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The Science Behind Personalized Nutrition

Nutrition advice has long been built on population averages, but every step of how you process food runs through enzymes coded by your genes. Nutrigenomics is why two people can eat identical diets and get completely different results.

By Mosaic Biodata1 min read
The Science Behind Personalized Nutrition

For decades, nutrition advice has been built on population averages — but your body may process nutrients completely differently from the average person those guidelines were built for. That's the premise behind nutrigenomics: the science of how your genes interact with what you eat, and why two people can follow the same diet and get opposite results.

Your genes affect how you process food

Every step of nutrition, digestion, absorption, transport, metabolism, and storage, involves enzymes coded by your genes. Different genetic variants mean different enzyme efficiency. This explains why two people can eat identical diets and have completely different outcomes.

Some people efficiently convert plant-based omega-3s into the forms their body uses. Others barely convert any and need direct sources of EPA and DHA. Some people handle saturated fat fine; others see dramatic cholesterol responses. Some thrive on higher carbohydrate intake; others do better with more fat.

Real examples from real genes

The APOA2 gene affects how your body responds to saturated fat. Certain variants are associated with weight gain on high-saturated-fat diets, while people with other variants show no such association. The FTO gene influences appetite and satiety signals. TCF7L2 affects how you process carbohydrates and your risk for blood sugar issues.

Then there's the lactase gene, the classic example. Most adults worldwide can't digest lactose well because the gene that produces lactase typically turns off after childhood. But some populations evolved a variant that keeps it active. Your genes literally determine whether dairy works for you.

Beyond macros: micronutrient needs

Genetic variants also affect your vitamin and mineral needs. BCMO1 influences how well you convert beta-carotene to Vitamin A. VDR and GC affect Vitamin D metabolism. MTHFR, perhaps the most well-known, affects folate processing. These aren't rare mutations; they're common variants that affect significant portions of the population.

The bottom line

Personalized nutrition isn't a fad; it's the logical application of what we now know about genetic variation. General guidelines are fine starting points, but they can't account for your individual biochemistry. When you know how your body actually processes nutrients, you can stop guessing and start optimizing, which is exactly what the Macronutrient Optimization section of your Mosaic report is for.

Keep exploring: the Insights Library breaks down the 108 traits Mosaic reads from your DNA, and the reports show how they come together.

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