LDL Cholesterol Calculator
Estimate your LDL cholesterol from total cholesterol, HDL, and triglycerides using the Sampson-NIH 2020 equation, with the classic Friedewald estimate shown alongside for comparison. Supports mg/dL and mmol/L. This is an informational reference using published formulas, not a diagnostic test.
Both estimates are calculated, not directly measured. The Sampson-NIH equation is valid up to triglycerides of 800 mg/dL; Friedewald becomes unreliable above about 400 mg/dL and is shown only for comparison. A direct LDL measurement is recommended when triglycerides are very high. Discuss your lipid results with a healthcare provider.
How LDL Cholesterol Is Estimated
On most lab reports, LDL cholesterol is not measured directly. It is calculated from the three values a standard lipid panel does measure: total cholesterol, HDL cholesterol, and triglycerides. For decades the Friedewald equation (1972) was the default, but it systematically underestimates LDL at low LDL levels and breaks down when triglycerides are high. In 2020, Sampson and colleagues at the NIH published a more accurate equation (JAMA Cardiology 5:540–548) that remains valid up to triglycerides of 800 mg/dL. This tool computes both so you can see them side by side.
LDL = TC/0.948 − HDL/0.971 − (TG/8.56 + TG×(TC−HDL)/2140 − TG²/16100) − 9.44Friedewald (1972), shown for comparison:
LDL = TC − HDL − TG/5 (mg/dL) or TC − HDL − TG/2.2 (mmol/L)
Published LDL Reference Context
The bands below reflect the LDL-C categories long used by the US National Cholesterol Education Program (NCEP ATP III). These are published reference categories, not a treatment plan; current guidelines individualise LDL goals by overall cardiovascular risk.
| LDL-C (mg/dL) | LDL-C (mmol/L) | NCEP ATP III category |
|---|---|---|
| Below 100 | Below 2.6 | Optimal |
| 100 – 129 | 2.6 – 3.3 | Near or above optimal |
| 130 – 159 | 3.4 – 4.1 | Borderline high |
| 160 – 189 | 4.1 – 4.9 | High |
| 190 and above | 4.9 and above | Very high |
When a Calculated LDL Can Be Misleading
- Very high triglycerides. Above 800 mg/dL even the Sampson equation is not validated, and a direct LDL measurement is preferred.
- Non-fasting samples. Triglycerides rise after eating, which shifts the calculated LDL. Many labs still prefer a fasting sample for the calculated value.
- Low LDL. Friedewald in particular underestimates LDL when it is low, which is exactly where treatment targets often sit; the Sampson equation was designed to fix this.