Associations of accumulated selected persistent organic pollutants in adipose tissue with insulin sensitivity and risk of incident type-2 diabetes
Metadatos
Afficher la notice complèteAuteur
Barrios Rodríguez, Rocío; Pérez Carrascosa, Francisco Miguel; Gómez Peña, Celia; Mustieles Miralles, Vicente; Salcedo Bellido, Inmaculada; Requena Méndez, María del Pilar; Martín Olmedo, Piedad; Jiménez Moleón, José Juan; Arrebola Moreno, Juan PedroEditorial
Elsevier
Materia
Persistent organic pollutants Type 2 diabetes mellitus HOMA Adipose tissue Glucose homeostasis
Date
2021-05-07Referencia bibliográfica
Rocío Barrios-Rodríguez... [et al.]. Associations of accumulated selected persistent organic pollutants in adipose tissue with insulin sensitivity and risk of incident type-2 diabetes, Environment International, Volume 155, 2021, 106607, ISSN 0160-4120, [https://doi.org/10.1016/j.envint.2021.106607]
Patrocinador
Ramon y Cajal Program (Ministerio de Economia, Industria y Competitividad, Spain) RYC-2016-20155; Instituto de Salud Carlos III; European Commission PI16/01858 PI18/01573 PI20/01568Résumé
Continuous exposure to low doses of persistent organic pollutant (POPs), such as those occurring in the general
population, might contribute to the burden of type 2 diabetes mellitus (T2DM). However, evidences from longitudinal
studies are scarce. We aimed to explore the associations of accumulated POP exposure with the
development of T2DM by means of 1) longitudinal associations with the 16-year incidence of the disease, and 2)
complementary cross-sectional analyses with markers of glucose homeostasis at recruitment. Organochlorine
pesticide and polychlorinated biphenyl (PCB) concentrations were analyzed in adipose tissue samples and
incident T2DM cases were retrieved from clinical records. Homeostatic model assessment values of insulin
sensitivity/resistance and β-cell function at recruitment were calculated. Linear and Cox-regression models were
performed. In individuals with normal weight/overweight (n = 293), we observed positive dose–response relationships
between the studied POPs and T2DM risk, particularly for hexachlorobenzene (HCB) [hazard ratio
(HR): 3.96 for 4th quartile versus 1st quartile (Q1); confidence interval (CI) 95%: 0.79, 19.71]. PCB-180 showed
a positive but seemingly non-linear association with T2DM risk [HR of 3er quartile (Q3) versus Q1: 6.48; CI 95%:
0.82, 51.29]. Unadjustment for body mass index considerably increased the magnitude of the associations. In the
cross-sectional study (n = 180), HCB and PCB-180 were inversely associated with insulin sensitivity and positively
associated with insulin resistance parameters. Our results suggest that a higher burden of specific POPs in
adipose tissue may disrupt glucose homeostasis, possibly contributing to increase T2DM risk, especially in nonobese
adults.