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Plasma Concentrations of Per- and Polyfluoroalkyl Substances at Baseline and Associations with Glycemic Indicators and Diabetes Incidence among High-Risk Adults in the Diabetes Prevention Program Trial

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ENVIRONMENTAL HEALTH PERSPECTIVES
卷 125, 期 10, 页码 -

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US DEPT HEALTH HUMAN SCIENCES PUBLIC HEALTH SCIENCE
DOI: 10.1289/EHP1612

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  1. National Institutes of Health [R01ES024765, K24HD069408]
  2. NIDDK
  3. General Clinical Research Center Program
  4. National Institute of Child Health and Human Development (NICHD)
  5. National Institute on Aging (NIA)
  6. Office of Research on Women's Health
  7. Office of Research on Minority Health
  8. CDC
  9. American Diabetes Association
  10. NIDDK Central Repositories [1X01DK104234]

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BACKGROUND: Several per- and polyfluoroalkyl substances (PFAS) are ubiquitous anthropogenic pollutants almost universally detected in humans. Experimental evidence indicates that PFAS alter glucose metabolism and insulin secretion. However, epidemiological studies have yielded inconsistent results. OBJECTIVE: We sought to examine associations between plasma PFAS concentrations, glycemic indicators, and diabetes incidence among high-risk adults. METHODS: Within the Diabetes Prevention Program (DPP), a trial for the prevention of type 2 diabetes among high-risk individuals, we quantified baseline plasma concentrations of nine PFAS among 957 participants randomized to a lifestyle intervention or placebo. We evaluated adjusted associations for plasma PEAS concentrations with diabetes incidence and key glycemic indicators measured at baseline and annually over up to 4.6 y. RESULTS: Plasma PFAS concentrations were similar to those reported in the U.S. population in 1999-2000. At baseline, in cross-sectional analysis, a doubling in plasma perfluorooctanesulfonic acid (PFOS) and perfluorooctanoic acid (PFOA) concentrations was associated with higher homeostatic model assessment of insulin resistance (HOMA-IR) [beta(PFOS) = 0.39; 95% confidence interval (CI): 0.13, 0.66; beta(PFOA) = 0.64; 95% CI: 0.34, 0.94], beta-cell function (HOMA-beta) (beta(PFOS) = 9.62; 95% CI: 1.55, 17.70; beta(PFOA) = 15.93; 95% CI: 6.78, 25.08), fasting proinsulin (beta(PFOS) = 1.37 pM; 95% CI: 0.50, 2.25; beta(PFOA) = 1.71 pM; 95% CI: 0.72, 2.71), and glycated hemoglobin (HbA(1c)) (beta(PFOS) = 0.03%; 95% CI: 0.002, 0.07; beta(PFOA) = 0.04%; 95% CI: 0.001, 0.07). There was no strong evidence of associations between plasma PFAS concentrations and diahetes incidence or prospective changes in glycemic indicators during the follow-up period. CONCLUSIONS: At baseline, several PFAS were cross-sectionally associated with small differences in markers of insulin secretion and function. However, there was limited evidence suggesting that PFAS concentrations are associated with diabetes incidence or changes in glycemic indicators during the follow-up period.

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