Evidence map›Paper›PMID 34063775›Full record

ArticleDiagnostics (Basel, Switzerland)2021

Molecular Characteristics of the Serological Weak D Phenotype in Koreans.

Dajeong Jeong, Sujin Oh, Eun Young Song, Yun Ji Hong, Kyoung Un Park

Open access · goldAbstract read
In one paragraph

Article in Diagnostics (Basel, Switzerland), 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.

0numbers the graph read from it
0cells of the map it votes in
2citing papers in PubMed
0.4field-weighted citation impact, top 38% 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

2 citing papers in PubMed, 8 citations in OpenAlex.

  1. Review
  2. Annals of laboratory medicine · 2023
    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

5 authors at 1 institution in 1 country.

Dajeong JeongDepartment of Laboratory Medicine, Seoul National University College of Medicine, Seoul 03080, Korea.ORCID 0000-0003-4848-668X
Sujin OhDepartment of Laboratory Medicine, Seoul National University College of Medicine, Seoul 03080, Korea.
Eun Young SongDepartment of Laboratory Medicine, Seoul National University College of Medicine, Seoul 03080, Korea.
Yun Ji HongDepartment of Laboratory Medicine, Seoul National University College of Medicine, Seoul 03080, Korea.
Kyoung Un ParkDepartment of Laboratory Medicine, Seoul National University College of Medicine, Seoul 03080, Korea.ORCID 0000-0002-2402-7633
Seoul National University · KR

Funding

Operation of the Korean Rare Blood Program from the KONOS, Ministry of Health and Welfare 800-20190023
6 · The paper itself

Abstract

Serological weak D is a reaction of 2+ or less to anti-D reagent and includes weak D and partial D phenotypes. Although identifying the RhD subtype is important for transfusion safety, serological tests are insufficient for defining the RhD subtype, and molecular tests are needed. To analyze the molecular characteristics of D variants in Koreans to facilitate the formulation of individualized transfusion strategies, molecular tests such as RhD genotyping using real-time polymerase chain reaction (PCR) and partial-D and/or weak-D sequence-specific amplification (SSP) were performed on 105 Korean Rare Blood Program (KRBP) patients exhibiting serological weak D. In total, 58 out of 68 serologically determined weak D KRBP patients were typed as having weak D or partial D phenotypes via RhD genotyping. In detail, eight (13.8%) were typed as partial DVa or DBS, nine (15.5%) as weak D type 15, and four others (6.8%) as partial DVI, partial DVII, weak D type 2, or weak D type 41 or 45, whereas the rest (n = 37, 63.8%) was typed as having either weak D or partial D. This suggests that serological weak D Koreans who require transfusion should be treated as D-negative.

Indexed as

partial DPCR-SSPreal-time PCRRhD variantweak D

Identifiers

PMID34063775
PMCPMC8223775
OpenAlexW3162786617

What OpenQuestion holds

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LicenceCC BY
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.