Evidence map›Paper›PMID 39234305›Full record

ArticleFrontiers in physiology2024

Short-term HIIT impacts HDL function differently in lean, obese, and diabetic subjects.

Lin Zhu, Julia An, Thao Luu, Sara M Reyna, Puntip Tantiwong, Apiradee Sriwijitkamol, Nicolas Musi, John M Stafford

Abstract read
In one paragraph

Article in Frontiers in physiology, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 8 papers.

0numbers the graph read from it
0cells of the map it votes in
8citing 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

8 citing papers in PubMed.

  1. Trial
  2. Review
  3. Effect of HIIT Training Modality in People with Pre-Diabetes.Journal of functional morphology and kinesiology · 2026
    Article
  4. Observational
  5. Article
  6. Article
  7. Article
  8. Review
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

8 authors.

Lin ZhuTennessee Valley Health System, Veterans Affairs, Nashville, TN, United States.
Julia AnDepartment of Medicine, Division of Diabetes, Endocrinology and Metabolism, Vanderbilt University Medical Center, Nashville, TN, United States.
Thao LuuDepartment of Medicine, Division of Diabetes, Endocrinology and Metabolism, Vanderbilt University Medical Center, Nashville, TN, United States.
Sara M ReynaDiabetes Division, University of Texas Health Science Center at San Antonio, San Antonio, TX, United States.
Puntip TantiwongDiabetes Division, University of Texas Health Science Center at San Antonio, San Antonio, TX, United States.
Apiradee SriwijitkamolDiabetes Division, University of Texas Health Science Center at San Antonio, San Antonio, TX, United States.
Nicolas MusiDiabetes Division, University of Texas Health Science Center at San Antonio, San Antonio, TX, United States.
John M StaffordTennessee Valley Health System, Veterans Affairs, Nashville, TN, United States.

Funding

Sex-Specific Risk of Metabolic and Cardiovascular DiseaseR01HL144846 · NHLBI · VANDERBILT UNIVERSITY MEDICAL CENTER · PI John Michael Stafford · 2019 to 2026
$4.1M
Therapeutic Potential of Estrogen-Regulated Metabolism and Cardiovascular RiskR01DK109102 · NIDDK · VANDERBILT UNIVERSITY MEDICAL CENTER · PI STAFFORD, JOHN MICHAEL · 2016 to 2024
$3.6M
Does Senescence Impair the Cardiovascular Benefits of Menopause Hormone Therapy?K01AG077038 · NIA · VANDERBILT UNIVERSITY MEDICAL CENTER · PI Lin Zhu · 2022 to 2026
$601k
Macrophage ERK Signaling and Its Application in Modulating Skeletal Muscle Insulin ResistanceSC2GM127272 · NIGMS · UNIVERSITY OF TEXAS RIO GRANDE VALLEY · PI REYNA, SARA M · 2018 to 2020
$436k
Role of NFkappaB Signaling in Edothelial Dysfunction in Insulin ResistanceF32HL086089 · NHLBI · UNIVERSITY OF TEXAS HLTH SCIENCE CENTER · PI REYNA, SARA M · 2006 to 2009
$131k
Cholesteryl ester transfer protein, a novel mediator of insulin sensitivityI01BX002223 · VA · VETERANS HEALTH ADMINISTRATION · PI STAFFORD, JOHN MICHAEL · 2014 to 2017
–
BLRD VA I01 BX002223NHLBI NIH HHS F32 HL086089NHLBI NIH HHS R01 HL144846NIA NIH HHS K01 AG077038NIDDK NIH HHS R01 DK109102NIGMS NIH HHS SC2 GM127272
6 · The paper itself

Abstract

Introduction: High density lipoproteins (HDL) exert cardiovascular protection in part through their antioxidant capacity and cholesterol efflux function. Effects of exercise training on HDL function are yet to be well established, while impact on triacylglycerol (TG)-lowering has been often reported. We previously showed that a short-term high-intensity interval training (HIIT) program improves insulin sensitivity but does not inhibit inflammatory pathways in immune cells in insulin-resistant subjects. The purpose of this study is to evaluate HDL function along with changes of lipoproteins after the short-term HIIT program in lean, obese nondiabetic, and obese type 2 diabetic (T2DM) subjects. Methods: All individuals underwent a supervised 15-day program of alternative HIIT for 40 minutes per day. VO Results: Blood lipid profile and HDL function were analyzed before and after the HIIT program. Along with improved blood lipid profiles in obese and T2DM subjects, the HIIT program affected circulating apolipoprotein amounts differently. The HIIT program increased HDL-cholesterol levels and improved the cholesterol efflux capacity only in lean subjects. Furthermore, the HIIT program improved the antioxidant capacity of HDL in all subjects. Data from multiple logistic regression analysis showed that changes in HDL antioxidant capacity were inversely associated with changes in atherogenic lipids and changes in HDL-TG content. Discussion: We show that a short-term HIIT program improves aspects of HDL function depending on metabolic contexts, which correlates with improvements in blood lipid profile. Our results demonstrate that TG content in HDL particles may play a negative role in the anti-atherogenic function of HDL.

Indexed as

antioxidant capacitycholesterol effluxHDL functionHIIT exercise traininghyperlipidemiaobese

Identifiers

PMID39234305
PMCPMC11371628

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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.