Endocrinology
North American Familial Chylomicronemia Score calculator
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Clinical inputs
Result
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Clinical inputs
- Age group and onset
- Body mass index
- Secondary factors
- Abdominal pain or pancreatitis
- Fasting triglycerides
- Triglyceride to total cholesterol ratio
- Apolipoprotein B
Primary source
Hegele RA et al. Development and validation of clinical criteria to identify familial chylomicronemia syndrome (FCS) in North America. J Clin Lipidol. DOI: 10.1016/j.jacl.2024.09.008. PMID: 39537503. Table 3 points, confirmed on the scenario grid in Table 2. Adolescent or adult with early hypertriglyceridemia onset 12. Child with hypertriglyceridemia 12. All fasting triglyceride readings severely elevated 13. High triglyceride/total cholesterol ratio 8. Low apolipoprotein B 12. BMI under 25.0 kg/m² in adults, or under the 85th percentile in children and adolescents, 9. Recurrent abdominal pain without pancreatitis 9. History of pancreatitis 16. No secondary factors 11. Interactions: high ratio and low apolipoprotein B 7; child and no secondary factors 7; high ratio and no secondary factors 5. Early onset is hypertriglyceridemia of at least 5 mmol/L (440 mg/dL) in infancy or childhood. Severe triglycerides are above 10 mmol/L (880 mg/dL) on all recent fasting samples. A high ratio is above 8 in mg/dL or above 3.5 in mmol/L. Low apolipoprotein B is under 1.0 g/L (100 mg/dL). In the validation, 60 or higher was definite classical FCS (specificity 100%, sensitivity 66.7%) and 45 or higher was likely FCS (specificity 96.9%, sensitivity 88.9%). (2024)
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