One hundred biomarkers. Read against each other.
Ten organ systems. Every panel on every member. The quarterly retest covers the subset where intra-year change is clinically meaningful — excluding genetic markers, antibodies, and stable indices.
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Cardiovascular
Lipid particles, vascular inflammation, and risk markers that drive long-term cardiovascular disease independent of conventional cholesterol.
13 markers- On quarterly retest
Total cholesterol
TC · mg/dLThe sum of all cholesterol carried in the blood across LDL, HDL, and VLDL particles.
A broad cardiovascular risk indicator. Elevated total cholesterol is associated with atherosclerotic disease, though particle-based markers (ApoB, LDL-P) offer more precise risk stratification.
Reference — < 200 optimal; 200-239 borderline; ≥ 240 elevated - On quarterly retest
Low-density lipoprotein cholesterol
LDL-C · mg/dLCholesterol carried in LDL particles. The principal modifiable risk factor for atherosclerotic cardiovascular disease.
Lower is better for long-term cardiovascular outcomes. Target ranges depend on baseline risk profile. Statin therapy and dietary intervention are the standard means of lowering LDL-C.
Reference — < 100 optimal; 100-129 near-optimal; 130-159 borderline; ≥ 160 elevated - On quarterly retest
High-density lipoprotein cholesterol
HDL-C · mg/dLCholesterol carried in HDL particles, involved in reverse cholesterol transport.
Higher values are historically considered cardio-protective, though extremely high HDL has been associated with increased risk in some cohorts. Interpret in context of overall lipid profile.
Reference — > 60 protective; 40-60 (men) / 50-60 (women) acceptable; < 40 (men) / < 50 (women) low - On quarterly retest
Triglycerides
TG · mg/dLCirculating fat molecules derived from dietary intake and hepatic synthesis.
Elevated triglycerides are a marker of insulin resistance, excess caloric intake, and, at very high levels, pancreatitis risk. Interpret alongside fasting glucose and HbA1c.
Reference — < 150 optimal; 150-199 borderline; 200-499 elevated; ≥ 500 very elevated - On quarterly retest
Non-HDL cholesterol
Non-HDL-C · mg/dLTotal cholesterol minus HDL-C, reflecting all atherogenic particles including LDL, VLDL, IDL, and Lp(a).
A stronger predictor of cardiovascular events than LDL-C alone, particularly in insulin-resistant states. Target is typically 30 mg/dL above the LDL-C target.
Reference — < 130 optimal; 130-159 borderline; ≥ 160 elevated - On quarterly retest
Apolipoprotein B
ApoB · mg/dLThe structural protein on every atherogenic lipoprotein particle — LDL, VLDL, IDL, and Lp(a).
A direct particle count for atherogenic particles. ApoB is increasingly favoured as the most actionable cardiovascular risk marker, especially where LDL-C and triglycerides are discordant.
Reference — < 80 optimal; 80-100 acceptable; ≥ 100 elevated - Full panel only
Lipoprotein(a)
Lp(a) · nmol/LA genetically determined lipoprotein strongly associated with cardiovascular risk independent of LDL.
Elevated Lp(a) is a causal risk factor for atherosclerotic cardiovascular disease. Levels are largely fixed at birth; testing once in a lifetime is sufficient for risk stratification.
Reference — < 75 optimal; 75-125 borderline; > 125 elevated - On quarterly retest
High-sensitivity C-reactive protein
hs-CRP · mg/LA sensitive measure of low-grade systemic inflammation.
Elevated hs-CRP is associated with cardiovascular risk and metabolic inflammation. Interpret only when no acute illness is present, as infection sharply elevates the value.
Reference — < 1.0 low risk; 1.0-3.0 moderate; > 3.0 elevated - On quarterly retest
Homocysteine
Hcy · µmol/LAn amino acid intermediate whose elevation reflects methylation dysfunction and B-vitamin status.
Moderately elevated homocysteine is associated with cardiovascular and cognitive risk. Often responds to B12, folate, and B6 repletion.
