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European Heart Journal· 2013Q1· Guideline

Familial hypercholesterolaemia is underdiagnosed and undertreated in the general population: guidance for clinicians to prevent coronary heart disease: Consensus Statement of the European Atherosclerosis Society

Børge G. Nordestgaard, M. John Chapman, Steve E. Humphries, Henry N. Ginsberg et al.

Short summary

Familial hypercholesterolaemia (FH) is severely underdiagnosed (<1% of estimated 1/500 prevalence) and undertreated, leading to up to 13-fold increased coronary heart disease (CHD) risk, necessitating urgent screening and aggressive treatment.

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Key points

  • Less than 1% of the estimated 14-34 million individuals worldwide with Familial Hypercholesterolaemia (FH) are diagnosed.
  • Individuals with FH have up to a 13-fold increased risk of coronary heart disease (CHD).
  • Screening is recommended for individuals with plasma cholesterol ≥8 mmol/L (adults) or ≥6 mmol/L (children), premature CHD, or family history of FH.
  • Treatment involves aggressive lipid-lowering therapies, including statins, ezetimibe, and bile acid binding resins, with specific LDL cholesterol targets based on age and CHD status.

AI-generated from the title and abstract; the full text is not read.

Abstract

AIMS: The first aim was to critically evaluate the extent to which familial hypercholesterolaemia (FH) is underdiagnosed and undertreated. The second aim was to provide guidance for screening and treatment of FH, in order to prevent coronary heart disease (CHD). METHODS AND RESULTS: Of the theoretical estimated prevalence of 1/500 for heterozygous FH, <1% are diagnosed in most countries. Recently, direct screening in a Northern European general population diagnosed approximately 1/200 with heterozygous FH. All reported studies document failure to achieve recommended LDL cholesterol targets in a large proportion of individuals with FH, and up to 13-fold increased risk of CHD. Based on prevalences between 1/500 and 1/200, between 14 and 34 million individuals worldwide have FH. We recommend that children, adults, and families should be screened for FH if a person or family member presents with FH, a plasma cholesterol level in an adult ≥8 mmol/L(≥310 mg/dL) or a child ≥6 mmol/L(≥230 mg/dL), premature CHD, tendon xanthomas, or sudden premature cardiac death. In FH, low-density lipoprotein cholesterol targets are <3.5 mmol/L(<135 mg/dL) for children, <2.5 mmol/L(<100 mg/dL) for adults, and <1.8 mmol/L(<70 mg/dL) for adults with known CHD or diabetes. In addition to lifestyle and dietary counselling, treatment priorities are (i) in children, statins, ezetimibe, and bile acid binding resins, and (ii) in adults, maximal potent statin dose, ezetimibe, and bile acid binding resins. Lipoprotein apheresis can be offered in homozygotes and in treatment-resistant heterozygotes with CHD. CONCLUSION: Owing to severe underdiagnosis and undertreatment of FH, there is an urgent worldwide need for diagnostic screening together with early and aggressive treatment of this extremely high-risk condition.

The authors' abstract, as published at the source. European Heart Journal, 2013 · DOI ↗

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Field: Surgery

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