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Where every number comes from

Biomarker Guide

What each biomarker actually does, what it measures, why anyone would test it, and what makes the number move. We are here to educate you on what the numbers mean, so every figure is referenced, and where there is no agreed number, we say so. The Body Guide is the other half and explains the systems these markers belong to. Between them you get the complete picture.

The latest science, constantly updated74 markers fully unpackedHealthcare, not sickcare

This guide contains two important but different types of numbers: population reference ranges and guideline thresholds.

A population reference range describes where most people in a reference group sit. It is a description, not a target, and the reference group is not always a healthy one. Sometimes a range is simply taken from the manufacturer or the published literature.

A guideline threshold is different: it is a line a professional body has drawn deliberately, for a stated purpose, and we name the body and the purpose every time one appears.

Neither of the above can claim to be the optimal level at which humans should be. And they likely never will. Not least of all because everyone is so different and blanket statements or ranges almost never work.

For most tests there is no single NHS reference range. Each hospital lab publishes its own, which is why the same test can read differently in 2 different hospitals. Some of that difference comes from the analysers and methods each lab uses, and creatinine is the clearest example. The same applies to any blood testing labs but UK labs have agreed common ranges for a list of tests since 2011, including things like magnesium, albumin, ALP, adjusted calcium, creatine kinase and uric acid. Either way, the range on your own report is the one that matters.

All personal blood results should be discussed with your doctor.

How much does a repeat have to move before it means anything

Every result carries 2 kinds of wobble. The analyser is not perfectly repeatable, and your own level genuinely varies from one day to the next. Together they set a figure called the reference change value, which is how far a second result has to sit from the first before the difference is real and not noise.

It is larger than most people expect and it differs enormously between markers. For some it runs well past 50%. This is the reason a low testosterone is repeated before anyone acts on it, and why up to 30% of men whose first one comes back low are normal on the second. The same logic applies to every number in this guide, which is why a small change between 2 tests is not always an actual change in you.

Supplementing biotin can affect your blood results

Biotin is vitamin B7. Hair, skin and nail supplements routinely contain 5mg, at least 100 times the reference intake in the UK (50mcg) and 150 times in the US (30mcg), and prescribed biotin therapy can go well beyond that at 100 mg a day or more. This matters because a large group of blood tests are built on a biotin-based chemistry, and enough circulating biotin bends the result.

It does not affect everything, and where it does it does not push in the same direction. The tests affected are the immunoassays. On this panel that is testosterone, oestradiol, progesterone, SHBG, prolactin, FSH, LH, cortisol, DHEA-sulphate, anti-Mullerian hormone, TSH, free T4, free T3, total T4, thyroid antibodies, PSA, ferritin, vitamin D, vitamin B12, active B12 and folate. Which way it pushes depends on how the test is built. Tests for small molecules read falsely HIGH, so testosterone, oestradiol, progesterone, cortisol, DHEA-sulphate, free T4, free T3, vitamin D, B12 and folate all read higher than they are. The thyroid antibodies also read falsely high even though they are large molecules. This is because their tests are built the same way as the small-molecule ones. Tests for large molecules read falsely LOW, so SHBG, prolactin, FSH, LH, TSH, anti-Mullerian hormone, active B12, ferritin and PSA all read lower than they are.

That is why a biotin-affected panel does not look obviously wrong. It looks contradictory, and the contradiction is a pattern that ordinarily means something. High sex hormones alongside suppressed pituitary hormones is the classic one. A falsely low SHBG next to a falsely high testosterone makes it worse, because calculated free testosterone and the free androgen index are both worked out from those 2 numbers, so both get pushed the same way twice.

The rest of the panel is not affected at all. Liver, kidney, lipids, glucose, serum iron and the iron binding capacities, hs-CRP, the full blood count and HbA1c are measured by methods that do not use biotin.

The usual advice is to leave at least 8 hours after an ordinary supplement dose (5-10mg) and at least 3 days after the very high doses (100mg+) or the tests that are more sensitive to biotin like folate and thyroid antibodies. Manufacturers have been reformulating these tests to tolerate more biotin, and how much any one of them now tolerates depends on which version your lab runs, so the safe move is unchanged. If you take biotin and nobody asked you about it before the draw, stop it and repeat.

