酒精使用障碍严重程度的影响因素及风险预测模型
Factors Influencing the Severity of Alcohol Use Disorders and Risk Prediction Modeling
投稿时间:2023-10-11  修订日期:2024-04-07
DOI:
中文关键词:  酒精使用障碍  疾病严重程度  临床特征  γ-谷氨酸酰胺转移酶  总胆红素
英文关键词:Alcohol use disorders  Disease severity  diagnostic trait  γ-Glutamyl transpeptidase  Total bilirubin
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作者单位地址
杨学智 1.广西医科大学公共卫生学院2.广西南宁市第五人民医院 广西南宁市邕武路7号
陆冰 广西南宁市第五人民医院 
魏菀 广西南宁市第五人民医院 
曾真 广西南宁市第五人民医院 
胡思贵 广西南宁市第五人民医院 
曹永康 广西南宁市第五人民医院 
马贞玉* 广西医科大学公共卫生学院 广西南宁双拥路22号
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中文摘要:
      【摘要】 背景 酒精使用障碍(AUD)是常见的慢性复发性精神疾病,重度酒精使用障碍需要早期快速识别并及时妥善处理以避免不可逆的伤害发生。目前对AUD严重程度的评估主要基于临床医师的精神检查,关于AUD严重程度影响因素及预测模型的研究有限。 目的 分析南宁市某精神专科医院酒精使用障碍患者疾病严重程度的影响因素,构建风险预测模型,为评估酒精使用障碍患者的疾病进展提供参考。方法 回顾性选取2017年1月1日—2022年12月31日南宁市第五人民医院收治的、符合《精神障碍诊断与统计手册(第5版)》(DSM-5)酒精使用障碍诊断标准的1 358例首次住院患者为研究对象,收集其基本资料,根据疾病严重程度分为轻中度组(n=330)和重度组(n=1 028),比较两组患者基本资料的差异。按7∶3将患者分为训练集和测试集,在训练集样本中构建Logistic回归模型,在测试集样本中采用受试者工作特征(ROC)曲线分析该模型对疾病严重程度的预测价值。结果 与轻中度组患者相比,重度组患者居住地在城市(?2 =7.804)、农民(?2=17.991)、饮酒频率高于1~2次/天(?2=35.267)的比例更高,初次饮酒年龄更大(t=-3.858),合并躯体疾病数量更多(Z=-22.782),γ-谷氨酸酰胺转移酶(?2=259.940)和总胆红素异常(?2=148.552)的比例更高(P<0.05或0.01)。在训练集中进行的Logistic分析结果表明,农民(OR=2.024,95% CI:1.352~3.029)、初次饮酒年龄较大(OR=1.075,95% CI:1.025~1.129)、用餐时间外也饮酒(OR=3.988,95% CI:2.408~6.606)、总胆红素异常(OR=1.034,95% CI:1.000~1.069)、合并更多的躯体疾病(OR=4.386,95% CI:2.636~7.298)是AUD患者疾病严重程度的危险因素。该模型在测试集样本中的曲线下面积(AUC)为0.906。 结论 在精神专科医院中,农民、初次饮酒年龄较大、用餐时间外也饮酒、总胆红素异常、合并更多的躯体疾病可能是重度AUD的危险因素。
英文摘要:
      【Abstract】 Background Alcohol use disorders are common chronic relapsing psychiatric disorders, and severe alcohol use disorders require early and rapid recognition and timely and appropriate management to avoid irreversible harm. Currently, the assessment of severity is based on psychiatric examination by the clinician, and there is limited research on the factors affecting AUD severity and prediction models. Objective Analyzing the factors influencing the severity of alcohol use disorder patients in a psychiatric hospital in Nanning, China, and constructing a risk prediction model to provide a reference for assessing the disease progression of alcohol use disorder patients. Methods Retrospectively selected 1 358 first-time hospitalized patients admitted to the Fifth People's Hospital of Nanning City from January 1, 2017 to December 31, 2022 who met the diagnostic criteria of Diagnostic and Statistical Manual of Mental Disorders (5th Edition) (DSM-5) for alcohol use disorders as the study subjects, collected their basic data, and were divided into the mild-moderate group according to the severity of the disease (n = 330) and severe group (n=1 028), and compared the differences in basic data between the two groups. The patients were divided into training and test sets according to 7:3, and a logistic regression model was constructed in the training set samples, and the predictive value of the model for disease severity was analyzed in the test set samples by using the subject's work characteristics (ROC) curve. Results Compared to patients in the mild-moderate group, patients in the severe group had a higher proportion of patients living in urban areas (χ2=7.804), farmers (χ2=17.991), a higher frequency of alcohol consumption higher than 1-2 drinks/day (χ2=35.267), a greater age of first drinking (t=-3.858), a greater greater number of comorbid somatic disorders (Z=-22.782), and higher proportions of gamma-glutamate aminotransferase (χ2=259.940) and total bilirubin abnormalities (χ2=148.552) (P<0.05 or 0.01). The results of the logistic analysis conducted in the training set showed that farmers (OR=2.024, 95% CI: 1.352~3.029), older age at first drinking (OR=1.075, 95% CI: 1.025~1.129), drinking also outside of mealtimes (OR=3.988, 95% CI: 2.408~6.606), total bilirubin abnormalities (OR=1.034, 95% CI: 1.000~1.069), and more comorbid somatic diseases (OR=4.386, 95% CI: 2.636~7.298) were risk factors for disease severity in AUD patients. The area under the curve (AUC) for this model in the test set sample was 0.906. Conclusion In psychiatric hospitals, farmers, older age at first drinking, drinking also outside meal times, abnormal total bilirubin, and comorbidities with more somatic illnesses may be risk factors for severe AUD.
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