OBJECTIVE:
Preterm premature rupture of fetal membranes is
responsible for 30% to 40% of preterm deliveries. Fetal
membranes are composed primarily of collagen. Matrix
metalloproteinases are enzymes capable of degrading
extracellular matrix macromolecules, including collagens.
Expression of matrix metalloproteinase-9 (gelatinase B, 92 kd)
and its tissue inhibitor (tissue inhibitor of metalloproteinase-1) has
been localized in amnion and chorion. The objective of this study
was to determine whether rupture of fetal membranes and
intrauterine infection are associated with changes in the
expression of matrix metalloproteinase-9 and tissue inhibitor of
metalloproteinase-1.
STUDY DESIGN:
Two hundred one women
in the following categories had amniotic fluid retrieved:
RESULTS:
Spontaneous rupture of membranes at
term is associated with a significant increase in the amniotic fluid
concentrations of matrix metalloproteinase-9 (premature rupture
of membranes, no labor: median 3.9 ng/mL, range 2. 7 to 11.1
ng/mL vs no premature rupture of membranes, no labor: median
<0.4 ng/mL, range <0.4 to 22.4 ng/mL; P <.001). Patients with
preterm premature rupture of the membranes had higher median
matrix metalloproteinase-9 concentrations than those with preterm
labor and intact membranes who were delivered at term (7.6
ng/mL, range <0.4 to 230.81 ng/mL vs <0.4 ng/mL, range <0.4 to
1650 ng/mL; P =.06). Women with microbial invasion of the
amniotic cavity had higher median matrix metalloproteinase-9
concentrations than did those without microbial invasion
regardless of membrane status (preterm labor: 54.5 ng/mL, range
<0.4 to 3910 ng/mL vs <0.4 ng/mL, range <0. 4 to 1650 ng/mL; P
<.01; preterm premature rupture of membranes: 179. 8 ng/mL,
range <0.4 to 611 ng/mL vs 7.6 ng/mL, range <0.4 to 230.81; P
<.001). CONCLUSION: Our data support a role for matrix
metalloproteinase-9 in the mechanisms responsible for membrane
rupture in term and preterm gestations.