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Ethnic and Racial Variation in Intracerebral Hemorrhage Risk Factors and Risk Factor Burden.
Kittner, Steven J; Sekar, Padmini; Comeau, Mary E; Anderson, Christopher D; Parikh, Gunjan Y; Tavarez, Tachira; Flaherty, Matthew L; Testai, Fernando D; Frankel, Michael R; James, Michael L; Sung, Gene; Elkind, Mitchell S V; Worrall, Bradford B; Kidwell, Chelsea S; Gonzales, Nicole R; Koch, Sebastian; Hall, Christiana E; Birnbaum, Lee; Mayson, Douglas; Coull, Bruce; Malkoff, Marc D; Sheth, Kevin N; McCauley, Jacob L; Osborne, Jennifer; Morgan, Misty; Gilkerson, Lee A; Behymer, Tyler P; Demel, Stacie L; Moomaw, Charles J; Rosand, Jonathan; Langefeld, Carl D; Woo, Daniel.
Afiliação
  • Kittner SJ; Geriatric Research and Education Clinical Center, Department of Neurology, Baltimore Veterans Administration Medical Center, University of Maryland School of Medicine, Baltimore.
  • Sekar P; Department of Neurology and Rehabilitation Medicine, University of Cincinnati College of Medicine, Cincinnati, Ohio.
  • Comeau ME; Department of Biostatistics and Data Science, Wake Forest University, Winston-Salem, North Carolina.
  • Anderson CD; Henry and Allison McCance Center for Brain Health and Center for Genomic Medicine, Massachusetts General Hospital, Boston.
  • Parikh GY; Department of Neurology, University of Maryland School of Medicine, Baltimore.
  • Tavarez T; Department of Neurological Sciences, Rush University Medical Center, Chicago, Illinois.
  • Flaherty ML; Department of Neurology and Rehabilitation Medicine, University of Cincinnati College of Medicine, Cincinnati, Ohio.
  • Testai FD; Department of Neurology and Rehabilitation Medicine, University of Illinois College of Medicine, Chicago, Illinois.
  • Frankel MR; Department of Neurology, Emory University, Grady Memorial Hospital, Atlanta, Georgia.
  • James ML; Departments of Anesthesiology and Neurology, Duke University, Durham, North Carolina.
  • Sung G; Neurocritical Care and Stroke Division, University of Southern California, Los Angeles.
  • Elkind MSV; Department of Neurology, Vagelos College of Physicians and Surgeons, Columbia University, New York, New York.
  • Worrall BB; Department of Epidemiology, Mailman School of Public Health, Columbia University, New York, New York.
  • Kidwell CS; Departments of Neurology and Public Health Sciences, University of Virginia, Charlottesville.
  • Gonzales NR; Department of Neurology, University of Arizona-Tucson.
  • Koch S; Department of Neurology, McGovern Medical School at UTHealth, Houston, Texas.
  • Hall CE; Department of Neurology, University of Miami Miller School of Medicine, Miami, Florida.
  • Birnbaum L; Department of Neurology and Neurotherapeutics, University of Texas-Southwestern, Dallas.
  • Mayson D; Department of Neurology, University of Texas-San Antonio.
  • Coull B; Department of Neurology, Medstar Georgetown University Hospital, Washington, DC.
  • Malkoff MD; Department of Neurology, University of Arizona-Tucson.
  • Sheth KN; Department of Neurology and Neurosurgery, University of Tennessee Health Sciences, Memphis.
  • McCauley JL; Department of Neurology, Yale University, New Haven, Connecticut.
  • Osborne J; John P. Hussman Institute for Human Genomics, University of Miami Miller School of Medicine, Miami, Florida.
  • Morgan M; Department of Neurology and Rehabilitation Medicine, University of Cincinnati College of Medicine, Cincinnati, Ohio.
  • Gilkerson LA; Department of Neurology and Rehabilitation Medicine, University of Cincinnati College of Medicine, Cincinnati, Ohio.
  • Behymer TP; Department of Neurology and Rehabilitation Medicine, University of Cincinnati College of Medicine, Cincinnati, Ohio.
  • Demel SL; Department of Neurology and Rehabilitation Medicine, University of Cincinnati College of Medicine, Cincinnati, Ohio.
  • Moomaw CJ; Department of Neurology and Rehabilitation Medicine, University of Cincinnati College of Medicine, Cincinnati, Ohio.
  • Rosand J; Department of Neurology and Rehabilitation Medicine, University of Cincinnati College of Medicine, Cincinnati, Ohio.
  • Langefeld CD; Henry and Allison McCance Center for Brain Health and Center for Genomic Medicine, Massachusetts General Hospital, Boston.
  • Woo D; Department of Biostatistics and Data Science, Wake Forest University, Winston-Salem, North Carolina.
JAMA Netw Open ; 4(8): e2121921, 2021 08 02.
Article em En | MEDLINE | ID: mdl-34424302
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.
Assuntos

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Etnicidade / Hemorragia Cerebral / Predisposição Genética para Doença / Fatores Raciais / Minorias Étnicas e Raciais Tipo de estudo: Etiology_studies / Observational_studies / Prognostic_studies / Risk_factors_studies Limite: Aged / Female / Humans / Male / Middle aged País/Região como assunto: America do norte Idioma: En Revista: JAMA Netw Open Ano de publicação: 2021 Tipo de documento: Article

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Etnicidade / Hemorragia Cerebral / Predisposição Genética para Doença / Fatores Raciais / Minorias Étnicas e Raciais Tipo de estudo: Etiology_studies / Observational_studies / Prognostic_studies / Risk_factors_studies Limite: Aged / Female / Humans / Male / Middle aged País/Região como assunto: America do norte Idioma: En Revista: JAMA Netw Open Ano de publicação: 2021 Tipo de documento: Article