Chronic Pain and Inflammatory Biomarkers in Obese Women: Impact of Adipose Phenotypes and Lipedema

Authors

  • Paulo André Dias da Silva Centro Universitário do Estado do Pará
  • Reginaldo Costa da Silva Junior Universidade Federal do Pará
  • Tiago dos Santos Brito Universidade Federal do Pará
  • Diórgenes Rodrigues Cardoso Universidade Federal do Pará
  • Yasmin Santiago Paixão Universidade Federal do Pará
  • Felipe de Castro dos Santos Universidade Federal do Pará
  • Israel Dias Nonato Universidade Federal do Pará
  • Igor Gomes de Oliveira Universidade Federal do Pará
  • Gabriel Jersemi Rodrigues Costa Universidade Federal do Pará
  • Manuel Dionizio Bentes Monteiro Neto Universidade Federal do Pará
  • Carolyna Tereza Brasil Papaléo Centro Universitário Metropolitano da Amazônia
  • Maria Eduarda de Lima Dacier Lobato Centro Universitário Metropolitano da Amazônia
  • José Rodrigo Moraes Teles Centro Universitário Metropolitano da Amazônia
  • Vitor Cayke Savedra Dias Centro Universitário Metropolitano da Amazônia
  • Amanda Beatriz Pinheiro Macedo Centro Universitário Metropolitano da Amazônia

DOI:

https://doi.org/10.36557/2674-8169.2026v8n2p869-884

Keywords:

Obesity, Lipedema, Inflammatory Biomarkers, Chronic Pain

Abstract

Background: Chronic pain in women with obesity may arise from interactions between fat distribution (android vs gynoid), systemic inflammation, and painful adipose-tissue phenotypes, including lipedema. Objective: To critically synthesize 2020–2025 evidence on the association between pain intensity and inflammatory biomarkers in women with obesity, contrasting android/gynoid phenotypes and incorporating lipedema as a confounder or distinct phenotype. Methods: Narrative review with a structured search in PubMed/MEDLINE and Google Scholar (2020–2025), combining terms for obesity, body fat distribution, chronic pain, inflammation, and lipedema; studies were selected for clinical/methodological relevance, and data were extracted on body composition phenotyping, pain outcomes, biomarker panels, and confounder control. Results: Findings are heterogeneous; variability in visceral vs subcutaneous adiposity measurement, biomarker selection, and adjustment strategies constrains cross-study comparability. Unrecognized lipedema may cluster pain within peripheral phenotypes and bias comparisons. Conclusions: Interpreting pain–inflammation relationships in women with obesity requires objective fat-distribution phenotyping and systematic lipedema screening to disentangle metabolic–inflammatory visceral mechanisms from subcutaneous painful-adipose mechanisms.

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References

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Published

2026-02-16

How to Cite

Silva, P. A. D. da, Junior, R. C. da S., Brito, T. dos S., Cardoso, D. R., Paixão, Y. S., Santos, F. de C. dos, Nonato, I. D., Oliveira, I. G. de, Costa, G. J. R., Neto, M. D. B. M., Papaléo, C. T. B., Lobato, M. E. de L. D., Teles, J. R. M., Dias, V. C. S., & Macedo, A. B. P. (2026). Chronic Pain and Inflammatory Biomarkers in Obese Women: Impact of Adipose Phenotypes and Lipedema. Brazilian Journal of Implantology and Health Sciences, 8(2), 869–884. https://doi.org/10.36557/2674-8169.2026v8n2p869-884