Fetomaternal incompatibility in
human platelet antigens (HPAs) can cause maternal alloimmunization, which in turn may lead to
thrombocytopenia with or without
intracranial hemorrhage (ICH) in the fetus or newborn. Retrospective studies suggest that boys from alloimmunized mothers may have higher risk of ICH and lower
birth weight than girls. The objective of this study was to assess how maternal
HPA-1a alloimmunization, sex of the neonate and
birth weight relates in a large prospective cohort. Through a national screening study in Poland (PREVFNAIT) involving HPA-1 typing of 24,259 pregnant women during 2013-2017, 606
HPA-1a negative pregnant women and their offspring were identified and included. Various multivariate models were used to assess if and how maternal
HPA-1a alloimmunization status was associated with
birth weight and risk of having a small for gestational age (SGA) neonate, and if and how sex of the neonate mattered. Most immunized pregnancies had male fetuses (69 %). Women carrying a male fetus had increased likelihood of having an SGA newborn if they were
HPA-1a alloimmunized compared to non-immunized mothers. Increasing maternal anti-HPA-1a antibody levels were significantly associated with reduced
birth weight and SGA risk among male-fetus pregnancies, but not if the fetus was female. In conclusion, anti-HPA-1a
antibodies in a male fetus pregnancy is associated with increased risk of SGA and lower
birth weight, especially if the antibody level is high. Sex of the fetus may therefore be considered as a new clinical predictor of more severe FNAIT neonatal outcome.