Evidence map›Paper›PMID 29710269›Full record

SynthesisJAMA neurology2018

Association of Sickle Cell Trait With Ischemic Stroke Among African Americans: A Meta-analysis.

Hyacinth I Hyacinth, Cara L Carty, Samantha R Seals, Marguerite R Irvin, Rakhi P Naik, Gregory L Burke, Neil A Zakai, James G Wilson, Nora Franceschini, Cheryl A Winkler and 18 more

Open access · bronzeAbstract readMeta-Analysis
In one paragraph

Synthesis in JAMA neurology, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 25 papers, 2 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
25citing papers in PubMed, 2 pooled it
3.3field-weighted citation impact, top 7% 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

25 citing papers in PubMed, 2 syntheses or guidelines pooled it, 32 citations in OpenAlex.

  1. Pooled it
  2. Pooled it
  3. Article
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  8. Article
  9. Review
  10. Article
  11. Article
  12. Review
  13. Review
  14. Article
  15. Unmasking hypertension in children and adolescents with sickle/beta-thalassemia.Journal of clinical hypertension (Greenwich, Conn.) · 2020
    Article
  16. Review
  17. Article
  18. Article
  19. Article
  20. The current state of sickle cell trait: implications for reproductive and genetic counseling.Hematology. American Society of Hematology. Education Program · 2018
    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

28 authors at 20 institutions in 1 country.

Hyacinth I HyacinthAflac Cancer and Blood Disorder Center, Emory Children's Center, Department of Pediatrics, Emory University School of Medicine, Atlanta, Georgia.
Cara L CartyWomen's Health Initiative, Fred Hutchinson Cancer Research Center, Seattle, Washington.
Samantha R SealsDepartment of Mathematics and Statistics, Hal Marcus College of Science and Engineering, University of West Florida, Pensacola.
Marguerite R IrvinDepartment of Epidemiology, School of Public Health, University of Alabama at Birmingham, Birmingham.
Rakhi P NaikDivision of Hematology, Department of Medicine, Johns Hopkins University, Baltimore, Maryland.
Gregory L BurkeDivision of Public Health Science, Wake Forest University, Winston-Salem, North Carolina.
Neil A ZakaiDepartment of Medicine, Larner College of Medicine at the University of Vermont, Burlington.
James G WilsonDepartment of Physiology and Biophysics, University of Mississippi Medical Center, Jackson.
Nora FranceschiniDepartment of Nephrology, University of North Carolina, Chapel Hill.
Cheryl A WinklerBasic Science Laboratory, Frederick National Laboratory for Cancer Research, Leidos Biomedical Research, National Cancer Institute, Frederick, Maryland.
Victor A DavidBasic Science Laboratory, Frederick National Laboratory for Cancer Research, Leidos Biomedical Research, National Cancer Institute, Frederick, Maryland.
Jeffrey B KoppNational Institute of Diabetes, Digestive, and Kidney Diseases, National Institutes of Health, Bethesda, Maryland.
Suzanne E JuddDepartment of Epidemiology, School of Public Health, University of Alabama at Birmingham, Birmingham.
Robert J AdamsStroke Center, Department of Neurology, Medical University of South Carolina, Charleston.
W T LongstrethDepartments of Neurology and Epidemiology, University of Washington, Seattle.
Leonard EgedeDivision of General Internal Medicine, Medical College of Wisconsin, Milwaukee.
Daniel T LacklandStroke Center, Department of Neurology, Medical University of South Carolina, Charleston.
Herman TaylorCardiovascular Research Institute, Morehouse School of Medicine, Atlanta, Georgia.
JoAnn E MansonBrigham and Women's Hospital, Harvard Medical School, Boston, Massachusetts.
Virginia HowardDepartment of Epidemiology, School of Public Health, University of Alabama at Birmingham, Birmingham.
Matthew AllisonDivision of Preventive Medicine, Department of Family Medicine and Public Health, University of California, San Diego.
Beatrice E GeeDepartment of Pediatrics, Morehouse School of Medicine, Atlanta, Georgia.
Adolfo CorreaJackson Heart Study, University of Mississippi Medical Center, Jackson.
Monika M SaffordDivision of General Internal Medicine, Weill Cornell Medicine, New York, New York.
Donna K ArnettCollege of Public Health, University of Kentucky College of Public Health, Lexington.
George HowardDepartment of Biostatistics, School of Public Health, University of Alabama at Birmingham, Birmingham.
Alexander P ReinerFred Hutchinson Cancer Research Center, University of Washington, Seattle.
Mary CushmanDepartment of Medicine, Larner College of Medicine at the University of Vermont, Burlington.
University of Alabama at Birmingham · USJackson Memorial Hospital · USLeidos (United States) · USMedical University of South Carolina · USMorehouse School of Medicine · USUniversity of Vermont · USCornell University · USEmory University · USFred Hutch Cancer Center · USHarvard University · USJohns Hopkins Medicine · USMedical College of Wisconsin · USNational Institute of Diabetes and Digestive and Kidney Diseases · USUniversity of California, San Diego · USUniversity of Kentucky · USUniversity of North Carolina at Chapel Hill · USUniversity of Washington · USUniversity of West Florida · USWake Forest University · USWomen's Health Initiative · US

