Evidence map›Paper›PMID 34581772›Full record

ArticleBlood advances2021

Impact of sickle cell trait on morbidity and mortality from SARS-CoV-2 infection.

Lauren E Merz, Kavita Mistry, Donna Neuberg, Revital Freedman, Gerda Menard, David M Dorfman, Hae Soo Park, Katherine Jolley, Maureen O Achebe

Open access · goldAbstract read
In one paragraph

Article in Blood advances, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 9 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
9citing papers in PubMed, 1 pooled it
1.7field-weighted citation impact, top 16% 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

9 citing papers in PubMed, 1 synthesis or guideline pooled it, 13 citations in OpenAlex.

  1. Pooled it
  2. Article
  3. Article
  4. Article
  5. Article
  6. COVID-19 outcomes in sickle cell disease and sickle cell trait.Best practice & research. Clinical haematology · 2022
    Review
  7. Review
  8. Article
  9. 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

9 authors at 2 institutions in 1 country.

Lauren E MerzDepartment of Internal Medicine, Brigham and Women's Hospital, Boston, MA.
Kavita MistryDepartment of Internal Medicine, Brigham and Women's Hospital, Boston, MA.
Donna NeubergDepartment of Data Science, Dana-Farber Cancer Institute, Boston, MA.
Revital FreedmanDivision of Hematology, Department of Internal Medicine, and.
Gerda MenardDepartment of Pathology, Brigham and Women's Hospital, Boston, MA; and.
David M DorfmanDepartment of Pathology, Brigham and Women's Hospital, Boston, MA; and.
Hae Soo ParkDivision of Hematology, Department of Internal Medicine, and.
Katherine JolleyDivision of Hematology, Department of Internal Medicine, and.
Maureen O AchebeDivision of Hematology, Department of Internal Medicine, and.
Brigham and Women's Hospital · USDana-Farber Cancer Institute · US

Funding

Novel Cilia Trafficking MechanismsR01DK084725 · NIDDK · UNIVERSITY OF MICHIGAN AT ANN ARBOR · PI MARGOLIS, BENJAMIN L · 2009 to 2010
$702k
NIDDK NIH HHS R01 DK084725
6 · The paper itself

Abstract

The COVID-19 pandemic has highlighted racial health disparities within the United States. Although social determinants of health are the most likely drivers of this disparity, it is possible that genetic traits enriched in the black population like sickle cell trait (SCT) could worsen the morbidity and mortality of infection with severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2). Patients admitted for SARS-CoV-2 infection who identified as black or African American were included in the study (n = 166). Blood remnants were tested for SCT, and clinical data were abstracted from the chart. There was no difference in mortality between those with SCT and those without. There was no difference in respiratory complications between groups, but those without SCT had a much higher burden of chronic lung disease (P = .004). Those with SCT had higher creatinine on admission (P = .004), but no difference in in-hospital renal complications (P = .532). Notably, 12% of the cohort had SCT, which is higher than the expected 7.31% (P = .025). Our study did not show any evidence of increased end organ damage, morbidity, or mortality from SARS-CoV-2 infection among patients with SCT but did show differences in admission creatinine and preexisting lung disease.

Indexed as

COVID-19Sickle Cell TraitHumansMorbidityPandemicsSARS-CoV-2United States

Identifiers

PMID34581772
PMCPMC8479384
OpenAlexW3097890649

What OpenQuestion holds

Textmetadata
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 OpenQuestion graph.