Conflicting headlines about coffee and heart health have confused patients and clinicians for years. The resolution lies not in the beverage itself, but in individual genetic variation. A single polymorphism in the CYP1A2 gene—the enzyme responsible for metabolizing 95% of ingested caffeine—determines whether coffee poses a cardiac risk. Approximately 45% of people are fast caffeine metabolisers, clearing the compound within 3 hours with no increased myocardial infarction risk, even at high intake. Conversely, 55% carry slow-metabolizer alleles, accumulating caffeine for 6–10 hours. For this majority population, consuming 4 or more cups daily correlates with a 64% increased odds of nonfatal MI. This precision medicine insight transforms coffee from a blanket health concern into a personalized clinical consideration.
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