Evidence map›Paper›PMID 33320903›Full record

ArticlePloS one2020

Associations between legal performance-enhancing substance use and future cardiovascular disease risk factors in young adults: A prospective cohort study.

Jason M Nagata, Kyle T Ganson, Mitchell L Cunningham, Deborah Mitchison, Jason M Lavender, Aaron J Blashill, Holly C Gooding, Stuart B Murray

Open access · goldAbstract read
In one paragraph

Article in PloS one, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 3 papers.

0numbers the graph read from it
0cells of the map it votes in
3citing papers in PubMed
0.4field-weighted citation impact, top 32% 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

3 citing papers in PubMed, 3 citations in OpenAlex.

  1. Review
  2. Review
  3. 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 at 8 institutions in 3 countries.

Jason M NagataDepartment of Pediatrics, University of California, San Francisco, San Francisco, California, United States of America.ORCID 0000-0002-6541-0604
Kyle T GansonFactor-Inwentash Faculty of Social Work, University of Toronto, Toronto, Ontario, Canada.ORCID 0000-0003-3889-3716
Mitchell L CunninghamSchool of Psychology, University of Sydney, Sydney, New South Wales, Australia.
Deborah MitchisonTranslational Health Research Institute, School of Medicine, Western Sydney University, Sydney, New South Wales, Australia.
Jason M LavenderMilitary Cardiovascular Outcomes Research Program (MiCOR), Department of Medicine, Uniformed Services University of the Health Sciences, Bethesda, Maryland, United States of America.
Aaron J BlashillDepartment of Psychology, San Diego State University, San Diego, California, United States of America.
Holly C GoodingDepartment of Pediatrics, Emory University School of Medicine, Atlanta, Georgia, United States of America.
Stuart B MurrayDepartment of Psychiatry & Behavioral Sciences, University of Southern California, Los Angeles, California, United States of America.
Emory University · USSan Diego State University · USThe University of Sydney · AUTranslational Research Institute · AUUniformed Services University of the Health Sciences · USUniversity of California, San Francisco · USUniversity of Southern California · USUniversity of Toronto · CA

Funding

Wave IV Data CollectionP01HD031921 · NICHD · UNIV OF NORTH CAROLINA CHAPEL HILL · PI HARRIS, KATHLEEN MULLAN · 1994 to 2020
$86.1M
Pediatric Scientist Development Program (PSDP) [K12]K12HD000850 · NICHD · YALE UNIVERSITY · PI Sallie R. Permar · 1987 to 2026
$44.1M
Fear Conditioning and Fear Extinction in Anorexia NervosaK23MH115184 · NIMH · UNIVERSITY OF SOUTHERN CALIFORNIA · PI MURRAY, STUART B · 2017 to 2021
$990k
Maintenance of Ideal Cardiovascular Health across the Life Course in WomenK23HL122361 · NHLBI · EMORY UNIVERSITY · PI GOODING, HOLLY CATHERINE · 2015 to 2019
$816k
NHLBI NIH HHS K23 HL122361NICHD NIH HHS K12 HD000850NICHD NIH HHS P01 HD031921NIMH NIH HHS K23 MH115184
6 · The paper itself

Abstract

backgroundLegal performance-enhancing substances (PES), such as creatine, are commonly used by adolescents and young adults. As PES are mostly unregulated by the US Food and Drug Administration, there has been limited empirical attention devoted to examining their long-term safety and health outcomes. Preliminary studies have demonstrated associations between PES use and severe medical events, including hospitalizations and death. PES could be linked to cardiovascular disease (CVD), the most common cause of mortality in the US, by altering the myocardium, vasculature, or metabolism. The objective of this study was to examine prospective associations between the use of legal PES in young adulthood and CVD risk factors at seven-year follow-up. MATERIALS AND

methodsNationally representative longitudinal cohort data from the National Longitudinal Study of Adolescent to Adult Health, Waves III (2001-2002) and IV (2008), were analyzed. Regression models determined the prospective association between the use of legal PES (e.g. creatine monohydrate) and CVD risk factors (e.g. body mass index, diabetes, hypertension, hyperlipidemia), adjusting for relevant covariates.

resultsAmong the diverse sample of 11,996 male and female participants, no significant differences by PES use in body mass index, diabetes, hypertension, or hyperlipidemia were noted at Wave III. In unadjusted comparisons, legal PES users (versus non-users) were more likely to be White, be male, be college educated, drink alcohol, and engage in weightlifting, exercise, individual sports, team sports, and other strength training. There were no significant prospective associations between legal PES use at Wave III and body mass index, hemoglobin A1c, systolic and diastolic blood pressure, and cholesterol (total, HDL, LDL, triglycerides) deciles at seven-year follow-up (Wave IV), adjusting for demographics, health behaviors, and Wave III CVD risk factors. Similarly, there were no significant prospective associations between legal PES use and diabetes, hypertension, or hyperlipidemia based on objective measures or self-reported medications and diagnoses, adjusting for demographics, health behaviors, and Wave III CVD risk.

conclusionsWe do not find evidence for a prospective association between legal PES use and CVD risk factors in young adults over seven years of follow-up, including BMI, diabetes, hypertension, or hyperlipidemia. It should be noted that legal PES use was operationalized dichotomously and as one broad category, which did not account for frequency, amount, or duration of use. Given the lack of regulation and clinical trials data, observational studies can provide much needed data to inform the safety and long-term health associations of legal PES use and, in turn, inform clinical guidance and policy.

Indexed as

AdolescentAdultBlood PressureCardiovascular DiseasesCholesterolCreatineDrug UtilizationExerciseFemaleHemoglobin AHumansLife StyleMalePerformance-Enhancing SubstancesCholesterolCreatineHemoglobin APerformance-Enhancing Substances

Identifiers

PMID33320903
PMCPMC7737961
OpenAlexW3111677383

What OpenQuestion holds

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Registered trials

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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.