Widening the phenotypic spectrum caused by pathogenic PDX1 variants in individuals with neonatal diabetes

BMJ Open Diabetes Res Care. 2024 Nov 14;12(6):e004439. doi: 10.1136/bmjdrc-2024-004439.

Abstract

Introduction: Biallelic PDX1 variants are a rare cause of isolated pancreatic agenesis and neonatal diabetes (NDM) without exocrine pancreatic insufficiency, with 17 cases reported in the literature.

Research design and methods: To determine the phenotypic variability caused by this rare genetic aetiology, we investigated 19 individuals with NDM resulting from biallelic disease-causing PDX1 variants.

Results: Of the 19 individuals, 8 (42%) were confirmed to have exocrine insufficiency requiring replacement therapy. Twelve individuals (63.2%) had extrapancreatic features, including 8 (42%) with conditions affecting the duodenum and/or hepatobiliary tract. Defects in duodenum development are consistent with previous Pdx1 ablation studies in mice which showed abnormal rostral duodenum development.

Conclusions: Our findings show that recessive PDX1 variants can cause a syndromic form of NDM, highlighting the need for clinical assessment of extrapancreatic features in individuals with NDM caused by PDX1 variants.

Keywords: Genetics.

MeSH terms

  • Diabetes Mellitus* / genetics
  • Female
  • Homeodomain Proteins* / genetics
  • Humans
  • Infant
  • Infant, Newborn
  • Male
  • Mutation
  • Pancreas* / abnormalities
  • Pancreas* / pathology
  • Pancreatic Diseases / congenital
  • Phenotype*
  • Prognosis
  • Trans-Activators* / genetics

Substances

  • pancreatic and duodenal homeobox 1 protein
  • Homeodomain Proteins
  • Trans-Activators

Supplementary concepts

  • Pancreatic Agenesis, Congenital