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炎症性和胰岛素血症性饮食模式的代谢潜能与2型糖尿病风险

The metabolic potential of inflammatory and insulinaemic dietary patterns and risk of type 2 diabetes.

作者信息

Lee Dong Hoon, Jin Qi, Shi Ni, Wang Fenglei, Bever Alaina M, Liang Liming, Hu Frank B, Song Mingyang, Zeleznik Oana A, Zhang Xuehong, Joshi Amit, Wu Kana, Jeon Justin Y, Meyerhardt Jeffrey A, Chan Andrew T, Eliassen A Heather, Clish Clary, Clinton Steven K, Giovannucci Edward L, Li Jun, Tabung Fred K

机构信息

Department of Sport Industry Studies, Yonsei University, Seoul, Republic of Korea.

Department of Nutrition, Harvard T.H. Chan School of Public Health, Boston, MA, USA.

出版信息

Diabetologia. 2024 Jan;67(1):88-101. doi: 10.1007/s00125-023-06021-3. Epub 2023 Oct 11.

Abstract

AIMS/HYPOTHESIS: Diets with higher inflammatory and insulinaemic potential have been associated with an increased risk of type 2 diabetes. However, it remains unknown whether plasma metabolomic profiles related to proinflammatory/hyperinsulinaemic diets and to inflammatory/insulin biomarkers are associated with type 2 diabetes risk.

METHODS

We analysed 6840 participants from the Nurses' Health Study and Health Professionals Follow-up Study to identify the plasma metabolome related to empirical dietary inflammatory pattern (EDIP), empirical dietary index for hyperinsulinemia (EDIH), four circulating inflammatory biomarkers and C-peptide. Dietary intakes were assessed using validated food frequency questionnaires. Plasma metabolomic profiling was conducted by LC-MS/MS. Metabolomic signatures were derived using elastic net regression. Multivariable Cox regression was used to examine associations of the metabolomic profiles with type 2 diabetes risk.

RESULTS

We identified 27 metabolites commonly associated with both EDIP and inflammatory biomarker z score and 21 commonly associated with both EDIH and C-peptide. Higher metabolomic dietary inflammatory potential (MDIP), reflecting higher metabolic potential of both an inflammatory dietary pattern and circulating inflammatory biomarkers, was associated with higher type 2 diabetes risk. The HR comparing highest vs lowest quartiles of MDIP was 3.26 (95% CI 2.39, 4.44). We observed a strong positive association with type 2 diabetes risk for the metabolomic signature associated with EDIP-only (HR 3.75; 95% CI 2.71, 5.17) or inflammatory biomarkers-only (HR 4.07; 95% CI 2.91, 5.69). In addition, higher metabolomic dietary index for hyperinsulinaemia (MDIH), reflecting higher metabolic potential of both an insulinaemic dietary pattern and circulating C-peptide, was associated with greater type 2 diabetes risk (HR 3.00; 95% CI 2.22, 4.06); further associations with type 2 diabetes were HR 2.79 (95% CI 2.07, 3.76) for EDIH-only signature and HR 3.89 (95% CI 2.82, 5.35) for C-peptide-only signature. The diet scores were significantly associated with risk, although adjustment for the corresponding metabolomic signature scores attenuated the associations with type 2 diabetes, these remained significant.

CONCLUSIONS/INTERPRETATION: The metabolomic signatures reflecting proinflammatory or hyperinsulinaemic diets and related biomarkers were positively associated with type 2 diabetes risk, supporting that these dietary patterns may influence type 2 diabetes risk via the regulation of metabolism.

摘要

目的/假设:具有较高炎症和胰岛素血症潜力的饮食与2型糖尿病风险增加有关。然而,与促炎/高胰岛素血症饮食以及炎症/胰岛素生物标志物相关的血浆代谢组学特征是否与2型糖尿病风险相关仍不清楚。

方法

我们分析了来自护士健康研究和卫生专业人员随访研究的6840名参与者,以确定与经验性饮食炎症模式(EDIP)、高胰岛素血症经验性饮食指数(EDIH)、四种循环炎症生物标志物和C肽相关的血浆代谢组。使用经过验证的食物频率问卷评估饮食摄入量。通过液相色谱-串联质谱法进行血浆代谢组学分析。使用弹性网络回归得出代谢组学特征。采用多变量Cox回归来检验代谢组学特征与2型糖尿病风险的关联。

结果

我们鉴定出27种代谢物通常与EDIP和炎症生物标志物z评分均相关,以及21种通常与EDIH和C肽均相关。较高的代谢组学饮食炎症潜力(MDIP),反映了炎症饮食模式和循环炎症生物标志物的较高代谢潜力,与较高的2型糖尿病风险相关。比较MDIP最高四分位数与最低四分位数的风险比为3.26(95%置信区间2.39,4.44)。我们观察到仅与EDIP相关的代谢组学特征(风险比3.75;95%置信区间2.71, 5.17)或仅与炎症生物标志物相关的代谢组学特征(风险比4.07;95%置信区间2.91, 5.69)与2型糖尿病风险呈强正相关。此外,较高的高胰岛素血症代谢组学饮食指数(MDIH),反映了胰岛素血症饮食模式和循环C肽的较高代谢潜力,与更大的2型糖尿病风险相关(风险比3.00;95%置信区间2.22, 4.06);仅与EDIH相关的特征与2型糖尿病的进一步关联风险比为2.79(95%置信区间2.07, 3.76),仅与C肽相关的特征风险比为3.89(95%置信区间2.82, 5.35)。饮食评分与风险显著相关,尽管对相应的代谢组学特征评分进行调整会减弱与2型糖尿病的关联,但这些关联仍然显著。

结论/解读:反映促炎或高胰岛素血症饮食及相关生物标志物的代谢组学特征与2型糖尿病风险呈正相关,支持这些饮食模式可能通过代谢调节影响2型糖尿病风险。

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