Six-marker cardiovascular panel — full lipid profile plus high-sensitivity CRP for comprehensive heart risk monitoring.
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A six-marker essential cardiovascular panel measuring total cholesterol, LDL, HDL, triglycerides, non-HDL, and high-sensitivity CRP.
Cardiovascular disease is the leading cause of death in the UK. Knowing your lipid profile and inflammation levels gives you the clearest picture of your personal cardiovascular risk. Blood lipid levels and systemic inflammation are the two most important modifiable risk factors detectable by a simple blood test.
The Essential Heart Health Check measures the five-part lipid panel — total cholesterol, LDL (the primary atherogenic driver), HDL (the protective fraction), triglycerides (reflecting carbohydrate and alcohol intake), and non-HDL cholesterol (a comprehensive atherogenic burden marker) — alongside high-sensitivity CRP, which captures the low-grade vascular inflammation that predicts cardiovascular events independently of cholesterol levels.
This panel is suitable from age 25 onwards as part of annual health monitoring, for those with a family history of heart disease, and for individuals tracking the impact of dietary or lifestyle changes on their cardiovascular risk profile. Home fingerstick kit available; fasted collection required for accurate triglycerides. GMC-physician reviewed results within 3 to 5 working days.
Understand what each marker measures, why it matters, and what the science says — not just a list of numbers.
Overall cholesterol burden; clinical significance depends on the breakdown between protective HDL and atherogenic LDL fractions.
Primary driver of atherosclerotic plaques; the main modifiable cardiovascular risk target.
Protective cholesterol that transports excess cholesterol back to the liver; higher levels reduce cardiovascular risk.
Blood fats elevated by refined carbohydrates, alcohol, and metabolic syndrome; an independent cardiovascular risk marker.
Total cholesterol minus HDL; captures all atherogenic lipoprotein fractions and is a superior risk indicator to LDL alone.
Sensitive vascular inflammation marker; predicts cardiovascular events independently of cholesterol levels.
This panel is designed for adults who want a comprehensive, evidence-based picture of their metabolic health — not a GP referral panel.
Adults over 25 wanting an annual cardiovascular risk baseline
Those with a family history of heart attack or stroke
People tracking the cardiovascular impact of dietary, exercise, or medication changes
Those on statins who want to monitor lipid levels between GP visits
Non-fasted triglyceride levels are significantly elevated by recent food intake; for accurate results, a 10 to 12 hour fast before collection is required. This panel does not include ApoB, Lp(a), or homocysteine — markers that provide additional cardiovascular risk data beyond the standard lipid panel. hsCRP is a non-specific inflammation marker; elevated values may reflect sources of inflammation other than cardiovascular risk (infection, autoimmune disease), and clinical context is required for interpretation. LDL is calculated using the Friedewald equation in this panel; at very low LDL values (below 1.5 mmol/L) or very high triglycerides (above 4.5 mmol/L), direct LDL measurement may be more accurate.
From order to physician-reviewed report in as little as three working days.
Three options designed to fit your schedule, location, and preference — all producing a laboratory-standard sample.
Adults 18+ in mainland UK. Not suitable if you have had a transfusion in the last 3 months.
Order anytime; kit dispatched within 24 hours Mon–Fri.
Allow 24–48 hours for sample transit on top of lab processing time.
Adults 18+ within 20 miles of a serviced city centre.
Mon–Sun, 06:00–20:00. Next-day booking typical.
Sample reaches the lab within 24 hours of collection.
Adults 16+ with photo ID. Paediatric draws by appointment at selected sites.
Mon–Fri, with Saturday hours at most metropolitan locations.
Samples processed same-day at the receiving clinic.
Every test is processed in a UKAS ISO 15189-accredited laboratory, overseen by GMC-registered physicians, and governed by UK GDPR. No overseas processing, no offshore data.
Follow these guidelines to ensure accurate, reproducible results. Most markers are sensitive to recent food, exercise, and sleep.
Can't find your answer? Our clinical support team is available Monday to Friday, 9am–5pm.
Contact supportUK NHS targets for cardiovascular risk prevention are: total cholesterol below 5.0 mmol/L; LDL below 3.0 mmol/L for primary prevention, and below 1.8 mmol/L (or at least 50% reduction from baseline) for high-risk individuals or those with established cardiovascular disease; HDL above 1.0 mmol/L in men and above 1.2 mmol/L in women; triglycerides below 1.7 mmol/L. Non-HDL cholesterol targets are typically 0.8 mmol/L higher than the corresponding LDL target. These are population-level benchmarks; your physician report will assess your individual risk profile, accounting for blood pressure, family history, smoking, diabetes, and other factors.
LDL (low-density lipoprotein) is the most atherogenic form — it penetrates arterial walls, oxidises, triggers inflammation, and forms plaques that can rupture and cause heart attacks or strokes. However, LDL alone is an imperfect measure because different people carry very different amounts of cholesterol within each LDL particle. ApoB, which counts the actual number of LDL particles, is more predictive of events than LDL cholesterol content, particularly in those with metabolic syndrome. Non-HDL cholesterol — which captures VLDL, IDL, and Lp(a) in addition to LDL — provides a more complete atherogenic picture than LDL alone within the standard lipid panel.
For many people, dietary changes alone can meaningfully reduce LDL by 10 to 20%. The most impactful dietary strategies include: replacing saturated fats (butter, cheese, fatty meat, coconut oil) with unsaturated fats (olive oil, nuts, oily fish); increasing soluble fibre (oats, beans, lentils, apples) which binds cholesterol in the gut; adding plant sterols and stanols (found in enriched spreads and some yoghurts); losing weight if overweight (particularly visceral fat); reducing refined carbohydrates and added sugar (to lower triglycerides and raise HDL); and moderating alcohol intake. For those with familial hypercholesterolaemia or high cardiovascular risk, medication is usually required alongside dietary changes.
Non-HDL cholesterol is calculated as total cholesterol minus HDL. It encompasses all atherogenic lipoprotein fractions — LDL, VLDL (which carries triglycerides), IDL, and Lp(a) — giving a more complete picture of atherogenic burden than LDL alone. It does not require the sample to be fasted (unlike calculated LDL), though fasting is still recommended for accurate triglyceride measurement. UK NICE guidelines recommend non-HDL as the preferred cholesterol target for cardiovascular risk management, particularly in people with diabetes or those being treated with statins.
hsCRP (high-sensitivity CRP) measures very low levels of C-reactive protein that reflect chronic low-grade vascular inflammation — distinct from the high CRP elevations seen in acute infections. Vascular inflammation is a key driver of atherosclerotic plaque formation and rupture. The JUPITER trial demonstrated that individuals with normal LDL but hsCRP above 2 mg/L had substantially higher cardiovascular event rates and benefited from statin therapy, leading to rosuvastatin being approved for primary cardiovascular prevention in this group. Values below 1 mg/L represent low inflammatory risk; 1 to 3 mg/L moderate risk; above 3 mg/L high risk in the cardiovascular risk context.
For adults with no known cardiovascular risk factors, testing every 2 to 3 years from age 25 is a reasonable baseline monitoring frequency. For those with elevated LDL, a family history of premature cardiovascular disease, diabetes, or hypertension, annual testing is more appropriate. Those on statin therapy or other lipid-modifying treatments should test 3 months after starting or adjusting medication to confirm the response, and then annually once stable. If you are making significant dietary or lifestyle changes, retesting at 3 to 6 months gives meaningful feedback on your cardiovascular response.