Evidence map›Paper›PMID 34424302›Full record

ArticleJAMA network open2021

Ethnic and Racial Variation in Intracerebral Hemorrhage Risk Factors and Risk Factor Burden.

Steven J Kittner, Padmini Sekar, Mary E Comeau, Christopher D Anderson, Gunjan Y Parikh, Tachira Tavarez, Matthew L Flaherty, Fernando D Testai, Michael R Frankel, Michael L James and 22 more

Open access · goldAbstract readComparative Study
In one paragraph

Article in JAMA network open, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 37 papers.

0numbers the graph read from it
0cells of the map it votes in
37citing papers in PubMed
4.1field-weighted citation impact, top 5% 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

37 citing papers in PubMed, 60 citations in OpenAlex.

  1. Article
  2. Genetics of intracerebral hemorrhage.Journal of cerebral blood flow and metabolism : official journal of the International Society of Cerebral Blood Flow and Metabolism · 2026
    Review
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  4. Article
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  10. Review
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  14. Two decades of trends in nontraumatic intracerebral hemorrhage care: A nationwide analysis.Journal of clinical neuroscience : official journal of the Neurosurgical Society of Australasia · 2025
    Article
  15. Observational
  16. Untreated and uncontrolled hypertension in Japanese patients with spontaneous intracerebral hemorrhage.Hypertension research : official journal of the Japanese Society of Hypertension · 2025
    Article
  17. Article
  18. Article
  19. Review
  20. 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

32 authors at 20 institutions in 1 country.

Steven J KittnerGeriatric Research and Education Clinical Center, Department of Neurology, Baltimore Veterans Administration Medical Center, University of Maryland School of Medicine, Baltimore.
Padmini SekarDepartment of Neurology and Rehabilitation Medicine, University of Cincinnati College of Medicine, Cincinnati, Ohio.
Mary E ComeauDepartment of Biostatistics and Data Science, Wake Forest University, Winston-Salem, North Carolina.
Christopher D AndersonHenry and Allison McCance Center for Brain Health and Center for Genomic Medicine, Massachusetts General Hospital, Boston.
Gunjan Y ParikhDepartment of Neurology, University of Maryland School of Medicine, Baltimore.
Tachira TavarezDepartment of Neurological Sciences, Rush University Medical Center, Chicago, Illinois.
Matthew L FlahertyDepartment of Neurology and Rehabilitation Medicine, University of Cincinnati College of Medicine, Cincinnati, Ohio.
Fernando D TestaiDepartment of Neurology and Rehabilitation Medicine, University of Illinois College of Medicine, Chicago, Illinois.
Michael R FrankelDepartment of Neurology, Emory University, Grady Memorial Hospital, Atlanta, Georgia.
Michael L JamesDepartments of Anesthesiology and Neurology, Duke University, Durham, North Carolina.
Gene SungNeurocritical Care and Stroke Division, University of Southern California, Los Angeles.
Mitchell S V ElkindDepartment of Neurology, Vagelos College of Physicians and Surgeons, Columbia University, New York, New York.
Bradford B WorrallDepartments of Neurology and Public Health Sciences, University of Virginia, Charlottesville.
Chelsea S KidwellDepartment of Neurology, University of Arizona-Tucson.
Nicole R GonzalesDepartment of Neurology, McGovern Medical School at UTHealth, Houston, Texas.
Sebastian KochDepartment of Neurology, University of Miami Miller School of Medicine, Miami, Florida.
Christiana E HallDepartment of Neurology and Neurotherapeutics, University of Texas-Southwestern, Dallas.
Lee BirnbaumDepartment of Neurology, University of Texas-San Antonio.
Douglas MaysonDepartment of Neurology, Medstar Georgetown University Hospital, Washington, DC.
Bruce CoullDepartment of Neurology, University of Arizona-Tucson.
Marc D MalkoffDepartment of Neurology and Neurosurgery, University of Tennessee Health Sciences, Memphis.
Kevin N ShethDepartment of Neurology, Yale University, New Haven, Connecticut.
Jacob L McCauleyJohn P. Hussman Institute for Human Genomics, University of Miami Miller School of Medicine, Miami, Florida.
Jennifer OsborneDepartment of Neurology and Rehabilitation Medicine, University of Cincinnati College of Medicine, Cincinnati, Ohio.
Misty MorganDepartment of Neurology and Rehabilitation Medicine, University of Cincinnati College of Medicine, Cincinnati, Ohio.
Lee A GilkersonDepartment of Neurology and Rehabilitation Medicine, University of Cincinnati College of Medicine, Cincinnati, Ohio.
Tyler P BehymerDepartment of Neurology and Rehabilitation Medicine, University of Cincinnati College of Medicine, Cincinnati, Ohio.
Stacie L DemelDepartment of Neurology and Rehabilitation Medicine, University of Cincinnati College of Medicine, Cincinnati, Ohio.
Charles J MoomawDepartment of Neurology and Rehabilitation Medicine, University of Cincinnati College of Medicine, Cincinnati, Ohio.
Jonathan RosandHenry and Allison McCance Center for Brain Health and Center for Genomic Medicine, Massachusetts General Hospital, Boston.
Carl D LangefeldDepartment of Biostatistics and Data Science, Wake Forest University, Winston-Salem, North Carolina.
Daniel WooDepartment of Neurology and Rehabilitation Medicine, University of Cincinnati College of Medicine, Cincinnati, Ohio.
University of Cincinnati Medical Center · USUniversity of Arizona · USUniversity of Maryland, Baltimore · USUniversity of Miami · USWake Forest University · USCenter for Pain and the Brain · USColumbia University · USDuke University · USGrady Memorial Hospital · USMassachusetts General Hospital · USMedStar Georgetown University Hospital · USRush University Medical Center · USThe University of Texas at San Antonio · USThe University of Texas Health Science Center at Houston · USThe University of Texas Southwestern Medical Center · USUniversity of Illinois Chicago · USUniversity of Southern California · USUniversity of Tennessee Health Science Center · USUniversity of Virginia · USYale University · US

