Impact of a 12-week personalized dietary intervention on vascular function and cardiovascular risk factors

IF 5.7 2区 医学 Q1 ENDOCRINOLOGY & METABOLISM Diabetes, Obesity & Metabolism Pub Date : 2025-02-27 DOI:10.1111/dom.16261
Lisa Wanders PhD, Anouk Gijbels PhD, Gabby B. Hul MSc, Edith J. M. Feskens PhD, Lydia A. Afman PhD, Ellen E. Blaak PhD, Maria T. E. Hopman PhD, Gijs H. Goossens PhD, Dick H. J. Thijssen PhD
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Abstract

Aims

Individuals with liver insulin-resistant (LIR) or muscle insulin-resistant (MIR) phenotypes may respond differently to dietary interventions. Given the interaction between insulin resistance and cardiovascular risk, this sub-analysis of the PERSON study examined whether a personalized diet according to MIR or LIR phenotypes improves vascular function and cardiovascular disease risk factors.

Materials and Methods

We randomized 119 participants to a 12-week low-fat, high-protein, high-fibre diet (LFHP; may be optimal for LIR) or Mediterranean diet (high in monounsaturated fat, HMUFA; may be optimal for MIR). Randomization linked the insulin-resistant (IR) phenotype to the proposed optimal diet, leading to PhenoDiet A (MIR-HMUFA and LIR-LFHP) and PhenoDiet B (MIR-LFHP and LIR-HMUFA). Before and after the intervention, vascular function (carotid artery reactivity) and cardiovascular risk factors (blood pressure, total cholesterol, HDL-cholesterol and Framingham risk score) were examined. A 7-point oral glucose tolerance test was performed to determine insulin resistance (Matsuda index and HOMA-IR) and disposition index.

Results

Following drop-out (n = 18), 101 participants finished the intervention (54 women, 61 ± 7 years, 27.6 [26.4;30.0] kg/m2), with n = 80 available for the primary outcome of vascular function. Overall, the dietary interventions significantly decreased blood pressure, total cholesterol, HDL-cholesterol and the Framingham risk score (all p < 0.05), while vascular function was not affected (p = 0.485). Insulin resistance (p ≤ 0.001), but not disposition index (p = 0.362), was significantly improved after intervention. The Matsuda index (p = 0.078) tended to increase more and total cholesterol (p = 0.052) tended to decrease more in PhenoDiet group B than A, but other changes in outcome parameters were not significantly different between PhenoDiet groups. The LFHP diet resulted in more pronounced improvements in cholesterol, diastolic blood pressure (DBP) and insulin resistance compared with the HMUFA diet (all p < 0.05).

Conclusion

A 12-week diet improves metabolic and cardiovascular outcomes, but not vascular function in insulin-resistant adults with overweight or obesity. Whilst the LFHP diet resulted in greater improvements in cardiometabolic risk markers than the HMUFA diet, we found no significant differences between the PhenoDiet groups.

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为期12周的个性化饮食干预对血管功能和心血管危险因素的影响
目的:肝脏胰岛素抵抗(LIR)或肌肉胰岛素抵抗(MIR)表型的个体可能对饮食干预有不同的反应。鉴于胰岛素抵抗和心血管风险之间的相互作用,这项PERSON研究的亚分析研究了根据MIR或LIR表型的个性化饮食是否能改善血管功能和心血管疾病风险因素。材料和方法:我们将119名参与者随机分为12周的低脂、高蛋白、高纤维饮食(LFHP;可能是LIR的最佳选择)或地中海饮食(高单不饱和脂肪,HMUFA;可能是MIR的最佳选择)。随机化将胰岛素抵抗(IR)表型与建议的最佳饮食联系起来,导致表型饮食A (MIR-HMUFA和LIR-LFHP)和表型饮食B (MIR-LFHP和LIR-HMUFA)。干预前后检测血管功能(颈动脉反应性)和心血管危险因素(血压、总胆固醇、高密度脂蛋白胆固醇、Framingham危险评分)。7点口服糖耐量试验测定胰岛素抵抗(Matsuda指数和HOMA-IR)和处置指数。结果:退出后(n = 18), 101名参与者完成了干预(54名女性,61±7岁,27.6 [26.4;30.0]kg/m2),血管功能的主要结局n = 80。总体而言,饮食干预显著降低了血压、总胆固醇、高密度脂蛋白胆固醇和Framingham风险评分(均为p)。结论:12周的饮食改善了超重或肥胖的胰岛素抵抗成人的代谢和心血管结局,但对血管功能没有改善。虽然LFHP饮食比HMUFA饮食对心脏代谢风险指标的改善更大,但我们发现表型饮食组之间没有显著差异。
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来源期刊
Diabetes, Obesity & Metabolism
Diabetes, Obesity & Metabolism 医学-内分泌学与代谢
CiteScore
10.90
自引率
6.90%
发文量
319
审稿时长
3-8 weeks
期刊介绍: Diabetes, Obesity and Metabolism is primarily a journal of clinical and experimental pharmacology and therapeutics covering the interrelated areas of diabetes, obesity and metabolism. The journal prioritises high-quality original research that reports on the effects of new or existing therapies, including dietary, exercise and lifestyle (non-pharmacological) interventions, in any aspect of metabolic and endocrine disease, either in humans or animal and cellular systems. ‘Metabolism’ may relate to lipids, bone and drug metabolism, or broader aspects of endocrine dysfunction. Preclinical pharmacology, pharmacokinetic studies, meta-analyses and those addressing drug safety and tolerability are also highly suitable for publication in this journal. Original research may be published as a main paper or as a research letter.
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