CLOCK genes are core components of the circadian rhythm and regulate numerous hormonal pathways, including those involved in reproduction. Animal models and observational human studies suggest that circadian disruption – e.g., from shift work or sleep deprivation – may impair fertility by altering sex hormone levels, menstrual cycle regularity, and oocyte quality. However, the evidence is largely mechanistic; robust clinical trials directly linking specific CLOCK variants to fertility outcomes are lacking. A consumer DNA test for CLOCK polymorphisms cannot diagnose or predict fertility. The interplay between circadian genes and reproduction is complex and influenced by many non-genetic factors. Individuals with fertility concerns should consult a healthcare provider rather than rely on genetic testing. The current evidence does not support clinical use of CLOCK genotyping for fertility assessment.
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