Department of Obstetrics and Gynecology, School of Medical Sciences, University of Campinas (UNICAMP), Campinas, Brazil.
Department of Translational Medicine, School of Medical Sciences, University of Campinas (UNICAMP), Campinas, Brazil.
Int J Gynaecol Obstet. 2024 Jun;165(3):1199-1209. doi: 10.1002/ijgo.15357. Epub 2024 Feb 1.
To evaluate gene expression associated with vaginal bleeding in the 52-mg hormonal intrauterine device (IUD) users.
We conducted a prospective study involving 100 women seeking to use the 52-mg hormonal IUD for contraception. We excluded women with a history or current condition of abnormal uterine bleeding and who were unable to attend a 1-year follow up. Women who expelled the device, removed it for reasons unrelated to vaginal bleeding, or were lost to follow up were discontinued. We collected endometrial biopsies immediately before IUD placement and assessed 20 selected genes using reverse transcription quantitative polymerase chain reaction. Users maintained a uterine bleeding diary for 12 months following IUD insertion. For statistical analysis, participants were categorized into groups with or without vaginal bleeding at 3 and 12 months.
Women with elevated CXCL9 expression had an 8.15-fold higher likelihood of experiencing vaginal bleeding at 3 months (odds ratio [OR] 8.15, 95% confidence interval [CI] 2.24-29.61, P = 0.001). At 12 months of follow up, women with increased TIMP1 expression had a 2.74-fold higher chance of experiencing vaginal bleeding (OR 2.74, 95% CI 1.08-6.95, P = 0.033). CXCL9 ≥ 1.5 and IL17A ≥ 0.68 were associated with a higher probability of vaginal bleeding at 3 months, while TIMP1 levels ≥0.943 were linked to an increased risk of bleeding at 12 months.
Users of the 52-mg hormonal IUD with elevated relative CXCL9 expression face an increased risk of vaginal bleeding at 3-month follow up, whereas those with heightened TIMP1 expression are more likely to experience vaginal bleeding at 12 months.
评估与 52 毫克激素宫内节育器(IUD)使用者阴道出血相关的基因表达。
我们进行了一项前瞻性研究,纳入了 100 名希望使用 52 毫克激素 IUD 避孕的女性。我们排除了有异常子宫出血病史或现病史且无法参加 1 年随访的女性,以及因阴道出血以外的原因取出 IUD 或失访的女性。我们在放置 IUD 前立即采集子宫内膜活检,并使用逆转录定量聚合酶链反应(qPCR)评估 20 个选定的基因。使用者在放置 IUD 后 12 个月内保持子宫出血日记。为了进行统计分析,我们将参与者分为放置 IUD 后 3 个月和 12 个月时出现或不出现阴道出血的两组。
CXCL9 表达升高的女性在放置 IUD 后 3 个月出现阴道出血的可能性增加 8.15 倍(比值比 [OR] 8.15,95%置信区间 [CI] 2.24-29.61,P=0.001)。在 12 个月的随访中,TIMP1 表达增加的女性出现阴道出血的可能性增加 2.74 倍(OR 2.74,95% CI 1.08-6.95,P=0.033)。CXCL9≥1.5 和 IL17A≥0.68 与放置 IUD 后 3 个月阴道出血的可能性增加相关,而 TIMP1 水平≥0.943 与放置 IUD 后 12 个月出血风险增加相关。
使用 52 毫克激素 IUD 的女性中,相对 CXCL9 表达升高者在 3 个月随访时阴道出血风险增加,而 TIMP1 表达升高者在 12 个月时阴道出血风险增加。