Reference — < 10 optimal; 10-15 borderline; > 15 elevated - Full panel only
LDL particle number
LDL-P · nmol/LThe total count of LDL particles in circulation, measured by NMR spectroscopy.
Where LDL-C and LDL-P are discordant (for example, in insulin resistance), LDL-P is the superior predictor of cardiovascular events.
Reference — < 1000 optimal; 1000-1299 near-optimal; 1300-1599 borderline; ≥ 1600 elevated - Full panel only
Small dense LDL
sdLDL · mg/dLA particularly atherogenic subfraction of LDL particles.
Elevated sdLDL is associated with increased cardiovascular risk and is characteristic of the atherogenic dyslipidaemia seen in metabolic syndrome.
Reference — < 20 optimal; 20-35 borderline; > 35 elevated - On quarterly retest
Total cholesterol to HDL ratio
TC:HDL · ratioCalculated ratio of total cholesterol to HDL cholesterol.
A simple composite cardiovascular risk ratio. Below 3.5 is considered optimal; above 5 suggests elevated risk.
Reference — < 3.5 optimal; 3.5-5.0 acceptable; > 5.0 elevated - On quarterly retest
Very low-density lipoprotein
VLDL · mg/dLCalculated as one-fifth of triglycerides when triglycerides are below 400 mg/dL.
A surrogate for triglyceride-rich atherogenic particles. Interpret alongside triglycerides and ApoB.
Reference — < 30
Metabolic
Glucose regulation, insulin sensitivity, and early markers of metabolic dysfunction.
10 markers- On quarterly retest
Fasting glucose
FBG · mg/dLBlood glucose concentration after an overnight fast.
A foundational marker for diabetes risk. Interpret alongside HbA1c and fasting insulin for a fuller picture of metabolic health.
Reference — 70-99 normal; 100-125 prediabetic; ≥ 126 diabetic (on two occasions) - On quarterly retest
Haemoglobin A1c
HbA1c · %The percentage of haemoglobin that has been glycated, reflecting average blood glucose over the prior ~3 months.
The gold-standard marker for chronic glycaemic status. Less affected by short-term dietary changes than fasting glucose.
Reference — < 5.7 normal; 5.7-6.4 prediabetic; ≥ 6.5 diabetic - On quarterly retest
Fasting insulin
Insulin · µIU/mLCirculating insulin concentration after an overnight fast.
Elevated fasting insulin is an early sign of insulin resistance, often preceding changes in fasting glucose or HbA1c by years.
Reference — < 10 optimal; 10-15 borderline; > 15 elevated - On quarterly retest
HOMA-IR
HOMA-IR · indexCalculated index of insulin resistance from fasting glucose and fasting insulin.
A composite insulin-resistance score. Rising HOMA-IR over time is actionable even when fasting glucose remains normal.
Reference — < 1.5 optimal; 1.5-2.5 borderline; > 2.5 insulin-resistant - On quarterly retest
Uric acid
UA · mg/dLA metabolic end product of purine degradation.
Elevated uric acid is associated with gout, metabolic syndrome, and cardiovascular risk. Levels reflect diet, alcohol intake, renal clearance, and fructose metabolism.
Reference — 3.4-7.0 (men) / 2.4-6.0 (women) normal - On quarterly retest
Triglyceride-glucose index
TyG · indexA calculated index from fasting triglycerides and fasting glucose, used as a surrogate marker of insulin resistance.
A simple and reliable insulin-resistance proxy. Useful when fasting insulin assay variability is a concern.
Reference — < 8.5 optimal; 8.5-9.0 borderline; > 9.0 elevated - Full panel only
C-peptide
C-peptide · ng/mLA by-product of endogenous insulin synthesis, released in equal molar amounts to insulin.
Distinguishes endogenous from exogenous insulin. Useful in evaluating hypoglycaemia and residual beta-cell function.
Reference — 0.8-3.9 - Full panel only
Fructosamine
Fructosamine · µmol/LGlycated serum proteins, reflecting average blood glucose over the prior 2-3 weeks.
