Kitada Ayako, Nakai Takehiro, Fukui Sho, Rokutanda Ryo, Okada Masato, Kusaoi Makio, Yamaji Ken, Tamura Naoto
83911St Luke's International Hospital, Tokyo, Japan.
Graduate School of Medicine, 12847Juntendo University, Tokyo, Japan.
Lupus. 2023 Mar;32(3):352-362. doi: 10.1177/09612033221148334. Epub 2023 Jan 12.
Tacrolimus is one of the drugs that can be used in pregnancies complicated with systemic lupus erythematosus (SLE), but there are still few reports on its pregnancy outcomes. Although tacrolimus has been reported to cause adverse events, such as increased blood pressure, abnormal glucose metabolism, and susceptibility to infection, there have been no studies on the impact of tacrolimus in SLE pregnancies at these points. We performed a retrospective observational study of pregnancies complicated by SLE at St Luke's International Hospital in Tokyo from April 2003 to August 2021.
Basic clinical information on SLE, pregnancy outcomes, disease activity before and after pregnancy, laboratory results, blood pressure, blood glucose levels, treatment regimens, and presence of infection was extracted from electronic medical records. We defined overall adverse pregnancy outcomes (APOs) as follows: (1) fetal death after 10 gestational weeks, (2) preterm delivery, (3) delivery due to hypertensive disorders of pregnancy, preeclampsia, or placental insufficiency, or (4) the diagnosis of small for gestational age infants. We also examined whether there was a statistical difference in APO incidence between patients treated with and without tacrolimus.
Pregnancy outcomes were obtained for 48 patients with a total of 60 pregnancies complicated by SLE. In 20 (33.3%) of these pregnancies, the patients took tacrolimus, and 28 (46.7%) of the pregnancies had APOs. APO incidence did not statistically differ between the tacrolimus and non-tacrolimus groups in the multivariate analysis ( = 1.00, adjusted OR 1, 95% CI: 0.23-4.39). Multiple regression analyses indicated that tacrolimus use did not significantly affect systolic blood pressure in the third trimester (B = -2.23, = .74) or blood glucose levels in the first trimester (B = 10.2, = .056). Incidence of infections did not significantly differ between patients treated with and without tacrolimus in the univariate analysis (10.8% vs. 21.1%, = .42).
Tacrolimus did not significantly affect pregnancy outcomes, blood pressure, or glucose levels. Further research is required to confirm its effects in a larger population.
他克莫司是可用于治疗合并系统性红斑狼疮(SLE)妊娠的药物之一,但关于其妊娠结局的报道仍较少。尽管有报道称他克莫司会引起不良事件,如血压升高、糖代谢异常和易感染,但尚未有关于他克莫司在这些方面对SLE妊娠影响的研究。我们对2003年4月至2021年8月在东京圣路加国际医院发生的合并SLE的妊娠进行了一项回顾性观察研究。
从电子病历中提取有关SLE的基本临床信息、妊娠结局、妊娠前后的疾病活动度、实验室检查结果、血压、血糖水平、治疗方案以及感染情况。我们将总体不良妊娠结局(APO)定义如下:(1)孕10周后胎儿死亡;(2)早产;(3)因妊娠高血压疾病、子痫前期或胎盘功能不全而分娩;或(4)诊断为小于胎龄儿。我们还检查了使用和未使用他克莫司的患者之间APO发生率是否存在统计学差异。
共获得48例合并SLE妊娠患者的60次妊娠结局。其中20次(33.3%)妊娠患者使用了他克莫司,28次(46.7%)妊娠出现了APO。在多因素分析中,他克莫司组和非他克莫司组的APO发生率无统计学差异(P = 1.00,校正OR为1,95%CI:0.23 - 4.39)。多元回归分析表明,使用他克莫司对孕晚期收缩压(B = -2.23,P = 0.74)或孕早期血糖水平(B = 10.2,P = 0.056)无显著影响。在单因素分析中,使用和未使用他克莫司的患者感染发生率无显著差异(10.8%对21.1%,P = 0.42)。
他克莫司对妊娠结局、血压或血糖水平无显著影响。需要进一步研究以在更大人群中证实其作用。