Evidence map›Paper›PMID 32004207›Full record

ArticleJournal of hypertension2020

An untargeted metabolomics study of blood pressure: findings from the Bogalusa Heart Study.

William J He, Changwei Li, Xuenan Mi, Mengyao Shi, Xiaoying Gu, Lydia A Bazzano, Alexander C Razavi, Jovia L Nierenberg, Kirsten Dorans, Hua He and 1 more

Open access · greenAbstract read
In one paragraph

Article in Journal of hypertension, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 32 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
32citing papers in PubMed, 1 pooled it
1.8field-weighted citation impact, top 15% 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

32 citing papers in PubMed, 1 synthesis or guideline pooled it, 41 citations in OpenAlex.

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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

11 authors at 5 institutions in 2 countries.

William J HeKrieger School of Arts and Sciences, Johns Hopkins University, Baltimore, Maryland.
Changwei LiDepartment of Epidemiology and Biostatistics, University of Georgia College of Public Health, Athens, Georgia, USA.
Xuenan MiDepartment of Epidemiology, Tulane University School of Public Health and Tropical Medicine, Tulane University, New Orleans, Louisiana.
Mengyao ShiDepartment of Epidemiology, Tulane University School of Public Health and Tropical Medicine, Tulane University, New Orleans, Louisiana.
Xiaoying GuInstitute of Clinical Medical Science, China-Japan Friendship Hospital, Beijing, China.
Lydia A BazzanoDepartment of Epidemiology, Tulane University School of Public Health and Tropical Medicine, Tulane University, New Orleans, Louisiana.
Alexander C RazaviDepartment of Epidemiology, Tulane University School of Public Health and Tropical Medicine, Tulane University, New Orleans, Louisiana.
Jovia L NierenbergDepartment of Epidemiology, Tulane University School of Public Health and Tropical Medicine, Tulane University, New Orleans, Louisiana.
Kirsten DoransDepartment of Epidemiology, Tulane University School of Public Health and Tropical Medicine, Tulane University, New Orleans, Louisiana.
Hua HeDepartment of Epidemiology, Tulane University School of Public Health and Tropical Medicine, Tulane University, New Orleans, Louisiana.
Tanika N KellyDepartment of Epidemiology, Tulane University School of Public Health and Tropical Medicine, Tulane University, New Orleans, Louisiana.
Tulane University · USChina-Japan Friendship Hospital · CNGeorgia College & State University · USJohns Hopkins University · USKelly Services (United States) · US

Funding

Tulane COBRE in Cardiometabolic Diseases Clinical Research CoreP20GM109036 · NIGMS · TULANE UNIVERSITY OF LOUISIANA · PI Tony Y. Hu · 2016 to 2026
$25.3M
Lifespan Cardiovascular Risk Exposures and Alzheimer-related brain health: Bogalusa Heart StudyRF1AG041200 · NIA · TULANE UNIVERSITY OF LOUISIANA · PI BAZZANO, LYDIA, CARMICHAEL, OWEN T. · 2019 to 2022
$4.2M
The Role of Vascular Aging in Cognitive and Physical Function - Diversity SupplementR01AG041200 · NIA · TULANE UNIVERSITY OF LOUISIANA · PI BAZZANO, LYDIA · 2012 to 2017
$2.9M
A novel research infrastructure enabling life-course studies of healthy agingR33AG057983 · NIA · TULANE UNIVERSITY OF LOUISIANA · PI BAZZANO, LYDIA · 2020 to 2022
$2.4M
Training in the Molecular & Genetic Epidemiology of CancerT32CA112355 · NCI · UNIVERSITY OF CALIFORNIA, SAN FRANCISCO · PI CHENG, IONA C, ZIV, ELAD · 2020 to 2024
$1.8M
The Roles of the Microbiome and Metabolome in Vascular AgingR21AG051914 · NIA · TULANE UNIVERSITY OF LOUISIANA · PI KELLY, TANIKA NICOLE · 2016 to 2017
$424k
The Roles of the Metabolome and Dietary Protein Intake in Left Ventricular Diastolic FunctionF30HL147486 · NHLBI · TULANE UNIVERSITY OF LOUISIANA · PI RAZAVI, ALEXANDER C. · 2019 to 2020
$97k
NCI NIH HHS T32 CA112355NHLBI NIH HHS F30 HL147486NIA NIH HHS R01 AG041200NIA NIH HHS R21 AG051914NIA NIH HHS R33 AG057983NIA NIH HHS RF1 AG041200NIGMS NIH HHS P20 GM109036
6 · The paper itself

Abstract

objectiveTo identify novel and confirm previously reported metabolites associated with SBP, DBP, and hypertension in a biracial sample of Bogalusa Heart Study (BHS) participants.

methodsWe employed untargeted, ultra-high performance liquid chromatography tandem mass spectroscopy metabolomics profiling among 1249 BHS participants (427 African-Americans and 822 whites) with BP and covariable data collected during the 2013 to 2016 visit cycle. A total of 1202 metabolites were tested for associations with continuous and binary BP phenotypes using multiple linear and logistic regression models, respectively, in overall and race-stratified analyses.

resultsA total of 24 novel metabolites robustly associated with BP, achieving Bonferroni-corrected P less than 4.16 × 10 in the overall analysis and consistent effect sizes across race groups. The identified metabolites included three amino acid and nucleotide metabolites from histidine, pyrimidine, or tryptophan metabolism sub-pathways, seven cofactor and vitamin or xenobiotic metabolites from the ascorbate and aldarate metabolism, bacterial/fungal, chemical, and food component sub-pathways, 10 lipid metabolites from the eicosanoid, phosphatidylcholine, phosphatidylethanolamine, and sphingolipid metabolism sub-pathways, and four still unnamed metabolites. Six previously described metabolites were robustly confirmed by our study (Bonferroni-corrected P < 4.95 × 10 and consistent effect directions across studies). Furthermore, previously reported metabolites for SBP, DBP, and hypertension demonstrated 5.92-fold, 4.77-fold, and 4.54-fold enrichment for nominally significant signals in the BHS (P = 3.08 × 10, 5.93 × 10, and 2.30 × 10, respectively).

conclusionIn aggregate, our study provides new information about potential molecular mechanisms underlying BP regulation. We also demonstrate reproducibility of findings across studies despite differences in study populations and metabolite profiling methods.

Indexed as

Blood PressureMetabolomicsAdultBiomarkersBlack or African AmericanChromatography, High Pressure LiquidFemaleHumansHypertensionLipidsLongitudinal StudiesMaleMiddle AgedPhenotypeRegression AnalysisReproducibility of ResultsBiomarkersLipids

Identifiers

PMID32004207
PMCPMC8805288
OpenAlexW3005411776

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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.