Monocyte chemotactic protein-1 is increased in the amnioticfluid of women who deliver preterm in the presence or absence of intra-amniotic infection
Monocyte chemotactic protein-1 is increased in the amnioticfluid of women who deliver preterm in the presence or absence of intra-amniotic infection
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DOI:
10.1080/14767050500141329
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发表时间:
2005-06-01
影响因子:
1.8
通讯作者:
Adashi, EY
中科院分区:
文献类型:
--
作者:
Esplin, MS;Romero, R;Adashi, EY
Objective. Pro-inflammatory chemokines have been associated with preterm parturition. Monocyte chemotactic protein-1 (MCP-1) is a chemokine capable of recruiting monocytes/macrophages into sites of inflammation, as well as stimulating the respiratory burst required for macrophage activation. MCP-1 transcripts and immuno-reactivity are expressed by uterine tissues (i.e., decidual cells and myometrium) and, thus, may participate in the process of labor. This study was conducted to determine if preterm labor leading to preterm delivery and intra-amniotic infection (IAI) are associated with changes in the amniotic fluid concentrations of MCP-1.Study design. A cross-sectional study was designed to examine the amniotic fluid concentrations of MCP-1 in women in two groups: 1) those presenting with preterm labor with intact membranes; and 2) those with preterm prelabor rupture of membranes ( PROM). Amniotic fluid was obtained by transabdominal amniocentesis from 131 women in preterm labor with intact membranes and 105 women with preterm PROM. IAI was defined by a positive amniotic fluid culture for microorganisms. Group 1 included women with preterm labor and intact membranes ( n = 131), and was subdivided into the following groups: a) delivery at term in the absence of IAI ( n= 42); b) preterm delivery ( 537 weeks) in the absence of IAI ( n = 58); and c) preterm delivery in the presence of IAI ( n = 31). Group 2 consisted of women with PROM ( n= 105), and was subdivided into women with ( n = 51) and without ( n = 54) IAI. Non-parametric statistics were used for data analysis.Results. 1) Immuno-reactive MCP-1 was detected in all amniotic fluid samples; 2) IAI, regardless of the membrane status, was associated with a significantly higher median amniotic fluid concentration of immuno-reactive MCP-1 than those without IAI (p