Complements HbA1c when short-term glycaemic change matters or when HbA1c interpretation is compromised (haemoglobinopathy, recent transfusion).
Reference — 200-285 - Full panel only
Leptin
Leptin · ng/mLAn adipocyte-derived hormone involved in satiety and energy balance.
Elevated leptin is common in obesity and indicates leptin resistance. Tested on indication.
Reference — Sex and BMI dependent - Full panel only
Adiponectin
Adiponectin · µg/mLAn adipocyte-derived hormone involved in insulin sensitivity.
Inversely correlated with visceral adiposity and insulin resistance. Low values add resolution to metabolic risk assessment.
Reference — Sex and BMI dependent
Hepatic
Liver enzyme activity, bile function, and synthetic capacity.
8 markers- On quarterly retest
Alanine aminotransferase
ALT · U/LAn enzyme released when hepatocytes are damaged.
The most specific routine marker of hepatocellular injury. Elevated ALT is commonly seen in non-alcoholic fatty liver disease, viral hepatitis, and drug-induced liver injury.
Reference — 7-45 (men) / 7-35 (women) - On quarterly retest
Aspartate aminotransferase
AST · U/LAn enzyme found in liver, heart, muscle, and red blood cells.
Less specific than ALT. Interpret alongside ALT: an AST:ALT ratio > 2 suggests alcoholic liver disease; ratio < 1 suggests non-alcoholic fatty liver disease.
Reference — 10-40 - On quarterly retest
Alkaline phosphatase
ALP · U/LAn enzyme from bile ducts, bone, and intestine.
Elevated ALP can indicate cholestasis, bile duct obstruction, or bone turnover. Fractionation distinguishes hepatic from bone origin when the cause is unclear.
Reference — 44-147 - On quarterly retest
Gamma-glutamyl transferase
GGT · U/LA biliary enzyme sensitive to alcohol, hepatic fat, and drug-induced injury.
An early and sensitive marker of hepatobiliary stress. Often the first liver enzyme to rise in response to alcohol intake.
Reference — 9-48 - On quarterly retest
Total bilirubin
T. Bili · mg/dLA pigment produced from haemoglobin breakdown, cleared by the liver.
Elevation can indicate hepatocellular dysfunction, haemolysis, or Gilbert's syndrome. Mild isolated elevation in an asymptomatic member is often benign Gilbert's.
Reference — 0.1-1.2 - On quarterly retest
Direct (conjugated) bilirubin
D. Bili · mg/dLThe conjugated fraction of bilirubin.
An elevated direct fraction suggests biliary obstruction or hepatocellular damage, distinguishing these causes from haemolysis.
Reference — 0.0-0.3 - On quarterly retest
Albumin
Alb · g/dLThe principal plasma protein, produced by the liver.
A marker of hepatic synthetic function and nutritional status. Low albumin suggests chronic illness, malnutrition, or advanced liver disease.
Reference — 3.5-5.0 - On quarterly retest
Total protein
TP · g/dLThe sum of albumin and globulins.
Interpretation requires albumin-globulin breakdown. Low total protein suggests malabsorption or synthetic failure; elevated globulin fraction can indicate inflammation or paraproteinaemia.
Reference — 6.0-8.3
Renal
Glomerular filtration, electrolyte balance, and nitrogen clearance.
9 markers- On quarterly retest
Creatinine
Cr · mg/dLA muscle breakdown product cleared by the kidneys.
A standard marker of renal filtration, best interpreted through the calculated eGFR. Muscle mass affects baseline values.
Reference — 0.74-1.35 (men) / 0.59-1.04 (women) - On quarterly retest
Estimated glomerular filtration rate
eGFR · mL/min/1.73m²A calculated estimate of glomerular filtration rate.
The primary measure of renal function. Chronic kidney disease staging depends on eGFR trend across repeated measurements.
Reference — ≥ 90 normal; 60-89 mild reduction; 30-59 moderate; < 30 severe - On quarterly retest
Blood urea nitrogen
BUN · mg/dLNitrogen carried in urea, a protein metabolism end product.
