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Maternal diabetes and renal agenesis/dysgenesis
Erin M Davis1, Jennifer David Peck, David Thompson
1The University of Oklahoma Health Sciences Center, Oklahoma City, Oklahoma 73104, USA.
Insights
Maternal diabetes significantly increases the risk of renal agenesis and dysgenesis in newborns. This study found a 3.1-fold higher odds of these congenital malformations in infants born to mothers with diabetes.
Area of Science:
- Perinatology
- Congenital Malformations
- Epidemiology
Background:
- Renal agenesis and dysgenesis are rare but severe congenital malformations affecting 2-5 infants per 10,000 live births.
- Limited research exists on risk factors, particularly the association between maternal diabetes and renal malformations.
Purpose of the Study:
- To investigate the association between maternal diabetes and the risk of renal agenesis/dysgenesis.
- To evaluate diabetes as a potential risk factor for these specific congenital anomalies.
Main Methods:
- A population-based case-control study was conducted in Texas from 2000-2002.
- 89 cases of renal agenesis/dysgenesis were identified from the Texas Birth Defects Registry.
- 356 controls were randomly selected and frequency matched to cases; maternal diabetes data was collected from vital records.
Main Results:
- Deliveries to mothers with diabetes had 3.1 times greater odds of renal agenesis/dysgenesis compared to those without diabetes (95% CI, 1.1-9.3).
- This association remained after controlling for matching factors.
Conclusions:
- Findings support previous limited research linking maternal diabetes to renal agenesis/dysgenesis.
- Maternal diabetes is suggested as a potential risk factor for congenital renal malformations, warranting further investigation into diabetes types.
Background:
Renal agenesis and dysgenesis are potentially lethal congenital malformations affecting 2 to 5 infants per 10,000 live births annually in the United States. The low prevalence of these malformations has complicated understanding of potential risk factors. Maternal diabetes (type 1, type 2, and gestational) has been evaluated extensively as a risk factor for other congenital malformations, but only a limited number of studies have assessed the association between diabetes and renal agenesis.
Methods:
We conducted a population-based case-control study of deliveries after 20 weeks gestation in Texas Health Service Region 6 (Houston/Galveston area) from January 1, 2000 to December 31, 2002. Cases of renal agenesis/dysgenesis (n = 89) were ascertained from the Texas Birth Defects Registry. Cumulative incidence sampling was used to randomly select, from birth and fetal death records, 356 controls frequency matched to cases by delivery year and vital status. Maternal diabetes and other covariates were collected from vital records.
Results:
The odds of renal agenesis/dysgenesis were 3.1 (95% confidence interval [CI], 1.1-9.3) times greater among deliveries of mothers with diabetes compared to deliveries of mothers without diabetes, controlling for matching factors.
Conclusions:
Our results are consistent with prior, but limited, research identifying diabetes as a risk factor for renal agenesis/dysgenesis. While these data did not differentiate diabetes diagnoses by type, the results suggest that maternal diabetes may be associated with renal malformations. Further study is warranted.
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