Pregnancy-induced hypertension (PIH) is a frequent cause of maternal a
nd neonatal morbidity and mortality. In the present study we focused o
n the pathophysiology of PIH, mainly on the role of mineralocorticoids
, reversed blood pressure patterns, and the resulting necessity of con
tinuous monitoring of the preeclamptic mother. Problems of antihyperte
nsive therapy are discussed and the first results of a pilot study wit
h Urapidil are presented. To examine the role of mineralocorticoids in
the pathophysiology of PIH, we studied plasma aldosterone and 18-hydr
oxy-corticosterone (18-OH-B) levels in 25 women with PIH and in 25 hea
lthy pregnant women. Furthermore, we evaluated the mineralocorticoid r
eceptor (MR) count in mononuclear leukocytes in the 2 groups. The MR-c
ount was significantly decreased in the PIH-group. The values of plasm
a aldosterone and 18-OH-B were also low. These results cannot be expla
ined by receptor down-regulation due to higher level of mineralocortic
oids of the zona glomerulosa. Perhaps deoxycorticosterone or a hithert
o unknown mineralocorticoid is responsible for the hypertension and al
tered MR-status. The first results of continuous blood pressure measur
ements with a noninvasive, real-time blood pressure monitor (Finapres)
are presented. The comparison of the obtained values with intraarteri
al measurements demonstrates a good correlation between the two method
s. We also report on the first experiences with Urapidil in the treatm
ent of hypertension in severe preeclampsia. The data show that hyperte
nsion in preeclamptic women can be treated by Urapidil without side ef
fects or reflextachycardia. Further studies will have to prove if Urap
idil is suited for prepartal treatment of PIH as well.