| Literature DB >> 27687742 |
Ruth Schübel1, Mirja E Graf1, Johanna Nattenmüller2, Diana Nabers3, Disorn Sookthai1, Laura F Gruner1, Theron Johnson1, Christopher L Schlett2, Oyunbileg von Stackelberg2, Romy Kirsten4, Nina Habermann5, Mario Kratz6, Hans-Ulrich Kauczor2, Cornelia M Ulrich7, Rudolf Kaaks1, Tilman Kühn8.
Abstract
Mechanistic studies suggest benefits of intermittent calorie restriction (ICR) in chronic disease prevention that may exceed those of continuous calorie restriction (CCR), even at equal net calorie intake. Despite promising results from first trials, it remains largely unknown whether ICR-induced metabolic alterations reported from experimental studies can also be observed in humans, and whether ICR diets are practicable and effective in real life situations. Thus, we initiated the HELENA Trial to test the effects of ICR (eu-caloric diet on five days and very low energy intake on two days per week) on metabolic parameters and body composition over one year. We will assess the effectiveness of ICR compared to CCR and a control diet over a 12-week intervention, 12-week maintenance phase and 24-week follow-up in 150 overweight or obese non-smoking adults (50 per group, 50% women). Our primary endpoint is the difference between ICR and CCR with respect to fold-changes in expression levels of 82 candidate genes in abdominal subcutaneous adipose tissue biopsies (SATb) during the intervention phase. The candidate genes represent pathways, which may link obesity-related metabolic alterations with the risk for major chronic diseases. In secondary and exploratory analyses, changes in metabolic, hormonal, inflammatory and metagenomic parameters measured in different biospecimens (SATb, blood, urine, stool) are investigated and effects of ICR/CCR/control on imaging-based measures of subcutaneous, visceral and hepatic fat are evaluated. Our study is the first randomized trial over one year testing the effects of ICR on metabolism, body composition and psychosocial factors in humans.Entities:
Keywords: Adipose tissue; Calorie restriction; Gene-expression; Intermittent fasting; Metabolism; Obesity
Mesh:
Year: 2016 PMID: 27687742 DOI: 10.1016/j.cct.2016.09.004
Source DB: PubMed Journal: Contemp Clin Trials ISSN: 1551-7144 Impact factor: 2.226