study question: What are the effects of dienogest (DNG) on midkine (MK) production in women with endometriosis? summary answer: DNG-mediated down-regulation of MK in vivo and in vitro. what is known already: DNG is an oral progestin that alleviates painful symptoms of women with endometriosis with a favourable tolerability and safety profile. Its effects on MK, a growth factor that plays an important role in endometriosis, have not yet been investigated. study design, size, duration: Prospective in vivo study on 283 patients subjected to laparoscopy for benign pathologies in a University hospital and in vitro cultures of primary endometrial stromal cells (ESC) from6 of thesewomenwith histologically confirmed endometriosis. participants/materials, setting, methods: MK concentrations in the peritoneal fluid (PF) of women were measured by ELISA and compared based on endometriosis status and the use of DNG. A subsequent in vitro analysis with ESC was used to confirm the direct influence of DNG and other progestins including, norethisterone acetate (NETA) and medroxyprogesterone acetate (MPA) on MK mRNA production. main results and the role of chance: The final study population consisted of 253 women.Of these, 165 suffered fromendometriosis, with 62 of them taking DNG (DNG group) and 103 taking no hormone treatment (non-DNG group) during at least 3 months before surgery. Another 88 women were endometriosis free (non-endometriosis group). The concentration of MK was highest in the PF of women in the non-DNG group (median 5.26 ng/ml, IQR 2.74–8.46). Significantly lower concentrations were found in the non-endometriosis group (median 3.51 ng/ml, IQR: 1.90–7.53, P ¼ 0.028). The lowest concentrationswere found in theDNGgroup (median 2.44 ng/ml, IQR: 1.12–4.70, P, 0.0001 versus non-DNG group, P ¼ 0.048 versus non-endometriosis group). The treatment of primary cultured ESC with DNG (1025 M) suppressed MK mRNA production (P ¼ 0.016), whereas MPA (P ¼ 0.109) and NETA (P ¼ 0.422) at same concentrations did not show a similar effect. limitations, reasons for caution: The non-randomized design of the study. wider implications of the findings: These findings could indicate a direct effect ofDNGon endometriotic cells that could contribute to its effectiveness in the treatment of this disease.

Study question: What are the effects of dienogest (DNG) on midkine (MK) production in women with endometriosis? summary answer: DNG-mediated down-regulation of MK in vivo and in vitro. what is known already: DNG is an oral progestin that alleviates painful symptoms of women with endometriosis with a favourable tolerability and safety profile. Its effects on MK, a growth factor that plays an important role in endometriosis, have not yet been investigated. study design, size, duration: Prospective in vivo study on 283 patients subjected to laparoscopy for benign pathologies in a University hospital and in vitro cultures of primary endometrial stromal cells (ESC) from6 of thesewomenwith histologically confirmed endometriosis. participants/materials, setting, methods: MK concentrations in the peritoneal fluid (PF) of women were measured by ELISA and compared based on endometriosis status and the use of DNG. A subsequent in vitro analysis with ESC was used to confirm the direct influence of DNG and other progestins including, norethisterone acetate (NETA) and medroxyprogesterone acetate (MPA) on MK mRNA production. main results and the role of chance: The final study population consisted of 253 women.Of these, 165 suffered fromendometriosis, with 62 of them taking DNG (DNG group) and 103 taking no hormone treatment (non-DNG group) during at least 3 months before surgery. Another 88 women were endometriosis free (non-endometriosis group). The concentration of MK was highest in the PF of women in the non-DNG group (median 5.26 ng/ml, IQR 2.74-8.46). Significantly lower concentrations were found in the non-endometriosis group (median 3.51 ng/ml, IQR: 1.90-7.53, P = 0.028). The lowest concentrationswere found in theDNGgroup (median 2.44 ng/ml, IQR: 1.12-4.70, P< 0.0001 versus non-DNG group, P = 0.048 versus non-endometriosis group). The treatment of primary cultured ESC with DNG (10-5 M) suppressed MK mRNA production (P = 0.016), whereas MPA (P = 0.109) and NETA (P = 0.422) at same concentrations did not show a similar effect. limitations, reasons for caution: The non-randomized design of the study. wider implications of the findings: These findings could indicate a direct effect ofDNGon endometriotic cells that could contribute to its effectiveness in the treatment of this disease. study funding/competing interest(s): Funding was received from Swiss National Science Foundation (Grant No. 320030-140774).M.D.M. has received fees for speaking at scientificmeetings fromBayer. The other authors have no conflicts of interest to declare. The authors state that the manufacturer of dienogest has in no way influenced the performance or outcomes of this study.

Dienogest mediates midkine suppression in endometriosis

CAGNACCI, Angelo;
2016

Abstract

study question: What are the effects of dienogest (DNG) on midkine (MK) production in women with endometriosis? summary answer: DNG-mediated down-regulation of MK in vivo and in vitro. what is known already: DNG is an oral progestin that alleviates painful symptoms of women with endometriosis with a favourable tolerability and safety profile. Its effects on MK, a growth factor that plays an important role in endometriosis, have not yet been investigated. study design, size, duration: Prospective in vivo study on 283 patients subjected to laparoscopy for benign pathologies in a University hospital and in vitro cultures of primary endometrial stromal cells (ESC) from6 of thesewomenwith histologically confirmed endometriosis. participants/materials, setting, methods: MK concentrations in the peritoneal fluid (PF) of women were measured by ELISA and compared based on endometriosis status and the use of DNG. A subsequent in vitro analysis with ESC was used to confirm the direct influence of DNG and other progestins including, norethisterone acetate (NETA) and medroxyprogesterone acetate (MPA) on MK mRNA production. main results and the role of chance: The final study population consisted of 253 women.Of these, 165 suffered fromendometriosis, with 62 of them taking DNG (DNG group) and 103 taking no hormone treatment (non-DNG group) during at least 3 months before surgery. Another 88 women were endometriosis free (non-endometriosis group). The concentration of MK was highest in the PF of women in the non-DNG group (median 5.26 ng/ml, IQR 2.74–8.46). Significantly lower concentrations were found in the non-endometriosis group (median 3.51 ng/ml, IQR: 1.90–7.53, P ¼ 0.028). The lowest concentrationswere found in theDNGgroup (median 2.44 ng/ml, IQR: 1.12–4.70, P, 0.0001 versus non-DNG group, P ¼ 0.048 versus non-endometriosis group). The treatment of primary cultured ESC with DNG (1025 M) suppressed MK mRNA production (P ¼ 0.016), whereas MPA (P ¼ 0.109) and NETA (P ¼ 0.422) at same concentrations did not show a similar effect. limitations, reasons for caution: The non-randomized design of the study. wider implications of the findings: These findings could indicate a direct effect ofDNGon endometriotic cells that could contribute to its effectiveness in the treatment of this disease.
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Utilizza questo identificativo per citare o creare un link a questo documento: http://hdl.handle.net/11390/1105895
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