Comprehensive biomarker analysis and personalised optimisation for peak performance
At 22.3%, Sarah is leaner than ~89% of UK women her age. Below the "healthy" range floor of 24% — this is athletic-level leanness.
A rating of 3 out of 59 is exceptional. Minimal internal organ fat, placing Sarah in the top 8% for metabolic health risk profile.
A metabolic age of 30 vs chronological 45 is a 33% reduction. This places Sarah in the top 5% — her body functions like someone 15 years younger.
At 20.9, Sarah sits in the ideal middle of the healthy range. Leaner than ~62% of UK women aged 40–49, where average BMI is 27.5.
40.5 kg at 54.9 kg body weight is an impressive 73.8% ratio. Above average for age group, indicating consistent strength training and good protein synthesis.
Scoring ~98 on the leg muscle scale, well above the age-reference curve. Strong lower body foundation — critical for longevity and fall prevention.
| Date | Weight | Body Fat % | Muscle | Visceral | BMI | Met. Age | Water % |
|---|---|---|---|---|---|---|---|
| 24 Feb 2026 Latest | 55.0 kg | 22.8% | 40.5 kg | 3 | 20.7 | 30 | 53.3% |
| 8 Feb 2026 | 55.4 kg | 23.3% | 40.5 kg | 3 | 20.9 | 30 | 53.0% |
| 25 Jan 2026 | 55.5 kg | 22.2% | 41.1 kg | 3 | 20.9 | 30 | 53.7% |
| 6 Jan 2026 | 56.5 kg | 23.5% | 41.9 kg | 3 | 21.3 | 30 | 52.8% |
| Date | Weight | Body Fat % | Muscle | Visceral | BMI | Met. Age | BMR | Water % | Bone |
|---|---|---|---|---|---|---|---|---|---|
| 24 Feb Latest | 54.9 kg | 22.3% | 40.5 kg | 3 | 20.9 | 30 | 1,212 | 53.3% | 2.2 kg |
| 8 Feb | 55.6 kg | 21.8% | 41.3 kg | 3 | 21.2 | 30 | 1,226 | 54.1% | 2.2 kg |
| 25 Jan | 56.6 kg | 23.6% | 41.1 kg | 3 | 21.6 | 30 | 1,229 | 52.7% | 2.2 kg |
| 6 Jan | 58.4 kg | 24.3% | 41.9 kg | 4 | 22.2 | 31 | 1,254 | 52.1% | 2.3 kg |
Muscle mass has dropped from 41.9 kg to 40.5 kg (−1.4 kg) over 7 weeks. Resistance training 2×/week with 88–110g daily protein is now the single most important intervention.
All 31 biomarkers within normal ranges. Excellent lipid profile with low triglycerides (0.71) and good HDL (1.49). Thyroid function optimal. Oestradiol at mid-cycle level consistent with menstrual phase. Iron and calcium within range. No flags requiring clinical intervention.
