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| Intensity | Drug & Dose | LDL↓ | PH Brand Names |
|---|---|---|---|
| High | Atorvastatin 40–80 mg | ≥50% |
Lipitor
Atostat
Atorvastatin (generics)
|
| High | Rosuvastatin 20–40 mg | ≥50% |
Crestor
Rosuphar
Rosuva (generics)
|
| Moderate | Atorvastatin 10–20 mg | 30–49% |
Lipitor
Atorvastatin (generics)
|
| Moderate | Rosuvastatin 5–10 mg | 30–49% |
Crestor
Rosuvastatin (generics)
|
| Moderate | Simvastatin 20–40 mg | 30–49% |
Zocor
Simtin
Simvastatin (generics)
|
| Moderate | Pravastatin 40–80 mg | 30–49% |
Pravachol
Pravastatin (generics)
|
| Moderate | Pitavastatin 2–4 mg | 30–49% |
Livalo
Pitava
|
| Low | Simvastatin 10 mg | <30% |
Simvastatin (generics)
|
| Low | Fluvastatin 20–40 mg | <30% |
Lescol
|
| Agent | Mechanism | LDL↓ | PH Brand | Notes |
|---|---|---|---|---|
| Ezetimibe 10 mg | NPC1L1 inhibitor (intestinal cholesterol absorption) | 15–25% | EzetrolZetia | Add-on to statin; also available as Vytorin (ezetimibe + simvastatin 10/20 or 10/40) |
| Evolocumab | PCSK9 inhibitor (monoclonal antibody) | 50–60% | Repatha | 140 mg SC q2w or 420 mg SC monthly; expensive — specialist referral |
| Alirocumab | PCSK9 inhibitor (monoclonal antibody) | 45–60% | Praluent | 75–150 mg SC q2w; limited local availability |
| Inclisiran | PCSK9 siRNA (gene silencing) | ~50% | Leqvio | 284 mg SC at 0, 3 mo, then q6 months; not yet widely available PH |
| Bempedoic acid | ATP-citrate lyase inhibitor | 15–25% | Limited PH availability | For statin-intolerant patients; avoid if eGFR <30 |
| Risk Category | LDL-C Goal | Non-HDL Goal | ApoB Goal |
|---|---|---|---|
| Secondary — Very High Risk (VHR) ≥2 events OR 1 event + high-risk features |
<55 mg/dL | <85 mg/dL | <55 mg/dL |
| Secondary — Not VHR 1 major ASCVD event, no high-risk features |
≤70 mg/dL | <100 mg/dL | <70 mg/dL |
| Primary — High Risk (≥10%) Including DM or FH |
<70 mg/dL | <100 mg/dL | <70 mg/dL |
| Primary — Intermediate (5–<10%) | <100 mg/dL | <130 mg/dL | <90 mg/dL |
| Primary — Borderline (3–<5%) Consider if risk enhancers present |
<100 mg/dL | <130 mg/dL | <90 mg/dL |
| Primary — Low Risk (<3%) | Lifestyle first; statin if LDL ≥190 | — | — |
| FH / LDL-C ≥190 mg/dL | <70 mg/dL or ≥50% ↓ | <100 mg/dL | <70 mg/dL |
| CAC Score | Implication | LDL Target |
|---|---|---|
| 0 (no detectable CAC) | Low risk — can defer statin in borderline/intermediate | Lifestyle modification; reassess in 5 yr |
| 1–99 Agatston Units | Mild coronary atherosclerosis | <100 mg/dL |
| 100–299 AU | Moderate atherosclerosis — treat as high-risk primary | <70 mg/dL |
| ≥300 AU (or ≥75th percentile for age/sex) | Extensive atherosclerosis | <70 mg/dL |
| ≥1000 AU | Very high coronary atherosclerosis burden | <55 mg/dL |
| Factor | Threshold | Clinical Impact |
|---|---|---|
| Lp(a) | ≥125 nmol/L (≥50 mg/dL) | Risk-enhancing — may upscale therapy in borderline/intermediate |
| Lp(a) (very high) | ≥250 nmol/L | Independent ≥2× CV risk increase; consider PCSK9i |
| hs-CRP | ≥2.0 mg/L | Inflammatory risk enhancer |
| ABI | <0.9 | Peripheral artery disease indicator — risk enhancer |
| Premature ASCVD | Men <55, women <65 | Strong family history — risk enhancer |
| Chronic inflammation | Autoimmune / HIV / psoriasis | Raises residual risk |
| Preeclampsia history | — | Women's risk enhancer |
| Metabolic syndrome | 3 of 5 criteria | Risk enhancer |