Literature DB >> 29753540

Risk Factors for Early Dialysis Dependency in Autosomal Recessive Polycystic Kidney Disease.

Kathrin Burgmaier1, Kevin Kunzmann2, Gema Ariceta3, Carsten Bergmann4, Anja Katrin Buescher5, Mathias Burgmaier6, Ismail Dursun7, Ali Duzova8, Loai Eid9, Florian Erger10, Markus Feldkoetter11, Matthias Galiano12, Michaela Geßner13, Heike Goebel14, Ibrahim Gokce15, Dieter Haffner16, Nakysa Hooman17, Bernd Hoppe11, Augustina Jankauskiene18, Guenter Klaus19, Jens König20, Mieczyslaw Litwin21, Laura Massella22, Djalila Mekahli23, Engin Melek24, Sevgi Mir25, Lars Pape16, Larisa Prikhodina26, Bruno Ranchin27, Raphael Schild28, Tomas Seeman29, Lale Sever30, Rukshana Shroff31, Neveen A Soliman32, Stella Stabouli33, Malgorzata Stanczyk34, Yilmaz Tabel35, Katarzyna Taranta-Janusz36, Sara Testa37, Julia Thumfart38, Rezan Topaloglu8, Lutz Thorsten Weber1, Dorota Wicher21, Elke Wühl39, Simone Wygoda40, Alev Yilmaz41, Katarzyna Zachwieja42, Ilona Zagozdzon43, Klaus Zerres44, Jörg Dötsch1, Franz Schaefer39, Max Christoph Liebau45.   

Abstract

OBJECTIVE: To identify prenatal, perinatal, and postnatal risk factors for dialysis within the first year of life in children with autosomal recessive polycystic kidney disease (ARPKD) as a basis for parental counseling after prenatal and perinatal diagnosis. STUDY
DESIGN: A dataset comprising 385 patients from the ARegPKD international registry study was analyzed for potential risk markers for dialysis during the first year of life.
RESULTS: Thirty-six out of 385 children (9.4%) commenced dialysis in the first year of life. According to multivariable Cox regression analysis, the presence of oligohydramnios or anhydramnios, prenatal kidney enlargement, a low Apgar score, and the need for postnatal breathing support were independently associated with an increased hazard ratio for requiring dialysis within the first year of life. The increased risk associated with Apgar score and perinatal assisted breathing was time-dependent and vanished after 5 and 8 months of life, respectively. The predicted probabilities for early dialysis varied from 1.5% (95% CI, 0.5%-4.1%) for patients with ARPKD with no prenatal sonographic abnormalities to 32.3% (95% CI, 22.2%-44.5%) in cases of documented oligohydramnios or anhydramnios, renal cysts, and enlarged kidneys.
CONCLUSIONS: This study, which identified risk factors associated with onset of dialysis in ARPKD in the first year of life, may be helpful in prenatal parental counseling in cases of suspected ARPKD.
Copyright © 2018 Elsevier Inc. All rights reserved.

Entities:  

Keywords:  PKHD1; ciliopathy; oligohydramnios; renal replacement therapy

Mesh:

Year:  2018        PMID: 29753540     DOI: 10.1016/j.jpeds.2018.03.052

Source DB:  PubMed          Journal:  J Pediatr        ISSN: 0022-3476            Impact factor:   4.406


  15 in total

1.  Perspectives on Drug Development in Autosomal Recessive Polycystic Kidney Disease.

Authors:  Max C Liebau; Erum A Hartung; Ronald D Perrone
Journal:  Clin J Am Soc Nephrol       Date:  2022-08-23       Impact factor: 10.614

2.  Phenotypic Variability in Siblings With Autosomal Recessive Polycystic Kidney Disease.

Authors:  Ramona Ajiri; Kathrin Burgmaier; Nurver Akinci; Ilse Broekaert; Anja Büscher; Ismail Dursun; Ali Duzova; Loai Akram Eid; Marc Fila; Michaela Gessner; Ibrahim Gokce; Laura Massella; Antonio Mastrangelo; Monika Miklaszewska; Larisa Prikhodina; Bruno Ranchin; Nadejda Ranguelov; Rina Rus; Lale Sever; Julia Thumfart; Lutz Thorsten Weber; Elke Wühl; Alev Yilmaz; Jörg Dötsch; Franz Schaefer; Max Christoph Liebau
Journal:  Kidney Int Rep       Date:  2022-05-04

3.  Neonatal Polycystic Kidney Disease in a One-Day-Old Baby: A Case Report.

Authors:  Deborah Mchaile; Philip Mrindoko; Matei Mselle; Elton Meleki; Elise Kimambo; Arnold Likiliwike; Jay Lodhia
Journal:  Pediatric Health Med Ther       Date:  2020-10-29

4.  Imaging of Kidney Cysts and Cystic Kidney Diseases in Children: An International Working Group Consensus Statement.

Authors:  Charlotte Gimpel; E Fred Avni; Luc Breysem; Kathrin Burgmaier; Anna Caroli; Metin Cetiner; Dieter Haffner; Erum A Hartung; Doris Franke; Jens König; Max C Liebau; Djalila Mekahli; Albert C M Ong; Lars Pape; Andrea Titieni; Roser Torra; Paul J D Winyard; Franz Schaefer
Journal:  Radiology       Date:  2019-01-01       Impact factor: 11.105

Review 5.  Prenatal genetic considerations of congenital anomalies of the kidney and urinary tract (CAKUT).

Authors:  Asha N Talati; Carolyn M Webster; Neeta L Vora
Journal:  Prenat Diagn       Date:  2019-08-05       Impact factor: 3.050

Review 6.  Autosomal Recessive Polycystic Kidney Disease-The Clinical Aspects and Diagnostic Challenges.

Authors:  Dorota Wicher; Łukasz Obrycki; Irena Jankowska
Journal:  J Pediatr Genet       Date:  2020-07-29

7.  Prenatal MR imaging features of Caroli syndrome in association with autosomal recessive polycystic kidney disease.

Authors:  Amanda Rivas; Monica Epelman; Enrico Danzer; N Scott Adzick; Teresa Victoria
Journal:  Radiol Case Rep       Date:  2018-11-26

8.  Neonatal polycystic kidney disease, a potential life-threatening condition at this age: A case report.

Authors:  Lorena Elena Meliţ; Cristina Oana Mărginean; Cristian Dan Mărginean; Maria Oana Mărginean; Cornel Aldea
Journal:  Medicine (Baltimore)       Date:  2019-11       Impact factor: 1.817

9.  Challenging Disease Ontology by Instances of Atypical PKHD1 and PKD1 Genetics.

Authors:  Jonathan de Fallois; Ria Schönauer; Johannes Münch; Mato Nagel; Bernt Popp; Jan Halbritter
Journal:  Front Genet       Date:  2021-06-25       Impact factor: 4.599

Review 10.  Predictors of progression in autosomal dominant and autosomal recessive polycystic kidney disease.

Authors:  Eric G Benz; Erum A Hartung
Journal:  Pediatr Nephrol       Date:  2021-01-21       Impact factor: 3.651

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