Elevated BUN can indicate dehydration, high protein intake, or renal dysfunction. Interpret with creatinine — BUN:Cr ratio distinguishes prerenal from intrinsic causes.
Reference — 7-25 - Full panel only
Cystatin C
CysC · mg/LA filtration marker less dependent on muscle mass than creatinine.
A more sensitive marker of early renal dysfunction, particularly in low-muscle-mass individuals and athletes where creatinine is misleading.
Reference — 0.53-0.95 - On quarterly retest
Sodium
Na · mmol/LThe principal extracellular cation.
Abnormalities reflect fluid balance and antidiuretic hormone function rather than dietary intake. Chronic hyponatraemia warrants investigation.
Reference — 135-145 - On quarterly retest
Potassium
K · mmol/LThe principal intracellular cation.
Abnormalities have cardiac implications and require attention. Spurious elevation from haemolysis during collection is common.
Reference — 3.5-5.1 - On quarterly retest
Chloride
Cl · mmol/LThe principal extracellular anion.
Typically shifts in parallel with sodium. Informs acid-base status when interpreted with bicarbonate.
Reference — 98-107 - On quarterly retest
Bicarbonate
HCO3 · mmol/LThe principal buffer in the blood, reflecting acid-base status.
Low bicarbonate suggests metabolic acidosis (renal, diabetic, or respiratory compensation). Elevated values suggest metabolic alkalosis.
Reference — 22-29 - On quarterly retest
Urine microalbumin / creatinine ratio
UACR · mg/gA urinary marker of early glomerular damage.
The earliest marker of diabetic and hypertensive nephropathy. Elevation precedes eGFR decline and warrants intervention.
Reference — < 30 normal; 30-300 microalbuminuria; > 300 macroalbuminuria
Thyroid
Thyroid hormone production, conversion, and autoimmune activity.
6 markers- On quarterly retest
Thyroid-stimulating hormone
TSH · mIU/LThe pituitary hormone that regulates thyroid output.
The most sensitive screening marker for thyroid dysfunction. Elevated TSH suggests hypothyroidism; suppressed TSH suggests hyperthyroidism.
Reference — 0.4-4.0 - On quarterly retest
Free triiodothyronine
Free T3 · pg/mLThe biologically active form of thyroid hormone.
Measures the unbound, active fraction of T3. Useful when symptoms suggest thyroid dysfunction despite a normal TSH.
Reference — 2.3-4.2 - On quarterly retest
Free thyroxine
Free T4 · ng/dLThe unbound fraction of the primary thyroid hormone T4.
Confirms and characterises TSH-flagged thyroid dysfunction. Normal Free T4 with elevated TSH defines subclinical hypothyroidism.
Reference — 0.8-1.8 - Full panel only
Reverse triiodothyronine
rT3 · ng/dLAn inactive metabolite of T4 produced under stress, illness, and caloric restriction.
Elevated rT3 with normal TSH can indicate thyroid hormone resistance, chronic stress, or severe illness. Interpretation is nuanced and requires clinical correlation.
Reference — 9.2-24.1 - Full panel only
Thyroid peroxidase antibody
TPO Ab · IU/mLAn autoantibody directed at thyroid peroxidase.
The principal marker of Hashimoto's thyroiditis. Once detected and characterised, repeat testing adds limited value over time.
Reference — < 35 - Full panel only
Thyroglobulin antibody
Tg Ab · IU/mLAn autoantibody directed at thyroglobulin.
Supports the diagnosis of autoimmune thyroid disease, particularly when TPO antibodies are borderline.
Reference — < 20
Reproductive hormones
Gonadal and pituitary hormones relevant to reproductive health, body composition, and mood.
12 markers- On quarterly retest
Total testosterone
Total T · ng/dLThe sum of free and bound testosterone in circulation.
The foundational marker of gonadal function in men. Age-appropriate ranges matter; a value of 400 is different at age 32 than at age 62.
Reference — 264-916 (men); 15-70 (women) - On quarterly retest
Free testosterone
Free T · pg/mLThe unbound, biologically active fraction of testosterone.
