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Reproductive Biomedicine
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Volume 12, Issue 4 (5-2014)
IJRM 2014, 12(4): 263-268 |
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Omrani M D, Azizi F, Rajabibazl M, Safavi Naini N, Omrani S, Mona Abbasi A et al . Can we rely on the multiplex ligation-dependent probe amplification method (MLPA) for prenatal diagnosis?. IJRM 2014; 12 (4) :263-268
URL: http://ijrm.ir/article-1-527-en.html
URL: http://ijrm.ir/article-1-527-en.html
Mir Davood Omrani1 
, Faezeh Azizi1 , Masoumeh Rajabibazl2 , Niloufar Safavi Naini1 , Sara Omrani3 , Arezo Mona Abbasi4 , Soraya Saleh Gargari * 5
, Faezeh Azizi1 , Masoumeh Rajabibazl2 , Niloufar Safavi Naini1 , Sara Omrani3 , Arezo Mona Abbasi4 , Soraya Saleh Gargari * 5
1- Department of Clinical Genetics, Faculty of Medicine, Shahid Beheshti University of Medical Sciences, Tehran, Iran
2- Department of Clinical Biochemistry, Faculty of Medicine, Shahid Beheshti University of Medical Sciences, Tehran, Iran
3- Faculty of Medicine, Shahid Beheshti University of Medical Sciences, Tehran, Iran
4- Edward Via College of Osteopathic Medicine, Virginia, USA
5- Feto-Maternal Unit, Mahdieh Hospital, Shahid Beheshti, University, Tehran, Iran ,Soraya_saleh2000@yahoo.co.uk
2- Department of Clinical Biochemistry, Faculty of Medicine, Shahid Beheshti University of Medical Sciences, Tehran, Iran
3- Faculty of Medicine, Shahid Beheshti University of Medical Sciences, Tehran, Iran
4- Edward Via College of Osteopathic Medicine, Virginia, USA
5- Feto-Maternal Unit, Mahdieh Hospital, Shahid Beheshti, University, Tehran, Iran ,
Abstract: (2668 Views)
Background: The major aneuploidies that are diagnosed prenatally involve the autosomal chromosomes 13, 18, and 21, as well as sex chromosomes, X and Y. Because multiplex ligation-dependent probe amplification (MLPA) is rapid and non-invasive, it has replaced traditional culture methods for the screening and diagnosis of common aneuploidies in some countries.
Objective: To evaluate the sensitivity and specificity of MLPA in a cross-sectional descriptive study for the detection of chromosomal aneuploidies in comparison to other methods.
Materials and Methods: Genomic DNA was extracted from the peripheral blood samples of 10 normal controls and the amniotic fluid of 55 patients. Aneuploidies screening of chromosomes 13, 18, 21, X and Y were carried out using specific MLPA probe mixes (P095-A2). For comparison purposes, samples were also tested by Quantitative Fluorescent-PCR (QF-PCR) and routine chromosomal culture method.
Results: Using this specific MLPA technique and data-analyzing software (Genemarker v1.85), one case was diagnosed with 45, X (e.g. Monosomy X or Turner’s Syndrome), and the remaining 54 cases revealed normal karyotypes. These results were concordant with routine chromosomal culture and QF-PCR findings.
Conclusion: The experiment demonstrates that MLPA can provide a rapid and accurate clinical method for prenatal identification of common chromosomal aneuploidies with 100% sensitivity and 100% specificity.
Objective: To evaluate the sensitivity and specificity of MLPA in a cross-sectional descriptive study for the detection of chromosomal aneuploidies in comparison to other methods.
Materials and Methods: Genomic DNA was extracted from the peripheral blood samples of 10 normal controls and the amniotic fluid of 55 patients. Aneuploidies screening of chromosomes 13, 18, 21, X and Y were carried out using specific MLPA probe mixes (P095-A2). For comparison purposes, samples were also tested by Quantitative Fluorescent-PCR (QF-PCR) and routine chromosomal culture method.
Results: Using this specific MLPA technique and data-analyzing software (Genemarker v1.85), one case was diagnosed with 45, X (e.g. Monosomy X or Turner’s Syndrome), and the remaining 54 cases revealed normal karyotypes. These results were concordant with routine chromosomal culture and QF-PCR findings.
Conclusion: The experiment demonstrates that MLPA can provide a rapid and accurate clinical method for prenatal identification of common chromosomal aneuploidies with 100% sensitivity and 100% specificity.
Type of Study: Original Article |
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