Funding

VCID and Stroke in a Bi-racial National CohortU01NS041588 · NINDS · UNIVERSITY OF ALABAMA AT BIRMINGHAM · PI CUSHMAN, MARY, HOWARD, GEORGE · 2002 to 2022
$96.0M
Institute for Clinical and Translational ResearchUL1TR001079 · NCATS · JOHNS HOPKINS UNIVERSITY · PI FORD, DANIEL ERNEST · 2013 to 2017
$60.1M
Tracking and Evaluation CoreU54GM115428 · NIGMS · UNIVERSITY OF MISSISSIPPI MED CTR · PI HALL, JOHN E · 2016 to 2025
$38.2M
UNC-CH CENTER FOR ENVIRONMENTAL HEALTH &SUSCEPTIBILITYP30ES010126 · NIEHS · UNIV OF NORTH CAROLINA CHAPEL HILL · PI Melissa A. Troester · 2001 to 2026
$36.3M
Role of obesity in preeclamptic pregnancy.P20GM121334 · NIGMS · UNIVERSITY OF MISSISSIPPI MED CTR · PI Pier Paolo Claudio, Babbette LaMarca · 2017 to 2026
$26.4M
Clinical and Translational Science AwardUL1TR000040 · NCATS · COLUMBIA UNIVERSITY HEALTH SCIENCES · PI GINSBERG, HENRY N · 2012 to 2015
$26.2M
SUBCLINICAL CARDIOVASCULAR DISEASE COORDINATING CENTERN01HC95159 · NHLBI · UNIVERSITY OF WASHINGTON · PI KRONMAL, RICHARD A · 2007 to 2014
$19.6M
Focal Segmental Glomerulosclerosis: Genetics & MechanismsZIADK043308 · NIDDK · NATIONAL INSTITUTE OF DIABETES AND DIGESTIVE AND KIDNEY DISEASES · PI KOPP, JEFFREY BURNETT · 2009 to 2024
$15.7M
REGARDS - MI StudyR01HL080477 · NHLBI · WEILL MEDICAL COLL OF CORNELL UNIV · PI LEVITAN, EMILY B, SAFFORD, MONIKA M · 2006 to 2020
$11.6M
Cellular and Molecular Mechanisms of Acute Lung Injury in Sickle Cell DiseaseU01HL117721 · NHLBI · EMORY UNIVERSITY · PI DEBAUN, MICHAEL R., JOINER, CLINTON H · 2013 to 2017
$9.4M
Genetics of Renal Disease in African AmericansZIABC010022 · NCI · DIVISION OF BASIC SCIENCES - NCI · PI WINKLER, CHERYL · 2009 to 2022
$8.9M
SUBCLINICAL CARDIOVASCULAR DISEASE STUDY--FIELD CENTERN01HC95160 · NHLBI · UNIVERSITY OF CALIFORNIA LOS ANGELES · PI WATSON, KAROL · 2007 to 2015
$7.7M
NCATS NIH HHS UL1 TR000040NCATS NIH HHS UL1 TR001079NHLBI NIH HHS HHSN268201100046CNHLBI NIH HHS HHSN268201300046CNHLBI NIH HHS HHSN268201300047CNHLBI NIH HHS HHSN268201300048CNHLBI NIH HHS HHSN268201300049CNHLBI NIH HHS HHSN268201300050CNHLBI NIH HHS K08 HL096841NHLBI NIH HHS K08 HL125100NHLBI NIH HHS N01HC95159NHLBI NIH HHS N01HC95160NHLBI NIH HHS N01HC95161NHLBI NIH HHS N01HC95162NHLBI NIH HHS N01HC95163NHLBI NIH HHS N01HC95164NHLBI NIH HHS N01HC95165NHLBI NIH HHS N01HC95166NHLBI NIH HHS N01HC95167NHLBI NIH HHS N01HC95168NHLBI NIH HHS N01HC95169NHLBI NIH HHS R01 HL080477NHLBI NIH HHS R01 HL130733NHLBI NIH HHS R01 HL132947NHLBI NIH HHS R01 HL136574NHLBI NIH HHS R01 HL138423NHLBI NIH HHS R21 HL123677NHLBI NIH HHS U01 HL117721NIA NIH HHS HHSN271201100004CNIDDK NIH HHS R01 DK117445NIDDK NIH HHS R56 DK104806NIEHS NIH HHS P30 ES010126NIGMS NIH HHS P20 GM121334NIGMS NIH HHS U54 GM115428NIH HHS HHSN263201500003INIMHD NIH HHS R01 MD012765NINDS NIH HHS U01 NS041588WHI NIH HHS HHSN268201100001CWHI NIH HHS HHSN268201100002CWHI NIH HHS HHSN268201100003CWHI NIH HHS HHSN268201100004C
6 · The paper itself