A better reflection of tissue-level androgen availability than total testosterone, particularly when SHBG is abnormal.
Reference — 9-30 (men); 0.3-1.9 (women) - On quarterly retest
Sex hormone-binding globulin
SHBG · nmol/LA liver-produced protein that binds sex hormones in circulation.
SHBG modifies the interpretation of total testosterone and estradiol. Low SHBG is associated with insulin resistance; high SHBG is seen with hyperthyroidism, oral estrogen, and hepatic dysfunction.
Reference — 10-57 (men); 18-144 (women) - On quarterly retest
Dehydroepiandrosterone sulfate
DHEA-S · µg/dLAn adrenal androgen precursor.
Declines with age. Low DHEA-S is associated with adrenal fatigue states; high DHEA-S in women warrants evaluation for adrenal or ovarian pathology.
Reference — Age and sex dependent; typically 80-560 (men 18-60); 35-430 (women 18-60) - On quarterly retest
Estradiol
E2 · pg/mLThe principal estrogen in women of reproductive age; present in lower concentrations in men.
Interpreted differently across the menstrual cycle and menopausal status in women. In men, elevated E2 from aromatisation of testosterone is a cause of gynaecomastia and mood changes.
Reference — Cycle-dependent in women; 10-40 in men - On quarterly retest
Progesterone
Prog · ng/mLA steroid hormone, elevated in the luteal phase and during pregnancy.
Luteal-phase progesterone confirms ovulation. Perimenopausal decline is associated with sleep disruption and mood changes.
Reference — Cycle-dependent; 5-20 in luteal phase; < 1 in postmenopause - Full panel only
Luteinising hormone
LH · mIU/mLA pituitary hormone driving gonadal steroid production.
Distinguishes primary from secondary hypogonadism. Elevated LH with low testosterone indicates primary testicular failure.
Reference — Cycle-dependent in women; 1.7-8.6 in men - Full panel only
Follicle-stimulating hormone
FSH · mIU/mLA pituitary hormone driving follicular development and spermatogenesis.
Elevated FSH in women is a key marker of diminished ovarian reserve and perimenopausal transition. In men, elevated FSH with normal testosterone suggests isolated spermatogenic failure.
Reference — Cycle-dependent in women; 1.5-12.4 in men - Full panel only
Prolactin
PRL · ng/mLA pituitary hormone.
Elevated prolactin can suppress gonadal function and warrants evaluation for pituitary adenoma, medication effect, or hypothyroidism.
Reference — 4-15 (men); 4-23 (women) - Full panel only
Anti-Müllerian hormone
AMH · ng/mLA marker of ovarian reserve in women.
Declines with age. A key fertility-planning marker. Interpretation is context-specific; tested by member request in the relevant demographic.
Reference — Age-dependent; 1.0-4.0 in women 25-35 - Full panel only
Prostate-specific antigen, total
PSA · ng/mLA prostate glycoprotein elevated in prostate disease.
Screening value in men over 45 with informed consent. Elevation requires urological follow-up. Interpretation nuanced by age and prostate volume.
Reference — < 4.0 for most men; age-adjusted thresholds apply - Full panel only
Free PSA
Free PSA · %The unbound fraction of PSA, expressed as a percentage of total PSA.
A lower free PSA percentage with elevated total PSA raises suspicion of prostate malignancy.
Reference — > 25% lower risk
Adrenal and longevity
Stress-axis hormones and growth factors associated with ageing and resilience.
5 markers- On quarterly retest
Cortisol, morning
Cortisol AM · µg/dLThe primary glucocorticoid, peaking in the early morning.
Assesses HPA-axis function. Markedly low AM cortisol warrants evaluation for adrenal insufficiency; markedly elevated values warrant evaluation for Cushing's syndrome.
Reference — 6.2-19.4 (AM draw) - Full panel only
Insulin-like growth factor 1
IGF-1 · ng/mLA growth factor mediating many effects of growth hormone.
A stable proxy for growth hormone status. Elevated IGF-1 with appropriate clinical picture raises concern for acromegaly; low IGF-1 with symptoms suggests adult growth hormone deficiency.