| Marker | Result | Unit | Range | Status | Position in Range |
|---|---|---|---|---|---|
| White Cell Count | 5.53 | ×10&sup9;/L | 4.0–10.0 | Normal | |
| Haemoglobin | 142 | g/L | 120–150 | Normal | |
| Platelet Count | 288 | ×10&sup9;/L | 150–410 | Normal | |
| Red Blood Cells | 4.54 | ×10¹²/L | 3.8–4.8 | Normal | |
| Haematocrit | 0.417 | L/L | 0.360–0.460 | Normal | |
| MCV | 91.9 | fL | 83–101 | Normal | |
| MCH | 31.3 | pg | 27–32 | Normal | |
| MCHC | 341 | g/L | 315–345 | Normal | |
| Neutrophils | 3.56 | ×10&sup9;/L | 2.0–7.0 | Normal | |
| Lymphocytes | 1.50 | ×10&sup9;/L | 1.0–3.0 | Normal | |
| Monocytes | 0.39 | ×10&sup9;/L | 0.2–1.0 | Normal | |
| Eosinophils | 0.03 | ×10&sup9;/L | 0.02–0.50 | Normal | |
| Basophils | 0.05 | ×10&sup9;/L | 0.02–0.10 | Normal |
| Marker | Result | Unit | Range | Status | Position in Range |
|---|---|---|---|---|---|
| Sodium | 137 | mmol/L | 133–146 | Normal | |
| Potassium | 4.6 | mmol/L | 3.5–5.3 | Normal | |
| Urea | 3.5 | mmol/L | 2.5–7.8 | Normal | |
| Creatinine | 62.0 | µmol/L | 45–84 | Normal | |
| eGFR | >90 | mL/min/1.73m² | — | Normal | |
| Total Protein | 75 | g/L | 60–80 | Normal | |
| Albumin | 46 | g/L | 35–50 | Normal | |
| Globulin | 29 | g/L | 19–33 | Normal | |
| Bilirubin | 10 | µmol/L | 0–21 | Normal | |
| Alk Phosphatase | 51 | u/L | 35–104 | Normal | |
| ALT | 8 | u/L | 0–40 | Normal |
| Marker | Result | Status |
|---|---|---|
| Total Cholesterol | 5.0 mmol/L | Normal |
| HDL Cholesterol | 1.49 mmol/L | Optimal |
| Triglycerides | 0.71 mmol/L | Normal |
| Marker | Result | Range | Status |
|---|---|---|---|
| TSH | 1.07 miu/L | 0.27–4.20 | Normal |
| Free T4 | 16.3 pmol/L | 12.0–22.0 | Normal |
| Free T3 | 3.9 pmol/L | 3.1–6.8 | Normal |
| Marker | Result | Range | Status |
|---|---|---|---|
| Oestradiol | 986 pmol/L | 222–1959 | Normal |
| Marker | Result | Range | Status |
|---|---|---|---|
| Serum Iron | 16 µmol/L | 5.83–34.5 | Normal |
| Calcium | 2.39 mmol/L | 2.00–2.60 | Normal |
| Adj. Calcium | 2.35 mmol/L | 2.20–2.60 | Normal |
| Gene | Variant | Effect | Impact |
|---|---|---|---|
| MTHFR (C677T) | CT | 40% reduced enzyme activity | Amber |
| MTRR | GG | Downregulated B12 recycling | Red |
| BHMT | AA | Downregulated homocysteine conversion | Red |
| PEMT | TT | Reduced choline synthesis | Red |
| TCN2 | GG | Reduced B12 transport | Red |
| CBS | AA | Upregulated — pulls homocysteine | Amber |
| GSS | TT | Reduced glutathione synthesis | Red |
| NOS3 | GT | Reduced nitric oxide production | Amber |
| SOD2 | CT | Reduced superoxide dismutase | Amber |
| VDR | CT | Impaired vitamin D metabolism | Amber |
| MAOA | GT | Slower neurotransmitter breakdown | Amber |
In plain English: Your body is 40% less efficient at converting the folate in food and standard supplements into the form your cells can actually use. Think of it like having a narrower fuel pipe — the engine works fine, but you need the right type of fuel (methylfolate) to get through the smaller opening. Regular folic acid (the cheap kind in multivitamins and fortified bread) actually makes this worse because it clogs the system. The fix is simple: take methylfolate instead of folic acid, and eat folate-rich whole foods like spinach, eggs, and liver.
Five interacting variants compound across B12 recycling, backup methylation, phospholipid synthesis, intestinal absorption, and cellular transport. Net effect: substantially reduced B12 bioavailability at the cellular level and compromised homocysteine recycling. Cyanocobalamin (cheapest supplement form) cannot be utilised efficiently.
Overactive CBS shunts homocysteine rapidly towards cysteine/sulphate, depleting SAMe. Combined with GSS TT reducing glutathione synthetase, antioxidant defence is compromised. High-dose sulphur supplements overwhelm this already accelerated pathway.
VDR CT reduces efficiency of cellular response to vitamin D. Standard 400–800 IU doses are inadequate for this genotype. Target serum level: 100–150 nmol/L (vs standard 50–75 nmol/L).
