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Clinical and risk factor analysis of cloacal defects in the National Birth Defects Prevention Study
Kim M Keppler-Noreuil1, Kristin M Conway2, Dereck Shen2
1Medical Genomics and Metabolic Genetics Branch, National Human Genome Research Institute, National Institutes of Health, Bethesda, Maryland.
Insights
Cloacal exstrophy (CE) and persistent cloaca (PC) share risk factors like fertility treatments, but may have different causes. Further research into these rare birth defects is needed.
Area of Science:
- Medical Genetics
- Pediatric Surgery
- Reproductive Medicine
Background:
- Cloacal exstrophy (CE) and persistent cloaca (PC) are major congenital cloacal defects.
- These defects are often studied together, potentially masking distinct etiologies.
- Understanding differences in risk factors and causes is crucial for clinical management.
Purpose of the Study:
- To investigate potential differing etiologies between CE and PC.
- To compare clinical features and risk factors for CE and PC.
- To identify maternal and infant characteristics associated with these cloacal defects.
Main Methods:
- Analysis of 47 CE and 54 PC cases from the National Birth Defects Prevention Study.
- Comparison of cases with 11,829 non-malformed controls using chi-square or Fisher's exact tests.
- Logistic regression analysis of maternal exposures (pre-pregnancy and periconceptional) and birth defect associations.
Main Results:
- Both CE and PC cases were more likely to be preterm compared to controls.
- CE cases had a higher likelihood of being from multiple births.
- Fertility medication or assisted reproductive technology use was associated with increased odds of CE and PC.
Conclusions:
- Findings suggest potential distinct etiologies for CE and PC.
- Fertility treatments are a significant risk factor for both CE and PC.
- Further research is warranted to elucidate the specific causes of these rare cloacal defects.
Abstract:
Cloacal exstrophy (CE) and persistent cloaca (PC) (alternatively termed urorectal septum malformation sequence [URSMS]), represent two major cloacal defects (CDs). Clinical characteristics and risk factors often are studied for both defects combined, rather than exploring if these defects have different etiologies. We enumerated clinical features for 47 CE and 54 PC (inclusive of URSMS) cases from the National Birth Defects Prevention Study. Thirty-three CE cases were classified as isolated and 14 as multiple (presence of unassociated major defects); respective totals for PC cases were 26 and 28. We compared selected child and maternal characteristics between 11,829 non-malformed controls and CE and PC cases using chi-square or Fisher's exact tests. Compared to controls, CE and PC cases were statistically more likely (p < 0.05) to be preterm; CE cases were more likely to be multiple births. We conducted logistic regression analysis to estimate odds ratios and 95% confidence intervals for any CD, CE, and PC with selected self-reported maternal prepregnancy and periconceptional (one month prior to 3 months following conception) exposures. In crude and adjusted analyses, we observed significant positive associations for any CD, CE, and PC with use of any fertility medication or assisted reproductive technology procedure. Significant positive associations observed only in crude analyses were any CD with maternal obesity or use of progesterone, any CD and CE with any x-ray, and any CD and PC with use of folate antagonist medications. Our findings provide some of the first insights into potential differing etiologies for CE and PC.
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