Kazemi Mahnaz, Lalooha Fatemeh, Nooshabadi Mohamadreza Rashidi, Haghighian Hossein Khadem
Department of Nutrition, School of Health, Qazvin University of Medical Sciences, Qazvin, Iran.
Department of Obstetrics and Gynecology, Faculty of Medicine, Qazvin University of Medical Sciences, Qazvin, Iran.
J Obstet Gynaecol Res. 2022 May;48(5):1212-1221. doi: 10.1111/jog.15196. Epub 2022 Mar 15.
This study aimed to evaluate the oleoylethanolamide (OEA) effects on oxidative stress and inflammatory factors in girls with primary dysmenorrhea.
This double-blind, placebo-controlled clinical trial was done on population consisted of female students who had dysmenorrhea pain based on the visual analogue scale (VAS) questionnaire. Patients were randomly allocated to groups consuming a capsule containing 125 mg of OEA per day (n = 22) or placebo (n = 22) for 2 months. The severity of the pain, total antioxidant capacity (TAC), malondialdehyde (MDA), C-reactive protein (CRP), and tumor necrosis factor alpha (TNF-α) were measured at the beginning and the end of the study. In this study, SPSS software was used to analyze the data.
According to the results, oral supplementation with OEA for 60 days significantly increased TAC (p = 0.022) and decreased the menstrual pain (p = 0.040), MDA (p = 0.011), CRP (p = 0.01), and TNF-α (p = 0.038) compared to the placebo group. Also, intragroup changes were statistically significant on the mean of pain (p = 0.042), TAC (p = 0.032), MDA (p = 0.023), CRP (p = 0.027), and TNF-α (p = 0.029) at the end of the study in the intervention group. Changes in the studied factors at the end of the study compared to the beginning of the study in the placebo group were not statistically significant.
Considering the reducing effects of OEA on menstrual pain, using of this supplement can be introduced as an alternative medicine to reduce the use of anti-inflammatory drugs.
本研究旨在评估油酰乙醇胺(OEA)对原发性痛经女孩氧化应激和炎症因子的影响。
本双盲、安慰剂对照临床试验针对基于视觉模拟量表(VAS)问卷有痛经疼痛的女学生群体进行。患者被随机分为两组,一组每天服用一粒含125毫克OEA的胶囊(n = 22),另一组服用安慰剂(n = 22),为期2个月。在研究开始和结束时测量疼痛严重程度、总抗氧化能力(TAC)、丙二醛(MDA)、C反应蛋白(CRP)和肿瘤坏死因子α(TNF-α)。本研究使用SPSS软件分析数据。
结果显示,与安慰剂组相比,口服OEA 60天可显著提高TAC(p = 0.022),减轻痛经(p = 0.040)、降低MDA(p = 0.011)、CRP(p = 0.01)和TNF-α(p = 0.038)。此外,干预组在研究结束时,疼痛平均值(p = 0.042)、TAC(p = 0.032)、MDA(p = 0.023)、CRP(p = 0.027)和TNF-α(p = 0.029)的组内变化具有统计学意义。安慰剂组在研究结束时与开始时相比,所研究因素的变化无统计学意义。
考虑到OEA对痛经的缓解作用,这种补充剂可作为减少抗炎药物使用的替代药物。