Evidence map›Paper›PMID 20644109›Full record

ArticleBlood2010

RH genotyping in a sickle cell disease patient contributing to hematopoietic stem cell transplantation donor selection and management.

Ross M Fasano, Alessandro Monaco, Emily Riehm Meier, Philippe Pary, A Hallie Lee-Stroka, John Otridge, Harvey G Klein, Francesco M Marincola, Naynesh R Kamani, Naomi L C Luban and 2 more

Open access · bronzeAbstract readCase Reports
In one paragraph

Article in Blood, 2010. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 27 papers.

0numbers the graph read from it
0cells of the map it votes in
27citing papers in PubMed
1.3field-weighted citation impact, top 20% 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

27 citing papers in PubMed, 46 citations in OpenAlex.

  1. Trial
  2. Article
  3. Article
  4. Article
  5. DNA Reference Reagents for Genotyping RH Variants.The Journal of molecular diagnostics : JMD · 2024
    Article
  6. Article
  7. Article
  8. Article
  9. Transfusion support for a woman withImmunohematology · 2022
    Article
  10. Article
  11. Proceed with care: the "uncommon" serologic weak D phenotypes.Blood transfusion = Trasfusione del sangue · 2021
    Article
  12. Article
  13. First Korean Case of Partial DAnnals of laboratory medicine · 2020
    Article
  14. Review
  15. Red Cell Transfusions in the Genomics Era.Seminars in hematology · 2019
    Review
  16. Article
  17. Article
  18. Article
  19. Observational
  20. Red cell genotyping precision medicine: a conference summary.Therapeutic advances in hematology · 2017
    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 2 institutions in 1 country.

Ross M FasanoChildren's National Medical Center, Washington, DC, USA.
Alessandro Monaco
Emily Riehm Meier
Philippe Pary
A Hallie Lee-Stroka
John Otridge
Harvey G Klein
Francesco M Marincola
Naynesh R Kamani
Naomi L C Luban
David Stroncek
Willy A Flegel
National Institutes of Health · USChildren's National · US

Funding

Structure and Function Granulocyte AntigensZIACL002095 · CLC · CLINICAL CENTER · PI STRONCEK, DAVID · 2009 to 2015
$0k
Immunogenetics of Vaccine TherapyZIACL002115 · CLC · CLINICAL CENTER · PI MARINCOLA, FRANCESCO M · 2009 to 2010
$0k
Immunogenetic Study of Infectious Diseases and CancerZIACL002118 · CLC · CLINICAL CENTER · PI MARINCOLA, FRANCESCO M · 2009 to 2012
$0k
Molecular Immunohematology in Ethiopian Sub-populationsZIACL002123 · CLC · CLINICAL CENTER · PI FLEGEL, WILLY · 2012 to 2025
$0k
6 · The paper itself

Abstract

African individuals harbor molecular RH variants, which permit alloantibody formation to high-prevalence Rh antigens after transfusions. Genotyping identifies such RH variants, which are often missed by serologic blood group typing. Comprehensive molecular blood group analysis using 3 genotyping platforms, nucleotide sequencing, and serologic evaluation was performed on a 7-year-old African male with sickle cell disease who developed an "e-like" antibody shortly after initiating monthly red blood cell (RBC) transfusions for silent stroke. Genotyping of the RH variant predicted a severe shortage of compatible RBCs for long-term transfusion support, which contributed to the decision for hematopoetic stem cell transplantation. RH genotyping confirmed the RH variant in the human leukocyte antigen-matched sibling donor. The patient's (C)ce(s) type 1 haplotype occurs in up to 11% of African American sickle cell disease patients; however, haplotype-matched RBCs were serologically incompatible. This case documents that blood unit selection should be based on genotype rather than one matching haplotype.

Indexed as

Hematopoietic Stem Cell TransplantationAnemia, Sickle CellBlack or African AmericanChildDonor SelectionErythrocyte TransfusionGenotypeHumansMalePolymorphism, GeneticRh-Hr Blood-Group SystemRh-Hr Blood-Group System

Identifiers

PMID20644109
PMCPMC2974591
OpenAlexW2000881443

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.