Evidence map›Paper›PMID 38972029›Full record

ArticleMetabolomics : Official journal of the Metabolomic Society2024

Broadcasters, receivers, functional groups of metabolites, and the link to heart failure by revealing metabolomic network connectivity.

Azam Yazdani, Raul Mendez-Giraldez, Akram Yazdani, Rui-Sheng Wang, Daniel J Schaid, Sek Won Kong, M Reza Hadi, Ahmad Samiei, Esmat Samiei, Clemens Wittenbecher and 9 more

Abstract read
In one paragraph

Article in Metabolomics : Official journal of the Metabolomic Society, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.

0numbers the graph read from it
0cells of the map it votes in
2citing papers in PubMed
–field-weighted citation impact
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

2 citing papers in PubMed.

  1. Article
  2. Article
4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

19 authors.

Azam YazdaniDivision of Preventive Medicine, Department of Medicine, Brigham Women's Hospital, Harvard Medical School, Boston, MA, 02115, USA. a.mandana.yazdani@gmail.com.
Raul Mendez-GiraldezBeckman Coulter, Brea, USA.
Akram YazdaniDivision of Clinical and Translational Sciences, Department of Internal Medicine, The University of Texas Health Science Center at Houston, McGovern Medical School, Houston, USA.
Rui-Sheng WangDepartment of Medicine, Brigham Women's Hospital, Harvard Medical School, Boston, MA, USA.
Daniel J SchaidDepartment of Quantitative Health Sciences, Mayo Clinic, Rochester, MN, 55902, USA.
Sek Won KongComputational Health Informatics Program, Boston Children's Hospital, Boston, MA, USA.
M Reza HadiSchool of Mathematics, University of Science and Technology of Iran, Tehran, Iran.
Ahmad SamieiDivision of Pulmonary Medicine, Boston Children's Hospital, Boston, USA.
Esmat SamieiGamelectronic, Tehran, Iran.
Clemens WittenbecherDivision of Food and Nutrition Science, Department of Life Sciences, Chalmers University of Technology, Gothenburg, Sweden.
Jessica Lasky-SuDepartment of Medicine, Brigham Women's Hospital, Harvard Medical School, Boston, MA, USA.
Clary B ClishBroad Institute of MIT and Harvard, Cambridge, USA.
Jochen D MuehlschlegelDepartment of Anesthesia, Brigham Women's Hospital, Harvard Medical School, Boston, MA, USA.
Francesco MarottaReGenera R&D International for Aging Intervention and Vitality & Longevity Medical Science Commission, Femtec, Milano, Italy.
Joseph LoscalzoThe Division of Cardiovascular Medicine, Department of Medicine, Brigham Women's Hospital, Harvard Medical School, Boston, MA, USA.
Samia MoraDepartment of Medicine, Brigham Women's Hospital, Harvard Medical School, Boston, MA, USA.
Daniel I ChasmanDepartment of Medicine, Brigham Women's Hospital, Harvard Medical School, Boston, MA, USA.
Martin G LarsonDepartment of Biostatistics, Boston University, Boston, MA, 02118, USA.
Sarah H ElseaBaylor College of Medicine, Houston, USA.

Funding

ROLE OF DIETARY CONSTITUENTS ON GENE EXPRESSION IN INTESTINAL EPITHELIUMP30DK040561 · NIDDK · MASSACHUSETTS GENERAL HOSPITAL · PI Takara Leah Stanley · 1994 to 2026
$31.6M
FRAMINGHAM HEART STUDY - YEAR 5 EXAM75N92019D00031 · NHLBI · BOSTON UNIVERSITY MEDICAL CAMPUS · 2019 to 2024
$29.8M
Metabolomic predictors of insulin resistance and diabetesR01DK081572 · NIDDK · VANDERBILT UNIVERSITY · PI CLISH, CLARY B, GERSZTEN, ROBERT E · 2008 to 2025
$9.3M
Cardiac Exosomes in myocardial Ischemic injuryR01HL150401 · NHLBI · JOHNS HOPKINS UNIVERSITY · PI MUEHLSCHLEGEL, JOCHEN DANIEL · 2020 to 2024
$3.3M
Preclinical Analyses of NAD Kinase as a Redox Vulnerability for the Treatment of Pancreatic CancerR01CA211176 · NCI · BAYLOR COLLEGE OF MEDICINE · PI ELSEA, SARAH H. · 2017 to 2021
$2.6M
Quantitative Methods for Genetic EpidemiologyR35GM140487 · NIGMS · MAYO CLINIC ROCHESTER · PI SCHAID, DANIEL J. · 2021 to 2025
$1.9M
Patient Centered Approaches to Preventing ASCVD EventsK24HL136852 · NHLBI · BRIGHAM AND WOMEN'S HOSPITAL · PI SAMIA MORA · 2018 to 2026
$1.1M
NCI NIH HHS R01 CA211176NHLBI NIH HHS 75N92019D00031NHLBI NIH HHS K24 HL136852NHLBI NIH HHS R01 HL150401NIDDK NIH HHS P30 DK040561NIDDK NIH HHS R01 DK081572NIGMS NIH HHS R35 GM140487
6 · The paper itself

Abstract

BACKGROUND AND

objectiveBlood-based small molecule metabolites offer easy accessibility and hold significant potential for insights into health processes, the impact of lifestyle, and genetic variation on disease, enabling precise risk prevention. In a prospective study with records of heart failure (HF) incidence, we present metabolite profiling data from individuals without HF at baseline.

methodsWe uncovered the interconnectivity of metabolites using data-driven and causal networks augmented with polygenic factors. Exploring the networks, we identified metabolite broadcasters, receivers, mediators, and subnetworks corresponding to functional classes of metabolites, and provided insights into the link between metabolomic architecture and regulation in health. We incorporated the network structure into the identification of metabolites associated with HF to control the effect of confounding metabolites.

resultsWe identified metabolites associated with higher and lower risk of HF incidence, such as glycine, ureidopropionic and glycocholic acids, and LPC 18:2. These associations were not confounded by the other metabolites due to uncovering the connectivity among metabolites and adjusting each association for the confounding metabolites. Examples of our findings include the direct influence of asparagine on glycine, both of which were inversely associated with HF. These two metabolites were influenced by polygenic factors and only essential amino acids, which are not synthesized in the human body and are obtained directly from the diet.

conclusionMetabolites may play a critical role in linking genetic background and lifestyle factors to HF incidence. Revealing the underlying connectivity of metabolites associated with HF strengthens the findings and facilitates studying complex conditions like HF.

Indexed as

Heart FailureMetabolomicsAgedFemaleHumansMaleMetabolic Networks and PathwaysMetabolomeMiddle AgedProspective StudiesCausal networksConfounding metabolitesData-driven or Bayesian networksGenetic variationHeart failureMetabolomicsStructural equation modeling

Identifiers

PMID38972029
PMCPMC12060728

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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.