Fetal growth restriction affected by formation of maternal gene

The current issue of the journal Pediatric and Developmental Pathology reports results of a study of 470 pairs of mothers and babies in Japan. Mothers and babies were genotyped using maternal and cord blood, and the weight, length, head circumference, and incidence of small-for-gestational age status were recorded for full-term newborn infants.

The renin-angiotensin system is a hormone system that regulates blood pressure and fluid balance in the body. The maternal renin-angiotensin system affects the regulation of uteroplacental blood flow. A disorder in the maternal system may contribute to reduced placental blood flow, preeclampsia, and intrauterine growth restriction.

This study focused on both maternal and fetal insertion or deletion polymorphism of the angiotensin-converting enzyme gene. Pairing of either insertion/insertion, insertion/deletion, or deletion/deletion gene alleles was identified. In adults, this insertion or deletion polymorphism is considered a marker of renin-angiotensin system function, and has been associated with cardiovascular disorders. Its role in incidents related to pregnancy has not been as clearly defined.

In this study, researchers found that the incidence of small-for-gestational age in babies whose mothers had one or two deletion alleles was greater than that in babies whose mothers had two insertion alleles. No significant differences between these groups were found when analyzing the infants' alleles.

This investigation provides evidence that the maternal renin-angiotensin system, rather than the fetal system, has a greater effect on fetal growth. Fetal growth may be restricted by reduced blood flow for a fetus whose mother has a D allele.