Evidence map›Paper›PMID 27136427›Full record

ArticleBlood transfusion = Trasfusione del sangue2017

Genotyping approach for non-invasive foetal RHD detection in an admixed population.

Carolina Trucco Boggione, Melina E Luján Brajovich, Stella M Mattaloni, René A Di Mónaco, Silvia E García Borrás, Claudia S Biondi, Carlos M Cotorruelo

Abstract read
In one paragraph

Article in Blood transfusion = Trasfusione del sangue, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 12 papers.

0numbers the graph read from it
0cells of the map it votes in
12citing papers in PubMed
2.3field-weighted citation impact, top 11% 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

12 citing papers in PubMed, 19 citations in OpenAlex.

  1. Trial
  2. Article
  3. Noninvasive fetal blood group antigen genotyping.Blood transfusion = Trasfusione del sangue · 2025
    Review
  4. Article
  5. Review
  6. Article
  7. Article
  8. Establishment of the first platelet-donor registry in Argentina.Blood transfusion = Trasfusione del sangue · 2020
    Article
  9. Usefulness of Non-Invasive Fetal RHD Genotyping towards Immunoprophylaxis Optimization.Transfusion medicine and hemotherapy : offizielles Organ der Deutschen Gesellschaft fur Transfusionsmedizin und Immunhamatologie · 2018
    Article
  10. Transfusion Medicine and Molecular Genetic Methods.International journal of preventive medicine · 2018
    Review
  11. Article
  12. Non-invasive foetal RhD genotyping in admixed populations.Blood transfusion = Trasfusione del sangue · 2017
    Article
4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

7 authors at 1 institution in 1 country.

Carolina Trucco BoggioneInstituto de Inmunología Clínica y Experimental Rosario-Consejo Nacional de Investigaciones Científicas y Tecnicas (IDICER-CONICET), Rosario, Argentina.
Melina E Luján BrajovichInstituto de Inmunología Clínica y Experimental Rosario-Consejo Nacional de Investigaciones Científicas y Tecnicas (IDICER-CONICET), Rosario, Argentina.
Stella M MattaloniInstituto de Inmunología Clínica y Experimental Rosario-Consejo Nacional de Investigaciones Científicas y Tecnicas (IDICER-CONICET), Rosario, Argentina.
René A Di MónacoFacultad de Medicina, Universidad Nacional de Rosario, Rosario, Argentina.
Silvia E García BorrásLaboratorio de Inmunohematologia, Facultad de Ciencias Bioquimicas y Farmacéuticas, Rosario, Argentina.
Claudia S BiondiLaboratorio de Inmunohematologia, Facultad de Ciencias Bioquimicas y Farmacéuticas, Rosario, Argentina.
Carlos M CotorrueloInstituto de Inmunología Clínica y Experimental Rosario-Consejo Nacional de Investigaciones Científicas y Tecnicas (IDICER-CONICET), Rosario, Argentina.
National University of Rosario · AR

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundNon-invasive foetal RHD genotyping can predict haemolytic disease of the foetus and the newborn in pregnancies with anti-D alloantibodies and also avoid antenatal anti-D prophylaxis in pregnant women carrying an RHD negative foetus. Considering that the Argentine genetic background is the result of generations of intermixing between several ethnic groups, we evaluated the diagnostic performance of a non-invasive foetal RHD determination strategy to guide targeted antenatal RhD immunoprophylaxis. This algorithm is based on the analysis of four regions of the RHD gene in cell-free foetal DNA in maternal plasma and maternal and paternal RHD genotyping. MATERIALS AND

methodsDNA from 298 serologically D negative pregnant women between 19-28 weeks gestation were RHD genotyped. Foetal RHD status was determined by real-time PCR in 296 maternal plasma samples. In particular cases, RHDΨ and RHD-CE-D

resultsOf the 298 maternal samples, 288 were D-/RHD- and 10 D-/RHD+ (2 RHD*DAR; 5 RHD-CE-D DISCUSSION: The protocol used for non-invasive prenatal RHD genotyping proved to be suitable to determine foetal RHD status in our admixed population. The knowledge of the genetic background of the population under study and maternal and paternal molecular analysis can reduce the number of inconclusive results when investigating foetal RHD status.

Indexed as

DNAFemaleFetal BloodFetusGenetic VariationGenotypeGenotyping TechniquesGestational AgeHumansImmunotherapyMalePregnancyPrenatal DiagnosisRh-Hr Blood-Group SystemDNARh-Hr Blood-Group System

Identifiers

PMID27136427
PMCPMC5269430
OpenAlexW2461239228

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.