用情况、合并结核感染、糖尿病、心血管病、营养状况是HIV/AIDS患者肝损伤的独立影响因素(
P
<
0.05)。基于上述影响因素构建HIV/AIDS患者肝损伤风险预测的列线图模型,模型组列线图模型预测HIV/AIDS患者肝损伤的受试者操作曲线下面积(area under the subject curve,AUC)为0.969(95%
CI
:0.904,0.988);验证组AUC为0.971(95%
CI
:0.905,0.992)。Bootstrap法重复抽样1 000次,并以验证组进行验证,校准曲线结果显示:模型组与验证组预测曲线与标准曲线基本拟合;H-L拟合优度检验结果显示,该列线图模型预测HIV/AIDS患者肝损伤的概率与实际概率比较,差异无统计学意义(
χ
2
=2.088,
P
=0.148)。模型组决策曲线分析结果显示:当该列线图模型预测HIV/AIDS患者肝损伤的概率阈值为0.15~0.95时,患者的净受益率>0;验证组决策曲线分析结果显示:当该列线图模型预测HIV/AIDS患者肝损伤的概率阈值为0.10~0.95时,患者的净受益率>
0。
结论
2
饮酒史、CD4
+
T淋巴细胞水平、抗真菌药物使用情况、合并结核感染、糖尿病、心血管病、营养状况是HIV/AIDS患者肝损伤的独立影响因素,基于上述因素构建的列线图模型用于HIV/AIDS肝损伤风险预测具有较高的准确度。
Objective
2
To investigate the occurrence of liver injury in HIV/AIDS patients
and establish and verify its prediction model.
Methods
2
A total of 290 newly-diagnosed HIV/AIDS patients admitted to Mianyang 404 Hospital from January to December 2021 were subjected
and then assigned into a test group (
n
=203) and validation group (
n
=87) at a ratio of 7 ∶3. The factors that may affect the liver injury in HIV/AIDS patients were collected. The patients were divided into 2 groups according to the presence or absence of liver injury. Their gender
age
BMI and other factors were compared between the 2 groups. LASSO regression analysis was used to screen variables
then multivariate logistic regression analysis was employed to screen out independent influencing factors
and a nomogram model was constructed according to the logistic regression results.
Results
2
There were statistical differences between the patients with and without liver injury in history of alcohol drinking
CD4
+
T lymphocyte level
use of antifungal drugs
other types of antiretroviral drugs and sulfonamides
complications of tuberculosis
diabetes
cardiovascular disease
and nutritional status (
P
<
0.05). LASSO regression model screened out 7 potential influencing factors
including drinking history
CD4
+
T lymphocyte level
antifungal drug use
comorbid tuberculosis infection
diabetes
cardiovascular disease
and nutritional status. Multivariate logistic regression analysis showed that drinking history
CD4
+
T lymphocyte level
use of antifungal drugs
comorbid tuberculosis
diabetes
cardiovascular disease
and nutritional status were independent
influencing factors of liver injury in HIV/AIDS patients (
P
<
0.05). Based on the above influencing factors
a nomogram model for predicting the risk of liver injury in HIV/AIDS patients was constructed. The results of ROC curve analysis showed that the area under the subject curve (AUC) of the model group was 0.969 (95%
CI
: 0.904~0.988)
and the AUC of the validation group was 0.971 (95%
CI
: 0.905~0.992) for predicting liver injury in HIV/AIDS patients. After Bootstrapping was conducted for repeated sampling 1 000 times
and the verification group was used for verification. The results of the calibration curve indicated that the prediction curve of the model group and the verification group basically fitted the standard curve. The results of the H-L goodness of fit test suggested that the nomogram model predicted the probability of liver injury in HIV/AIDS patients was not significantly different from the actual probability (
Chi
-square=2.088
P
=0.148). The analysis results of decision curve of model group showed that when the probability threshold of predicting liver injury of HIV/AIDS patients by the nomograph model was 0.15~0.95
the net benefit rate of patients was greater than 0. While
the analysis results of the decision curve of the validation group showed that when the probability threshold of predicting the liver injury of HIV/AIDS patients by the nomograph model was 0.10~0.95
the net benefit rate of the patients was greater than 0.
Conclusion
2
History of drinking
CD4
+
T lymphocyte level
use of antifungal drugs
comorbid tuberculosis infection
diabetes
cardiovascular disease
and nutritional status are independent influencing factors of liver injury in HIV/AIDS patients. Our nomogram model constructed based on the above factors has high accuracy and discrimination for HIV/AIDS liver injury risk prediction.
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