论文已发表
注册即可获取德孚的最新动态
IF 收录期刊
慢性疼痛伴认知障碍的危险因素和诊断模型构建
Authors Zhang C, Su Y, Zeng X, Zhu X, Gao R, Liu W, Du R, Chen C , Liu J
Received 9 October 2024
Accepted for publication 6 December 2024
Published 17 December 2024 Volume 2024:17 Pages 4331—4342
DOI https://doi.org/10.2147/JPR.S485000
Checked for plagiarism Yes
Review by Single anonymous peer review
Peer reviewer comments 2
Editor who approved publication: Dr Jonathan Greenberg
Changteng Zhang,1,2,* Ying Su,1,2,* Xianzheng Zeng,3 Xiaoyu Zhu,1,2 Rui Gao,1,2 Wangyang Liu,1,2 Runzi Du,1,2 Chan Chen,1,2 Jin Liu1,2
1Department of Anesthesiology, West China Hospital, Sichuan University, Chengdu, People’s Republic of China; 2The Research Units of West China (2018RU012)-Chinese Academy of Medical Sciences, West China Hospital, Sichuan University, Chengdu, People’s Republic of China; 3Department of Pain Management, West China Hospital, Sichuan University, Chengdu, People’s Republic of China
*These authors contributed equally to this work
Correspondence: Chan Chen, Email chenchan@scu.edu.cn; xychenchan@gmail.com
Background: Cognitive impairment (CI) is frequently observed in patients with chronic pain (CP). CP progression increases the risk of dementia and accelerates Alzheimer’s disease pathogenesis. However, risk diagnostic models and biomarkers for CP-related CI remain insufficient. Previous research has highlighted the relationships between several complete blood count parameters for CP or CI-related diseases, such as Alzheimer’s disease, while the specific values of complete blood count parameters in CP-related CI patients remain unclear. This study aimed to explore the correlation between complete blood count parameters and CP-related CI to establish a risk diagnostic model for the early detection of CP-related CI.
Methods: This cross-sectional study was conducted at West China Hospital, Sichuan University. The Montreal Cognitive Assessment (MoCA) was used to classify patients into either the CP with CI group or the CP without CI group. Univariate analysis and multivariate logistic regression analysis were used to screen the related factors of CP-related CI for constructing a risk diagnostic model, and the model was evaluated using receiver operating characteristic (ROC) curve analysis.
Results: The study ultimately included 163 eligible patients. Based on analysis, age (OR, 1.037 [95% CI, 1.007– 1.070]; P=0.018), duration of pain (OR, 2.546 [95% CI, 1.099– 6.129]; P=0.032), VAS score (OR, 1.724 [95% CI, 0.819– 3.672]; P=0.153), LMR (OR, 0.091 [95% CI, 0.024– 0.275]; P< 0.001), absolute neutrophil value (OR, 0.306 [95% CI, 0.115– 0.767]; P=0.014), and lymphocyte percentage (OR, 6.551 [95% CI, 2.143– 25.039]; P=0.002) were identified as critical factors of CP-related CI. The diagnostic model was evaluated by the ROC curve, demonstrating good diagnostic value with an area under the curve (AUC) of 0.803, a sensitivity of 0.603 and a specificity of 0.871.
Conclusion: The risk diagnostic model developed in this study for CP-related CI has significant value and enables clinicians to customize interventions based on each patient’s needs.
Keywords: cognitive impairment, chronic pain, diagnostic model, complete blood count parameters, risk factors