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Updated: Oct 2, 2026

Flow Cytometric Analysis of Biomarkers for Detecting Human Sperm Functional Defects
Published on: April 21, 2022
Sperm AluY Epimutations in Male Partners of Couples with Unexplained Recurrent Pregnancy Loss
Elango Kamaraj1, Jordan Moore2, Mykle Keni2
1Department of Obstetrics and Gynecology, University of Texas Health, San Antonio, TX, USA.
Abstract:
Recurrent pregnancy loss (RPL) affects 5% of couples worldwide. Over half of cases remain unexplained (uRPL) as paternal factors are rarely clinically evaluated or studied. This study presents data showing that sperm DNA methylation is a putative contributor to RPL. Using ONT direct whole methylome sequencing, we generated the largest cohort of locus-resolved, single-molecule sperm methylome maps from men with uRPL. We identified 294 differentially methylated regions (DMRs), of which 158 (53.7%) overlapped AluY repetitive elements, representing significant enrichment (z=40.9); most were hypomethylated in uRPL sperm and spanned the full length of individual AluY insertions. Because of single-molecule resolution, we show that the methylation differences found in uRPL sperm occur in a subpopulation of sperm rather than a uniform DNA methylation change across all sperm. AluY epimutation represents a previously unrecognized, predominant signature of paternal epigenetic perturbation in uRPL, establishing repetitive elements as a new axis of sperm epigenetic risk.
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