Funding

Yale Clinical and Translational Science Award (U Component)UL1TR001863 · NCATS · YALE UNIVERSITY · PI John H. Krystal, LUCILA OHNO-MACHADO · 2016 to 2026
$102.9M
NSTN National Clinical Coordinating CenterU01NS086872 · NINDS · UNIVERSITY OF CINCINNATI · PI Joseph Paul Broderick, Pooja Khatri · 2013 to 2026
$32.3M
Cerebrovascular Fellowship Training ProgramT32NS047996 · NINDS · UNIVERSITY OF CINCINNATI · PI Joseph Paul Broderick, Stacie Demel · 2006 to 2026
$3.7M
Genetics of Early-Onset Ischemic Stroke ConsortiumR01NS105150 · NINDS · UNIVERSITY OF MARYLAND BALTIMORE · PI KITTNER, STEVEN J, MITCHELL, BRAXTON D · 2018 to 2022
$3.0M
NCATS NIH HHS UL1 TR001863NINDS NIH HHS T32 NS047996NINDS NIH HHS U01 NS086872
6 · The paper itself

Abstract

Importance: Black and Hispanic individuals have an increased risk of intracerebral hemorrhage (ICH) compared with their White counterparts, but no large studies of ICH have been conducted in these disproportionately affected populations. Objective: To examine the prevalence, odds, and population attributable risk (PAR) percentage for established and novel risk factors for ICH, stratified by ICH location and racial/ethnic group. Design, Setting, and Participants: The Ethnic/Racial Variations of Intracerebral Hemorrhage Study was a case-control study of ICH among 3000 Black, Hispanic, and White individuals who experienced spontaneous ICH (1000 cases in each group). Recruitment was conducted between September 2009 and July 2016 at 19 US sites comprising 42 hospitals. Control participants were identified through random digit dialing and were matched to case participants by age (±5 years), sex, race/ethnicity, and geographic area. Data analyses were conducted from January 2019 to May 2020. Main Outcomes and Measures: Case and control participants underwent a standardized interview, physical measurement for body mass index, and genotyping for the ɛ2 and ɛ4 alleles of APOE, the gene encoding apolipoprotein E. Prevalence, multivariable adjusted odds ratio (OR), and PAR percentage were calculated for each risk factor in the entire ICH population and stratified by racial/ethnic group and by lobar or nonlobar location. Results: There were 1000 Black patients (median [interquartile range (IQR)] age, 57 [50-65] years, 425 [42.5%] women), 1000 Hispanic patients (median [IQR] age, 58 [49-69] years; 373 [37.3%] women), and 1000 White patients (median [IQR] age, 71 [59-80] years; 437 [43.7%] women). The mean (SD) age of patients with ICH was significantly lower among Black and Hispanic patients compared with White patients (eg, lobar ICH: Black, 62.2 [15.2] years; Hispanic, 62.5 [15.7] years; White, 71.0 [13.3] years). More than half of all ICH in Black and Hispanic patients was associated with treated or untreated hypertension (PAR for treated hypertension, Black patients: 53.6%; 95% CI, 46.4%-59.8%; Hispanic patients: 46.5%; 95% CI, 40.6%-51.8%; untreated hypertension, Black patients: 45.5%; 95% CI, 39.%-51.1%; Hispanic patients: 42.7%; 95% CI, 37.6%-47.3%). Lack of health insurance also had a disproportionate association with the PAR percentage for ICH in Black and Hispanic patients (Black patients: 21.7%; 95% CI, 17.5%-25.7%; Hispanic patients: 30.2%; 95% CI, 26.1%-34.1%; White patients: 5.8%; 95% CI, 3.3%-8.2%). A high sleep apnea risk score was associated with both lobar (OR, 1.68; 95% CI, 1.36-2.06) and nonlobar (OR, 1.62; 95% CI, 1.37-1.91) ICH, and high cholesterol was inversely associated only with nonlobar ICH (OR, 0.60; 95% CI, 0.52-0.70); both had no interactions with race and ethnicity. In contrast to the association between the ɛ2 and ɛ4 alleles of APOE and ICH in White individuals (eg, presence of APOE ɛ2 allele: OR, 1.84; 95% CI, 1.34-2.52), APOE alleles were not associated with lobar ICH among Black or Hispanic individuals. Conclusions and Relevance: This study found sleep apnea as a novel risk factor for ICH. The results suggest a strong contribution from inadequately treated hypertension and lack of health insurance to the disproportionate burden and earlier onset of ICH in Black and Hispanic populations. These findings emphasize the importance of addressing modifiable risk factors and the social determinants of health to reduce health disparities.

Indexed as

Genetic Predisposition to DiseaseAgedBlack or African AmericanCase-Control StudiesCerebral HemorrhageEthnic and Racial MinoritiesEthnicityFemaleHispanic or LatinoHumansMaleMiddle AgedOdds RatioRace FactorsRisk FactorsUnited States

Identifiers

PMID34424302
PMCPMC8383133
OpenAlexW3193664840

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.