Fasting for Ramadan can affect your blood results

Ramadan is a lunar month in which observant Muslims take no food or drink, water included, from dawn to sunset, and in a UK summer that daily fast can run past 18 hours.

Most of the panel holds still across the month. In healthy adults, fasting insulin and the insulin resistance worked out from it are unchanged, fasting glucose falls by a trivial amount, and the average movement in the lipid panel is smaller than the analytical variation of the test itself. Weight falls by about 1 kg and is back within a few weeks of the month ending.

What does move is concentration rather than the thing being measured. A sample drawn late in a fasting day is more concentrated, because a long fast without water thickens the blood, so creatinine and urea read higher and eGFR reads lower, and haematocrit, haemoglobin, albumin and adjusted calcium shift the same way. Drinking more overnight brings them back, which is what shows this is concentration and not damage. Bilirubin goes the other way and rises with fasting in everyone, which matters most in Gilbert's syndrome and is covered in the Liver section.

In practice a test taken during Ramadan is usually done in the evening after eating, which is a fed sample. Anything that asks for a fast, so glucose and triglycerides, will not be a fasting value on that draw. A morning sample is drawn a few hours after suhoor and is not a fasting value either. If you want a clean fasting result, the week before the month or the week after it is the straightforward answer. This is behaviour and not ethnicity, so it applies to anybody who fasts this way.

This guide is reviewed regularly and updated to reflect current guidance and new evidence.

Last reviewed: 5 October 2026.

Every marker, grouped by system. Pick a section, or go straight to a marker.

Hormones

Testosterone | Free testosterone | Free androgen index | Oestradiol | Progesterone | Sex Hormone Binding Globulin | Follicle Stimulating Hormone | Luteinising Hormone | Prolactin | DHEA-Sulphate | Cortisol | Anti-Müllerian Hormone

Thyroid

Thyroid Stimulating Hormone | Free T4 | Free T3 | Thyroid Antibodies

Iron

Iron | Total Iron Binding Capacity | Unsaturated Iron Binding Capacity | Transferrin saturation | Ferritin

Full blood count

Haemoglobin | Haematocrit | Red blood cell count | MCV | MCH | MCHC | RDW | White blood cell count | Neutrophils | Lymphocytes | Monocytes | Eosinophils | Basophils | Platelet count | MPV

Liver

ALT | AST | ALP | GGT | Total bilirubin | Total protein | Albumin | Globulin | Lipase

Kidney

Urea | Creatinine | eGFR | Sodium | Potassium | Cystatin C | Uric acid

Lipids and cardiovascular

Total cholesterol | HDL cholesterol | LDL cholesterol | Non-HDL cholesterol | HDL as a percentage of total cholesterol | Triglycerides | Apolipoprotein B | Apolipoprotein A1 | Lipoprotein(a)

Blood sugar

HbA1c | Glucose

Inflammation

High-Sensitivity CRP | Erythrocyte Sedimentation Rate

Vitamins and minerals

Vitamin D | Total Vitamin B12 | Active Vitamin B12 | Folate | Magnesium | Zinc | Adjusted Calcium

Other

Creatine Kinase | Prostate-Specific Antigen

References

Where a threshold, a reference range or a guideline position appears in this section, the body that published it is named alongside it in the text. Where the evidence and current guidance disagree, the entry says so instead of picking a side. The sources are listed here by marker.

