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地中海饮食中低升糖指数和高升糖指数对成年男女性的血糖和胰岛素水平的影响不同:来自 MEDGI-Carb 随机临床试验的数据。

The effects of Mediterranean diets with low or high glycemic index on plasma glucose and insulin profiles are different in adult men and women: Data from MEDGI-Carb randomized clinical trial.

机构信息

Diabetes, Nutrition and Metabolism Unit, Department of Clinical Medicine and Surgery, Federico II University, 80138 Naples, Italy.

Diabetes, Nutrition and Metabolism Unit, Department of Clinical Medicine and Surgery, Federico II University, 80138 Naples, Italy.

出版信息

Clin Nutr. 2023 Oct;42(10):2022-2028. doi: 10.1016/j.clnu.2023.08.016. Epub 2023 Aug 25.

Abstract

BACKGROUND & AIMS: Recent evidence suggests that the ability to regulate glucose and insulin homeostasis is different in men and women. Against this background, it has been hypothesized that the impact on daily plasma glucose and insulin profiles of the glycemic index (GI) of the habitual diet may differ according to sex. The aim of this study is to evaluate whether 8-h average plasma glucose and insulin profiles during a low- or a high-GI diet in individuals at high risk of developing type 2 diabetes are influenced by sex.

METHODS

We conducted a randomized, controlled, parallel group dietary intervention, comparing high-versus low-GI diets in a multi-national (Italy, Sweden, and the United States) sample of 156 adults at risk for type 2 diabetes. For 12 weeks, 82 vs 74 participants consumed either a low-GI or high-GI Mediterranean diet, respectively. The two experimental diets contained the same quantity of available carbohydrate (270 g/d) and fiber (35 g/d) and the same foods and beverages, except for the major sources of starch that was specific to the low-GI and high-GI groups (pasta, brown rice, flatbread, all bran, and wheat bread plus rye and seeds, vs jasmine rice, potato, couscous, wholegrain bread, and rusks). At baseline and after the intervention plasma glucose and insulin profiles were evaluated for 8 h in the two intervention groups - separately for men and women - with both breakfast and lunch resembling food choices of the assigned diet.

RESULTS

One hundred fifty-six adults (82 women, 74 men) with at least two traits of the metabolic syndrome completed the intervention. In women, the high-GI induced significantly higher (23%, p < 0.05) 8-h average plasma glucose concentrations in comparison to the low-GI diet already on the first day of the intervention; the difference increased up to 37% (p < 0.05) after 12 weeks of diet. Conversely, there were no significant differences between the two diets in men. These results were confirmed by the two-way analysis of variance showing a statistically significant interaction between the effects of sex and diet on the glucose profile after breakfast and lunch (F = 7.887, p = 0.006).

CONCLUSION

The results of our intervention show that women, compared to men, are more sensitive to the metabolic effects of the dietary GI. This has a strong clinical and scientific relevance and, if confirmed in further studies, it might have important implications for dietary strategies for diabetes and cardiovascular disease prevention in the context of personalized nutrition.

REGISTRATION NUMBER OF CLINICAL TRIAL

Clinicaltrials.gov n. NCT03410719.

摘要

背景与目的

最近的证据表明,男性和女性调节血糖和胰岛素稳态的能力不同。在此背景下,有人假设习惯性饮食的血糖指数(GI)对日常血浆葡萄糖和胰岛素谱的影响可能因性别而异。本研究旨在评估在患有 2 型糖尿病风险较高的个体中,低 GI 或高 GI 饮食对 8 小时平均血浆葡萄糖和胰岛素谱的影响是否受性别影响。

方法

我们进行了一项随机、对照、平行组饮食干预研究,比较了高 GI 与低 GI 饮食对来自意大利、瑞典和美国的 156 名高危 2 型糖尿病患者的影响。在 12 周的时间里,82 名参与者和 74 名参与者分别食用低 GI 或高 GI 的地中海饮食。两种实验饮食均含有相同数量的可利用碳水化合物(270 克/天)和纤维(35 克/天),以及相同的食物和饮料,只是高 GI 和低 GI 组的主要淀粉来源不同(意大利面、糙米、薄饼、全麦、小麦面包加黑麦和种子,vs 茉莉香米、土豆、古斯米、全麦面包、饼干)。在基线和干预后,两组干预组 - 分别为男性和女性 - 评估了 8 小时的血浆葡萄糖和胰岛素谱,其中早餐和午餐均类似于指定饮食的食物选择。

结果

156 名成年人(82 名女性,74 名男性)至少有两种代谢综合征特征完成了干预。在女性中,高 GI 饮食在干预的第一天就导致 8 小时平均血浆葡萄糖浓度显著升高(23%,p<0.05);12 周饮食后,差异增加至 37%(p<0.05)。相比之下,男性在两种饮食之间没有显著差异。这一结果通过早餐和午餐后血糖谱的双向方差分析得到证实,表明性别和饮食对血糖谱的影响存在统计学显著的相互作用(F=7.887,p=0.006)。

结论

我们的干预结果表明,与男性相比,女性对饮食 GI 的代谢影响更为敏感。这具有很强的临床和科学意义,如果在进一步的研究中得到证实,它可能对个性化营养背景下的糖尿病和心血管疾病预防的饮食策略具有重要意义。

临床试验注册号

Clinicaltrials.gov n. NCT03410719。

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