Reference — Age-dependent; typically 100-300 in adults 30-50 - Full panel only
Dehydroepiandrosterone (free)
DHEA · ng/mLThe unconjugated adrenal androgen precursor.
Complements DHEA-S as a marker of adrenal reserve. Interpretation combined with cortisol and DHEA-S.
Reference — Age and sex dependent - Full panel only
Pregnenolone
Preg · ng/dLA precursor to all steroid hormones.
Low pregnenolone can suggest an upstream steroidogenesis limitation. Tested on indication.
Reference — 10-200 - Full panel only
Parathyroid hormone
PTH · pg/mLThe primary regulator of serum calcium.
Evaluates the calcium-PTH-vitamin D axis. Elevated PTH with elevated calcium suggests primary hyperparathyroidism.
Reference — 15-65
Haematology
Complete blood count and differential — red cells, white cells, platelets.
18 markers- On quarterly retest
White blood cell count
WBC · 10³/µLTotal leukocyte count.
Elevated in infection, inflammation, leukaemia, and corticosteroid use. Low WBC warrants evaluation for marrow suppression, viral illness, or autoimmune disease.
Reference — 4.0-11.0 - On quarterly retest
Red blood cell count
RBC · 10⁶/µLTotal erythrocyte count.
Interpret alongside haemoglobin and MCV. Distinguishes absolute erythrocytosis from haemoconcentration.
Reference — 4.5-5.9 (men); 4.0-5.2 (women) - On quarterly retest
Haemoglobin
Hb · g/dLThe oxygen-carrying protein in red blood cells.
The principal marker for anaemia. Interpretation requires MCV classification to identify the underlying cause.
Reference — 13.5-17.5 (men); 12.0-15.5 (women) - On quarterly retest
Haematocrit
Hct · %The proportion of blood volume occupied by red cells.
Tracks with haemoglobin. Useful for assessing plasma volume shifts and erythrocytosis.
Reference — 41-53 (men); 36-46 (women) - On quarterly retest
Mean corpuscular volume
MCV · fLThe average volume of a red blood cell.
Classifies anaemia as microcytic (iron deficiency, thalassaemia), normocytic (acute blood loss, chronic disease), or macrocytic (B12/folate deficiency, alcohol).
Reference — 80-100 - On quarterly retest
Mean corpuscular haemoglobin
MCH · pgThe average mass of haemoglobin per red blood cell.
Complements MCV in characterising anaemia. Low MCH is seen in iron deficiency and thalassaemia.
Reference — 27-33 - On quarterly retest
Mean corpuscular haemoglobin concentration
MCHC · g/dLThe average concentration of haemoglobin within red blood cells.
Elevated MCHC is seen in hereditary spherocytosis. Low MCHC is seen with iron deficiency.
Reference — 32-36 - On quarterly retest
Red cell distribution width
RDW · %Variation in red cell size.
Elevated RDW indicates heterogeneity in red cell volumes and is often the earliest sign of evolving iron, B12, or folate deficiency before MCV becomes abnormal.
Reference — 11.5-14.5 - On quarterly retest
Platelet count
Plt · 10³/µLTotal platelet count.
Low platelet count affects bleeding risk and warrants evaluation for drug effect, viral illness, or marrow disease. Elevated platelet count can be reactive (inflammation) or clonal.
Reference — 150-450 - On quarterly retest
Mean platelet volume
MPV · fLAverage platelet volume.
Elevated MPV indicates higher platelet turnover. Provides context in thrombocytopenia evaluation.
Reference — 7.5-11.5 - On quarterly retest
Neutrophils, absolute
ANC · 10³/µLAbsolute neutrophil count.
The primary infection-fighting leukocyte. Elevated in bacterial infection and acute stress; severely low ANC is associated with infection risk.
Reference — 1.8-7.7 - On quarterly retest
Lymphocytes, absolute
ALC · 10³/µLAbsolute lymphocyte count.
Elevated in viral infection and lymphoproliferative disease. Low in stress, corticosteroid exposure, and some viral infections.
