TY - JOUR
T1 - Environmental and parental risk factors for congenital solitary functioning kidney — a case–control study
AU - Groen in ‘t Woud, Sander
AU - Roeleveld, Nel
AU - van Rooij, Iris A.L.M.
AU - Feitz, Wout F.J.
AU - Schreuder, Michiel F.
AU - van der Zanden, Loes F.M.
AU - van Wijk, J. A.E.
AU - Westland, R.
AU - Renkema, K. Y.
AU - Lilien, M. R.
AU - Keijzer-Veen, M. G.
AU - Kloosterman, F. J.
AU - Steffens, M. G.
AU - Gracchi, V.
AU - Zegers, B.
AU - Jira, P. E.
AU - van der Deure, H.
AU - van Rooij, R. W.G.
AU - Wijnands - van den Berg, E.
AU - Breukels, M.
AU - de Pont, S. M.H.B.
AU - Harnisch, E.
AU - van Dael, C. M.L.
AU - Creemers, D.
AU - de Moor, R.
AU - Konijnenberg, A. Y.
AU - Knots, E.
AU - van der Kuur, E. C.
AU - Jacobs, M. J.
AU - Koppejan-Stapel, M.
AU - Pijning, A.
AU - Dorresteijn, E.
AU - Leunissen, R. W.J.
AU - Rijlaarsdam, R.
AU - del Canho, R.
AU - Semmekrot, B.
AU - Dings-Lammertink, A.
AU - Nijhuis, I. J.M.
AU - van Ledden-Klok, M. J.
AU - van den Broek, L. M.
AU - Jansen, C. Meine
AU - Beeren, M. C.G.
AU - Blokland-Loggers, H. E.
AU - Dorrepaal, C.
AU - Pierik, L. J.W.M.
AU - Tanja, A. L.
N1 - Funding Information:
We would like to thank all participating children and their parents for their contribution to this study. Furthermore, we are thankful for the support in the identification of patients and collection of data provided by many pediatricians, pediatric nephrologists, urologists, and other colleagues. The following collaborators are included as non-authors in the SOFIA study group: J.A.E. van Wijk and R. Westland (Emma Children’s Hospital, Amsterdam UMC), K.Y. Renkema, M.R. Lilien and M.G. Keijzer-Veen (Wilhelmina Children’s Hospital, University Medical Center Utrecht), F.J. Kloosterman and M.G. Steffens (Isala Klinieken), V. Gracchi (Beatrix Children’s Hospital, University Medical Center Groningen), B. Zegers (Máxima MC), P.E. Jira (Jeroen Bosch Ziekenhuis), H. van der Deure (Deventer Ziekenhuis), R.W.G. van Rooij (LUMC Willem Alexander Children’s Hospital), E. Wijnands—van den Berg (Medisch Spectrum Twente (currently Isala Klinieken)), M. Breukels (Elkerliek ziekenhuis), S.M.H.B. de Pont (Amphia Ziekenhuis), E. Harnisch (Franciscus Gasthuis & Vlietland), C.M.L. van Dael (VieCuri/Maastricht UMC +), D. Creemers (Rijnstate (currently Deventer Ziekenhuis)), R. de Moor (Elisabeth-TweeSteden Ziekenhuis), A.Y. Konijnenberg (Ziekenhuis St Jansdal), E. Knots (Catharina Ziekenhuis Eindhoven), E.C. van der Kuur (Streekziekenhuis Koningin Beatrix), M.J. Jacobs (Maasziekenhuis Pantein), M. Koppejan-Stapel (Ziekenhuis Gelderse Vallei), A. Pijning (Slingeland Ziekenhuis), E. Dorresteijn (Erasmus MC), R.W.J. Leunissen (Haaglanden Medisch Centrum), R. Rijlaarsdam (ZGT), R. del Canho (Maasstad Ziekenhuis), B. Semmekrot (CWZ), A. Dings-Lammertink (Gelre ziekenhuizen loc Zutphen), I.J.M. Nijhuis (Wilhelmina Ziekenhuis Assen), M.J. van Ledden-Klok (Van Weel-Bethesda), L.M. van den Broek (St Jans Gasthuis), C. Meine Jansen (Groene Hart Ziekenhuis), M.C.G. Beeren (St Anna Zorggroep), H.E. Blokland-Loggers and C. Dorrepaal (St Antonius Ziekenhuis), L.J.W.M. Pierik (Ommelander Ziekenhuis Groningen), and A.L. Tanja (Martini Ziekenhuis).
