{
  "abstract": "Background Heterozygous Familial Hypercholesterolaemia (HeFH) is caused by pathogenic variants in LDLR, APOB, APOE or PCSK9, leading to elevated low-density lipoprotein-cholesterol and increased cardiovascular risk. In the UK, HeFH affects ~1 in 288 individuals. The 100 000 Genomes Project (100KGP) generated whole genome sequencing (WGS) data from >85 000 participants recruited primarily with cancer or rare inherited disorders. We analysed WGS data to assess the prevalence and spectrum of FH-causing variants.Methods Variants in LDLR, APOB, APOE and PCSK9 were extracted from 100KGP WGS data and annotated using expert-reviewed ClinGen curation. Demographic, ancestry and linked health records were incorporated. Analyses were restricted to unrelated individuals.Results Among 54 818 unrelated participants, 167 were heterozygote for an FH-causing variant, giving a prevalence of 1:328 (95% CI 1:285 to 1:386). Prevalence was similar across ancestries, including African (1:388) and South Asian (1:276). Variant distribution was: LDLR 67%, APOB 26.5%, APOE 3.5% and PCSK9 3%. Two individuals carried two FH variants, consistent with homozygous FH. Among 22 442 genetic relatives, 77 also carried an FH variant. Of all variant carriers, 53% were female, mean age at recruitment was 41.3 years, with 43 younger than 18 years, and 54.3% had documented hypercholesterolaemia.Conclusions The prevalence and gene distribution of FH-causing variants in 100KGP are consistent with UK estimates. Differences in variant spectrum across ancestries were observed; however, FH prevalence was similar. Participants who consented to the return of actionable findings were informed, providing direct clinical benefit from genomic research.",
  "authors": [
    {
      "affiliations": [
        "Cardiovascular and Genomics Research Institute, School of Health & Medical Sciences, City St George’s University of London, London, UK",
        "Institute of Cardiovascular Science, Faculty of Population Health, University College London, London, UK"
      ],
      "name": "Marta Futema"
    },
    {
      "affiliations": [
        "Cardiovascular and Genomics Research Institute, School of Health & Medical Sciences, City St George’s University of London, London, UK",
        "Clinical Pharmacology and Precision Medicine, William Harvey Research Institute, Queen Mary University of London, London, UK"
      ],
      "name": "Martin Bird"
    },
    {
      "affiliations": [
        "Oxford Genetic Laboratories, Oxford University Hospitals NHS Foundation Trust, The Churchill Hospital, Oxford, UK"
      ],
      "name": "Ash Haeger"
    },
    {
      "affiliations": [
        "Oxford Genetic Laboratories, Oxford University Hospitals NHS Foundation Trust, The Churchill Hospital, Oxford, UK"
      ],
      "name": "Ellen Pinder"
    },
    {
      "affiliations": [
        "Oxford Genetic Laboratories, Oxford University Hospitals NHS Foundation Trust, The Churchill Hospital, Oxford, UK"
      ],
      "name": "Anthony O’Rourke"
    },
    {
      "affiliations": [
        "Cardiovascular and Genomics Research Institute, School of Health & Medical Sciences, City St George’s University of London, London, UK"
      ],
      "name": "Elijah R Behr"
    },
    {
      "affiliations": [
        "Institute of Cardiovascular Science, Faculty of Population Health, University College London, London, UK"
      ],
      "name": "Steve E Humphries"
    }
  ],
  "title": "Frequency of familial hypercholesterolaemia-causing genetic variants in the 100 000 Genomes Project cohort: whole genome sequencing analyses of 77 260 participants",
  "uid": "0107467b-424d-51b5-ae7b-79917c565927"
}