“… [22] This study showed that the amniotic fluid L-FABP level was strongly associated with fetal blood flow abnormalities without being affected by other factors and was a useful predictor of the fetal condition, specifically fetal hypoxia, which is similar to the finding of a previous report. [5] Additionally, the L-FABP level was not associated with HDP, but it tended to be associated with PE, which is the more severe category of HDP, causing maternal hypoperfusion. [24] L-FABP is expressed in human placenta, [25] and we speculated that increased expression of L-FABP in placenta caused by maternal hypoperfusion due to PE might lead to an elevated amniotic fluid L-FABP level.…”