Meden does not read your variants in isolation. Every genetic marker is interpreted in the context of every other — because your biology does not work in isolation either. This is the science behind your longevity protocol.
Consumer genetic testing gives you data. Meden gives you interpretation. There is a significant difference between knowing you carry a COMT Val158Met variant and understanding what that means alongside your MAOA, your BDNF, your NR3C1, and your current bloodwork.
Every Meden report begins with a full read of your genetic architecture — all 133+ markers across all 12 domains — before a single recommendation is written. The goal is not to flag individual variants. It is to understand how your unique biological system is wired.
The genetic architecture of how your cells age — and what slows it. FOXO3 longevity variants, SIRT1 cellular stress response, APOE Alzheimer's and cardiovascular risk, telomere maintenance genes.
Mitochondrial efficiency, ATP production capacity, endurance vs power architecture, VO2max genetics, and recovery speed between training sessions.
Oestrogen metabolism and clearance, testosterone pathway genetics, cortisol sensitivity and HPA axis regulation, thyroid function, and sex hormone binding globulin.
Collagen production and degradation genetics, UV damage response, antioxidant capacity, inflammatory skin response, and the genetic factors behind skin ageing rate.
Dopamine clearance rate, neuroplasticity and BDNF expression, mood architecture, memory pathway genetics, stress resilience, and neurodegenerative risk markers.
Circadian rhythm genetics, cortisol sensitivity and awakening response, sleep architecture predispositions, and the genetic factors that govern HPA axis resilience.
Baseline inflammatory tone, cytokine production genetics, immune regulation variants, and the markers that predict how aggressively your body responds to cellular stress.
MTHFR and the full methylation cycle, sulfur metabolism, glutathione production capacity, phase I and II detoxification pathways, and histamine clearance genetics.
Lipid metabolism genetics, homocysteine pathway variants, thrombosis risk, blood pressure regulation, and the genetic architecture behind long-term cardiovascular health.
Dietary fat and carbohydrate metabolism, insulin sensitivity genetics, appetite regulation, circadian eating patterns, and obesity risk architecture.
Lactose and gluten tolerance genetics, gut permeability predispositions, microbiome diversity markers, and food sensitivity architecture.
Cytochrome P450 enzyme genetics, caffeine and alcohol metabolism, nutrient absorption variants, and the pharmacogenomic markers that determine how your body processes what you take.
Every consumer genetics platform runs your SNPs through an algorithm. The algorithm produces the same report structure for every client — with your data filled in. Meden works differently. A genetics and bioengineering specialist reads your full genomic picture before writing a single word. The interactions between your variants — the ones no algorithm captures — are where your most important insights live.
Available in The Living Blueprint and The Meden Protocol, bloodwork interpretation connects your current biomarkers to your genetic findings — revealing what is actually happening in your body today, in the context of how it is genetically wired.
"Your labs are normal. But normal is not optimal. And optimal is different for every genome."
Standard lab reference ranges are built on population averages. Meden interprets your bloodwork against functional optimal ranges — the levels at which research shows the body performs best — and connects every result to your genetic context.
Every Meden programme begins with your raw DNA file from 23andMe or AncestryDNA. If you already have data, you can begin today.