Evidence map›Paper›PMID 35967820›Full record

ArticleFrontiers in nutrition2022

Dietary adaptation for weight loss maintenance at Yale (DAWLY): Protocol and predictions for a randomized controlled trial.

Xi Fang, Xue Davis, Kyle D Flack, Chavonn Duncan, Fangyong Li, Marney White, Carlos Grilo, Dana M Small

Registry-linked trialOpen access · goldAbstract read
In one paragraph

Article in Frontiers in nutrition, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. It is linked to trial NCT04614233 (Targeting the Gut-brain Axis to Facilitate Weight Loss in High Fat Diet Consumers), which is not on this map. Cited by 1 paper.

0numbers the graph read from it
0cells of the map it votes in
1citing papers in PubMed
–field-weighted citation impact, top 87% of its field
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

NCT04614233 phase4terminatednot on this map

Targeting the Gut-brain Axis to Facilitate Weight Loss in High Fat Diet Consumers

TypeinterventionalSponsorYale UniversityRan2021 to 2024Enrolled64ConditionsOverweight and ObesityArmsRiduZone (90% OEA), Placebo
3 · Its place in the literature

Who cites it

1 citing paper in PubMed, 0 citations in OpenAlex.

  1. Article
4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

8 authors at 3 institutions in 1 country.

Xi FangModern Diet and Physiology Research Center, New Haven, CT, United States.
Xue DavisModern Diet and Physiology Research Center, New Haven, CT, United States.
Kyle D FlackDepartment of Dietetics and Human Nutrition, College of Agriculture, Foods, and Environment, University of Kentucky, Lexington, KY, United States.
Chavonn DuncanModern Diet and Physiology Research Center, New Haven, CT, United States.
Fangyong LiYale Center for Analytical Sciences, Yale School of Public Health, New Haven, CT, United States.
Marney WhiteDepartment of Psychiatry, Yale University School of Medicine, New Haven, CT, United States.
Carlos GriloDepartment of Psychiatry, Yale University School of Medicine, New Haven, CT, United States.
Dana M SmallModern Diet and Physiology Research Center, New Haven, CT, United States.
Modern Diet and Physiology Research Center · USYale University · USUniversity of Kentucky · US

Funding

Yale Clinical and Translational Science Award (U Component)UL1TR001863 · NCATS · YALE UNIVERSITY · PI John H. Krystal, LUCILA OHNO-MACHADO · 2016 to 2026
$102.9M
Targeting the gut-brain axis to facilitate weight loss in high fat diet consumersR01DK126295 · NIDDK · YALE UNIVERSITY · PI SMALL, DANA M · 2021 to 2023
$2.1M
NCATS NIH HHS UL1 TR001863NIDDK NIH HHS R01 DK126295
6 · The paper itself

Abstract

Background: Current therapies for obesity treatment are effective at producing short-term weight loss, but weight loss maintenance remains a significant challenge. Here we investigate the impact of pre-intervention dietary fat intake on the efficacy of a dietary supplement to support weight loss maintenance. Preclinical work demonstrates that a vagal afferent pathway critical for sensing dietary lipids is blunted by a high-fat diet (HFD), resulting in a reduced preference for a low-fat emulsion and severe blunting of the dopamine (DA) response to the gastric infusion of lipids. Infusion of the gut lipid messenger oleoylethanolamide (OEA), which is also depleted by HFD, immediately reverses this DA blunting and restores preference for the low-fat emulsion. Studies of OEA supplementation for weight loss in humans have had limited success. Given the strong effect of HFD on this pathway, we designed a study to test whether the efficacy of OEA as a weight loss treatment is related to pre-intervention habitual intake of dietary fat. Methods/Design: We employed a randomized, double-blind, placebo-controlled trial in which 100 adults with overweight/obesity (OW/OB) were randomized to receive either OEA or placebo daily for 16 months. Following a baseline evaluation of diet, metabolic health, adiposity, and brain response to a palatable an energy dense food, participants in both groups underwent a 4-month behavioral weight loss intervention (LEARN Discussion: Focusing on interventions that target the gut-brain axis is supported by mounting evidence for the role of gut-brain signaling in food choice and the modulation of this circuit by diet. If successful, this work will provide support for targeting the gut-brain pathway for weight loss maintenance using a precision medicine approach that is easy and inexpensive to implement. Clinical Trial Registration: [www.ClinicalTrials.gov], identifier [NCT04614233].

Indexed as

dietary intakeobesityoleoylethanolamideoverweightrandomized controlled trialRiduzonesupplementationweight loss

Identifiers

PMID35967820
PMCPMC9369668
OpenAlexW4288426938

What OpenQuestion holds

Textmetadata
LicenceCC BY
Read underepoch 390

Registered trials

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.