Management of Hyperlipidaemia Based on Targets
The management of hyperlipidaemia should be based on risk stratification with LDL-C as the primary target, aiming for <1.8 mmol/L (70 mg/dL) in very high-risk patients and <2.6 mmol/L (100 mg/dL) in high-risk patients, or a reduction of at least 50% from baseline if these targets cannot be achieved.
Risk Stratification and Target Setting
Risk assessment is the first step in determining appropriate lipid targets:
Very High Risk 1:
- Documented cardiovascular disease (CVD)
- Diabetes with target organ damage
- Moderate to severe chronic kidney disease (GFR <60 mL/min/1.73m²)
- SCORE ≥10% for 10-year risk
- Target: LDL-C <1.8 mmol/L (70 mg/dL) or ≥50% reduction if baseline is 1.8-3.5 mmol/L
High Risk 1:
- Markedly elevated single risk factors (e.g., familial hyperlipidaemias, severe hypertension)
- SCORE ≥5% and <10% for 10-year risk
- Target: LDL-C <2.6 mmol/L (100 mg/dL) or ≥50% reduction if baseline is 2.6-5.1 mmol/L
Moderate Risk:
- SCORE ≥1% and <5% at 10 years
- Target: Consider LDL-C <3.0 mmol/L (115 mg/dL)
Low Risk:
- SCORE <1%
- Target: Consider LDL-C <3.0 mmol/L (115 mg/dL)
Secondary Targets
While LDL-C is the primary target, other lipid parameters should also be monitored 1, 2:
- Triglycerides: Target <150 mg/dL (1.7 mmol/L)
- HDL-C: Target >40 mg/dL (1.0 mmol/L) in men and >50 mg/dL (1.3 mmol/L) in women
- Non-HDL-C: Secondary target in patients with diabetes
- Very high risk: <2.6 mmol/L (<100 mg/dL)
- High risk: <3.4 mmol/L (<130 mg/dL)
Special Populations
Diabetes Patients 1, 2:
- Type 1 diabetes with microalbuminuria/renal disease: LDL-C reduction of at least 50% regardless of baseline
- Type 2 diabetes with CVD or CKD: LDL-C <1.8 mmol/L (<70 mg/dL)
- Type 2 diabetes without additional risk factors: LDL-C <2.6 mmol/L (<100 mg/dL)
Familial Hypercholesterolaemia 1:
- Suspect in patients with:
- CHD before age 55 (men) or 60 (women)
- Family history of premature CVD
- Tendon xanthomas
- Severely elevated LDL-C (>5 mmol/L or 190 mg/dL in adults)
- Require aggressive treatment with high-dose statins, often in combination with ezetimibe
Treatment Approach
- Statins at the highest recommended or tolerated dose
- High-intensity statins (atorvastatin 40-80 mg or rosuvastatin 20-40 mg) for very high-risk patients
- Assess LDL-C as early as 4 weeks after initiation
If targets not achieved 1, 2, 4:
- Add ezetimibe 10 mg daily (provides additional 15-25% LDL-C reduction)
- Consider PCSK9 inhibitors for very high-risk patients not achieving targets despite maximally tolerated statin plus ezetimibe
For elevated triglycerides 1, 2:
- Optimize glycemic control in diabetic patients
- Consider fibrates if HDL is low and LDL-C at goal
Monitoring and Follow-up
- Check lipid levels 4-12 weeks after initiating or changing therapy 2
- Monitor liver enzymes 8-12 weeks after starting statin therapy
- Once target levels achieved, annual lipid profile monitoring is recommended
- Assess for muscle symptoms at each follow-up visit
Common Pitfalls and Caveats
- Statin intolerance: Often overreported; consider rechallenge at lower doses or different statin before abandoning therapy
- Drug interactions: Be cautious with statin-fibrate combinations due to increased myopathy risk
- Pregnancy: Statins are generally not recommended during pregnancy
- Elderly patients: Benefit from statins similar to younger patients; treatment decisions should be based on risk assessment rather than age alone
- Acute coronary syndrome: High-dose statins should be given early after admission regardless of baseline LDL-C values
The most recent evidence strongly supports an aggressive approach to lipid management based on cardiovascular risk assessment, with LDL-C as the primary target and statins as the cornerstone of therapy.