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High incidences of chromosomal aberrations and Y chromosome micro-deletions as prominent causes for recurrent pregnancy losses in highly ethnic and consanguineous population.
Pandith, Arshad A; Manzoor, Usma; Amin, Ina; Ahmad, Abida; Rashid, Masarat; Zargar, Mahrukh H; Rah, Shayesta; Dar, Fayaz A; Qasim, Iqbal; Sanadhya, Dheera.
  • Pandith AA; Advanced Centre for Human Genetics, Sher-I-Kashmir Institute of Medical Sciences (SKIMS), Srinagar, J&K, India. arshaajiz@gmail.com.
  • Manzoor U; Advanced Centre for Human Genetics, Sher-I-Kashmir Institute of Medical Sciences (SKIMS), Srinagar, J&K, India.
  • Amin I; School of Life and Basic Sciences, Jaipur National University, Jaipur, 302025, India.
  • Dil-Afroze; Advanced Centre for Human Genetics, Sher-I-Kashmir Institute of Medical Sciences (SKIMS), Srinagar, J&K, India.
  • Ahmad A; Department of Clinical Biochemistry, University of Kashmir, J&K, India.
  • Rashid M; Advanced Centre for Human Genetics, Sher-I-Kashmir Institute of Medical Sciences (SKIMS), Srinagar, J&K, India.
  • Zargar MH; Department of Obstetrics and Gynecology, SKIMS, Srinagar, J&K, India.
  • Rah S; Department of Obstetrics and Gynecology, SKIMS, Srinagar, J&K, India.
  • Dar FA; Advanced Centre for Human Genetics, Sher-I-Kashmir Institute of Medical Sciences (SKIMS), Srinagar, J&K, India.
  • Qasim I; Department of Obstetrics and Gynaecology, LD Hospital, Srinagar, J&K, India.
  • Sanadhya D; Advanced Centre for Human Genetics, Sher-I-Kashmir Institute of Medical Sciences (SKIMS), Srinagar, J&K, India.
Arch Gynecol Obstet ; 305(6): 1393-1408, 2022 06.
Article en En | MEDLINE | ID: mdl-34542677
ABSTRACT

PURPOSE:

Recurrent Miscarriages (RM) commonly complicates the reproductive outcome where prominently chromosomal aberrations and molecular factors lead to recurrent miscarriages. We investigated couples with RM for cytogenetic abnormalities and Y chromosome microdeletions in males along with detection of aneuploidies de novo in the product of conception from a highly ethnic consanguineous population (Kashmir, North India) . STUDY

DESIGN:

Chromosomal analysis was done by Karyotyping on peripheral blood lymphocyte cultures and analyzed by Cytovision software Version 3.9. Microdeletion in Y chromosome was performed by STS-PCR and QF-PCR was used to detect aneuploidy in the product of conception.

RESULTS:

Of the 380 samples (190 couples) screened for cytogenetic analysis, 50 (13.1%) chromosomal aberrations were detected in both couples. Numerical aberrations were detected in 16.0%, inversions 22%, duplications 16.0% and translocations were found in 26.0% with three unique reciprocal translocations in males. The couples bonded consanguineously had 32% chromosomal changes with a significant difference in chromosomal inversions (37.5% vs. 14.7%) and translocations (37.5% vs. 20.6%) for consanguineous and non-consanguineous group, respectively (p < 0.05). Further, translocations and inversions (44.5% and 33.3%) were significantly implicated in couples with a positive family history of RM (p < 0.05). Y chromosome deletions were found in 2.1% cases of males.

CONCLUSION:

We conclude 15.2% couples affected either by chromosomal or Y chromosome deletions contribute hugely in the diagnosis and management of repeated pregnancy losses. It is recommended that couples that belong to consanguineous and multigenerational group of RM should be considered for cytogenetic and molecular testing after two abortions for successful pregnancy outcomes and management of RM.
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Texto completo: 1 Banco de datos: MEDLINE Asunto principal: Aborto Habitual / Aberraciones Cromosómicas Tipo de estudio: Etiology_studies / Incidence_studies / Prognostic_studies / Risk_factors_studies Límite: Female / Humans / Male / Pregnancy Idioma: En Año: 2022 Tipo del documento: Article

Texto completo: 1 Banco de datos: MEDLINE Asunto principal: Aborto Habitual / Aberraciones Cromosómicas Tipo de estudio: Etiology_studies / Incidence_studies / Prognostic_studies / Risk_factors_studies Límite: Female / Humans / Male / Pregnancy Idioma: En Año: 2022 Tipo del documento: Article