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Reliability of Potential Pain Biomarkers in the Saliva of Healthy Subjects: Inter-Individual Differences and Intersession Variability

Abstract Aim
Salivary cortisol, α-amylase (sAA), secretory IgA (sIgA), testosterone, and soluble fraction of receptor II of TNFα (sTNFαRII) could serve as objective pain measures, but the normal variability of these potential biomarkers is unknown.
Patients & Methods
Saliva was collected with the passive secretion method from 34, pain-free subjects in two single samples at least 24 hours apart. Biomarker variation and intersession reliability were assessed with the intraclass correlation coefficient (ICC). Also, we calculated the within-subject standard deviation (Sw) and the reproducibility (2.77 × Sw) of intersession measures.
Results
Salivary cortisol, sAA, sIgA, testosterone, and sTNFαRII yielded the following ICCs: 0.53, 0.003, 0.88, 0.42 and 0.83, respectively. We found no statistically significant systematic differences between sessions in any biomarker except for testosterone, which showed a decrease on the second day (p<0.001). The reproducibility for salivary cortisol, sAA, sIgA, testosterone, and sTNFαRII were 0.46 ng/ml, 12.88 U/ml, 11.7 μg/ml, 14.54 pg/ml and 18.29 pg/ml, respectively. Cortisol, testosterone and TNFαRII measurement variability showed a positive correlation with the magnitude (p<0.002), but no relationship was found for sAA and sIgA.
Conclusions
Salivary sIgA and sTNFαRII show a remarkable good reproducibility and, therefore, could be useful as pain biomarkers. When using the passive secretion method, intersession variations in salivary sIgA of more than 11.7 μg/ml may reflect true biomarker change. In the case of sTNFαRII this will depend of the magnitude. The estimates herein provided should help investigators and clinicians differentiate actual biomarker modification from measurement variability.

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Estradiol Saliva Testosterone Saliva Eva M. Sobas,1,2,* Roberto Reinoso,1,3,5 Rubén Cuadrado-Asensio,1,4 Itziar Fernández,1,5 Miguel J. Maldonado,1,4 and José C. Pastor1,4,6

Author Information

Urs M. Nater, Editor
1. Instituto Universitario de Oftalmobiología Aplicada (IOBA), Universidad de Valladolid, Valladolid, Spain
2. Escuela de Enfermería, Universidad de Valladolid, Valladolid, Spain
3. Visión I+D, Valladolid, Spain
4. Departamento de Cirugía, Oftalmología, Otorrinolaringología y Fisioterapia, Facultad de Medicina, Universidad de Valladolid, Valladolid, Spain
5. Networking Research Center on Bioengineering, Biomaterials and Nanomedicine (CIBER-BBN), Valladolid, Spain
6. Department of Ophthalmology, Hospital Clinico Universitario, Valladolid, Spain, University of Marburg, GERMANY
Competing Interests: Dr. Roberto Reinoso is employed by Vision I+D. This does not alter our adherence to PLOS ONE policies on sharing data and materials.
PLoS One. 2016; 11(12): e0166976. Published online 2016 Dec 1. doi:  10.1371/journal.pone.0166976
PMCID: PMC5132231
Link: https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5132231/

by Gary Khodanian | Dec 1, 2016

 
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