A classic twin study of lower urinary tract obstruction: Report of 3 cases and literature review.


Journal

Lower urinary tract symptoms
ISSN: 1757-5672
Titre abrégé: Low Urin Tract Symptoms
Pays: Australia
ID NLM: 101506777

Informations de publication

Date de publication:
Apr 2019
Historique:
received: 06 11 2017
revised: 06 02 2018
accepted: 25 02 2018
pubmed: 18 4 2018
medline: 18 12 2019
entrez: 18 4 2018
Statut: ppublish

Résumé

The aim of the present study was to investigate genetic effects in the formation of congenital lower urinary tract obstruction (LUTO) comprising posterior urethral valves (PUV), urethral atresia, and urethras with variable degrees of stenosis. A classic twin study was performed by assessing LUTO twin pairs from the literature. Furthermore, data regarding 3 previously unreported twin pairs with PUV from University of Bonn, Essen and Wrocławs own in-house databases were added. Both pair- and probandwise concordance rates were calculated and compared for monozygotic (MZ) and dizygotic (DZ) twin pairs. The pairwise concordance rates for all LUTO were 53% (95% confidence interval [CI] 32%-73%) and 17% (95% CI 3%-56%) for MZ and DZ twin pairs, respectively (P = .180). The probandwise concordance rates were 69% (95% CI 51%-83%) and 29% (CI 95% 8%-64%) for MZ and DZ twin pairs respectively (P = .084). The MZ/DZ ratios of the pair- and probandwise concordance rates were 3.1 and 2.4, respectively. The present study did not show significant differences in comparisons of concordance rates of MZ and DZ twin pairs, probably due to the small number of twin pairs reported. However, the more than 2-fold higher pair- and probandwise concordance rates for MZ versus DZ twin pairs are very suggestive of a contribution of genetic factors to the development of LUTO.

Identifiants

pubmed: 29664229
doi: 10.1111/luts.12222
doi:

Types de publication

Case Reports Journal Article Review Twin Study

Langues

eng

Sous-ensembles de citation

IM

Pagination

O85-O88

Subventions

Organisme : BONFOR - Gerok
ID : O-149.0123

Informations de copyright

© 2018 John Wiley & Sons Australia, Ltd.

Auteurs

Sandra Frese (S)

Children's Hospital, University of Bonn, Bonn, Germany.

Alexander Weigert (A)

Department of Pediatrics, Division of Pediatric Nephrology, University Hospital Bonn, Bonn, Germany.

Bernd Hoppe (B)

Department of Pediatrics, Division of Pediatric Nephrology, University Hospital Bonn, Bonn, Germany.

Markus Feldkötter (M)

Department of Pediatrics, Division of Pediatric Nephrology, University Hospital Bonn, Bonn, Germany.

Michael Ludwig (M)

Department of Clinical Chemistry and Clinical Pharmacology, University of Bonn, Bonn, Germany.

Stefanie Weber (S)

University Children's Hospital Marburg, Philipps-University, Marburg, Germany.

Katarzyna Kiliś-Pstrusińska (K)

Department of Pediatric Nephrology, Medical University, Wrocław, Poland.

Marcin Zaniew (M)

Children's Hospital, Poznań, Poland.

Heiko Reutter (H)

Institute of Human Genetics, University of Bonn, Bonn, Germany.
Department of Neonatology and Pediatric Intensive Care, Children's Hospital, University of Bonn, Bonn, Germany.

Alina C Hilger (AC)

Children's Hospital, University of Bonn, Bonn, Germany.
Institute of Human Genetics, University of Bonn, Bonn, Germany.

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Classifications MeSH