Reference — 1.0-4.0 - On quarterly retest
Monocytes, absolute
AMC · 10³/µLAbsolute monocyte count.
Elevated in chronic inflammation, tuberculosis, and some malignancies.
Reference — 0.1-0.9 - On quarterly retest
Eosinophils, absolute
AEC · 10³/µLAbsolute eosinophil count.
Elevated in allergy, atopic disease, helminth infection, and drug reactions.
Reference — 0.0-0.5 - On quarterly retest
Basophils, absolute
ABC · 10³/µLAbsolute basophil count.
Rarely elevated in routine practice. Persistent elevation raises concern for chronic myeloid leukaemia.
Reference — 0.0-0.2 - Full panel only
Reticulocyte count
Retic · %The percentage of immature red cells in circulation.
Distinguishes hypoproliferative anaemia from anaemia with appropriate marrow response. Essential in anaemia workup.
Reference — 0.5-2.5 - On quarterly retest
Creatine kinase
CK · U/LAn enzyme released from skeletal and cardiac muscle.
Elevation suggests muscle injury. Interpret in the context of exercise, statin use, and symptoms.
Reference — 30-200 (men); 20-180 (women) - On quarterly retest
Lactate dehydrogenase
LDH · U/LA cytoplasmic enzyme released on cell turnover or damage.
A non-specific marker of tissue damage. Elevation warrants clinical correlation.
Reference — 125-220
Iron and nutrients
Iron kinetics, key vitamins, and mineral status.
17 markers- On quarterly retest
Serum iron
Fe · µg/dLCirculating iron bound to transferrin.
Interpret alongside TIBC and ferritin. A single value in isolation is of limited meaning.
Reference — 65-175 (men); 50-170 (women) - On quarterly retest
Total iron-binding capacity
TIBC · µg/dLThe total capacity of transferrin to bind iron.
Elevated in iron deficiency. Suppressed in chronic inflammation and hepatic disease.
Reference — 240-450 - On quarterly retest
Transferrin saturation
TSAT · %The proportion of transferrin occupied by iron.
A percentage below 20 suggests iron deficiency. Persistent elevation above 45 warrants evaluation for haemochromatosis.
Reference — 20-50 - On quarterly retest
Ferritin
Ferritin · ng/mLAn intracellular iron storage protein whose circulating level correlates with iron stores.
Low ferritin confirms iron deficiency. Elevated ferritin is non-specific — interpret in the context of inflammation (hs-CRP) before concluding iron overload.
Reference — 30-400 (men); 15-200 (women) - On quarterly retest
Vitamin D, 25-hydroxy
25(OH)D · ng/mLThe circulating storage form of vitamin D.
Widespread insufficiency in India despite sun exposure. Optimal range for musculoskeletal and immune function is 40 to 60 ng/mL.
Reference — 30-100 sufficient; 20-29 insufficient; < 20 deficient - On quarterly retest
Vitamin B12
B12 · pg/mLCirculating cobalamin.
Low B12 causes macrocytic anaemia and neurological symptoms. Vegetarian and vegan Indian members are particularly at risk; active B12 (holotranscobalamin) and MMA refine interpretation at borderline values.
Reference — 200-1100 - On quarterly retest
Folate
Folate · ng/mLCirculating folate.
Required for methylation and red cell production. Deficiency produces macrocytic anaemia and elevated homocysteine.
Reference — ≥ 5.4 - On quarterly retest
Magnesium
Mg · mg/dLSerum magnesium concentration.
Serum magnesium reflects only ~1% of body stores and often underestimates tissue deficiency. Interpret alongside symptoms (cramping, poor sleep, arrhythmia risk).
Reference — 1.7-2.3 - On quarterly retest
Phosphorus
P · mg/dLSerum phosphate concentration.
Interpret alongside calcium, vitamin D, and parathyroid hormone when indicated. Rarely abnormal in healthy adults.
Reference — 2.5-4.5 - Full panel only
Methylmalonic acid
MMA · nmol/LA metabolite that accumulates in functional B12 deficiency.