Reference ranges and guideline thresholds

Berg J, Lane V. Pathology Harmony; a pragmatic and scientific approach to unfounded variation in the clinical laboratory. Ann Clin Biochem 2011;48(3):195-197

Berg J. The UK Pathology Harmony initiative; The foundation of a global model. Clin Chim Acta 2014;432:22-26

How much does a repeat have to move before it means anything

Harris EK, Yasaka T. On the calculation of a "reference change" for comparing two consecutive measurements. Clin Chem 1983;29(1):25-30

Fraser CG. Biological Variation: From Principles to Practice. Washington DC: AACC Press, 2001

Aarsand AK, Fernandez-Calle P, Webster C, Coskun A, Gonzalez-Lao E, Diaz-Garzon J, et al. The EFLM Biological Variation Database. European Federation of Clinical Chemistry and Laboratory Medicine

Mairesse A, Wauthier L, Courcelles L, Luyten U, Burlacu MC, Maisin D, et al. Biological variation and analytical goals of four thyroid function biomarkers in healthy European volunteers. Clin Endocrinol (Oxf) 2021;94(5):845-850

Carobene A, Aarsand AK, Coskun A, Diaz-Garzon J, Locatelli M, Fernandez-Calle P, et al. Biological variation of serum iron from the European biological variation study (EuBIVAS). Clin Chem Lab Med 2022;61(3):e57-e60

Brambilla DJ, O'Donnell AB, Matsumoto AM, McKinlay JB. Intraindividual variation in levels of serum testosterone and other reproductive and adrenal hormones in men. Clin Endocrinol (Oxf) 2007;67(6):853-862

Bhasin S, Brito JP, Cunningham GR, Hayes FJ, Hodis HN, Matsumoto AM, et al. Testosterone Therapy in Men With Hypogonadism: An Endocrine Society Clinical Practice Guideline. J Clin Endocrinol Metab 2018;103(5):1715-1744

Corona G, Morgado LA, Boeri L, et al. EAU Guidelines on Sexual and Reproductive Health: A Summary of the 2026 Recommendations for Measurement and Biochemical Confirmation of Hypogonadism. Eur Urol Focus 2026 (online 23 May 2026)

Grossmann M, Jayasena CN, Anawalt BD. Approach to the Patient: The Evaluation and Management of Men >=50 Years With Low Serum Testosterone Concentration. J Clin Endocrinol Metab 2023;108(9):e871-e884

Brambilla DJ, Matsumoto AM, Araujo AB, McKinlay JB. The effect of diurnal variation on clinical measurement of serum testosterone and other sex hormone levels in men. J Clin Endocrinol Metab 2009;94(3):907-913

Supplementing biotin can affect your blood results

Li D, Ferguson A, Cervinski MA, Lynch KL, Kyle PB. AACC Guidance Document on Biotin Interference in Laboratory Tests. J Appl Lab Med 2020;5(3):575-587

Trambas C, Lu Z, Yen T, Sikaris K. Characterization of the scope and magnitude of biotin interference in susceptible Roche Elecsys competitive and sandwich immunoassays. Ann Clin Biochem 2018;55(2):205-215

Institute of Medicine (US) Standing Committee on the Scientific Evaluation of Dietary Reference Intakes. Dietary Reference Intakes for Thiamin, Riboflavin, Niacin, Vitamin B6, Folate, Vitamin B12, Pantothenic Acid, Biotin, and Choline. Washington DC: National Academies Press, 1998, Chapter 11 (Biotin)

Roche Diagnostics. Elecsys Anti-TPO method sheet, V11.0, 2025-04; Roche Diagnostics. Elecsys Anti-Tg method sheet, V2.0, 2024-11 (doc 09004998500)

National Institute for Health and Care Excellence. Thyroid disease: assessment and management. NICE guideline NG145, published 20 November 2019, last updated 12 October 2023, recommendation 1.2.11

Campi I, Feldt-Rasmussen U, Gruson D, Halsall D, Raverot V, van den Berg S, Moran C. 2026 ETA guideline on interference in immunoassay measurements used in assessment of thyroid function. Eur Thyroid J 2026;15(4):e260011

Roche Diagnostics. Elecsys Ferritin method sheet, V7.0, 2023-12 (GB)

Roche Diagnostics. Elecsys Vitamin D total, Elecsys Vitamin B12, Elecsys Folate III and Elecsys Active-B12 (holotranscobalamin) method sheets

US Food and Drug Administration. Biotin Interference with Troponin Lab Tests - Assays Subject to Biotin Interference. Last updated 21 June 2022

