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在前瞻性代谢和胰岛细胞评估(PROMISE)队列中,NEFA 组成与胰岛素敏感性和β细胞功能的关系。

Association of NEFA composition with insulin sensitivity and beta cell function in the Prospective Metabolism and Islet Cell Evaluation (PROMISE) cohort.

机构信息

Department of Nutritional Sciences, Faculty of Medicine, University of Toronto, FitzGerald Building, 150 College Street, Toronto, ON, M5S 3E2, Canada.

Centre for Studies in Family Medicine, University of Western Ontario, London, ON, Canada.

出版信息

Diabetologia. 2018 Apr;61(4):821-830. doi: 10.1007/s00125-017-4534-6. Epub 2017 Dec 24.

Abstract

AIMS/HYPOTHESIS: Our aim was to determine the longitudinal associations of individual NEFA with the pathogenesis of diabetes, specifically with differences in insulin sensitivity and beta cell function over 6 years in a cohort of individuals who are at risk for diabetes.

METHODS

In the Prospective Metabolism and Islet Cell Evaluation (PROMISE) longitudinal cohort, 477 participants had serum NEFA measured at the baseline visit and completed an OGTT at three time points over 6 years. Outcome variables were calculated using the OGTT values. At each visit, insulin sensitivity was assessed using the HOMA2 of insulin sensitivity (HOMA2-%S) and the Matsuda index, while beta cell function was assessed using the insulinogenic index over HOMA-IR (IGI/IR) and the insulin secretion-sensitivity index-2 (ISSI-2). Generalised estimating equations were used, adjusting for time, waist, sex, ethnicity, baseline age, alanine aminotransferase (ALT) and physical activity. NEFA were analysed as both concentrations (nmol/ml) and proportions (mol%) of the total fraction.

RESULTS

Participants' (73% female, 70% with European ancestry) insulin sensitivity and beta cell function declined by 14-21% over 6 years of follow-up. In unadjusted models, several NEFA (e.g. 18:1 n-7, 22:4 n-6) were associated with lower insulin sensitivity, however, nearly all of these associations were attenuated in fully adjusted models. In adjusted models, total NEFA, 16:0, 18:1 n-9 and 18:2 n-6 (as concentrations) were associated with 3.7-8.0% lower IGI/IR and ISSI-2, while only 20:5 n-3 (as mol%) was associated with 7.7% higher HOMA2-%S.

CONCLUSIONS/INTERPRETATION: Total NEFA concentration was a strong predictor of lower beta cell function over 6 years. Our results suggest that the association with beta cell function is due to the absolute size of the serum NEFA fraction, rather than the specific fatty acid composition.

摘要

目的/假设:我们的目的是确定个体非酯化脂肪酸(NEFA)与糖尿病发病机制的纵向关联,特别是在糖尿病风险人群中,6 年内胰岛素敏感性和β细胞功能的差异。

方法

在前瞻性代谢和胰岛细胞评估(PROMISE)纵向队列中,477 名参与者在基线访视时测量血清 NEFA,并在 6 年内的 3 个时间点完成口服葡萄糖耐量试验(OGTT)。使用 OGTT 值计算结局变量。在每次访视时,使用 HOMA2 胰岛素敏感性(HOMA2-%S)和 Matsuda 指数评估胰岛素敏感性,使用胰岛素原指数超过 HOMA-IR(IGI/IR)和胰岛素分泌敏感性指数-2(ISSI-2)评估β细胞功能。使用广义估计方程,调整时间、腰围、性别、种族、基线年龄、丙氨酸氨基转移酶(ALT)和体力活动。NEFA 以总分数的浓度(nmol/ml)和比例(mol%)进行分析。

结果

参与者(73%为女性,70%为欧洲血统)的胰岛素敏感性和β细胞功能在 6 年的随访中下降了 14-21%。在未调整模型中,几种 NEFA(如 18:1n-7、22:4n-6)与较低的胰岛素敏感性相关,但在完全调整模型中,几乎所有这些关联都减弱了。在调整模型中,总 NEFA、16:0、18:1n-9 和 18:2n-6(作为浓度)与 IGI/IR 和 ISSI-2 降低 3.7-8.0%相关,而只有 20:5n-3(作为 mol%)与 HOMA2-%S 升高 7.7%相关。

结论/解释:总 NEFA 浓度是 6 年内β细胞功能下降的强有力预测指标。我们的结果表明,与β细胞功能的关联是由于血清 NEFA 分数的绝对大小,而不是特定脂肪酸的组成。

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