Evidence mapPaperPMID 31087608Full record

Trial reportDiabetes, obesity & metabolism2019

Mechanisms underlying the cardiometabolic protective effect of walnut consumption in obese people: A cross-over, randomized, double-blind, controlled inpatient physiology study.

Dario Tuccinardi, Olivia M Farr, Jagriti Upadhyay, Sabrina M Oussaada, Maria I Klapa, Marco Candela, Simone Rampelli, Sylvain Lehoux, Iolanda Lázaro, Aleix Sala-Vila and 3 more

Open access · greenAbstract readRandomized Controlled Trial
In one paragraph

Trial report in Diabetes, obesity & metabolism, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 30 papers, 4 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
30citing papers in PubMed, 4 pooled it
4.3field-weighted citation impact, top 5% 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.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

30 citing papers in PubMed, 4 syntheses or guidelines pooled it, 52 citations in OpenAlex.

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  20. Valorization of Traditional Italian Walnut (Plants (Basel, Switzerland) · 2022
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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

13 authors at 4 institutions in 4 countries.

Dario TuccinardiDivision of Endocrinology, Department of Medicine, Beth Israel Deaconess Medical Centre/Harvard Medical School, Boston, Massachusetts.ORCID 0000-0002-9139-7159
Olivia M FarrDivision of Endocrinology, Department of Medicine, Beth Israel Deaconess Medical Centre/Harvard Medical School, Boston, Massachusetts.ORCID 0000-0002-5182-3432
Jagriti UpadhyayDivision of Endocrinology, Department of Medicine, Beth Israel Deaconess Medical Centre/Harvard Medical School, Boston, Massachusetts.ORCID 0000-0003-2969-1602
Sabrina M OussaadaDivision of Endocrinology, Department of Medicine, Beth Israel Deaconess Medical Centre/Harvard Medical School, Boston, Massachusetts.
Maria I KlapaDepartment of Chemical & Biomolecular Engineering & Bioengineering, Metabolic Engineering and Systems Biology Laboratory, Institute of Chemical Engineering Sciences, Foundation for Research and Technology-Hellas, Patras, Greece.
Marco CandelaDepartment of Pharmacy and Biotechnology, University of Bologna, Bologna, Italy.
Simone RampelliDepartment of Pharmacy and Biotechnology, University of Bologna, Bologna, Italy.
Sylvain LehouxDepartment of Surgery, Beth Israel Deaconess Medical Centre, Harvard Medical School, Boston, Massachusetts.
Iolanda LázaroCIBERde Fisiopatología de la Obesidad y la Nutrición (CIBEROBN), Instituto de Salud Carlos III, Madrid, Spain.
Aleix Sala-VilaCIBERde Fisiopatología de la Obesidad y la Nutrición (CIBEROBN), Instituto de Salud Carlos III, Madrid, Spain.
Patrizia BrigidiDepartment of Pharmacy and Biotechnology, University of Bologna, Bologna, Italy.
Richard D CummingsDepartment of Pharmacy and Biotechnology, University of Bologna, Bologna, Italy.
Christos S MantzorosDivision of Endocrinology, Department of Medicine, Beth Israel Deaconess Medical Centre/Harvard Medical School, Boston, Massachusetts.ORCID 0000-0003-3755-8158
Beth Israel Deaconess Medical Center · USUniversity of Bologna · ITInstituto de Salud Carlos III · ESFoundation for Research and Technology Hellas · GR

Funding

NCRR NIH HHS UL1 RR025758NIDDK NIH HHS K24 DK081913NIGMS NIH HHS P41 GM103694
6 · The paper itself

Abstract

aimsTo assess the effects of walnuts on cardiometabolic outcomes in obese people and to explore the underlying mechanisms using novel methods including metabolomic, lipidomic, glycomic and microbiome analysis, integrated with lipid particle fractionation, appetite-regulating hormones and haemodynamic measurements. MATERIALS AND

methodsA total of 10 obese individuals were enrolled in this cross-over, randomized, double-blind, placebo-controlled clinical trial. The participants had two 5-day inpatient stays, during which they consumed a smoothie containing 48 g walnuts or a macronutrient-matched placebo smoothie without nuts, with a 1-month washout period between the two visits.

resultsWalnut consumption improved aspects of the lipid profile; it reduced fasting small and dense LDL particles (P < 0.02) and increased postprandial large HDL particles (P < 0.01). Lipoprotein insulin resistance score, glucose and the insulin area under the curve (AUC) decreased significantly after walnut consumption (P < 0.01, P < 0.02 and P < 0.04, respectively). Consuming walnuts significantly increased 10 N-glycans, with eight of them carrying a fucose core. Lipidomic analysis showed a robust reduction in harmful ceramides, hexosylceramides and sphingomyelins, which have been shown to mediate effects on cardiometabolic risk. The peptide YY AUC significantly increased after walnut consumption (P < 0.03). No major significant changes in haemodynamic or metabolomic analysis or in microbiome host health-promoting bacteria such as Faecalibacterium were found.

conclusionsThese data provide a more comprehensive mechanistic perspective of the effect of dietary walnut consumption on cardiometabolic variables. Lipidomic and lipid nuclear magnetic resonance spectroscopy analysis showed an early but significant reduction in ceramides and other atherogenic lipids with walnut consumption, which may explain the longer-term benefits of walnuts or other nuts on insulin resistance, cardiovascular risk and mortality.

Indexed as

JuglansCardiovascular DiseasesCross-Over StudiesDietDouble-Blind MethodEatingFastingFemaleHumansInpatientsInsulin ResistanceLipidsMaleMiddle AgedObesityPeptide YYLipidsPeptide YYcardiovascular riskceramidesglycomicslipidomicsMediterranean dietmetabolomicsmicrobiotanutrigenomicswalnuts

Identifiers

PMID31087608
PMCPMC6684390
OpenAlexW2945362271

What Socratic holds

Textmetadata
LicenceTDM
Read underepoch 390

Registered trials

None linked

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 Socratic graph.