Abstract

Importance: African Americans and individuals of African ancestry have a higher risk of stroke compared with non-Hispanic white individuals. Identifying the source of this disparity could provide an opportunity for clinical stroke risk stratification and more targeted therapy. Whether sickle cell trait (SCT) is an indicator of increased risk of ischemic stroke among African Americans is still unclear. Objective: To examine whether SCT is associated with a higher risk of incident ischemic stroke among African Americans. Design, Setting, and Participants: This meta-analysis assessed the association of SCT with the risk of incident ischemic stroke. Four large, prospective, population-based studies with African American cohorts were assessed: Jackson Heart Study (September 1, 2005, through December 31, 2012), Multi-Ethnic Study of Atherosclerosis (July 1, 2002, through December 31, 2012), Reasons for Geographic and Racial Differences in Stroke (January 1, 2003, through December 31, 2014), and Women's Health Initiative (October 1, 1998, through December 31, 2012). Using a Cox proportional hazards regression model adjusted for major stroke risk factors, this study estimated the hazard ratio for incident ischemic stroke associated with SCT. Data analysis was performed from July 10, 2016, to February 2, 2017. Interventions or Exposures: Participants' SCT status determined by polymerase chain reaction assay genotyping or a combination of whole-exome sequencing and imputation. Main Outcomes and Measures: Incident ischemic stroke. Results: This meta-analysis included 19 464 African American individuals (1520 with SCT, 17 944 without SCT, and 620 with ischemic stroke) from 4 studies, with a mean (SD) age of 60.0 (13.0) years (5257 [27.0%] men and 14 207 [73.0%] women). No differences were found in the distribution of risk factors for ischemic stroke comparing participants with and those without SCT at study visit 1 in each cohort. The crude incidence of ischemic stroke was 2.9 per 1000 person-years (95% CI, 2.2-4.0 per 1000 person-years) among those with SCT and 3.2 per 1000 person-years (95% CI, 2.7-3.8 per 1000 person-years) among those without SCT. After stroke risk factors were adjusted for, the hazard ratio of incident ischemic stroke independently associated with SCT in the meta-analysis of all 4 cohorts was 0.80 (95% CI, 0.47-1.35; P = .82). The results of the meta-analysis were similar to those of individual cohorts, in which the results were also similar. Conclusions and Relevance: Sickle cell trait may not be associated with incidence of ischemic stroke among African Americans. The results of this study suggest performing a more thorough clinical evaluation of a stroke patient with SCT rather than assuming that SCT is the etiologic factor for the stroke.

Indexed as

AgedBlack or African AmericanBrain IschemiaFemaleHemoglobinsHeterozygoteHumansIncidenceMaleMiddle AgedMutationSickle Cell TraitStrokeUnited StatesHemoglobins

Identifiers

PMID29710269
PMCPMC6145767
OpenAlexW2802853072

What OpenQuestion holds

Textmetadata
Read underepoch 390

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.