The American journal of clinical nutrition · 2026
Peanuts-derived plasma lipids and lower risk of type 2 diabetes: association mediated by body mass index-an intervention and case-cohort study.
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Domínguez-López Inés, Eichelmann Fabian, Parilli-Moser Isabella, Hurtado-Barroso Sara, Lamuela-Raventós Rosa M, Schulze Matthias B
Аннотация
BACKGROUND: Cardiometabolic risk can be modified by dietary factors, including fat quality. Peanuts have a distinctive fatty acid (FA) composition rich in very long-chain saturated fatty acids (VLCSFA), with potentially favorable effects on cardiometabolic health.
OBJECTIVES: This study aimed to characterize the effects of peanut consumption on the circulating lipidome and examine associations of the resulting changes with cardiovascular disease (CVD) and type 2 diabetes (T2D).
METHODS: We integrated data from the clinical trial ARISTOTLE and the prospective, population-based European Prospective Investigation into Cancer and Nutrition (EPIC)-Potsdam cohort. ARISTOTLE randomly assigned 63 healthy young adults to 25 g/d skin-roasted peanuts, 32 g/d peanut butter, or 32 g/d control butter with peanut oil for 6 mo. EPIC-Potsdam included case-cohort samples for T2D (774 cases) and CVD (545 cases). Plasma lipids were measured preintervention and postintervention in ARISTOTLE and at baseline in EPIC-Potsdam. Linear mixed models identified within-class FA sums responsive to peanut fat-pooling all participants-in ARISTOTLE, which were combined to derive a peanut lipidomic signature (PeLS) in EPIC-Potsdam. Multivariable Cox models were used to estimate hazard ratios (HRs) for PeLS and individual lipids with incident T2D and CVD. Hypothesis-generating mediation by body mass index (BMI) was assessed.
RESULTS: The ARISTOTLE intervention modified 51 within-class FA sums, predominantly VLCSFA-containing lipids, particularly sphingolipids. The resulting PeLS was modestly associated with lower risk of T2D [HR: 0.89 per 1-standard deviation (SD) increase in PeLS; 95% confidence interval (CI): 0.80, 0.99], but not CVD (HR: 1.01 per 1-SD increase in PeLS; 95% CI: 0.90, 1.15), in EPIC-Potsdam, with BMI identified as a potential mediator of this association (proportion explainable of 89%, 95% CI: 57%, 100%).
CONCLUSIONS: Peanut consumption induces changes in the circulating lipidome, largely involving VLCSFA-containing lipids, which are associated with lower T2D risk partly through BMI. These results highlight peanuts as a source of dietary fats that may be linked to lower risk of T2D. This study was registered at clinicaltrials.gov as NCT04324749.
OBJECTIVES: This study aimed to characterize the effects of peanut consumption on the circulating lipidome and examine associations of the resulting changes with cardiovascular disease (CVD) and type 2 diabetes (T2D).
METHODS: We integrated data from the clinical trial ARISTOTLE and the prospective, population-based European Prospective Investigation into Cancer and Nutrition (EPIC)-Potsdam cohort. ARISTOTLE randomly assigned 63 healthy young adults to 25 g/d skin-roasted peanuts, 32 g/d peanut butter, or 32 g/d control butter with peanut oil for 6 mo. EPIC-Potsdam included case-cohort samples for T2D (774 cases) and CVD (545 cases). Plasma lipids were measured preintervention and postintervention in ARISTOTLE and at baseline in EPIC-Potsdam. Linear mixed models identified within-class FA sums responsive to peanut fat-pooling all participants-in ARISTOTLE, which were combined to derive a peanut lipidomic signature (PeLS) in EPIC-Potsdam. Multivariable Cox models were used to estimate hazard ratios (HRs) for PeLS and individual lipids with incident T2D and CVD. Hypothesis-generating mediation by body mass index (BMI) was assessed.
RESULTS: The ARISTOTLE intervention modified 51 within-class FA sums, predominantly VLCSFA-containing lipids, particularly sphingolipids. The resulting PeLS was modestly associated with lower risk of T2D [HR: 0.89 per 1-standard deviation (SD) increase in PeLS; 95% confidence interval (CI): 0.80, 0.99], but not CVD (HR: 1.01 per 1-SD increase in PeLS; 95% CI: 0.90, 1.15), in EPIC-Potsdam, with BMI identified as a potential mediator of this association (proportion explainable of 89%, 95% CI: 57%, 100%).
CONCLUSIONS: Peanut consumption induces changes in the circulating lipidome, largely involving VLCSFA-containing lipids, which are associated with lower T2D risk partly through BMI. These results highlight peanuts as a source of dietary fats that may be linked to lower risk of T2D. This study was registered at clinicaltrials.gov as NCT04324749.