Evidence map›Paper›PMID 38823353›Full record

ArticleAtherosclerosis2024

Associations of an HDL apolipoproteomic index with cardiometabolic risk factors before and after exercise training in the HERITAGE Family Study.

J Sebastian Miranda Maravi, Eric C Leszczynski, Charles S Schwartz, Prasun K Dev, Jacob L Barber, Riley J Reasons, Ryan W Pearce, Michael J McPhaul, Robert J Konrad, Jeremy M Robbins and 5 more

Abstract read
In one paragraph

Article in Atherosclerosis, 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

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

15 authors.

J Sebastian Miranda MaraviDepartment of Exercise Science, University of South Carolina, Columbia, SC, USA.
Eric C LeszczynskiDepartment of Exercise Science, University of South Carolina, Columbia, SC, USA.
Charles S SchwartzDepartment of Exercise Science, University of South Carolina, Columbia, SC, USA.
Prasun K DevDepartment of Exercise Science, University of South Carolina, Columbia, SC, USA.
Jacob L BarberCardioVascular Institute, Beth Israel Deaconess Medical Center, Boston, MA, USA.
Riley J ReasonsDepartment of Exercise Science, University of South Carolina, Columbia, SC, USA.
Ryan W PearceQuest Diagnostics Cardiometabolic Center of Excellence at Cleveland HeartLab, Cleveland, OH, USA.
Michael J McPhaulQuest Diagnostics Cardiometabolic Center of Excellence at Cleveland HeartLab, Cleveland, OH, USA.
Robert J KonradLilly Research Laboratories, Eli Lilly and Company, Indianapolis, IN, USA.
Jeremy M RobbinsCardioVascular Institute, Beth Israel Deaconess Medical Center, Boston, MA, USA; Division of Cardiovascular Medicine, Beth Israel Deaconess Medical Center, Boston, MA, USA.
Robert E GersztenCardioVascular Institute, Beth Israel Deaconess Medical Center, Boston, MA, USA; Division of Cardiovascular Medicine, Beth Israel Deaconess Medical Center, Boston, MA, USA.
Timothy S CollierQuest Diagnostics Cardiometabolic Center of Excellence at Cleveland HeartLab, Cleveland, OH, USA.
Claude BouchardHuman Genomics Laboratory, Pennington Biomedical Research Center, Baton Rouge, LA, USA.
Anand RohatgiDivision of Cardiology, Department of Internal Medicine, UT Southwestern Medical Center, Dallas, TX, USA.
Mark A SarzynskiDepartment of Exercise Science, University of South Carolina, Columbia, SC, USA. Electronic address: sarz@mailbox.sc.edu.

Funding

HERITAGE STUDY: GENETICS, EXERCISE &RISK FACTORSR01HL045670 · NHLBI · LSU PENNINGTON BIOMEDICAL RESEARCH CTR · PI RANKINEN, TUOMO · 1992 to 2010
$6.8M
UofSC Postbaccalaureate Research Education ProgramR25GM066526 · NIGMS · UNIVERSITY OF SOUTH CAROLINA AT COLUMBIA · PI ARMSTRONG, ALISSA RICHMOND, ELY, BERT · 2004 to 2024
$5.4M
Molecular Basis of Exercise-induced Changes in HDL FunctionR01HL146462 · NHLBI · UNIVERSITY OF SOUTH CAROLINA AT COLUMBIA · PI SARZYNSKI, MARK ANDREW · 2019 to 2023
$3.6M
Biochemical profiling to identify cardiometabolic responsiveness to an endurance exercise interventionR01NR019628 · NINR · BETH ISRAEL DEACONESS MEDICAL CENTER · PI GERSZTEN, ROBERT E, SARZYNSKI, MARK ANDREW · 2021 to 2025
$2.7M
Training Program in Cardiovascular ResearchT32HL160522 · NHLBI · BETH ISRAEL DEACONESS MEDICAL CENTER · PI Jennifer E Ho · 2022 to 2026
$2.7M
HERITAGE STUDY: GENETICS, EXERCISE &RISK FACTORSR01HL047317 · NHLBI · WASHINGTON UNIVERSITY · PI RAO, DABEERU C · 1992 to 2003
$1.8M
HERITAGE STUDY: GENETICS, EXERCISE &RISK FACTORSR01HL047327 · NHLBI · INDIANA UNIVERSITY BLOOMINGTON · PI SKINNER, JAMES STANFORD · 1992 to 2003
$106k
HERITAGE STUDY: GENETICS, RESP. TO EXERCISE/RISK FACTORSR01HL047323 · NHLBI · UNIVERSITY OF MINNESOTA TWIN CITIES · PI LEON, ARTHUR S · 1992 to 2003
$100k
NHLBI NIH HHS R01 HL045670NHLBI NIH HHS R01 HL047317NHLBI NIH HHS R01 HL047323NHLBI NIH HHS R01 HL047327NHLBI NIH HHS R01 HL146462NHLBI NIH HHS T32 HL160522NIGMS NIH HHS R25 GM066526NINR NIH HHS R01 NR019628
6 · The paper itself

Abstract

BACKGROUND AND

aimsPrevious studies have derived and validated an HDL apolipoproteomic score (pCAD) that predicts coronary artery disease (CAD) risk. However, the associations between pCAD and markers of cardiometabolic health in healthy adults are not known, nor are the effects of regular exercise on pCAD.

methodsA total of 641 physically inactive adults free of cardiovascular disease from the HERITAGE Family Study completed 20 weeks of exercise training. The pCAD index (range 0-100) was calculated using measurements of apolipoproteins A-I, C-I, C-II, C-III, and C-IV from ApoA-I-tagged serum (higher index = higher CAD risk). The associations between pCAD index and cardiometabolic traits at baseline and their training responses were assessed with Spearman correlation and general linear models. A Bonferroni correction of p < 8.9 × 10

resultsThe mean ± SD baseline pCAD index was 29 ± 32, with 106 (16.5 %) participants classified as high CAD risk. At baseline, pCAD index was positively associated with blood pressure, systemic inflammation, and body composition. HDL size, VO

conclusionsA higher pCAD index was associated with a worse cardiometabolic profile at baseline but improved with regular exercise. The results from this study highlight the potential role of HDL apolipoproteins as therapeutic targets for lifestyle interventions, particularly in high-risk individuals.

Indexed as

BiomarkersCardiometabolic Risk FactorsExerciseAdultApolipoproteinsCholesterol, HDLCoronary Artery DiseaseExercise TherapyFemaleHumansLipoproteins, HDLMaleMiddle AgedProteomicsRisk AssessmentSedentary BehaviorApolipoproteinsBiomarkersCholesterol, HDLLipoproteins, HDLBiomarkerCoronary artery diseaseHigh-density lipoproteinpCADProteomics

Identifiers

PMID38823353
PMCPMC11254543

What Socratic holds

Textmetadata
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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.