Karolina Chmaj-Wierzchowska, Małgorzata Kampioni, Maciej Wilczak, Stefan Sajdak, Tomasz Opala
Vol 86, No 2 (2015)
ARTICLES
Abstract
Objectives: Endometriosis is a chronic disease manifested as peritoneal endometrial implants and adhesions, as well as endometrial cysts, with pain as the dominant component.
The aim: The aim of the study was to evaluate the role of chemokine (MCP-1, MCP-2, MIP-1α, MIP-1β and RANTES) and non-chemokine (urocortin, ghrelin, and leptin) factors in the intensity of pelvic pain in women with endometrial cysts.
Material and methods: A total of 86 women, aged 18-38, treated laparoscopically between September 2009 and November 2012, due to adnexal changes, i.e. endometrial cysts and mature teratomas, were recruited for the study. On a numeric rating scale, i.e. PSS (Pain Sensation Scale – according to Johnson), the patients rated pain intensity. The level of pain-related stress was investigated with the Pain Distress Scale (PDS, according to Johnson).
Results: Medians for MCP-1, MCP-2, MIP-1α, MIP-1β and RANTES concentrations were not statistically significantly different. The respondents rated pain intensity during menses as 6 and 3 points in the E and T groups, respectively (6 vs. 3 points; p=0.001). Statistically significant differences were also observed for pain intensity during work (apart from menses), (2 vs. 2 points, p=0,014) and during sexual intercourse (apart from menses) (3 vs. 1
points, p=0.006). Pain-related stress levels were higher in the T group as compared to the E group (3 vs. 5 points; p=0.007).
Conclusions: It seems safe to conclude that chemokines and leptin may play a significant role in the occurrence of pain complaints among women with endometrial cysts. Further research might result in implementation of new treatment methods for pain management, especially in terms of pharmacotherapy.
Abstract
Objectives: Endometriosis is a chronic disease manifested as peritoneal endometrial implants and adhesions, as well as endometrial cysts, with pain as the dominant component.
The aim: The aim of the study was to evaluate the role of chemokine (MCP-1, MCP-2, MIP-1α, MIP-1β and RANTES) and non-chemokine (urocortin, ghrelin, and leptin) factors in the intensity of pelvic pain in women with endometrial cysts.
Material and methods: A total of 86 women, aged 18-38, treated laparoscopically between September 2009 and November 2012, due to adnexal changes, i.e. endometrial cysts and mature teratomas, were recruited for the study. On a numeric rating scale, i.e. PSS (Pain Sensation Scale – according to Johnson), the patients rated pain intensity. The level of pain-related stress was investigated with the Pain Distress Scale (PDS, according to Johnson).
Results: Medians for MCP-1, MCP-2, MIP-1α, MIP-1β and RANTES concentrations were not statistically significantly different. The respondents rated pain intensity during menses as 6 and 3 points in the E and T groups, respectively (6 vs. 3 points; p=0.001). Statistically significant differences were also observed for pain intensity during work (apart from menses), (2 vs. 2 points, p=0,014) and during sexual intercourse (apart from menses) (3 vs. 1
points, p=0.006). Pain-related stress levels were higher in the T group as compared to the E group (3 vs. 5 points; p=0.007).
Conclusions: It seems safe to conclude that chemokines and leptin may play a significant role in the occurrence of pain complaints among women with endometrial cysts. Further research might result in implementation of new treatment methods for pain management, especially in terms of pharmacotherapy.
Keywords
MCP-1 / MCP-2 / MIP-1α / MIP-1β i RANTES / pain / endometriomas /
Title
The role of chemokine and non-chemokine factors in pain-related complaints in patients
with endometrial cysts
Journal
Ginekologia Polska
Issue
Vol 86, No 2 (2015)
Page views
687
Article views/downloads
629
DOI
10.17772/gp/1994
Bibliographic record
Ginekol Pol 2015;86(2).
Keywords
MCP-1 / MCP-2 / MIP-1α / MIP-1β i RANTES / pain / endometriomas /
Authors
Karolina Chmaj-Wierzchowska
Małgorzata Kampioni
Maciej Wilczak
Stefan Sajdak
Tomasz Opala