Cargando…

Cytogenetic investigation of couples with recurrent spontaneous miscarriages

BACKGROUND & OBJECTIVE: Spontaneous pregnancy loss has always been the frustrating experience for the couples and concern clinician. Chromosomal abnormality in either of the parent is considered to be the one of the leading cause of recurrent spontaneous miscarriages. This study was designed to...

Descripción completa

Detalles Bibliográficos
Autores principales: Hanif, Misbah Iqbal, Khan, Ayesha, Arif, Afsheen, Shoeb, Erum
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Professional Medical Publications 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6717443/
https://www.ncbi.nlm.nih.gov/pubmed/31489019
http://dx.doi.org/10.12669/pjms.35.5.678
_version_ 1783447559458521088
author Hanif, Misbah Iqbal
Khan, Ayesha
Arif, Afsheen
Shoeb, Erum
author_facet Hanif, Misbah Iqbal
Khan, Ayesha
Arif, Afsheen
Shoeb, Erum
author_sort Hanif, Misbah Iqbal
collection PubMed
description BACKGROUND & OBJECTIVE: Spontaneous pregnancy loss has always been the frustrating experience for the couples and concern clinician. Chromosomal abnormality in either of the parent is considered to be the one of the leading cause of recurrent spontaneous miscarriages. This study was designed to evaluate the possible chromosomal etiology of miscarriage and the subsequent intimacy of maternal or paternal genetic abnormality. METHODS: This case-control study was conducted between January 2016 and October 2016 at a tertiary care hospital in Karachi. A total of thirty-two couples were selected who had suffered with recurrent spontaneous miscarriages (RSM). Using conventional cytogenetic technique karyotyping was performed on all of the subjects. For the control twenty couples were also selected with no history of pregnancy loss. All the karyotypes were recorded on the standard method. Data was analyzed through SPSS version 22. RESULTS: Among thirty-two cases nine cases were found to have abnormal karyotype. In which sex chromosomal trisomy=02 (46,XY/47,XXY), marker chromosome=01 (47,XX,+mar), Robertsonian translocation=01 (45,XY,der,(14:21),(q10;q10)), reciprocal translocation=01 (46,XX,t(11;22)(q23;q11.2)), inversion=02 (46,XX,inv(9)(p11q13)) and minor structural abnormalities=02 (46,XX,15PS+) were found. Approximately equal ratio with 1:1.25 was observed among male and female carrier respectively. Non-significant difference was found between the ages of both carriers (p=0.34). Though a significant different value was calculated in the case of number of miscarriage (p=0.004*). Moreover, no significant association was found among spontaneous miscarriage (SM) and recurrent spontaneous miscarriage (RSM) with respect to maternal age (p= 0.157). CONCLUSION: In the recent study possible chromosomal abnormalities suggested the evaluation of the patient with the history of recurrent spontaneous miscarriage must include conventional cytogenetic. Moreover, probe development and extended investigation can ease the prognosis among pregnancy related complication.
format Online
Article
Text
id pubmed-6717443
institution National Center for Biotechnology Information
language English
publishDate 2019
publisher Professional Medical Publications
record_format MEDLINE/PubMed
spelling pubmed-67174432019-09-06 Cytogenetic investigation of couples with recurrent spontaneous miscarriages Hanif, Misbah Iqbal Khan, Ayesha Arif, Afsheen Shoeb, Erum Pak J Med Sci Original Article BACKGROUND & OBJECTIVE: Spontaneous pregnancy loss has always been the frustrating experience for the couples and concern clinician. Chromosomal abnormality in either of the parent is considered to be the one of the leading cause of recurrent spontaneous miscarriages. This study was designed to evaluate the possible chromosomal etiology of miscarriage and the subsequent intimacy of maternal or paternal genetic abnormality. METHODS: This case-control study was conducted between January 2016 and October 2016 at a tertiary care hospital in Karachi. A total of thirty-two couples were selected who had suffered with recurrent spontaneous miscarriages (RSM). Using conventional cytogenetic technique karyotyping was performed on all of the subjects. For the control twenty couples were also selected with no history of pregnancy loss. All the karyotypes were recorded on the standard method. Data was analyzed through SPSS version 22. RESULTS: Among thirty-two cases nine cases were found to have abnormal karyotype. In which sex chromosomal trisomy=02 (46,XY/47,XXY), marker chromosome=01 (47,XX,+mar), Robertsonian translocation=01 (45,XY,der,(14:21),(q10;q10)), reciprocal translocation=01 (46,XX,t(11;22)(q23;q11.2)), inversion=02 (46,XX,inv(9)(p11q13)) and minor structural abnormalities=02 (46,XX,15PS+) were found. Approximately equal ratio with 1:1.25 was observed among male and female carrier respectively. Non-significant difference was found between the ages of both carriers (p=0.34). Though a significant different value was calculated in the case of number of miscarriage (p=0.004*). Moreover, no significant association was found among spontaneous miscarriage (SM) and recurrent spontaneous miscarriage (RSM) with respect to maternal age (p= 0.157). CONCLUSION: In the recent study possible chromosomal abnormalities suggested the evaluation of the patient with the history of recurrent spontaneous miscarriage must include conventional cytogenetic. Moreover, probe development and extended investigation can ease the prognosis among pregnancy related complication. Professional Medical Publications 2019 /pmc/articles/PMC6717443/ /pubmed/31489019 http://dx.doi.org/10.12669/pjms.35.5.678 Text en Copyright: © Pakistan Journal of Medical Sciences http://creativecommons.org/licenses/by/3.0 This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/3.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Original Article
Hanif, Misbah Iqbal
Khan, Ayesha
Arif, Afsheen
Shoeb, Erum
Cytogenetic investigation of couples with recurrent spontaneous miscarriages
title Cytogenetic investigation of couples with recurrent spontaneous miscarriages
title_full Cytogenetic investigation of couples with recurrent spontaneous miscarriages
title_fullStr Cytogenetic investigation of couples with recurrent spontaneous miscarriages
title_full_unstemmed Cytogenetic investigation of couples with recurrent spontaneous miscarriages
title_short Cytogenetic investigation of couples with recurrent spontaneous miscarriages
title_sort cytogenetic investigation of couples with recurrent spontaneous miscarriages
topic Original Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6717443/
https://www.ncbi.nlm.nih.gov/pubmed/31489019
http://dx.doi.org/10.12669/pjms.35.5.678
work_keys_str_mv AT hanifmisbahiqbal cytogeneticinvestigationofcoupleswithrecurrentspontaneousmiscarriages
AT khanayesha cytogeneticinvestigationofcoupleswithrecurrentspontaneousmiscarriages
AT arifafsheen cytogeneticinvestigationofcoupleswithrecurrentspontaneousmiscarriages
AT shoeberum cytogeneticinvestigationofcoupleswithrecurrentspontaneousmiscarriages