OBJECTIVE: Multiple pituitary hormone deficiency (MPHD) may result from defects of transcription factors that govern early pituitary development. We aimed to establish the prevalence of HESX1, PROP1, and POU1F1 gene defects in a population-based cohort of patients with MPHD and to analyse the phenotype of affected individuals. DESIGN AND METHODS: Genomic analysis was carried out on 74 children and adults with MPHD from the Czech Republic (including four sibling pairs). Phenotypic data were collected from medical records and referring physicians. RESULTS: One patient carried a heterozygous mutation of POU1F1 (71C > T), and 18 patients (including three sibling pairs) had a PROP1 mutation (genotypes 150delA/301delGA/9/, 301delGA/301-delGA/8/, or 301delGA/349T > A/1/). A detailed longitudinal phenotypic analysis was performed for patients with PROP1 mutations (n = 17). The mean ( +/-s.d.) birth length SDS of these patients (0.12 +/- 0.76) was lower than expected based on their mean ( +/-s.d.) birth weight SDS (0.63 +/- 1.27; P = 0.01). Parental heights were normal. The patients' mean ( +/-s.d.) height SDS declined to -1.5 +/- 0.9, -3.6 +/- 1.3 and -4.1 +/- 1.2 at 1.5, 3 and 5 years of age, respectively. GH therapy, initiated at 6.8 +/- 3.2 years of age (mean dose: 0.022 mg/kg per day), led to substantial growth acceleration in all patients. Mean adult height (n = 7) was normal when adjusted for mid-parental height. ACTH deficiency developed in two out of seven young adult patients. CONCLUSIONS: PROP1 defects are a prevalent cause of MPHD. We suggest that testing for PROP1 mutations in patients with MPHD might become standard practice in order to predict risk of additional pituitary hormone deficiencies.
- MeSH
- dítě MeSH
- DNA vazebné proteiny genetika MeSH
- DNA genetika chemie MeSH
- dospělí MeSH
- fenotyp MeSH
- financování organizované MeSH
- homeodoménové proteiny genetika MeSH
- hypofyzární hormony nedostatek MeSH
- kohortové studie MeSH
- lidé MeSH
- longitudinální studie MeSH
- mladiství MeSH
- mutace MeSH
- nemoci hypofýzy genetika MeSH
- polymerázová řetězová reakce MeSH
- retrospektivní studie MeSH
- sekvenční analýza DNA MeSH
- senioři MeSH
- tělesná výška fyziologie MeSH
- transkripční faktor Pit-1 MeSH
- transkripční faktory genetika MeSH
- Check Tag
- dítě MeSH
- dospělí MeSH
- lidé MeSH
- mladiství MeSH
- mužské pohlaví MeSH
- senioři MeSH
- ženské pohlaví MeSH
- MeSH
- dítě MeSH
- finanční podpora výzkumu jako téma MeSH
- genetická transkripce MeSH
- geny MeSH
- hypofýza anatomie a histologie MeSH
- hypofyzární hormony genetika nedostatek MeSH
- lidé MeSH
- magnetická rezonanční tomografie metody MeSH
- mutace MeSH
- růstový hormon genetika nedostatek MeSH
- Check Tag
- dítě MeSH
- lidé MeSH
- Publikační typ
- abstrakt z konference MeSH
