Evidence map›Paper›PMID 31133557›Full record

Trial reportJournal of lipid research2019

Plasma apoM and S1P levels are inversely associated with mortality in African Americans with type 2 diabetes mellitus.

Mingxia Liu, Cecilia Frej, Carl D Langefeld, Jasmin Divers, Donald W Bowden, J Jeffrey Carr, Abraham K Gebre, Jianzhao Xu, Benny Larsson, Björn Dahlbäck and 2 more

Open access · hybridAbstract readClinical Trial
In one paragraph

Trial report in Journal of lipid research, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 17 papers.

0numbers the graph read from it
0cells of the map it votes in
17citing papers in PubMed
1.4field-weighted citation impact, top 19% 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

17 citing papers in PubMed, 27 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

12 authors at 4 institutions in 2 countries.

Mingxia LiuSection on Molecular Medicine, Department of Internal Medicine, Wake Forest School of Medicine, Winston-Salem, NC.
Cecilia FrejDepartment of Translational Medicine Skåne University Hospital, Lund University, Malmö, Sweden.
Carl D LangefeldDivision of Public Health Sciences, Department of Biostatistics and Data Science Wake Forest School of Medicine, Winston-Salem, NC.
Jasmin DiversDivision of Public Health Sciences, Department of Biostatistics and Data Science Wake Forest School of Medicine, Winston-Salem, NC.
Donald W BowdenDepartment of Biochemistry, Wake Forest School of Medicine, Winston-Salem, NC.
J Jeffrey CarrDepartment of Radiology Vanderbilt University Medical Center, Nashville, TN.
Abraham K GebreSection on Molecular Medicine, Department of Internal Medicine, Wake Forest School of Medicine, Winston-Salem, NC.
Jianzhao XuDepartment of Biochemistry, Wake Forest School of Medicine, Winston-Salem, NC.
Benny LarssonDepartment of Clinical Chemistry Skåne University Hospital, Lund, Sweden.
Björn DahlbäckDepartment of Translational Medicine Skåne University Hospital, Lund University, Malmö, Sweden.
Barry I FreedmanSection on Nephrology, Department of Internal Medicine, Wake Forest School of Medicine, Winston-Salem, NC bfreedma@wakehealth.edu jparks@wakehealth.edu.
John S ParksSection on Molecular Medicine, Department of Internal Medicine, Wake Forest School of Medicine, Winston-Salem, NC bfreedma@wakehealth.edu jparks@wakehealth.edu.
Wake Forest University · USSkåne University Hospital · SELund University · SEVanderbilt University Medical Center · US

Funding

Subclinical CVD in African American Type 2 DiabeticsR01DK071891 · NIDDK · WAKE FOREST UNIVERSITY HEALTH SCIENCES · PI FREEDMAN, BARRY IRA · 2007 to 2016
$4.5M
The Role of Hepatocyte ABCA1 in Lipid Mobilization and TransportR01HL119962 · NHLBI · WAKE FOREST UNIVERSITY HEALTH SCIENCES · PI PARKS, JOHN S · 2013 to 2022
$3.9M
Integrative Lipid Metabolism, Inflammation, and Chronic DiseasesT32HL091797 · NHLBI · WAKE FOREST UNIVERSITY HEALTH SCIENCES · PI PARKS, JOHN S · 2008 to 2017
$1.8M
NHLBI NIH HHS R01 HL119962NHLBI NIH HHS T32 HL091797NIDDK NIH HHS R01 DK071891
6 · The paper itself

Abstract

apoM is a minor HDL apolipoprotein and carrier for sphingosine-1-phosphate (S1P). HDL apoM and S1P concentrations are inversely associated with atherosclerosis progression in rodents. We evaluated associations between plasma concentrations of S1P, plasma concentrations of apoM, and HDL apoM levels with prevalent subclinical atherosclerosis and mortality in the African American-Diabetes Heart Study participants (N = 545). Associations between plasma S1P, plasma apoM, and HDL apoM with subclinical atherosclerosis and mortality were assessed using multivariate parametric, nonparametric, and Cox proportional hazards models. At baseline, participants' median (25th percentile, 75th percentile) age was 55 (49, 62) years old and their coronary artery calcium (CAC) mass score was 26.5 (0.0, 346.5). Plasma S1P, plasma apoM, and HDL apoM were not associated with CAC. After 64 (57.6, 70.3) months of follow-up, 81 deaths were recorded. Higher concentrations of plasma S1P [odds ratio (OR) = 0.14,

Indexed as

Black or African AmericanApolipoproteins MBiomarkersDiabetes Mellitus, Type 2Disease-Free SurvivalFemaleHumansLysophospholipidsMaleMiddle AgedSphingosineSurvival RateApolipoproteins MAPOM protein, humanBiomarkersLysophospholipidsSphingosinesphingosine 1-phosphateapolipoprotein Mapolipoproteinsatherosclerosisclinical studiesethnicityhigh density lipoproteinsphingosine-1-phosphate

Identifiers

PMID31133557
PMCPMC6672033
OpenAlexW2947948369

What OpenQuestion holds

Textmetadata
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 OpenQuestion graph.