TY - JOUR
T1 - A risk prediction model for post-stroke depression in Chinese stroke survivors based on clinical and socio-psychological features
AU - Liu, Rui
AU - Yue, Yingying
AU - Jiang, Haitang
AU - Lu, Jian
AU - Wu, Aiqin
AU - Geng, Deqin
AU - Wang, Jun
AU - Lu, Jianxin
AU - Li, Shenghua
AU - Tang, Hua
AU - Lu, Xuesong
AU - Zhang, Kezhong
AU - Liu, Tian
AU - Yuan, Yonggui
AU - Wang, Qiao
N1 - Publisher Copyright:
© Liu et al.
PY - 2017
Y1 - 2017
N2 - Background: Post-stroke depression (PSD) is a frequent complication that worsens rehabilitation outcomes and patient quality of life. This study developed a risk prediction model for PSD based on patient clinical and socio-psychology features for the early detection of high risk PSD patients. Results: Risk predictors included a history of brain cerebral infarction (odds ratio [OR], 3.84; 95% confidence interval [CI], 2.22-6.70; P < 0.0001) and four sociopsychological factors including Eysenck Personality Questionnaire with Neuroticism/ Stability (OR, 1.18; 95% CI, 1.12-1.20; P < 0.0001), life event scale (OR, 0.99; 95% CI, 0.98-0.99; P = 0.0007), 20 items Toronto Alexithymia Scale (OR, 1.06; 95% CI, 1.02-1.10; P = 0.002) and Social Support Rating Scale (OR, 0.91; 95% CI, 0.87-0.90; P < 0.001) in the logistic model. In addition, 11 rules were generated in the tree model. The areas under the curve of the ROC and the accuracy for the tree model were 0.85 and 0.86, respectively. Methods: This study recruited 562 stroke patients in China who were assessed for demographic data, medical history, vascular risk factors, functional status poststroke, and socio-psychological factors. Multivariate backward logistic regression was used to extract risk factors for depression in 1-month after stroke. We converted the logistic model to a visible tree model using the decision tree method. Receiver operating characteristic (ROC) was used to evaluate the performance of the model. Conclusion: This study provided an effective risk model for PSD and indicated that the socio-psychological factors were important risk factors of PSD.
AB - Background: Post-stroke depression (PSD) is a frequent complication that worsens rehabilitation outcomes and patient quality of life. This study developed a risk prediction model for PSD based on patient clinical and socio-psychology features for the early detection of high risk PSD patients. Results: Risk predictors included a history of brain cerebral infarction (odds ratio [OR], 3.84; 95% confidence interval [CI], 2.22-6.70; P < 0.0001) and four sociopsychological factors including Eysenck Personality Questionnaire with Neuroticism/ Stability (OR, 1.18; 95% CI, 1.12-1.20; P < 0.0001), life event scale (OR, 0.99; 95% CI, 0.98-0.99; P = 0.0007), 20 items Toronto Alexithymia Scale (OR, 1.06; 95% CI, 1.02-1.10; P = 0.002) and Social Support Rating Scale (OR, 0.91; 95% CI, 0.87-0.90; P < 0.001) in the logistic model. In addition, 11 rules were generated in the tree model. The areas under the curve of the ROC and the accuracy for the tree model were 0.85 and 0.86, respectively. Methods: This study recruited 562 stroke patients in China who were assessed for demographic data, medical history, vascular risk factors, functional status poststroke, and socio-psychological factors. Multivariate backward logistic regression was used to extract risk factors for depression in 1-month after stroke. We converted the logistic model to a visible tree model using the decision tree method. Receiver operating characteristic (ROC) was used to evaluate the performance of the model. Conclusion: This study provided an effective risk model for PSD and indicated that the socio-psychological factors were important risk factors of PSD.
KW - Decision tree
KW - Logistic regression
KW - Post-stroke depression
KW - Risk prediction model
KW - Socio-psychological factor
UR - https://www.scopus.com/pages/publications/85029783760
U2 - 10.18632/oncotarget.16907
DO - 10.18632/oncotarget.16907
M3 - 文章
C2 - 28968957
AN - SCOPUS:85029783760
SN - 1949-2553
VL - 8
SP - 62891
EP - 62899
JO - Oncotarget
JF - Oncotarget
IS - 38
ER -