First-trimester spontaneous pregnancy loss - molecular analysis using multiplex ligation-dependent probe amplification

被引:12
作者
Zimowski, J. G. [1 ]
Massalska, D. [2 ]
Pawelec, M. [1 ]
Bijok, J. [2 ]
Michalowska, A. [2 ]
Roszkowski, T. [2 ]
机构
[1] Inst Psychiat & Neurol, Dept Genet, Warsaw, Poland
[2] Med Ctr Postgrad Educ, Dept Obstet & Gynecol, Czerniakowska 231, PL-00416 Warsaw, Poland
关键词
aneuploidies; miscarriage; molecular diagnosis; multiplex ligation-dependent probe amplification (MLPA); COMPARATIVE GENOMIC HYBRIDIZATION; RECURRENT MISCARRIAGE; SPONTANEOUS-ABORTIONS; KARYOTYPE ANALYSIS; MLPA; ANEUPLOIDY; PRODUCTS; PROFILE; EMBRYO; TISSUE;
D O I
10.1111/cge.12727
中图分类号
Q3 [遗传学];
学科分类号
071007 ; 090102 ;
摘要
Spontaneous miscarriages are the most frequent complications of pregnancy and, in at least half of cases, are caused by chromosomal abnormalities, mainly aneuploidies. We present the preliminary results of the implementation of multiplex ligation-dependent probe amplification (MLPA) in the detection of chromosomal aberrations in the tissue derived from first-trimester miscarriage and evaluate the limitations and requirements of the method. We studied 181 MLPA analyses with subtelomeric and subcentromeric probe kits for all chromosomes (SALSA P070 and SALSA P181) performed on the first-trimester spontaneous miscarriage products in our Department of Genetics between September 2012 and December 2014. Conclusive MLPA results were obtained in 97.2% of samples. Chromosomal aberrations were detected in 40.3% of samples: 61.8% samples of good quality and 12.6% samples of poor quality (p < 0.001). The normal female karyotype was detected in 14.7% of good quality samples and 84.8% of poor quality samples (p < 0.001). MLPA is a useful tool for the detection of chromosomal aberrations in first-trimester miscarriage products. However, the tissue has to be well prepared before testing and the results 46,XX should be interpreted with caution.
引用
收藏
页码:620 / 624
页数:5
相关论文
共 26 条
[1]   Profile of chromosomal aberrations in different gestational age spontaneous abortions detected by comparative genomic hybridization [J].
Azmanov, Dimitar N. ;
Milachich, Tania V. ;
Zaharieva, Boriana M. ;
Michailova, Gergana I. ;
Dimitrova, Violeta G. ;
Karagiozova, Zivka H. ;
Maznejkova, Valentina T. ;
Chernev, Todor A. ;
Toncheva, Draga I. .
EUROPEAN JOURNAL OF OBSTETRICS GYNECOLOGY AND REPRODUCTIVE BIOLOGY, 2007, 131 (02) :127-131
[2]   High-throughput analysis of chromosome abnormality in spontaneous miscarriage using an MLPA subtelomere assay with an ancillary FISH test for polyploidy [J].
Bruno, Damien L. ;
Burgess, Trent ;
Ren, Hua ;
Nouri, Sara ;
Pertile, Mark D. ;
Francis, David I. ;
Norris, Fiona ;
Kenney, Bronwyn K. ;
Schouten, Jan ;
Choo, K. H. Andy ;
Slater, Howard R. .
AMERICAN JOURNAL OF MEDICAL GENETICS PART A, 2006, 140A (24) :2786-2793
[3]   Trisomy 13 due to rea(13q;13q) is caused by i(13) and not rob(13;13)(q10;q10) in the majority of cases [J].
Bugge, M ;
deLozier-Blanchet, C ;
Bak, M ;
Brandt, CA ;
Hertz, JM ;
Nielsen, JB ;
Duprez, L ;
Petersen, MB .
AMERICAN JOURNAL OF MEDICAL GENETICS PART A, 2005, 132A (03) :310-313
[4]   EXTRA EMBRYONIC FETAL KARYOTYPIC DISCORDANCE DURING DIAGNOSTIC CHORIONIC VILLUS SAMPLING [J].
CALLEN, DF ;
KORBAN, G ;
DAWSON, G ;
GUGASYAN, L ;
KRUMINS, EJM ;
EICHENBAUM, S ;
PETRASS, J ;
PURVISSMITH, S ;
SMITH, A ;
DULK, GD ;
MARTIN, N .
PRENATAL DIAGNOSIS, 1988, 8 (06) :453-460
[5]  
Carp HJA, 2008, ISR MED ASSOC J, V10, P229
[6]  
Daniely M, 2001, Early Pregnancy, V5, P153
[7]   Evaluation of Array Comparative Genomic Hybridization for Genetic Analysis of Chorionic Villus Sampling from Pregnancy Loss in Comparison to Karyotyping and Multiplex Ligation-Dependent Probe Amplification [J].
Deshpande, Maitreyee ;
Harper, Joyce ;
Holloway, Melissa ;
Palmer, Rodger ;
Wang, Rubin .
GENETIC TESTING AND MOLECULAR BIOMARKERS, 2010, 14 (03) :421-424
[8]   MLPA as a screening method of aneuploidy and unbalanced chromosomal rearrangements in spontaneous miscarriages [J].
Diego-Alvarez, Dan ;
de Alba, Marta Rodriguez ;
Cardero-Merlo, Rocio ;
Diaz-Recasens, Joaquin ;
Ayuso, Carmen ;
Ramos, Carmen ;
Lorda-Sanchez, Isabel .
PRENATAL DIAGNOSIS, 2007, 27 (08) :765-771
[9]   Combined QF-PCR and MLPA molecular analysis of miscarriage products: an efficient and robust alternative to karyotype analysis [J].
Donaghue, Celia ;
Mann, Kathy ;
Docherty, Zoe ;
Mazzaschi, Roberto ;
Fear, Claudine ;
Ogilvie, Caroline .
PRENATAL DIAGNOSIS, 2010, 30 (02) :133-137
[10]   Cytogenetic Profile in 1,921 Cases of Trisomy 21 Syndrome [J].
Flores-Ramirez, Francisco ;
Palacios-Guerrero, Claudia ;
Garcia-Delgado, Constanza ;
Berenice Morales-Jimenez, Ariadna ;
Martin Arias-Villegas, Christian ;
Cervantes, Alicia ;
Fabiola Moran-Barrosoa, Veronica .
ARCHIVES OF MEDICAL RESEARCH, 2015, 46 (06) :484-489