EventsThe 2nd International Electronic Conference on Genes
Published
This submission belongs to the session C. Human Genomics and Genetic Diseases of the event The 2nd International Electronic Conference on Genes
Published date
09 Dec, 2024
Academic Editor
author-avatarLaurent Metzinger
Citation
Maria-Anna Kyrgiafini, Chrysi Kontse, Alexia Chatziparasidou, Zissis Mamuris, Whole-genome profile of Greek patients with asthenozoospermia: Identification of candidate variants and genes, in Proceedings of The 2nd International Electronic Conference on Genes, 11 December–13 December 2024, MDPI: Basel, Switzerland
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Whole-genome profile of Greek patients with asthenozoospermia: Identification of candidate variants and genes

Chrysi Kontse 1
1. Laboratory of Genetics, Comparative and Evolutionary Biology, Department of Biochemistry and Biotechnology, University of Thessaly, Larissa, Greece, Greece
2. Embryolab IVF Unit, Thessaloniki, Greece
Abstract

Introduction: Nowadays, infertility represents a multifaceted health issue that significantly impacts numerous couples, giving rise to notable psychological and social complexities. Notably, one in six couples experience infertility, with approximately 50% of cases attributed to male factors. Male infertility, a complex disorder influenced by both environmental factors and genetic predisposition, involves the interplay of various genes contributing to its manifestation. It can be categorized into specific subtypes, including asthenozoospermia. The primary aim of this study was to identify novel variants associated with asthenozoospermia within the Greek population and to elucidate the roles of the genes involved. Materials and Methods: Whole-genome sequencing (WGS) was conducted on both normozoospermic and asthenozoospermic individuals. Following the identification of variants exclusively present in asthenozoospermic men, an extensive range of tools, functional assessments, and predictive algorithms were employed to prioritize these variants. Results: The investigation unveiled numerous polymorphisms, comprising 155 classified as high-impact and 715 classified as moderate-impact. While several of these variants were found within genes previously linked to male infertility, a notable subset was associated with asthenozoospermia for the first time. Furthermore, pathway enrichment analysis and Gene ontology (GO) analyses revealed polymorphisms on genes implicated in teratozoospermia through various mechanisms and pathways. Conclusions: This study reaffirms the involvement of previously studied genes in male infertility, while also shedding light on novel molecular mechanisms. By providing a comprehensive list of variants and candidate genes associated with asthenozoospermia within the Greek population, this research contributes significantly to our understanding of male infertility and paves the road for future studies.

Keywords
male infertility
genetics
asthenozoospermia
variant
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