Incidence of Yq Microdeletion among Chattishgarh Population and Cast based distribution

Author:

Sinha Manisha B1,Dada Rima2,Patel Suprava3,Mohapatra Eli4,Bagde NilajKumar5,Sinha Human Prasad6,Gupta Sonam7

Affiliation:

1. Additional Professor, Lab of Molecular and Cytogenetics, Department of Anatomy, All India Institute of Medical Sciences,Raipur, CG, India

2. Sr Professor, Lab of Molecular and Cytogenetics, Department of Anatomy, All India Institute of Medical Sciences, Delhi, India

3. Additional Professor, Department of Biochemistry, All India Institute of Medical Sciences, Raipur, CG, India

4. Professor, Department of Biochemistry, All India Institute of Medical Sciences, Raipur, CG, India

5. Additional Professor, Department of Obstetrics and Gynaecology, All India Institute of Medical Sciences, Raipur, CG, India

6. Senior Consultant Neurologist, Department of Neurology, NH MMI Super Speciality Hospital, Raipur, CG, India

7. X-Project Fellow, Lab of Molecular and Cytogenetics, Department of Anatomy, All India Institute of Medical Sciences, Raipur, CG, India

Abstract

Abstract Background: Millions of individuals in their reproductive years are affected by infertility on a global scale, potentially exerting a significant influence on their lives and family dynamics. The coexistence of abnormal seminogram and Yq microdeletion synergistically affects infertility. Therefore, the study was designed to determine the frequency of distribution of Yq microdeletion in abnormal semen parametric infertility cases. Methodology: Seventy-five cases of infertility and 78 controls with known fertility were enrolled for the cross-sectional study. In the collected blood sample, DNA was isolated and a polymerase chain reaction (PCR) mix for various markers was prepared. After running in a thermocycler, PCR products were analyzed by gel electrophoresis. Results: The distribution of deletion among different subtypes: azoospermic, severe oligozoospermic, oligozoospermic, and normozoospermic cases was 35%, 33%, 35%, and 33%, respectively. The most common deletion type in the Chhattisgarh population was azoospermia factor c. Caste-based distribution among the study group was quite uniform. Conclusion: Y chromosome microdeletion would be an essential test after seminogram in cases of male infertility, especially to prevent the transmission or inheritance of infertility to offspring. Due to the high frequency of microdeletions, it is a very useful test to identify male infertility in Chhattisgarh.

Publisher

Medknow

Reference31 articles.

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2. Y choromosomal microdeletion screening in the workup of male infertility and its current status in India;Suganthi;Int J Fertil Steril,2014

3. Prevalence of Y chromosome microdeletion in azoospermia factor subregions among infertile men from West Bengal, India;Dutta;Mol Genet Genomic Med,2021

4. The human Y chromosome:The biological role of a “functional Wasteland”;Quintana-Murci;J Biomed Biotechnol,2001

5. Double-blind Y chromosome microdeletion analysis in men with known sperm parameters and reproductive hormone profiles:Microdeletions are specific for spermatogenic failure;Krausz;J Clin Endocrinol Metab,2001

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