Rare variant genetic landscape of familial chylomicronemia syndrome (FCS) in the United Kingdom.

PURPOSE

Familial chylomicronemia syndrome (FCS) is a rare autosomal recessive disorder. This study aimed to analyze the genotype distribution of FCS-causing genes in the United Kingdom.

METHODS

Data were anonymously collated from 2 genetic testing laboratories providing national genetic diagnosis services for severe hypertriglyceridemia in the United Kingdom.

RESULTS

As of December 2023, 880 individuals underwent genetic testing for FCS. The mean (SD) age at the time of genetic testing was 42.5 (15.3) years. After genotyping, 12.9% of the individuals ( = 114) received a genetic diagnosis of FCS. The detection rate of variant-positive multifactorial chylomicronemia syndrome, ie, heterozygous for pathogenic/likely pathogenic (P/LP) variants in 1 of the 5 canonical genes was 11.4% ( = 100).Among 114 genetically proven FCS individuals, 52.6% ( = 60) had biallelic P/LP variants (ie, LPL-FCS), 45.6% ( = 52) had biallelic non- P/LP variants (ie, non--FCS) and 1.7% ( = 2) individuals were digenic. Among non--FCS ( = 52), the most common gene implicated was (42.3%, = 22), followed by (32.7%, = 17), (13.5%, = 7) and (11.5%, = 6). Most variant-positive multifactorial chylomicronemia syndrome harbored P/LP variants in (61%) or (37%).The geographical distribution of FCS demonstrated regional variability, where the Northwest of England had the highest number of FCS cases per million population. Individuals of European geographic ancestry predominantly had LPL-FCS (60.9%); however, genotype was more diverse in individuals of non-European origin ( 47.1%, 30.9%, 8.8%, 7.4%, and 4.4%). Variants in specific causal genes, and , were predominantly observed in non-European FCS individuals.

CONCLUSION

The genetic architecture of FCS in the United Kingdom is complex, with a substantial proportion affected by non- FCS-causing genes. It also displays a significant regional and ethnic variations.