Human Reproduction · 2003 · 194 citations · 35 references
MedicineGeneticsMolecular GeneticsInfertilityMitochondrial GeneticsReproductive MedicineMale InfertilityMitochondrial HaplogroupsSemen AnalysisSperm BiologySperm Morphology AssessmentSperm Motility AssessmentDensity SeparationHaplogroup-specific MutationsMitochondrial Dna MutationsMitochondrial Dna Point MutationsNormal Sperm MorphologyPoint MutationsQuantitative Pcr DetectionSperm Quality Abnormalities
BACKGROUND: There is increasing evidence that mitochondrial DNA (mtDNA) anomalies in sperm may lead to infertility. Point mutations, deletions and the presence of a specific mtDNA haplogroup have been associated with poor sperm quality, but little attention has been paid to the role of mtDNA content. METHODS: Using density gradient separation and swim-up methods, we selected motile sperm from 32 normal and 35 abnormal sperm samples. The mtDNA/beta-globin gene ratio was determined by real-time quantitative PCR. RESULTS: The average mtDNA/beta-globin ratio of sperm collected from 100% density layers was 1.4 for normal sperm, 6.1 for sperm samples presenting at least one abnormal criterion [among the three criteria established by World Health Organization (1999), i.e. sperm count, motility and morphology], and 9.1 for sperm samples presenting two or more of these abnormal criteria. These differences are very highly significant (P < 0.0001). The mtDNA numbers were also much greater in sperm collected from the 40% density gradient layers (mean: 17.1, P < 0.001), known to contain the most abnormal sperm of the sperm samples, than in those collected from the 100% layers known to contain sperm with the best fertilizing ability. CONCLUSION: Our results showed significant mtDNA amplification in sperm collected from abnormal sperm samples.
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