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Allostatic load and chronic pain: a prospective finding from the national survey of midlife development in the United States, 2004-2014. | LitMetric

Allostatic load and chronic pain: a prospective finding from the national survey of midlife development in the United States, 2004-2014.

BMC Public Health

Institute for Social and Economic Research, University of Essex, Wivenhoe Park, Colchester, Essex, CO4 3SQ, UK.

Published: February 2024

AI Article Synopsis

  • Previous research shows a link between chronic stress and chronic pain, but few studies connect this to allostatic load (AL), which is the biological response to stress.
  • The study identified three AL phenotypes—low biological dysregulation, parasympathetic dysregulation, and metabolic dysregulation—and used statistical models to assess their links to chronic pain outcomes.
  • Results indicated that individuals with metabolic dysregulation were at a higher risk for significant chronic pain interference and multiple pain sites, suggesting that targeting metabolic dysfunction could help reduce chronic pain issues in the future.

Article Abstract

Background: Previous research has demonstrated a correlation between chronic stress and chronic pain (CP). However, there have been few studies examining the prospective association of allostatic load (AL)-the biological processes related to stress-with CP.

Methods: We firstly conducted latent class analysis to identify phenotypes of AL using a community-dwelling sample, the Midlife in the United States. Multinomial logistic regression models were used to examine the prospective association between phenotypes of AL at MIDUS 2 biomarker project and the presence of CP, CP interference and the number of CP sites at MIDUS 3.

Results: Three phenotypes of AL, low biological dysregulation, parasympathetic dysregulation and metabolic dysregulation, were identified. Compared to low biological dysregulation group, participants experiencing metabolic dysregulation phenotype of AL at MIDUS 2 had higher risks of having high-interference CP (RRR = 2.00, 95% CI: 1.06, 3.79, P < 0.05) and 3 or more CP sites (RRR = 2.03, 95% CI: 1.08, 3.83, P < 0.05) at MIDUS 3.

Conclusion: The findings indicate that focusing on mitigating the metabolic dysfunction phenotype of AL has the potential to be an efficacious strategy for alleviating future CP bodily widespreadness and high CP interference.

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Source
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC10854121PMC
http://dx.doi.org/10.1186/s12889-024-17888-1DOI Listing

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