Department of Pathology, School of Basic Medical Sciences, Heilongjiang University of Chinese Medicine, Harbin, Heilongjiang 150040, China.
Department of Cardiovascular Medicine, Ezhou Central Hospital, Hubei Province, Ezhou, Hubei 436000, China.
Eur J Obstet Gynecol Reprod Biol. 2023 Jun;285:59-68. doi: 10.1016/j.ejogrb.2023.04.004. Epub 2023 Apr 10.
Several randomized controlled trials (RCTs) have explored the impact of 17β-estradiol plus norethisterone acetate administration on blood pressure and inflammation markers, however, their findings have often been contradictory. Thus, we conducted a systematic review and meta-analysis of RCTs to assess the effects of this drug combination on systolic blood pressure (SBP), diastolic blood pressure (DBP) and C-reactive protein (CRP) concentrations.
The Cochrane Library, PubMed/Medline, Scopus, and Google Scholar were searched to identify relevant published RCTs. The pooled mean change and standard deviation (SD) of the outcomes were calculated using the STATA software (version 14) for Statistical Computing.
A total of 18 publications were included in the current meta-analysis. In total, there were 12 RCT arms on SBP, 12 RCT arms on DBP, and 6 RCT arms on CRP levels. The administration of 17β-estradiol plus norethisterone acetate intake increased SBP (WMD: 3.48 mmHg, 95% CI: 0.73, 6.23, P = 0.013), particularly in subjects aged ≥ 60 years (WMD: 5.89 mmHg, 95% CI: 1.71, 10.07, P = 0.006) or with a body mass index (BMI) < 30 kg/m (WMD: 6.55 mmHg, 95% CI: 2.64, 10.46, P = 0.012), as well as in the RCTs which lasted ≥ 6 months (WMD: 6.47 mmHg, 95% CI: 3.03, 9.90, P < 0.001),when 17β-estradiol dosages were ≥ 2 mg/day (WMD: 4.12 mmHg, 95% CI: 1.03, 7.22, P = 0.009; I = 99%, P < 0.001) and in RCTs conducted on healthy postmenopausal women (WMD: 4.22 mmHg, 95% CI: 0.43, 8.01, P = 0.02; I = 94%, P < 0.001). DBP decreased following this drug combination in the RCTs which lasted < 6 months (WMD: -1.42 mmHg, 95% CI: -2.27, -0.57, P = 0.001). CRP concentrations increased following the use of this drug combination (WMD: 1.01 mg/L, 95% CI: 0.62, 1.41, P < 0.001), especially in participants aged < 60 years (WMD: 1.22 mg/L, 95% CI: 0.77, 1.68, P < 0.001) or with a BMI < 30 kg/m (WMD: 0.97 mg/L, 95% CI: 0.67, 1.27, P < 0.001), as well as in RCTs with a duration of ≥ 6 months (WMD: 1.15 mg/L, 95% CI: 0.57, 1.73, P < 0.001), when 17β-estradiol dosages were ≥ 2 mg/day (WMD: 0.97 mg/L, 95% CI: 0.67, 1.27, P < 0.001; I = 55%, P = 0.107) and in RCTs conducted on healthy postmenopausal women (WMD: 1.22 mg/L, 95% CI: 0.77, 1.68, P < 0.001; I = 90%, P < 0.001).
The administration of 17β-estradiol plus norethisterone acetate increases SBP and CRP concentrations and, when prescribed for less than 6 months, decreases DBP. However, despite being statistically significant, the impact of this drug combination on SBP and DBP is not clinically relevant as the variation in blood pressure values was low.
多项随机对照试验(RCT)已经探讨了 17β-雌二醇加去氧孕烯醋酸酯给药对血压和炎症标志物的影响,但结果往往相互矛盾。因此,我们进行了系统评价和荟萃分析,以评估该药物组合对收缩压(SBP)、舒张压(DBP)和 C 反应蛋白(CRP)浓度的影响。
检索 Cochrane 图书馆、PubMed/Medline、Scopus 和 Google Scholar,以确定相关的已发表 RCT。使用 STATA 软件(版本 14)计算结局的汇总平均变化和标准差(SD)。
共有 18 篇文献纳入了本次荟萃分析。总共包括 12 个 SBP 的 RCT 臂,12 个 DBP 的 RCT 臂和 6 个 CRP 水平的 RCT 臂。17β-雌二醇加去氧孕烯醋酸酯的给药增加了 SBP(WMD:3.48mmHg,95%CI:0.73,6.23,P=0.013),尤其是在年龄≥60 岁的受试者(WMD:5.89mmHg,95%CI:1.71,10.07,P=0.006)或 BMI<30kg/m 的受试者(WMD:6.55mmHg,95%CI:2.64,10.46,P=0.012),以及持续时间≥6 个月的 RCT(WMD:6.47mmHg,95%CI:3.03,9.90,P<0.001)中,当 17β-雌二醇剂量≥2mg/天时(WMD:4.12mmHg,95%CI:1.03,7.22,P=0.009;I=99%,P<0.001)和在健康绝经后妇女的 RCT 中(WMD:4.22mmHg,95%CI:0.43,8.01,P=0.02;I=94%,P<0.001)。该药物组合降低了 DBP,尤其是在持续时间<6 个月的 RCT 中(WMD:-1.42mmHg,95%CI:-2.27,-0.57,P=0.001)。使用该药物组合后 CRP 浓度升高(WMD:1.01mg/L,95%CI:0.62,1.41,P<0.001),尤其是在年龄<60 岁的参与者(WMD:1.22mg/L,95%CI:0.77,1.68,P<0.001)或 BMI<30kg/m 的参与者(WMD:0.97mg/L,95%CI:0.67,1.27,P<0.001),以及持续时间≥6 个月的 RCT(WMD:1.15mg/L,95%CI:0.57,1.73,P<0.001)中,当 17β-雌二醇剂量≥2mg/天时(WMD:0.97mg/L,95%CI:0.67,1.27,P<0.001;I=55%,P=0.107)和在健康绝经后妇女的 RCT 中(WMD:1.22mg/L,95%CI:0.77,1.68,P<0.001;I=90%,P<0.001)。
17β-雌二醇加去氧孕烯醋酸酯的给药增加了 SBP 和 CRP 浓度,并且当使用时间少于 6 个月时,会降低 DBP。然而,尽管具有统计学意义,但该药物组合对 SBP 和 DBP 的影响在临床上并不相关,因为血压值的变化很小。