A more sensitive indicator of tissue B12 deficiency than serum B12, particularly when B12 is borderline (200-400 pg/mL).
Reference — 73-376 - On quarterly retest
Calcium
Ca · mg/dLTotal serum calcium.
Interpret with albumin (corrected calcium). Persistent elevation warrants evaluation for parathyroid or malignant causes.
Reference — 8.6-10.3 - Full panel only
Zinc
Zn · µg/dLPlasma zinc concentration.
Relevant to immune function, wound healing, and testosterone synthesis. Interpretation requires morning draw and attention to acute-phase confounding.
Reference — 60-120 - Full panel only
Vitamin A (retinol)
Vit A · µg/dLCirculating retinol.
Deficiency is uncommon in well-nourished adults but seen in malabsorption. Excess from supplementation is hepatotoxic.
Reference — 20-80 - Full panel only
Vitamin E (alpha-tocopherol)
Vit E · mg/LThe principal fat-soluble antioxidant vitamin.
Deficiency is uncommon; levels are affected by lipid status. Interpret alongside lipids.
Reference — 5.5-17.0 - Full panel only
Selenium
Se · µg/LA trace element involved in antioxidant enzymes and thyroid hormone metabolism.
Insufficient selenium impairs thyroid hormone conversion and antioxidant capacity. Widespread mild insufficiency in parts of India.
Reference — 70-150 - Full panel only
Copper
Cu · µg/dLA trace element and acute-phase reactant.
Persistent elevation warrants investigation. Low values are seen with zinc excess and in Menkes disease. Test on indication.
Reference — 70-140 (men); 80-155 (women) - Full panel only
Vitamin B6 (pyridoxal-5-phosphate)
B6 (PLP) · nmol/LThe active form of vitamin B6.
Required for homocysteine metabolism and neurotransmitter synthesis. Deficiency is common in chronic alcohol use and malabsorption.
Reference — 20-125
Inflammation and immunity
Systemic inflammation, immune activation, and omega balance.
7 markers- On quarterly retest
Erythrocyte sedimentation rate
ESR · mm/hrA non-specific marker of inflammation.
Slower to rise and fall than hs-CRP. Useful for tracking chronic inflammatory conditions over time.
Reference — 0-22 (men); 0-29 (women) - On quarterly retest
Ferritin (inflammatory context)
Ferritin-I · ng/mLThe same ferritin measurement, interpreted as an acute-phase reactant.
Markedly elevated ferritin (> 500 ng/mL) in the absence of iron overload can indicate systemic inflammation or infection. Context from hs-CRP and ESR is essential.
Reference — Interpretation varies by inflammatory context - On quarterly retest
Omega-3 index
Ω-3 index · %The percentage of EPA + DHA in red blood cell membranes.
Below 4% is associated with cardiovascular risk; above 8% is targeted for cardioprotection. Responsive to dietary and supplemental omega-3 intake.
Reference — > 8 optimal; 4-8 intermediate; < 4 elevated risk - Full panel only
Interleukin-6
IL-6 · pg/mLA cytokine central to the acute-phase inflammatory response.
Chronically elevated IL-6 is associated with cardiovascular risk, sarcopenia, and accelerated ageing. Tested on indication where chronic inflammation is suspected.
Reference — < 7 - On quarterly retest
Fibrinogen
Fibrinogen · mg/dLA clotting factor and acute-phase reactant.
Elevated fibrinogen contributes to thrombotic risk and tracks with inflammation. Adds resolution to cardiovascular risk assessment.
Reference — 200-400 - Full panel only
Anti-tissue transglutaminase IgA
anti-tTG IgA · U/mLAn autoantibody used in coeliac disease screening.
Elevated values raise suspicion of coeliac disease and warrant gastroenterology referral. Requires concurrent total IgA to interpret reliably.
Reference — < 20 - Full panel only
Immunoglobulin A
IgA · mg/dLTotal serum IgA concentration.
IgA deficiency affects interpretation of anti-tTG IgA. Elevated IgA can indicate chronic infection or inflammation.
Reference — 70-400
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