Reduced nitric oxide production affects vasodilation, blood pressure, and endothelial health. The dietary nitrate pathway (oral bacteria convert nitrate → nitrite → NO) is a powerful bypass — but depends on oral bacteria remaining intact.
SOD2 CT reduces mitochondrial antioxidant defence. Combined with high inflammatory skin response and reduced phase I/II detoxification, this creates elevated baseline oxidative burden — accelerating cellular ageing, amplifying inflammatory responses (especially skin), and reducing toxin clearance. This is the primary driver of Sarah’s elevated intrinsic skin ageing score.
Not generic advice — these are problematic specifically because of your variant combination
Designed by Mike | Push/Pull compound split | Tracked via MiLife
For a full-time surgeon, two quality strength sessions per week is optimal for muscle preservation. Research shows twice-weekly resistance training produces 80–90% of the gains of three sessions, with significantly better recovery and compliance.
Your slow genetic recovery profile (Stride DNA) supports this — more recovery time between sessions means better muscular adaptation and lower injury risk.
For days you can’t get to the gym. Same muscle groups, same push/pull pattern.
Your DNA flags slow recovery. The days between strength sessions are adaptation days, not just rest days. Light movement accelerates recovery.
Compound exercises recruit multiple muscle groups simultaneously. They are more time-efficient, produce a greater hormonal response, and are essential for maintaining functional strength as you age.
Your Stride DNA shows a high injury predisposition and slow recovery profile. Always include prehabilitative exercises (banded work, mobility drills), allow 48–72 hours between strength sessions for the same muscle group, and never skip warm-ups. Prioritise connective tissue health with collagen peptides and vitamin C.
450ml kefir + 5g creatine (existing habit ✓). Add: 15 min morning light exposure (circadian reset). Glass of water with lemon.
5-MTHF 400mcg, Methylcobalamin B12 1000mcg, Vitamin D3 4000 IU + K2 200mcg, Omega-3 1000mg. Take with breakfast for fat-soluble absorption.
High-protein: eggs + spinach + avocado, or Greek yoghurt + berries + walnuts. 25–30g protein target.
5 min walk or stretching (prevent >2 hour sedentary periods for NOS3). Nasal breathing throughout.
Protein-rich meal with beetroot/rocket salad (nitric oxide support). Last caffeine intake before 14:00.
Astaxanthin 4mg, Vitamin C 500mg. Optional: green tea (last caffeinated drink).
Strength training or walking session (see Exercise plan). 10 min warm-up mandatory (high injury predisposition).
Wild salmon/chicken + sweet potato + greens. Tryptophan-rich protein for serotonin/melatonin production. Last meal ≥2.5 hrs before bed.
Blue light filter on. Dim ambient lighting. Optional: tart cherry juice.
Magnesium glycinate 200–400mg. Warm bath with Epsom salts. 4-7-8 breathwork ×10. Screens off.
Room 16–18°C, complete darkness, consistent timing ±30 min. Track with Ultrahuman Ring.
Morning
Kefir — 150ml with breakfast
Live cultures to seed gut microbiome. Particularly beneficial given MTHFR status — gut health supports methylation pathways.
Supplements with food
Take all fat-soluble supplements (D3, Omega-3, Collagen) with a fat-containing meal for optimal absorption.
Nasal breathing — 5 minutes
Box breathing or simple nasal-only breathing upon waking. Activates parasympathetic tone before the clinical day begins.
Natural light exposure — first 30 min
Outdoor light within 30 minutes of waking anchors circadian rhythm and supports cortisol awakening response.
Genetics-Led
MTHFR note: Use methylfolate specifically — standard folic acid is poorly metabolised with your MTHFR variant.
Daytime
1.6–2.0g per kg bodyweight. Prioritise leucine-rich sources: meat, fish, eggs, Greek yoghurt.
Front-load morning. Electrolytes if in theatre or prolonged clinical work. Avoid caffeine after 14:00.
Accumulate throughout the clinical day — parking further away, stairs, and short lunchtime walks all count.
Caffeine cutoff — 14:00
COMT GG means you process dopamine rapidly — caffeine can still disrupt sleep architecture if taken late. Hard stop at 2pm.
