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Prevalence and cardiometabolic correlates of ketohexokinase gene variants among UK Biobank participants.
- Source :
-
PloS one [PLoS One] 2021 Feb 23; Vol. 16 (2), pp. e0247683. Date of Electronic Publication: 2021 Feb 23 (Print Publication: 2021). - Publication Year :
- 2021
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Abstract
- Essential fructosuria (EF) is a benign, asymptomatic, autosomal recessive condition caused by loss-of-function variants in the ketohexokinase gene and characterized by intermittent appearance of fructose in the urine. Despite a basic understanding of the genetic and molecular basis of EF, relatively little is known about the long-term clinical consequences of ketohexokinase gene variants. We examined the frequency of ketohexokinase variants in the UK Biobank sample and compared the cardiometabolic profiles of groups of individuals with and without these variants alone or in combination. Study cohorts consisted of groups of participants defined based on the presence of one or more of the five ketohexokinase gene variants tested for in the Affymetrix assays used by the UK Biobank. The rs2304681:G>A (p.Val49Ile) variant was present on more than one-third (36.8%) of chromosomes; other variant alleles were rare (<1%). No participants with the compound heterozygous genotype present in subjects exhibiting the EF phenotype in the literature (Gly40Arg/Ala43Thr) were identified. The rs2304681:G>A (p.Val49Ile), rs41288797 (p.Val188Met), and rs114353144 (p.Val264Ile) variants were more common in white versus non-white participants. Otherwise, few statistically or clinically significant differences were observed after adjustment for multiple comparisons. These findings reinforce the current understanding of EF as a rare, benign, autosomal recessive condition.<br />Competing Interests: The authors have read the journal’s policy and have the following conflicts: JJ, DN, PB, SC, YC and JM are employees of Eli Lilly and own stock in Eli Lilly. Eli Lilly holds a patent (“Disubstituted Pyrazole Compounds as Ketohexokinase Inhibitors”; WO 2020/257171 A1) related to inhibition of the ketohexokinase enzyme which is pertinent to the content of this article and is developing molecules that act by this mechanism. This does not alter our adherence to the PLOS ONE policies on sharing data and materials.
Details
- Language :
- English
- ISSN :
- 1932-6203
- Volume :
- 16
- Issue :
- 2
- Database :
- MEDLINE
- Journal :
- PloS one
- Publication Type :
- Academic Journal
- Accession number :
- 33621267
- Full Text :
- https://doi.org/10.1371/journal.pone.0247683