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Pilot Application of an Inflammation and Physiological Dysregulation Index Based on Noninvasive Salivary Biomarkers

Overview
Journal BMC Res Notes
Publisher Biomed Central
Date 2025 Feb 5
PMID 39910646
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Abstract

Background And Objective: Noninvasive salivary biomarkers can be used to assess the cumulative subclinical health impacts of social and environmental stressors. We evaluated seven salivary biomarkers of neuroendocrine and immune functions and a group index of physiological dysregulation based on these biomarkers in a pilot survey in a socioeconomically disadvantaged population.

Results: Participants recruited at subsidized public housing projects in Denver, Colorado, completed a sociodemographic, behavioral, and health questionnaire and used passive drool samplers to collect five saliva samples over the course of 1 day. Samples were tested for the neuroendocrine biomarkers alpha-amylase, cortisol, and dehydroepiandrosterone (DHEA) as well as immune system/inflammation biomarkers C-reactive protein (CRP), interleukin (IL)-1β, IL-6 and total immunoglobulin A (IgA). A composite Inflammation and Physiological Dysregulation Index (IPDI) was calculated as a count of potentially unhealthy values of dichotomized biomarkers. In 20 individuals who completed the survey (average age 46 years, 75% females), allergy to house dust was significantly associated with increased IPDI (adjusted for age) and significantly increased odds of potentially unhealthy values of total IgA, IL-1β, and CRP. Age, obesity, diabetes, allergy to pollen, recent loss of employment, and depression, anxiety, and stress scores from the standard DASS-21 questionnaire were positively but not significantly (0.05 < p < 0.2) associated with IPDI. This project demonstrated an application of a composite index based on noninvasive salivary biomarkers to assess subclinical health impacts of chronic social stressors.

References
1.
Nater U, Rohleder N, Schlotz W, Ehlert U, Kirschbaum C . Determinants of the diurnal course of salivary alpha-amylase. Psychoneuroendocrinology. 2007; 32(4):392-401. DOI: 10.1016/j.psyneuen.2007.02.007. View

2.
Campbell C, Padmanabhan N, Romero D, Joe J, Gebremeskel M, Manjula N . Quantitative serology for SARS-CoV-2 using self-collected saliva and finger-stick blood. Sci Rep. 2022; 12(1):6560. PMC: 9021827. DOI: 10.1038/s41598-022-10484-6. View

3.
Chovatiya R, Medzhitov R . Stress, inflammation, and defense of homeostasis. Mol Cell. 2014; 54(2):281-8. PMC: 4048989. DOI: 10.1016/j.molcel.2014.03.030. View

4.
Arbeev K, Cohen A, Arbeeva L, Milot E, Stallard E, Kulminski A . Optimal Versus Realized Trajectories of Physiological Dysregulation in Aging and Their Relation to Sex-Specific Mortality Risk. Front Public Health. 2016; 4:3. PMC: 4725219. DOI: 10.3389/fpubh.2016.00003. View

5.
Miller A, Spencer S . Obesity and neuroinflammation: a pathway to cognitive impairment. Brain Behav Immun. 2014; 42:10-21. DOI: 10.1016/j.bbi.2014.04.001. View