BACKGROUND AND OBJECTIVES: The chromosomal abnormalities are one of the important causes of male infertility.
In view of the genetic risks for the next generation, the importance of careful evaluation of karyotype is essential. The objective of this study was to determine the frequency of chromosomal abnormalities in infertile men with primary infertility from Indian population.
MATERIALS AND METHODS: The 78 infertile men with primary infertility, out of which 26 men were azoospermic, 19 men were oligospermic, 4 men were asthenospermic and 29 men were oligoasthenospermic were studied. Karyoptying was performed on peripheral blood lymphocytes by using the Giemsa trypsin banding (GTG) banding technique. Additional data was collected from published studies in Indian population leading to a total of 1814 cases.
RESULTS: Chromosome analysis of 78 infertile males showed major chromosome abnormalities in 10.2%, with 6.4% in autosomal chromosome abnormalities and 3.8% in sex chromosome abnormalities. The incidence of major chromosome abnormalities in oligospermic males were 21% and azoospermic males were 15.4 %. Chromosomal polymorphic variants were identified to be 16.7%. Combining the data from other published studies identified 153/ 1814 (8.4%) infertile men of chromosomal abnormalities; with 10.8% in azoospermia, 7.3% in oligospermia and 7.3% in oligoasthenoteratospermic from India.
INTERPRETATION AND CONCLUSION: The overall high prevalence of chromosomal abnormalities in infertile males suggests that the conventional chromosomal analysis is an important investigative tool for male infertility, especially prior to use of any assisted reproductive techniques.
Written by:
Kate UV, Pokale YS, Jadhav AM, Gangane SD. Are you the author?
Senior Scientific Officer & Quality Manager, Department of Cytogenetics, PreventiNe Life Care Pvt Ltd., Mumbai, India; Scientific Officer, Department of Cytogenetics, PreventiNe Life Care Pvt Ltd., Mumbai, India; Head of Department, Genetic Division, Department of Anatomy, Grant Medical College & Sir J.J. Group of Hospitals, Mumbai, India.
Reference: J Clin Diagn Res. 2014 Oct;8(10):SC01-6.
doi: 10.7860/JCDR/2014/8644.4933
PubMed Abstract
PMID: 25478430