Luteal blood flow as a predictive factor for methotrexate treatment outcomes in women with unruptured tubal pregnancy

Ectopic pregnancy (EP) occurs when blastocysts are implanted outside the uterine cavity, and EP may result in severe complications, including rupture of the fallopian tube, hemorrhagic shock, and even death [1, 2]. It has been reported that the incidence of EP represents 1–2% of all pregnancies and is the main reason of death in the first trimester of pregnancy [3]. Fallopian tubes are the most common site for blastocyst implantation [4]. At present, most EPs can be diagnosed in the early stage because of the improvement and popularization of transvaginal ultrasound (TVUS) [5]. Once a definitive diagnosis of EP has been made, the patient should be monitored closely and treated with surgical, medical or expectant management. The selection of the therapeutic plan depends on the serum human chorionic gonadotropin (hCG) level, size of the ectopic mass and foetal cardiac activity (FCA). Methotrexate (MTX) is widely used as a first-line treatment for women diagnosed with unruptured EP with a low serum hCG concentration, a small ectopic mass and stable haemodynamics. In appropriately selected women, the success rates of single-dose MTX for tubal EP treatment ranged from 65 to 95%, and 3 to 27% of the patients needed a second dose [6].

The blood flow in the corpus luteum can be detected by transvaginal colour-pulsed Doppler ultrasonography. The luteal blood flow increases gradually after ovulation, and the corpus luteum is filled with blood [7]. Previous studies have found that insufficiency of the corpus luteum during pregnancy was associated with infertility and spontaneous abortion in the first trimester of pregnancy [8, 9]. In addition, blood flow in the corpus luteum is closely related to luteal function. Some drug treatments could improve corpus luteum function by increasing its blood supply [10]. However, to the best of our knowledge, the impact of luteal blood flow on MTX treatment in women with unruptured tubal pregnancy has not been reported. Our research aims to observe the impact of luteal blood flow on MTX treatment outcomes in women with unruptured tubal pregnancy.

A total of 129 women were assessed for MTX treatment, and of these, we excluded 3 women who underwent surgical intervention, 5 women who underwent expectant management, 2 women who were lost to follow-up, and 4 women who declined to participate. Finally, 115 women were included in the study, and these women were divided into 2 groups according to the luteal blood flow. Fifty-six women were successfully treated with MTX in the poor luteal blood flow group, and 59 women were successfully treated with MTX in the abundant luteal blood flow group (Fig. 2).

Table 1 illustrates the baseline characteristics of the women in the two groups. No significant difference was found when comparing maternal age, BMI, number of pregnancies and deliveries, pregnancy method, risk factors of ectopic pregnancy, duration of pregnancy, clinical symptoms, serum β-hCG level before treatment, or ultrasound findings (P > 0.05). However, the serum progesterone level before treatment was significantly higher in women with abundant luteal blood flow than in those with poor luteal blood flow (P = 0.041).

No significant difference was found when comparing the volume of the corpus luteum (P = 0.058); however, the VI (P = 0.019), FI (P = 0.042) and VFI (P = 0.031) of the corpus luteum were significantly higher in women with abundant luteal blood flow than in women with poor luteal blood flow (Fig. 3).

The serum β-hCG level 4 days, 1 week and 2 weeks after MTX treatment in women with abundant luteal blood flow were significantly higher than those in women in the poor luteal blood flow group (P < 0.05). Moreover, the time of serum β-hCG clearance in women with abundant luteal blood flow was significantly longer (P = 0.029). The average diameter of the ectopic mass 1 week, 2 weeks and 3 weeks after MTX treatment in women with abundant luteal blood flow was significantly larger (P < 0.05), and the time required for ectopic mass disappearance was significantly longer (P = 0.043) compared with that in women in the poor luteal blood flow group (Fig. 4).

In women with poor luteal blood flow, 55 women (98.2%) received one dose of MTX treatment, and 1 woman (1.8%) received a second dose of MTX treatment because her serum β-hCG level did not decline by 15% between days 4 and 7. However, in women with abundant luteal blood flow, 52 women (88.1%) received one dose of MTX treatment, and 7 women (11.9%) received a second dose of MTX treatment. There was a significant difference in the dose of MTX used in the two groups (P = 0.034). Eight women with poor luteal blood flow reported side effects versus 11 in the abundant luteal blood flow group, and the laboratory results showed a minor rise in alanine aminotransferase (ALT) and aspartate transaminase (AST) levels, which ranged from 45 to 64 U/L. These side effects were mild and disappeared within 2 weeks after MTX treatment. No significant difference was found when comparing the side effects of MTX between the two groups (P = 0.529) (Table 2).

