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The effect of pycnogenol on patients with dysmenorrhea using low-dose oral contraceptives
OBJECTIVE: Menstrual symptoms such as dysmenorrhea usually occur during the hormone-free interval in oral contraceptive users. Progestin withdrawal activates NF-κB transcription factor, which upregulates both vascular endothelial growth factor (VEGF) and Cox-2 expression in the endometrium. The use...
Autores principales: | , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Dove Medical Press
2014
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4266261/ https://www.ncbi.nlm.nih.gov/pubmed/25525393 http://dx.doi.org/10.2147/IJWH.S75389 |
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author | Maia, Hugo Haddad, Clarice Casoy, Julio |
author_facet | Maia, Hugo Haddad, Clarice Casoy, Julio |
author_sort | Maia, Hugo |
collection | PubMed |
description | OBJECTIVE: Menstrual symptoms such as dysmenorrhea usually occur during the hormone-free interval in oral contraceptive users. Progestin withdrawal activates NF-κB transcription factor, which upregulates both vascular endothelial growth factor (VEGF) and Cox-2 expression in the endometrium. The use of natural NF-κB inhibitors such as pycnogenol may block this response, improving dysmenorrhea. PATIENTS AND METHODS: Twenty-four patients with severe dysmenorrhea were allocated to one of two treatment groups. In Group A (n=13), women were treated with an oral contraceptive containing 15 μg of ethinyl estradiol and 60 mg of gestodene (Adoless(®)) in a 24/4 regimen for three consecutive cycles. Women in Group B (n=11) used the same contraceptive regimen together with 100 mg of pycnogenol (Flebon(®)) continuously for 3 months. Pain scores were graded using a visual analog scale (VAS) before and during the hormone-free interval at the end of the third treatment cycle. RESULTS: Before treatment, VAS pain scores for dysmenorrhea were 8 and 9 in Groups A and B, respectively. However, by the end of the third treatment cycle, pain scores had decreased significantly (P<0.05) both in groups A and B. The final pain scores were 6 in Group A and 2 in Group B, a difference that was statistically significant (P<0.0001). In Group B, 27% of the patients became pain-free, while in Group A, none of the women reported complete disappearance of this symptom. The number of bleeding days was also lower in Group B. DISCUSSION: Pycnogenol effectively decreased pain scores and the number of bleeding days when administered concomitantly with a low-dose 24/4 oral contraceptive containing gestodene. |
format | Online Article Text |
id | pubmed-4266261 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2014 |
publisher | Dove Medical Press |
record_format | MEDLINE/PubMed |
spelling | pubmed-42662612014-12-18 The effect of pycnogenol on patients with dysmenorrhea using low-dose oral contraceptives Maia, Hugo Haddad, Clarice Casoy, Julio Int J Womens Health Original Research OBJECTIVE: Menstrual symptoms such as dysmenorrhea usually occur during the hormone-free interval in oral contraceptive users. Progestin withdrawal activates NF-κB transcription factor, which upregulates both vascular endothelial growth factor (VEGF) and Cox-2 expression in the endometrium. The use of natural NF-κB inhibitors such as pycnogenol may block this response, improving dysmenorrhea. PATIENTS AND METHODS: Twenty-four patients with severe dysmenorrhea were allocated to one of two treatment groups. In Group A (n=13), women were treated with an oral contraceptive containing 15 μg of ethinyl estradiol and 60 mg of gestodene (Adoless(®)) in a 24/4 regimen for three consecutive cycles. Women in Group B (n=11) used the same contraceptive regimen together with 100 mg of pycnogenol (Flebon(®)) continuously for 3 months. Pain scores were graded using a visual analog scale (VAS) before and during the hormone-free interval at the end of the third treatment cycle. RESULTS: Before treatment, VAS pain scores for dysmenorrhea were 8 and 9 in Groups A and B, respectively. However, by the end of the third treatment cycle, pain scores had decreased significantly (P<0.05) both in groups A and B. The final pain scores were 6 in Group A and 2 in Group B, a difference that was statistically significant (P<0.0001). In Group B, 27% of the patients became pain-free, while in Group A, none of the women reported complete disappearance of this symptom. The number of bleeding days was also lower in Group B. DISCUSSION: Pycnogenol effectively decreased pain scores and the number of bleeding days when administered concomitantly with a low-dose 24/4 oral contraceptive containing gestodene. Dove Medical Press 2014-12-11 /pmc/articles/PMC4266261/ /pubmed/25525393 http://dx.doi.org/10.2147/IJWH.S75389 Text en © 2014 Maia Jr et al. This work is published by Dove Medical Press Limited, and licensed under Creative Commons Attribution – Non Commercial (unported, v3.0) License The full terms of the License are available at http://creativecommons.org/licenses/by-nc/3.0/. Non-commercial uses of the work are permitted without any further permission from Dove Medical Press Limited, provided the work is properly attributed. |
spellingShingle | Original Research Maia, Hugo Haddad, Clarice Casoy, Julio The effect of pycnogenol on patients with dysmenorrhea using low-dose oral contraceptives |
title | The effect of pycnogenol on patients with dysmenorrhea using low-dose oral contraceptives |
title_full | The effect of pycnogenol on patients with dysmenorrhea using low-dose oral contraceptives |
title_fullStr | The effect of pycnogenol on patients with dysmenorrhea using low-dose oral contraceptives |
title_full_unstemmed | The effect of pycnogenol on patients with dysmenorrhea using low-dose oral contraceptives |
title_short | The effect of pycnogenol on patients with dysmenorrhea using low-dose oral contraceptives |
title_sort | effect of pycnogenol on patients with dysmenorrhea using low-dose oral contraceptives |
topic | Original Research |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4266261/ https://www.ncbi.nlm.nih.gov/pubmed/25525393 http://dx.doi.org/10.2147/IJWH.S75389 |
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