Evidence map›Paper›PMID 28792998›Full record

ArticleClinics (Sao Paulo, Brazil)2017

Validation of QF-PCR for prenatal diagnoses in a Brazilian population.

Renata Wendel de Moraes, Mario Henrique Burlacchini de Carvalho, Antonio Gomes de Amorim-Filho, Rossana Pulcineli Vieira Francisco, Renata Moscolini Romão, José Eduardo Levi, Marcelo Zugaib

Abstract readComparative StudyValidation Study
In one paragraph

Article in Clinics (Sao Paulo, Brazil), 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 7 papers.

0numbers the graph read from it
0cells of the map it votes in
7citing papers in PubMed
–field-weighted citation impact
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

7 citing papers in PubMed.

  1. Article
  2. Review
  3. Article
  4. Review
  5. Article
  6. Article
  7. Graft versus host disease and microchimerism in aAllergy, asthma, and clinical immunology : official journal of the Canadian Society of Allergy and Clinical Immunology · 2019
    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

7 authors.

Renata Wendel de MoraesDepartamento de Ginecologia e Obstetrícia, Faculdade de Medicina FMUSP, Universidade de São Paulo, São Paulo, SP, BR.
Mario Henrique Burlacchini de CarvalhoDepartamento de Ginecologia e Obstetrícia, Faculdade de Medicina FMUSP, Universidade de São Paulo, São Paulo, SP, BR.
Antonio Gomes de Amorim-FilhoDepartamento de Ginecologia e Obstetrícia, Faculdade de Medicina FMUSP, Universidade de São Paulo, São Paulo, SP, BR.
Rossana Pulcineli Vieira FranciscoDepartamento de Ginecologia e Obstetrícia, Faculdade de Medicina FMUSP, Universidade de São Paulo, São Paulo, SP, BR.
Renata Moscolini RomãoDepartamento de Ginecologia e Obstetrícia, Faculdade de Medicina FMUSP, Universidade de São Paulo, São Paulo, SP, BR.
José Eduardo LeviFundação Pró-Sangue, Hemocentro de São Paulo, SP, BR.
Marcelo ZugaibDepartamento de Ginecologia e Obstetrícia, Faculdade de Medicina FMUSP, Universidade de São Paulo, São Paulo, SP, BR.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

objectives: Quantitative fluorescence polymerase chain reaction (QF-PCR) is a rapid and reliable method for screening aneuploidies, but in Brazil, it is not used in public services. We investigated the accuracy of QF-PCR for the prenatal recognition of common aneuploidies and compared these results with cytogenetic results in our laboratory.

method: A ChromoQuant QF-PCR kit containing 24 primer pairs targeting loci on chromosomes 21, 13, 18, X and Y was employed to identify aneuploidies of the referred chromosomes.

results: A total of 162 amniotic fluid samples analyzed using multiplex QF-PCR were compared with karyotyping analysis. The QF-PCR results were consistent with the results of cytogenetic analysis in 95.4% of all samples.

conclusion: QF-PCR was demonstrated to be efficient and reliable for prenatal aneuploidy screening. This study suggests that QF-PCR can be used as a rapid diagnostic method. However, rearrangements and some mosaic samples cannot be detected with this test; thus, those exceptions must undergo cytogenetic analysis.

Indexed as

AneuploidyAdolescentAdultBrazilCytogenetic AnalysisFemaleFluorescenceHumansKaryotypingMiddle AgedPolymerase Chain ReactionPregnancyPrenatal DiagnosisProspective StudiesYoung Adult

Identifiers

PMID28792998
PMCPMC5525164

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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.