Since the first application by Tanaka et al. [13], MTX has become the primary treatment for unruptured EP [14]. The successful treatment of EP depends on several factors, including the serum hCG level, route of MTX administration, size of the ectopic mass and FCA [15‐17]. However, the effect of luteal blood flow during pregnancy on MTX treatment in women with EP has not been previously reported. Transvaginal colour Doppler ultrasound is a useful and noninvasive technique for the detection of blood flow around the corpus luteum [18]. Previous studies reported that luteal blood flow was associated with luteal vascularization and luteal function [19, 20], which is essential for the support of early pregnancy. Therefore, we speculate that the blood supply of the corpus luteum may be related to the treatment outcomes of unruptured tubal pregnancy.

The present study observed 115 women with unruptured tubal pregnancy who were treated successfully with MTX. Women in the study were divided into 2 groups according to their luteal blood flow. Our data revealed that women with abundant luteal blood flow had a significantly higher serum β-hCG level 4 days, 1 week and 2 weeks after MTX treatment compared with women with poor luteal blood flow. Moreover, the average diameter of the ectopic mass 1 week, 2 weeks and 3 weeks after MTX treatment in women with abundant luteal blood flow was significantly larger, and the time required for serum β-hCG clearance and ectopic mass disappearance were significantly longer in comparison with that in women with poor luteal blood flow. These findings illustrated that luteal blood flow impacted the therapeutic outcomes in women with unruptured tubal pregnancy, and those with abundant luteal blood flow needed a second dose of MTX treatment and a longer recovery time.

Previous studies confirmed that the crucial role of angiogenesis in corpus luteum is maintenance of luteal function [21]. Ovulation is triggered through a peak of luteinizing hormone (LH) in blood, which is secreted and released by hypothalamus. The pressure in the follicular cavity decreases after ovulation, and the avascular granulosa cell layer is invaded by the vascular endothelial cells of the theca cell layer, and then the blood flow in the corpus luteum increase rapidly [22]. In fact, vascularization and abundant blood flow in the corpus luteum are important for the development of the corpus luteum and progesterone secretion, which play an important role in the improvement of endometrial receptivity, embryo implantation and successful pregnancy.

Blood vessels are maintained in the corpus luteum until 10 weeks of gestation. The function of the corpus luteum is mainly used for the secretion of progesterone and its release into the blood. Previous studies displayed that the removal of the corpus luteum in the first trimester of pregnancy leads to a decline in blood progesterone level, which further causes miscarriages [21]. Multiple studies have confirmed that the blood supply of the corpus luteum is correlated with the serum progesterone level, and the blood supply of the corpus luteum is decreased in women with luteal phase defects compared with that in women with normal luteal function [10, 18, 20]. Progesterone maintains embryonic development during pregnancy in a variety of ways, such as by increasing the excitatory threshold of uterine smooth muscle, inhibiting uterine contraction, participating in the maintenance of the maternal-foetal microenvironment, and promoting maternal-foetal tolerance [23‐26]. The data in our study demonstrated that the serum progesterone level before treatment and the VI, FI and VFI of the corpus luteum were significantly higher in women with abundant luteal blood flow than those in women in the poor luteal blood flow group. These findings indicated that luteal blood flow was an important factor in regulating progesterone levels and affected luteal function and pregnancy outcomes. Low blood supply to the corpus luteum was associated with luteal function defects, which is consistent with previous reports [20].

This study has some limitations. Corpus luteum function is affected by factors other than the corpus luteal blood flow according to this study design. In addition, if an ectopic pregnancy had already been aborted due to falling β-hCG levels, this may not have had any effect on intervention with MTX. Therefore, the repeatability of the results of this study needs to be confirmed after excluding other factors that affect luteal function and therapeutic effect.

In conclusion, the present study showed the impact of luteal blood flow during pregnancy on MTX treatment in women with unruptured tubal pregnancy. Those with abundant luteal blood flow needed a second dose of MTX treatment and a longer recovery time. The blood supply of the corpus luteum may be an important clinical factor for assessing the prognosis of women with EP.