Berry-Bibee Erin N, Kim Myong-Jin, Tepper Naomi K, Riley Halley E M, Curtis Kathryn M
Division of Reproductive Health, Centers for Disease Control and Prevention, Atlanta, GA, USA.
Office of Clinical Pharmacology, U.S. Food and Drug Administration, Silver Spring, MD, USA.
Contraception. 2016 Dec;94(6):668-677. doi: 10.1016/j.contraception.2016.07.010. Epub 2016 Jul 18.
St. John's wort (SJW) is a known strong inducer of the cytochrome P450 (CYP) 3 A4 enzyme, and both the ethinyl estradiol and progestin components of hormonal contraceptives are substrates of CYP3A4. This systematic review examined whether the co-administration of SJW and hormonal contraceptives leads to significant safety or efficacy concerns.
Systematic review.
PubMed and Cochrane Library databases were searched for articles of any comparative study design (clinical or pharmacokinetic) that examined potential interactions between SJW and hormonal contraceptives in women of reproductive age.
Of the 48 identified articles, four studies met inclusion criteria and compared use of combined oral contraceptives (COCs) alone to the use of COCs co-administered with SJW. Two studies demonstrated no change in markers of ovulation, but one study demonstrated increased follicular growth and probable ovulation when COCs were co-administered with SJW. Three studies demonstrated an increased risk of breakthrough bleeding with COCs and SJW. Three studies showed changes in at least one pharmacokinetic parameter that suggested a significantly decreased exposure to hormone concentrations when COCs were co-administered with SJW. The only study that did not demonstrate any significant pharmacokinetic differences examined a SJW product containing a low amount of hypericin.
Limited evidence showing increased risk of ovulation and breakthrough bleeding raises concern for decreased contraceptive efficacy when COCs are co-administered with SJW. The pharmacokinetic evidence is mixed but suggests that SJW administration may be associated with weak to moderate induction of the metabolism of COCs.
圣约翰草是一种已知的细胞色素P450(CYP)3A4酶的强效诱导剂,而激素避孕药中的炔雌醇和孕激素成分均为CYP3A4的底物。本系统评价旨在研究圣约翰草与激素避孕药联合使用是否会引发重大的安全性或有效性问题。
系统评价。
检索PubMed和Cochrane图书馆数据库,查找任何比较研究设计(临床或药代动力学)的文章,这些文章研究了圣约翰草与激素避孕药在育龄女性中的潜在相互作用。
在48篇已识别的文章中,有4项研究符合纳入标准,比较了单独使用复方口服避孕药(COC)与COC联合圣约翰草使用的情况。两项研究表明排卵指标无变化,但一项研究表明COC与圣约翰草联合使用时卵泡生长增加且可能排卵。三项研究表明COC与圣约翰草联合使用时突破性出血风险增加。三项研究显示至少一项药代动力学参数发生变化,表明COC与圣约翰草联合使用时激素浓度暴露显著降低。唯一一项未显示任何显著药代动力学差异的研究检测的是一种金丝桃素含量低的圣约翰草产品。
有限的证据表明排卵和突破性出血风险增加,这引发了人们对COC与圣约翰草联合使用时避孕效果降低的担忧。药代动力学证据不一,但表明圣约翰草的使用可能与COC代谢的弱至中度诱导有关。