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Environmental and parental risk factors for congenital solitary functioning kidney - a case-control study
Sander Groen In 't Woud1,2, Nel Roeleveld1, Iris A L M van Rooij1
1Department for Health Evidence, Radboud University Medical Center, P.O. Box 9101, 6500 HB, Nijmegen, The Netherlands.
Insights
Maternal stress and in vitro fertilization are new risk factors for congenital solitary functioning kidney (CSFK). Optimizing maternal health and lifestyle may reduce CSFK risk.
Area of Science:
- Pediatric Nephrology
- Developmental Biology
- Epidemiology
Background:
- The causes of congenital solitary functioning kidney (CSFK) are not fully understood.
- CSFK is a condition where an individual is born with only one functional kidney.
- Identifying risk factors is crucial for understanding CSFK development.
Purpose of the Study:
- To investigate potential environmental and parental risk factors for CSFK.
- To compare exposures between children with CSFK and healthy controls.
Main Methods:
- A case-control study involving 434 children with CSFK and 1302 healthy controls.
- Data collected via parental questionnaires on risk factor exposure.
- Statistical analysis using odds ratios, confidence intervals, and multiple imputation for missing data.
Main Results:
- Maternal stress identified as a novel risk factor for CSFK (aOR 2.1).
- Confirmed associations include in vitro fertilization, maternal infections, smoking, and parental CAKUT.
- Folic acid supplementation and younger maternal age showed protective effects.
Conclusions:
- Environmental and parental factors play a role in CSFK development.
- Future research should explore genetic and gene-environment interactions.
- Maternal health optimization before conception is recommended to potentially reduce CSFK risk.
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. A higher-resolution version of the Graphical abstract is available as Supplementary information.
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