Rare Heterozygous PCSK1 Variants in Human Obesity: The Contribution of the p.Y181H Variant and a Literature Review

Genes (Basel). 2022 Sep 27;13(10):1746. doi: 10.3390/genes13101746.

Abstract

Recently, it was reported that heterozygous PCSK1 variants, causing partial PC1/3 deficiency, result in a significant increased risk for obesity. This effect was almost exclusively generated by the rare p.Y181H (rs145592525, GRCh38.p13 NM_000439.5:c.541T>C) variant, which affects PC1/3 maturation but not enzymatic capacity. As most of the identified individuals with the heterozygous p.Y181H variant were of Belgian origin, we performed a follow-up study in a population of 481 children and adolescents with obesity, and 486 lean individuals. We identified three obese (0.62%) and four lean (0.82%) p.Y181H carriers (p = 0.506) through sanger sequencing and high resulting melting curve analysis, indicating no association with obesity. Haplotype analysis was performed in 13 p.Y181H carriers, 20 non-carriers (10 with obesity and 10 lean), and two p.Y181H families, and showed identical haplotypes for all heterozygous carriers (p < 0.001). Likewise, state-of-the-art literature concerning the role of rare heterozygous PCSK1 variants implies them to be rarely associated with monogenic obesity, as first-degree carrier relatives of patients with PC1/3 deficiency are mostly not reported to be obese. Furthermore, recent meta-analyses have only indicated a robust association for scarce disruptive heterozygous PCSK1 variants with obesity, while clinical significance is less or sometimes lacking for most nonsynonymous variants.

Keywords: founder mutation; obesity; overweight; proprotein convertase subtilisin/kexin type 1 (PCSK1); rare variants.

Publication types

  • Review
  • Research Support, Non-U.S. Gov't

MeSH terms

  • Adolescent
  • Child
  • Follow-Up Studies
  • Heterozygote
  • Humans
  • Obesity* / genetics
  • Proprotein Convertase 1* / genetics

Substances

  • PCSK1 protein, human
  • Proprotein Convertase 1

Grants and funding

This research was funded by a Methusalem-OEC grant—“GENOMED” (Grant Number: FFB190208). Evelien Van Dijck is supported by a GOA-grant (FFB180348/36572) and a FWO-grant (Fonds Wetenschappelijk Onderzoek) (Grant Number: 11E6921N). The Methusalem-OEC grant and the GOA-grant are both from the University of Antwerp. The APC was funded by a grant from the university of Antwerp to WVH.