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Updated: Jun 4, 2025

Determining Pain Detection and Tolerance Thresholds Using an Integrated, Multi-Modal Pain Task Battery
Published on: April 14, 2016
Risk Factors and Diagnostic Model Construction of Chronic Pain with Cognitive Impairment
Changteng Zhang1,2, Ying Su1,2, Xianzheng Zeng3
1Department of Anesthesiology, West China Hospital, Sichuan University, Chengdu, People's Republic of China.
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.
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