Your wearable data reveals a picture of cardiovascular fitness and recovery that places you in the top tier for women your age.
Elite athlete range for your age is 50–55 bpm. You are right at that threshold.
Healthy population range is 95–100%. Your oxygen saturation is optimal.
How your metrics compare against average women aged 45 in the UK.
What these biometric numbers mean for your day-to-day health and longevity.
Real-world impact of a 20-year biological advantage
"This is what 2 days a week in the gym buys you — not just a better body now, but decades more of living life on your own terms."
GlycanAge measures the biological age of your immune system using a highly precise blood analysis of IgG glycosylation patterns — the sugar molecules attached to your antibodies. As we age, these glycan structures shift in a predictable way. The test captures where you sit on that spectrum.
Your result: 20. Exceptionally rare in a 45-year-old. Places your immune biological age in the top percentile for your age group. Reflects low systemic inflammation, strong immune regulation, and a lifestyle actively slowing the biological clock.
GlycanAge testing, Body Composition body composition scans, and a full personalised health report — all available through our clinic.
DoctoriumGP • Derby • CQC Registered
Based on your Stride DNA results, this profile maps your genetic predispositions across eight core skin health markers.
Genetic predisposition to faster collagen breakdown — skin ages more quickly without active intervention.
Elevated free radical activity accelerates cell damage — antioxidant support is essential.
Heightened immune-linked inflammatory signalling — increases sensitivity, redness risk, and reactive skin conditions.
Standard UV protection is sufficient — but given your high ageing risk, consistent SPF use is especially important.
Good baseline genetic capacity for moisture retention — maintain with standard hydration support.
Elevated contact dermatitis risk from nickel-containing metals, jewellery, and certain cosmetic ingredients.
Slower clearance of environmental toxins and skin metabolic by-products.
Moderate tendency for sugar molecules to cross-link with collagen — dietary sugar reduction supports skin firmness.
Your genetic profile presents a clear challenge: two high-risk markers (intrinsic ageing and inflammatory response) compounded by raised oxidative stress and reduced detoxification. Your skin is genetically primed to break down collagen faster, react more sensitively to environmental triggers, and clear damaging compounds more slowly than average.
Your strategy is therefore anti-ageing and anti-inflammatory led: prioritise collagen defence, antioxidant loading, and inflammation control. The genetic disadvantages are highly manageable with consistency.
Personalised to your genetic skin profile
DoctoriumGP SkinScope uses AI-powered imaging to assess your skin in detail — measuring texture, pores, pigmentation, hydration levels, and early signs of photoageing with clinical precision.
Professional lab-grade VO2 max testing to establish your true aerobic capacity and personalise training zones. Your Stride DNA shows medium VO2max potential with a balanced power/endurance profile — VO2 testing will reveal your actual fitness age and unlock precise heart rate zones for training.
| Supplement | Dose | Timing | Rationale |
|---|---|---|---|
| 5-MTHF (Methylfolate) | 400–800 mcg | Morning | MTHFR C677T reduces folate conversion 40%. Methylated form bypasses genetic block |
| Methylcobalamin (B12) | 1000 mcg | Morning | Triple B12 impairment: MTRR GG + TCN2 GG + FUT2 AG |
| Vitamin D3 + K2 | 2000–4000 IU | Morning with fat | VDR CT impairs metabolism. UK climate. Test levels every 6 months |
| Omega-3 (EPA/DHA) | 2000 mg | With meals | Raised genetic need + high inflammatory response + slow recovery |
| Vitamin C | 500–1000 mg | Split AM/PM | Raised genetic need + collagen support (high skin ageing) + antioxidant |
| Vitamin E (alpha-tocopherol) | 200 IU | With fat | Raised genetic need + telomere protection + cellular defence |
| Magnesium Glycinate | 300–400 mg | Evening | Supports methylation, sleep quality (genetically low), muscle recovery |
| Zinc | 15 mg | With food | Supports BHMT pathway (impaired), immune function, skin repair |
