A QST‐based Pain Phenotype in Adults With Sickle Cell Disease: Sensitivity and Specificity of Quality Descriptors. Issue 2 (18th October 2019)

• Record Type: Journal Article
• Authors: Dyal, Brenda W.; Ezenwa, Miriam O.; Yoon, Saunjoo L.; Fillingim, Roger B.; Yao, Yingwei; Schlaeger, Judith M.; Suarez, Marie L.; Wang, Zaijie J.; Molokie, Robert E.; Wilkie, Diana J.
• Is Part Of: Pain practice. Volume 20:Issue 2(2020)
• Page Start: 168
• Page End: 178
• Publication Date: 2019-10-18
• Subjects: Pain -- Treatment -- Periodicals; 616.0472
• DOI: 10.1111/papr.12841
• Languages: English
• ISSNs: 1530-7085

Abstract

Abstract: Background: We sought to refine a screening measure for discriminating a sensitized or normal sensation pain phenotype among African American adults with sickle cell disease (SCD). Objective: To develop scoring schemes based on sensory pain quality descriptors; evaluate their performance on classifying patients with SCD who had sensitization or normal sensation, and compare with scores on the Self‐report Leeds Assessment of Neuropathic Symptoms and Signs (S‐LANSS) and the Neuropathic Pain Symptom Inventory (NPSI). Methods: Participants completed PAIN Report It, quantitative sensory testing (QST), S‐LANSS, and NPSI. Conventional binary logistic regression and least absolute shrinkage and selection operator (lasso) regression were used to obtain 2 sets of weights resulting in 2 scores: the PR‐Logistic (PAIN Report It score weighted by conventional binary logistic regression coefficients) and PR‐Lasso (PAIN Report It score weighted by lasso regression coefficients). Performance of the proposed scores and the existing scores were evaluated. Results: Lasso regression resulted in a parsimonious model with non‐zero weights assigned to 2 neuropathic descriptors, cold and spreading. We found positive correlations between the PR‐Lasso and other scores: S‐LANSS ( r = 0.22, P < 0.01), NPSI ( r = 0.22, P < 0.01), and PR‐Logistic ( r = 0.35, P < 0.01). The NPSI and PR‐Lasso performed similarly at different levels of required specificity and outperformed the S‐LANSS and PR‐Logistic at the various specificity points. Conclusion: The PR‐Lasso offers a way to discriminate a SCD pain phenotype.