4.7 Article

Dietary Protein Restriction Improves Metabolic Dysfunction in Patients with Metabolic Syndrome in a Randomized, Controlled Trial

期刊

NUTRIENTS
卷 14, 期 13, 页码 -

出版社

MDPI
DOI: 10.3390/nu14132670

关键词

protein restriction; caloric restriction; type 2 diabetes; insulin resistance; metabolic syndrome; cardiovascular disease

资金

  1. Sao Paulo Research Foundation (FAPESP) [2015/12133-0, 2017/01184-9]
  2. Innovation Fund Denmark [7043-00015B]
  3. Novo Nordisk Foundation Center for Basic Metabolic Research (CBMR)
  4. Novo Nordisk Foundation [NNF18CC0034900]
  5. Danish Diabetes Academy - Novo Nordisk Foundation [NNF17SA0031406]

向作者/读者索取更多资源

This study aimed to investigate the benefits of dietary restriction in patients with metabolic syndrome and determine whether it is the calorie or protein restriction that mediates the effects. The findings showed that isocaloric dietary protein restriction can achieve similar clinical outcomes as calorie restriction, making it a more attractive and less drastic dietary strategy for patients with metabolic syndrome and has potential as an adjuvant therapy.
Dietary restriction (DR) reduces adiposity and improves metabolism in patients with one or more symptoms of metabolic syndrome. Nonetheless, it remains elusive whether the benefits of DR in humans are mediated by calorie or nutrient restriction. This study was conducted to determine whether isocaloric dietary protein restriction is sufficient to confer the beneficial effects of dietary restriction in patients with metabolic syndrome. We performed a prospective, randomized controlled dietary intervention under constant nutritional and medical supervision. Twenty-one individuals diagnosed with metabolic syndrome were randomly assigned for caloric restriction (CR; n = 11, diet of 5941 +/- 686 KJ per day) or isocaloric dietary protein restriction (PR; n = 10, diet of 8409 +/- 2360 KJ per day) and followed for 27 days. Like CR, PR promoted weight loss due to a reduction in adiposity, which was associated with reductions in blood glucose, lipid levels, and blood pressure. More strikingly, both CR and PR improved insulin sensitivity by 62.3% and 93.2%, respectively, after treatment. Fecal microbiome diversity was not affected by the interventions. Adipose tissue bulk RNA-Seq data revealed minor changes elicited by the interventions. After PR, terms related to leukocyte proliferation were enriched among the upregulated genes. Protein restriction is sufficient to confer almost the same clinical outcomes as calorie restriction without the need for a reduction in calorie intake. The isocaloric characteristic of the PR intervention makes this approach a more attractive and less drastic dietary strategy in clinical settings and has more significant potential to be used as adjuvant therapy for people with metabolic syndrome.

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