Evidence mapPaperPMID 38445515Full record

ArticleJournal of the American Heart Association2024

Dyslipidemia in American Indian Adolescents and Young Adults: Strong Heart Family Study.

Jessica A Reese, Mary J Roman, Jason F Deen, Tauqeer Ali, Shelley A Cole, Richard B Devereux, Amanda M Fretts, Wm James Howard, Elisa T Lee, Kimberly Malloy and 2 more

Open access · goldAbstract readMulticenter Study
In one paragraph

Article in Journal of the American Heart Association, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 18 papers.

0numbers the graph read from it
0cells of the map it votes in
18citing papers in PubMed
7.2field-weighted citation impact, top 2% 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

18 citing papers in PubMed, 18 citations in OpenAlex.

  1. Review
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  15. Cardiovascular Disease Risk Factors in the Native American Population.Journal of cardiovascular development and disease · 2025
    Review
  16. Article
  17. Article
  18. Intersectionality and Social Drivers of Health in Cardiovascular Care.Methodist DeBakey cardiovascular journal · 2024
    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

12 authors at 5 institutions in 1 country.

Jessica A ReeseCenter for American Indian Health Research, Department of Biostatistics and Epidemiology, Hudson College of Public Health University of Oklahoma Health Sciences Center Oklahoma City OK USA.ORCID 0000-0002-6640-6543
Mary J RomanWeill Cornell Medicine New York NY USA.ORCID 0000-0003-0183-6769
Jason F DeenDepartments of Pediatrics and Medicine University of Washington Seattle WA USA.
Tauqeer AliCenter for American Indian Health Research, Department of Biostatistics and Epidemiology, Hudson College of Public Health University of Oklahoma Health Sciences Center Oklahoma City OK USA.ORCID 0000-0002-9176-879X
Shelley A ColePopulation Health Texas Biomedical Research Institute San Antonio TX USA.ORCID 0000-0002-2651-0127
Richard B DevereuxWeill Cornell Medicine New York NY USA.
Amanda M FrettsDepartment of Epidemiology University of Washington Seattle WA USA.ORCID 0000-0002-5358-2345
Wm James HowardGeorgetown-Howard Universities Center for Clinical and Translational Science Washington DC USA.
Elisa T LeeCenter for American Indian Health Research, Department of Biostatistics and Epidemiology, Hudson College of Public Health University of Oklahoma Health Sciences Center Oklahoma City OK USA.ORCID 0000-0003-1826-3602
Kimberly MalloyCenter for American Indian Health Research, Department of Biostatistics and Epidemiology, Hudson College of Public Health University of Oklahoma Health Sciences Center Oklahoma City OK USA.
Jason G UmansMedStar Health Research Institute Hyattsville MD USA.ORCID 0000-0002-2746-3350
Ying ZhangCenter for American Indian Health Research, Department of Biostatistics and Epidemiology, Hudson College of Public Health University of Oklahoma Health Sciences Center Oklahoma City OK USA.ORCID 0000-0001-6945-3743
University of Oklahoma Health Sciences Center · USCornell University · USGeorgetown-Howard Universities Center for Clinical and Translational Science · USUniversity of Washington · USTexas Biomedical Research Institute · US

Funding

The Southwest National Primate Research CenterP51OD011133 · TEXAS BIOMEDICAL RESEARCH INSTITUTE · 2025 to 2025
$7.5M
STRONG HEART STUDY (SHS)- COORDINATING CENTER (CC)- TASK ORDER 00175N92019D00027 · UNIVERSITY OF OKLAHOMA HLTH SCIENCES CTR · 2025 to 2025
$1.9M
NHLBI NIH HHS 75N92019D00027NIH HHS P51 OD011133
6 · The paper itself

Abstract

backgroundAlthough many studies on the association between dyslipidemia and cardiovascular disease (CVD) exist in older adults, data on the association among adolescents and young adults living with disproportionate burden of cardiometabolic disorders are scarce. METHODS AND

resultsThe SHFS (Strong Heart Family Study) is a multicenter, family-based, prospective cohort study of CVD in an American Indian populations, including 12 communities in central Arizona, southwestern Oklahoma, and the Dakotas. We evaluated SHFS participants, who were 15 to 39 years old at the baseline examination in 2001 to 2003 (n=1440). Lipids were measured after a 12-hour fast. We used carotid ultrasounds to detect plaque at baseline and follow-up in 2006 to 2009 (median follow-up=5.5 years). We identified incident CVD events through 2020 with a median follow-up of 18.5 years. We used shared frailty proportional hazards models to assess the association between dyslipidemia and subclinical or clinical CVD, while controlling for covariates. Baseline dyslipidemia prevalence was 55.2%, 73.6%, and 78.0% for participants 15 to 19, 20 to 29, and 30 to 39 years old, respectively. Approximately 2.8% had low-density lipoprotein cholesterol ≥160 mg/dL, which is higher than the recommended threshold for lifestyle or medical interventions in young adults of 20 to 39 years old. During follow-up, 9.9% had incident plaque (109/1104 plaque-free participants with baseline and follow-up ultrasounds), 11.0% had plaque progression (128/1165 with both baseline and follow-up ultrasounds), and 9% had incident CVD (127/1416 CVD-free participants at baseline). Plaque incidence and progression were higher in participants with total cholesterol ≥200 mg/dL, low-density lipoprotein cholesterol ≥160 mg/dL, or non-high-density lipoprotein cholesterol ≥130 mg/dL, while controlling for covariates. CVD risk was independently associated with low-density lipoprotein cholesterol ≥160 mg/dL.

conclusionsDyslipidemia is a modifiable risk factor that is associated with both subclinical and clinical CVD, even among the younger American Indian population who have unexpectedly high rates of significant CVD events. Therefore, this population is likely to benefit from a variety of evidence-based interventions including screening, educational, lifestyle, and guideline-directed medical therapy at an early age.

Indexed as

Cardiovascular DiseasesDyslipidemiasPlaque, AtheroscleroticAdolescentAdultAmerican Indian or Alaska NativeCholesterolHumansLipoproteins, LDLProspective StudiesRisk FactorsYoung AdultCholesterolLipoproteins, LDLadolescentAmerican Indianatherosclerosiscardiovascular diseasedyslipidemiaStrong Heart Family Studyyoung adult

Identifiers

PMID38445515
PMCPMC11010025
OpenAlexW4392509459

What Socratic holds

Textmetadata
LicenceCC BY-NC-ND
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.