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Inflammatory biomarkers and risk of breast cancer among young women in Latin America: a case-control study

BACKGROUND: Breast cancer incidence is increasing rapidly in Latin America, with a higher proportion of cases among young women than in developed countries. Studies have linked inflammation to breast cancer development, but data is limited in premenopausal women, especially in Latin America. METHODS...

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Detalles Bibliográficos
Autores principales: Fontvieille, Emma, His, Mathilde, Biessy, Carine, Navionis, Anne-Sophie, Torres-Mejía, Gabriela, Ángeles-Llerenas, Angélica, Alvarado-Cabrero, Isabel, Sánchez, Gloria Inés, Navarro, Edgar, Cortes, Yorlany Rodas, Porras, Carolina, Rodriguez, Ana Cecilia, Garmendia, Maria Luisa, Soto, José Luis, Moyano, Leonor, Porter, Peggy L., Lin, Ming Gang, Guenthoer, Jamie, Romieu, Isabelle, Rinaldi, Sabina
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9367082/
https://www.ncbi.nlm.nih.gov/pubmed/35948877
http://dx.doi.org/10.1186/s12885-022-09975-6
Descripción
Sumario:BACKGROUND: Breast cancer incidence is increasing rapidly in Latin America, with a higher proportion of cases among young women than in developed countries. Studies have linked inflammation to breast cancer development, but data is limited in premenopausal women, especially in Latin America. METHODS: We investigated the associations between serum biomarkers of chronic inflammation (interleukin (IL)-6, IL-8, IL-10, tumor necrosis factor-α (TNF-α), interferon-γ (IFN-γ), leptin, adiponectin) and risk of premenopausal breast cancer among 453 cases and 453 matched, population-based controls from Chile, Colombia, Costa Rica, and Mexico. Odds ratios (OR) were estimated using conditional logistic regression models. Analyses were stratified by size and hormonal receptor status of the tumors. RESULTS: IL-6 (OR(per standard deviation (SD)) = 1.33 (1.11–1.60)) and TNF-α (OR(per SD) = 1.32 (1.11–1.58)) were positively associated with breast cancer risk in fully adjusted models. Evidence of heterogeneity by estrogen receptor (ER) status was observed for IL-8 (P-homogeneity = 0.05), with a positive association in ER-negative tumors only. IL-8 (P-homogeneity = 0.06) and TNF-α (P-homogeneity = 0.003) were positively associated with risk in the largest tumors, while for leptin (P-homogeneity = 0.003) a positive association was observed for the smallest tumors only. CONCLUSIONS: The results of this study support the implication of chronic inflammation in breast cancer risk in young women in Latin America. Largest studies of prospective design are needed to confirm these findings in premenopausal women. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1186/s12885-022-09975-6.