Autosomal dominant tubulointerstitial kidney disease (ADTKD) in Ireland
Jazyk angličtina Země Velká Británie, Anglie Médium print
Typ dokumentu časopisecké články, multicentrická studie
Grantová podpora
Wellcome Trust - United Kingdom
PubMed
31509055
PubMed Central
PMC6746258
DOI
10.1080/0886022x.2019.1655452
Knihovny.cz E-zdroje
- Klíčová slova
- ADTKD, HNF-1B, MUC-1, UMOD, chronic kidney disease, frameshift, genetic, urinary smear,
- MeSH
- chronické selhání ledvin epidemiologie genetika patologie MeSH
- dominantní geny * MeSH
- dospělí MeSH
- genetické testování statistika a číselné údaje MeSH
- hepatocytární jaderný faktor 1-beta genetika MeSH
- ledvinové kanálky patologie MeSH
- lidé středního věku MeSH
- lidé MeSH
- mucin 1 genetika MeSH
- mutace MeSH
- prevalence MeSH
- průřezové studie MeSH
- senioři MeSH
- uromodulin genetika MeSH
- Check Tag
- dospělí MeSH
- lidé středního věku MeSH
- lidé MeSH
- mužské pohlaví MeSH
- senioři MeSH
- ženské pohlaví MeSH
- Publikační typ
- časopisecké články MeSH
- multicentrická studie MeSH
- Geografické názvy
- Irsko epidemiologie MeSH
- Názvy látek
- hepatocytární jaderný faktor 1-beta MeSH
- HNF1B protein, human MeSH Prohlížeč
- MUC1 protein, human MeSH Prohlížeč
- mucin 1 MeSH
- UMOD protein, human MeSH Prohlížeč
- uromodulin MeSH
Introduction: Autosomal dominant tubulointerstitial kidney disease (ADTKD) is a rare genetic cause of renal impairment resulting from mutations in the MUC1, UMOD, HNF1B, REN, and SEC61A1 genes. Neither the national or global prevalence of these diseases has been determined. We aimed to establish a database of patients with ADTKD in Ireland and report the clinical and genetic characteristics of these families. Methods: We identified patients via the Irish Kidney Gene Project and referral to the national renal genetics clinic in Beaumont Hospital who met the clinical criteria for ADTKD (chronic kidney disease, bland urinary sediment, and autosomal dominant inheritance). Eligible patients were then invited to undergo genetic testing by a variety of methods including panel-based testing, whole exome sequencing and, in five families who met the criteria for diagnosis of ADTKD but were negative for causal genetic mutations, we analyzed urinary cell smears for the presence of MUC1fs protein. Results: We studied 54 individuals from 16 families. We identified mutations in the MUC1 gene in three families, UMOD in five families, HNF1beta in two families, and the presence of abnormal MUC1 protein in urine smears in three families (one of which was previously known to carry the genetic mutation). We were unable to identify a mutation in 4 families (3 of whom also tested negative for urinary MUC1fs). Conclusions: There are 4443 people with ESRD in Ireland, 24 of whom are members of the cohort described herein. We observe that ADTKD represents at least 0.54% of Irish ESRD patients.
Clinical Research Centre Royal College of Surgeons Dublin Ireland
Department of Medicine Boston Children's Hospital Harvard Medical School Boston MA USA
Department of Medicine Royal College of Surgeons Dublin Ireland
Nephrology Department Beaumont Hospital Dublin Ireland
Pathology Department Beaumont Hospital Dublin Ireland
Section on Nephrology Wake Forest School of Medicine Winston Salem NC USA
Trinity Health Kidney Centre Tallaght Hospital Dublin Ireland
Trinity Health Kidney Centre Trinity Translational Medicine Institute Dublin Ireland
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Autosomal dominant tubulointerstitial kidney disease: A review