| NAC (N-Acetyl Cysteine) | 600 mg | Morning | Glutathione precursor — GSS TT reduces glutathione synthesis |
| Astaxanthin | 4–12 mg | With fat | Reduces MMP expression — targets high intrinsic skin ageing |
| Creatine Already Taking | 5 g | Morning | Muscle preservation, cognitive function, methylation support |
| Kefir Already Taking | 450 ml | Morning | Gut health, probiotics, B12 absorption support |
| Test | Frequency | Next Due | Notes |
|---|---|---|---|
| Blood Tests | Every 6 months | Aug 2026 | Add: homocysteine, vitamin D, B12, folate, ferritin |
| Body Composition Body Composition | Monthly | Mar 2026 | Track muscle mass preservation |
| GlycanAge | 9–12 months | Feb–May 2026 | Retest to confirm maintenance |
| Ultrahuman Ring | Daily | Ongoing | HRV, sleep quality, readiness scores |
| tTG Antibody Test | Once | Next bloods | Rule out active coeliac disease (raised genetic predisposition) |
| Homocysteine | Every 6 months | Aug 2026 | Key methylation marker |
| Vitamin D levels | Every 6 months | Aug 2026 | VDR CT impairs metabolism |
Stride DNA reveals a raised genetic predisposition for coeliac disease. This does NOT mean coeliac is present — it means the genetic risk exists. Monitor for symptoms: bloating, fatigue, or brain fog after gluten. A tTG antibody blood test can rule out active disease. No need to eliminate gluten unless symptomatic, but awareness is key.
GlycanAge biological age of 20 vs chronological age 44 is an extraordinary result. Combined with a metabolic age of 30 from Body Composition, this paints a picture of someone ageing at roughly half the expected rate. Glycan Shield at the 95th percentile confirms exceptional immune regulation and minimal chronic inflammation.
Stride DNA reveals an impaired Methionine Cycle with 7 raised nutrient needs. MTHFR C677T (40% reduced), MTRR GG, BHMT AA, and PEMT TT variants mean methylated B vitamins, choline, and targeted supplementation are essential — not optional. Homocysteine monitoring every 6 months is strongly recommended.
Muscle mass dropped 1.4 kg over 11 weeks (41.9 → 40.5 kg), accelerating in the last scan. Combined with the slow genetic recovery profile and high injury predisposition, resistance training 2x/week (compound movements with Mike, plus home dumbbell alternatives) combined with 88–110g daily protein is now the single most important intervention. Prehabilitation exercises are essential every session.
Ultrahuman Ring data confirms outstanding cardiovascular health: resting HR 56 bpm, HRV 137 ms (top decile for age 45), SpO2 98%. Blood tests corroborate with perfect lipid panel (total cholesterol 5.0, HDL 1.49, triglycerides 0.71). The one area to watch is the Glycan Median (G1) at the 23rd percentile, suggesting slightly reduced vascular resilience.
Stride Skin DNA shows high intrinsic ageing, raised oxidative stress, and high inflammatory response — a triple challenge. However, this is highly actionable: daily SPF 50+, topical vitamin C and retinol, oral astaxanthin (4–12 mg), and an antioxidant-rich diet can significantly slow extrinsic ageing. Nickel sensitivity warrants awareness with jewellery and accessories.
Genetic sleep quality is at the lower end of the scale, with higher caffeine sensitivity compounding the issue. Despite this, HRV data shows excellent night-time recovery (121 ms average) — suggesting current habits are partially compensating. No caffeine after noon, consistent schedule, cool bedroom, and magnesium before bed are the key levers. The warrior (GG) genotype means stress resilience is strong, but needs challenge to perform.
Across 8 data sources and over 100 biomarkers, Sarah presents an extraordinary health profile for a 45-year-old female. A biological age of 20 (GlycanAge), metabolic age of 30 (Body Composition), textbook blood panel, and HRV in the top decile all confirm someone ageing at roughly half the expected rate. The key actionable areas are: preserving muscle mass through resistance training and higher protein, targeted methylation support via methylated B vitamins, and proactive skin defence against the high intrinsic ageing genetics. With the personalised supplement protocol and lifestyle optimisations now in place, the trajectory is set for long-term exceptional health.