Introduction: Increased active Matrix Metalloprotease (MMP) - 9 and decreased active MMP-2 have been associated with premature rupture of membranes and increased risk of preterm delivery. Administration of Lactoferrin (LF), a glycoprotein with anti-inflammatory properties, is able to decrease the amniotic fluid (AF) concentration of IL-6, with protective role against abortion secondary to amniocentesis (1). Therefore, we aimed to verify the efficacy of LF to modulate the production of active MMP-9 and MMP-2 and their tissue inhibitors (TIMP-1 and TIMP-2, respectively) following amniocentesis. Methods: One-hundred and six women were divided into two groups: 61 patients were controls; 45 patients were treated with vaginal LF, 4 hours before amniocentesis. Amniotic fluid was collected and stored at -80°C until assay. Active MMP-9 and MMP-2, TIMP-1 and TIMP-2 were determined by commercially available activity assays and ELISAs. The values were normalized by AF creatinine concentration. The Mann-Whitney U test was used to compare untreated and treated patients. A p<0.05 was considered significant. Results: Active MMP-9 and its inhibitor TIMP-1 were significantly lower in the AF of patients treated with LF than the controls (p<0.05 and p<0.005, respectively). However, the MMP-9/TIMP-1 molar ratio was not different between the two groups. On the contrary, we observed an increase in the levels of both active MMP- 2 and TIMP-2 in the patients treated with LF compared to the controls (p<0.0001 and p<0.05, respectively), with a simultaneous increase in the MMP-2/TIMP-2 molar ratio (p<0.005). Conclusions: As previously demonstrated, transvaginal LF administration is able to decrease the inflammation by decreasing AF IL-6 levels. To check the modulation of production of MMP-9 and MMP-2 and their tissue inhibitors, might be an adjunctive and useful tool against the increased risk of abortion that the procedure entails.

Lactoferrin administration prior to genetic amniocentesis dampens the intraamniotic inflammatory response

TRENTINI, Alessandro;MANFRINATO, Maria Cristina;PEZZUTO, Marina;MARITATI, Martina;VESCE, Fortunato;HANAU, Stefania;DALLOCCHIO, Franco Pasquale Filippo;CONTINI, Carlo;BELLINI, Tiziana
2015

Abstract

Introduction: Increased active Matrix Metalloprotease (MMP) - 9 and decreased active MMP-2 have been associated with premature rupture of membranes and increased risk of preterm delivery. Administration of Lactoferrin (LF), a glycoprotein with anti-inflammatory properties, is able to decrease the amniotic fluid (AF) concentration of IL-6, with protective role against abortion secondary to amniocentesis (1). Therefore, we aimed to verify the efficacy of LF to modulate the production of active MMP-9 and MMP-2 and their tissue inhibitors (TIMP-1 and TIMP-2, respectively) following amniocentesis. Methods: One-hundred and six women were divided into two groups: 61 patients were controls; 45 patients were treated with vaginal LF, 4 hours before amniocentesis. Amniotic fluid was collected and stored at -80°C until assay. Active MMP-9 and MMP-2, TIMP-1 and TIMP-2 were determined by commercially available activity assays and ELISAs. The values were normalized by AF creatinine concentration. The Mann-Whitney U test was used to compare untreated and treated patients. A p<0.05 was considered significant. Results: Active MMP-9 and its inhibitor TIMP-1 were significantly lower in the AF of patients treated with LF than the controls (p<0.05 and p<0.005, respectively). However, the MMP-9/TIMP-1 molar ratio was not different between the two groups. On the contrary, we observed an increase in the levels of both active MMP- 2 and TIMP-2 in the patients treated with LF compared to the controls (p<0.0001 and p<0.05, respectively), with a simultaneous increase in the MMP-2/TIMP-2 molar ratio (p<0.005). Conclusions: As previously demonstrated, transvaginal LF administration is able to decrease the inflammation by decreasing AF IL-6 levels. To check the modulation of production of MMP-9 and MMP-2 and their tissue inhibitors, might be an adjunctive and useful tool against the increased risk of abortion that the procedure entails.
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Utilizza questo identificativo per citare o creare un link a questo documento: https://hdl.handle.net/11392/2337896
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