Funding Information:
This research was funded by a Junior Investigator Grant from the Radboud Institute for Health Sciences. Sander Groen in ‘t Woud and Loes van der Zanden are funded by a Consortium Grant of the Dutch Kidney Foundation (20OC002). Loes van der Zanden received additional funding from a Veni grant (91618036) from the Dutch Research Council (NWO). Michiel Schreuder is funded by a Vidi grant (016.156.454) from the Dutch Research Council (NWO). The funders or the authors’ institutions had no role in the study design; collection, analysis, and interpretation of data; writing the report; and the decision to submit the report for publication.
Publisher Copyright:
© 2023, The Author(s).
PY - 2023/8
Y1 - 2023/8
N2 - Background: The etiology of congenital solitary functioning kidney (CSFK) is largely unknown but likely includes various risk factors. We performed a case–control study to compare exposure to environmental and parental risk factors during embryonic kidney development between children with CSFK and healthy controls. Methods: We included 434 children with CSFK and 1302 healthy controls from the AGORA data- and biobank matched on year of birth. Exposure to potential risk factors was investigated using parental questionnaire data. Crude and adjusted odds ratios (aORs) with 95% confidence intervals (CIs) were estimated for each potential risk factor. Multiple imputation was used to deal with missing values. Confounders for each potential risk factor were selected using directed acyclic graphs. Results: Maternal stress was newly identified as a risk factor for CSFK (aOR 2.1, 95% CI 1.2–3.5). Known associations with conception using in vitro fertilization/intracytoplasmic sperm injection (aOR 1.8, 95% CI 1.0–3.2), maternal infections during pregnancy (aOR 2.5, 95% CI 1.4–4.7), smoking during pregnancy (aOR 1.4, 95% CI 1.0–2.0), and parental CAKUT (aOR 6.6, 95% CI 2.9–15.1) were confirmed, but previous associations with diabetes and obesity could not be replicated. Folic acid supplement use and younger maternal age seemed to reduce the risk of CSFK (aORs 0.7, 95% CI 0.5–1.0, and 0.8, 95% CI 0.6–1.0, respectively). Conclusions: Environmental and parental risk factors are likely to be involved in the development of CSFK and future studies should combine genetic, environmental, and gene-environment interaction analyses. Women wanting to become pregnant should consider optimizing their health and lifestyle. Graphical abstract: [Figure not available: see fulltext.]
AB - Background: The etiology of congenital solitary functioning kidney (CSFK) is largely unknown but likely includes various risk factors. We performed a case–control study to compare exposure to environmental and parental risk factors during embryonic kidney development between children with CSFK and healthy controls. Methods: We included 434 children with CSFK and 1302 healthy controls from the AGORA data- and biobank matched on year of birth. Exposure to potential risk factors was investigated using parental questionnaire data. Crude and adjusted odds ratios (aORs) with 95% confidence intervals (CIs) were estimated for each potential risk factor. Multiple imputation was used to deal with missing values. Confounders for each potential risk factor were selected using directed acyclic graphs. Results: Maternal stress was newly identified as a risk factor for CSFK (aOR 2.1, 95% CI 1.2–3.5). Known associations with conception using in vitro fertilization/intracytoplasmic sperm injection (aOR 1.8, 95% CI 1.0–3.2), maternal infections during pregnancy (aOR 2.5, 95% CI 1.4–4.7), smoking during pregnancy (aOR 1.4, 95% CI 1.0–2.0), and parental CAKUT (aOR 6.6, 95% CI 2.9–15.1) were confirmed, but previous associations with diabetes and obesity could not be replicated. Folic acid supplement use and younger maternal age seemed to reduce the risk of CSFK (aORs 0.7, 95% CI 0.5–1.0, and 0.8, 95% CI 0.6–1.0, respectively). Conclusions: Environmental and parental risk factors are likely to be involved in the development of CSFK and future studies should combine genetic, environmental, and gene-environment interaction analyses. Women wanting to become pregnant should consider optimizing their health and lifestyle. Graphical abstract: [Figure not available: see fulltext.]
KW - Congenital anomalies of the kidney and urinary tract
KW - Environmental risk factors
KW - Etiology
KW - Kidney development
KW - Solitary functioning kidney
UR - http://www.scopus.com/inward/record.url?scp=85148500704&partnerID=8YFLogxK
U2 - 10.1007/s00467-023-05900-6
DO - 10.1007/s00467-023-05900-6
M3 - Article
C2 - 36808305
AN - SCOPUS:85148500704
SN - 0931-041X
VL - 38
SP - 2631
EP - 2641
JO - Pediatric Nephrology
JF - Pediatric Nephrology
IS - 8
ER -