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Use of real time PCR for rapid detection of Del phenotype in Taiwan

  • Chien Feng Sun*
  • , Jui Ping Liu
  • , Ding Ping Chen
  • , Wei Ting Wang
  • , Tyng Tyng Yang
  • *Corresponding author for this work
  • Chang Gung Memorial Hospital
  • Chang Gung University
  • Hsin Chu Blood Donation Center

Research output: Contribution to journalJournal Article peer-review

17 Scopus citations

Abstract

During routine serologic procedures, Rh Del blood is often not identified and subsequently labeled as RhD-negative. Recently, several reports have shown the ability of Del blood to induce anti-D in RhD-negative recipients. Among Korean, Japanese, and Chinese, almost all individuals with Del blood have a nucleotide change in the RHD gene of 1227G>A (RHDK407K). Thus, nucleotide 1227A at RHD exon 9 can be used as a marker for the Del phenotype in Asians. Real-time PCR for single nucleotide polymorphisms has been useful in biallelic discrimination of genomic sequence. Use of this methodology to identify 1227A will facilitate identification of blood units with the Del blood type and thus prevent potential sensitization of the RhD-negative recipients. In this study, real-time PCR-melting curve analysis at nucleotide 1227 of RHD exon 9 was performed on 990 leftover blood samples. PCR analysis identified 22 samples with the 1227G+A pattern, 965 samples with the 1227G pattern, and 3 with negative real-time results. The RHDEL allele frequency is 0.0116 (22/1980) among Taiwanese. These real-time PCR patterns were validated through DNA sequencing analyses of RHD exon 9 on 22 samples with the 1227G+A pattern and on 50 randomly selected samples from 1227G individuals. The real-time PCR test was then analyzed in 118 apparently RhD-negative Taiwanese donors, including 38 Del and 80 true RhD-negative donors, for efficiency studies. All of the Del samples (38, 100%) were found to have the 1227A pattern. Among the 80 serologic true RhD-negative samples, 77 were negative for real-time PCR results [1227A(-) /1227G(-)], 2 had the 1227G pattern [1227A(-)/1227G(+)], and one had the 1227A pattern [1227A(+)/1227G(-)]. Results of the melting curve analysis of RHD 1227A for the detection of Del among apparent RhD-negative individuals in Taiwan had the following characteristics: 100% sensitivity; 98.75% specificity, positive predictive value of 97.44%; negative predictive value of 100%; and an efficiency of 99.15%. Melting curve analysis using RHD 1227A for detection of Del phenotype can be efficiently applied in eastern Asian countries, since almost all the Del type in eastern Asians have the characteristic 1227A mutation.

Original languageEnglish
Pages (from-to)258-263
Number of pages6
JournalAnnals of Clinical and Laboratory Science
Volume38
Issue number3
StatePublished - 06 2008
Externally publishedYes

Keywords

  • D blood group
  • Melting curve analysis
  • Real-time PCR
  • Transfusion medicine

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