CDC/NCHS. NHANES Laboratory Procedure Manual: Creatine Phosphokinase (CPK) in Serum, Roche cobas 8000 c502. 2021 cycle

Ghosh A, Russell A, Dasgupta A. Newly reformulated total and free PSA immunoassay on cobas e411 analyzer is virtually free from biotin interference. Ann Clin Lab Sci 2022;52(3):504-506

Fasting for Ramadan can affect your blood results

Faris MAE, Jahrami H, BaHammam A, Kalaji Z, Madkour M, Hassanein M. A systematic review, meta-analysis, and meta-regression of the impact of diurnal intermittent fasting during Ramadan on glucometabolic markers in healthy subjects. Diabetes Res Clin Pract 2020;165:108226

Faris MAE, Abdelrahim DN, El Herrag SE, Khaled MB, Shihab KA, AlKurd R, Madkour M. Cardiometabolic and obesity risk outcomes of dawn-to-dusk, dry intermittent fasting: Insights from an umbrella review. Clin Nutr ESPEN 2025;67:127-145

Mirmiran P, Bahadoran Z, Gaeini Z, Moslehi N, Azizi F. Effects of Ramadan intermittent fasting on lipid and lipoprotein parameters: An updated meta-analysis. Nutr Metab Cardiovasc Dis 2019;29(9):906-915

Fernando HA, Zibellini J, Harris RA, Seimon RV, Sainsbury A. Effect of Ramadan Fasting on Weight and Body Composition in Healthy Non-Athlete Adults: A Systematic Review and Meta-Analysis. Nutrients 2019;11(2):478

Jahrami HA, Alsibai J, Clark CCT, Faris MAE. A systematic review, meta-analysis, and meta-regression of the impact of diurnal intermittent fasting during Ramadan on body weight in healthy subjects aged 16 years and above. Eur J Nutr 2020;59(6):2291-2316

Tarabeih M, Qaddumi J, Hamdan Z, Hassan M, Jebrin K, Khazneh E, et al. Increasing Overnight Fluid Intake and Kidney Function During Ramadan Fasting: A Randomized Controlled Trial. Transplant Proc 2023;55(1):80-86

Bello AK, Lloyd A, Osman MA, Kurzawa J, Chambers T, Habib S, et al. Impact of Ramadan fasting on kidney function and related outcomes in chronic kidney disease and kidney transplant recipients: a systematic review and meta-analysis. BMJ Open 2024;14(11):e085329

Nasiri A, Alahmadi A, Alshammari M, et al. Ramadan fasting and hematological disorders: clinical considerations, risks, and management strategies. Clin Hematol Int 2025;7(4):41-53

Faris MAE, Jahrami H, Abdelrahim D, Bragazzi N, BaHammam A. The effects of Ramadan intermittent fasting on liver function in healthy adults: A systematic review, meta-analysis, and meta-regression. Diabetes Res Clin Pract 2021;178:108951

Kamal S, Abdelhakam S, Ghoraba D, Massoud Y, Abdel Aziz K, Hassan H, et al. The frequency, clinical course, and health related quality of life in adults with Gilbert's syndrome: a longitudinal study. BMC Gastroenterol 2019;19:22

Maughan RJ, Shirreffs SM. Hydration and performance during Ramadan. J Sports Sci 2012;30 Suppl 1:S33-41

Chowdhury A, Khan H, Lasker SS, Chowdhury TA. Fasting outcomes in people with diabetes and chronic kidney disease in East London during Ramadan 2018: The East London diabetes in Ramadan survey. Diabetes Res Clin Pract 2019;152:166-170

Boobes Y, Afandi B, AlKindi F, et al. Consensus recommendations on fasting during Ramadan for patients with kidney disease: review of available evidence and a call for action (RaK Initiative). BMC Nephrol 2024;25(1):84

This page is general information about what lab tests measure. It is not medical advice, it is not a diagnosis, and it is not a substitute for speaking to a clinician about your own results.


Dr Abir Awan PhD

Specialist Haematology Pharmacist

Doctorate in Molecular Pharmacology

Independent Prescriber