Administration of a dietary supplement (N-oleyl-phosphatidylethanolamine and epigallocatechin-3-gallate formula) enhances compliance with diet in healthy overweight subjects: a randomized controlled trial

Many studies have found that N-oleyl-ethanolamine (NOE), a metabolite of N-oleyl-phosphatidylethanolamine (NOPE), and epigallocatechin-3-gallate (EGCG) inhibit food intake. The main aim of this study was to evaluate the efficacy of 2 months of administration of an oily NOPE–EGCG complex (85 mg NOPE...

Full description

Saved in:
Bibliographic Details
Published inBritish journal of nutrition Vol. 101; no. 3; pp. 457 - 464
Main Authors Rondanelli, Mariangela, Opizzi, Annalisa, Solerte, Sebastiano Bruno, Trotti, Rosita, Klersy, Catherine, Cazzola, Roberta
Format Journal Article
LanguageEnglish
Published Cambridge, UK Cambridge University Press 01.02.2009
Subjects
men
Online AccessGet full text

Cover

Loading…
More Information
Summary:Many studies have found that N-oleyl-ethanolamine (NOE), a metabolite of N-oleyl-phosphatidylethanolamine (NOPE), and epigallocatechin-3-gallate (EGCG) inhibit food intake. The main aim of this study was to evaluate the efficacy of 2 months of administration of an oily NOPE–EGCG complex (85 mg NOPE and 50 mg EGCG per capsule) and its effect on compliance with diet in healthy, overweight people. Secondary end-points of the study were to compare body composition, metabolic parameters, sensation of appetite, depressive symptoms and severity of binge eating. Using a parallel-arm, double-blind, placebo-controlled design, 138 healthy, overweight women (106) and men (thirty-two) were randomly assigned to one of two groups: (1) the treatment group (seventy-one patients: fifty-three females, eighteen males) taking two capsules per day of an oral supplement or (2) the placebo group (sixty-seven patients: fifty-three females, fourteen males). Both groups observed a 3344 kJ/d energy restriction. All parameters were assessed both before onset and after 2 months on the supplement. Dropout was 6 % in the NOPE–EGCG group and 27 % in the placebo group (P < 0·001). The treatment induced a significant weight reduction in both groups ( − 3·28 kg and − 2·67 kg in NOPE–EGCG and placebo, respectively); the weight changes were not significantly different between the groups. NOPE–EGCG treatment improved insulin resistance (P < 0·001), the sensation feelings of fullness (P < 0·05), depressive symptoms (P < 0·004) and severity of binge eating (P < 0·0001).
Bibliography:http://dx.doi.org/10.1017/S0007114508024008
PII:S0007114508024008
istex:8C25AF2C135EDFB21BDE505DDC497020B0FBE4EA
Abbreviations: EGCG, epigallocatechin-3-gallate; HOMA, homeostasis model assessment; NOE, N-oleyl-ethanolamide; NOPE, N-oleyl-phosphatidylethanolamine; QUICKI, quantitative insulin sensitivity check index
ArticleID:02400
ark:/67375/6GQ-MMMQ5CXK-7
ObjectType-Article-1
SourceType-Scholarly Journals-1
ObjectType-Feature-2
content type line 14
ObjectType-Article-2
ObjectType-Feature-1
content type line 23
ObjectType-Undefined-3
ISSN:0007-1145
1475-2662
1475-2662
DOI:10.1017/S0007114508024008