{"paper_id":"b8fe8b4e-a181-4484-91e1-c1a9f6effcf3","body_text":"1 Department of Gynecology, Women’s Hospital, Zhejiang University School of Medicine, 310006 Hangzhou, Zhejiang, China\nAbstract\nBackground: The adverse perinatal outcome caused by adenomyosis has\nbeen widely concerned recently, but little attention has been paid to whether the\npositional relationship between placenta and adenomyotic lesion influences the\nmaternal and perinatal outcomes. Methods: A total of 311 women with\nadenomyosis who were pregnant greater than 20 weeks gestation and delivered at\nWomen’s Hospital, Zhejiang University School of Medicine between January 2010 and\nDecember 2021 were recruited. The positional relationships between placenta and\nadenomyotic lesions were determined. The patients were divided into two\nsubgroups: group 1, placenta located on or above the adenomyotic lesion; and\ngroup 2, placenta located far away from the adenomyotic lesion. The clinical data\nof two groups were retrospectively analyzed. Results: We found a higher\nrate of diffuse adenomyosis (62.65% vs. 46.21%, p = 0.01),\ncoexisting endometriosis (31.93% vs. 15.86%, p = 0.002),\npreterm delivery (34.94% vs.15.17%, p\nKeywords\n- adenomyosis\n- pregnancy\n- perinatal outcome\n- placenta\n- adenomyotic lesion\nAdenomyosis, an estrogen-dependent chronic inflammatory gynecological benign disease, is defined as the presence of endometrial glands and stroma within the myometrium of the uterus, resulting in dysmenorrhea and infertility [1, 2, 3]. The exact pathogenesis of adenomyosis remains unclear, although the incidence of adenomyosis tends to occur in younger women and is rising [4, 5, 6]. Although there are many mechanisms to explain infertility caused by adenomyosis, such as abnormal endometrial receptivity and oviduct peristalsis, it is still not clear whether infertility is the result or the cause of adenomyosis [6, 7, 8, 9]. Recently, as more women delay their first pregnancy, adenomyosis, like endometriosis, is attracting more attention because of its increasing impact on fertility and pregnancy outcomes [10, 11, 12, 13, 14, 15, 16, 17]. Consequently, it is necessary to identify the high risk factors affecting the fertility and reproductive outcomes of patients with adenomyosis prior to pregnancy in order to minimize obstetric complications.\nIncreasing evidence from recent studies has demonstrated that many factors,\nincluding age, uterine size, disease severity, subtype and concomitant diseases,\ncan affect the pregnancy outcomes of women with adenomyosis [18, 19, 20, 21, 22, 23, 24]. One study of\nuterus-sparing surgery for patients with adenomyosis by Kishi et al.\n[18] showed that the clinical pregnancy rate of women\nMany obstetric complications in pregnant women with adenomyosis, such as preeclampsia, preterm birth, premature rupture of membrane, small for gestational age, malpresentation and abruption have received more attention in recent years [25, 26, 27, 28]. More recently, a study by Ono et al. [29] of the positional relationship between the placenta and the adenomyosis lesion influenced the perinatal outcomes demonstrating that placental localization near or above adenomyotic lesions increased the risk of perinatal complications. Based on previous research, we performed a retrospective study [30], and found that our results were consistent with those reported by Ono et al. [29]. There was a significant increase in the obstetric morbidity and lower birth weight when the placenta overlaid an adenomyosis lesion. If women with severe diffuse adenomyosis do not have normal myometrium, their placenta will be implanted on the adenomyotic lesions. This may be the cause of infertility or pregnancy failure in patients with severe diffuse adenomyosis.\nWe investigated if the positional relationship between placenta and adenomyotic lesions could be identified in pregnant women with adenomyosis, and all patients were divided into two subgroups (Group 1: placenta on or above the adenomyotic lesion; Group 2: placenta far away from the adenomyotic lesion) according to the relationship between placental implantation site and the adenomyotic lesion. A comparative analysis was performed so as to clarify the influence of the relationship between placental implantation site and adenomyosis lesion on perinatal complications.\nBetween January 2010 and December 2021, a total of 688 pregnant women with adenomyosis who delivered at Women’s Hospital, School of Medicine, Zhejiang University were recruited for this study. The clinical data of all pregnant women with adenomyosis, including age, gravidity, parity, history of surgery, hormone therapy, adenomyosis subtype, gestational age, natural pregnancy, assisted reproductive technology (ART) pregnancy, comorbidity, pregnancy induced hypertension (PIH), gestational diabetes mellitus (GDM), fetal growth restriction (FGR), placental abnormalities, premature rupture of fetal membranes (PROM), preterm birth, mode of delivery, size of the placenta, neonatal birth weight, and postpartum hemorrhage were retrospectively obtained and recorded from the original electronic medical record (EMR) of hospitalized pregnant women with adenomyosis. This study was approved by the Ethics Committee of Women’s Hospital, School of Medicine, Zhejiang University (No. IRB-20210310-R). All patients were exempt from informed consent because this study was retrospective.\nOf the 688 pregnant women with adenomyosis, 332 were excluded because there were\nno nuchal translucency (NT) ultrasound records during 11–13\nFlow chart of patient inclusion.\nThe diagram of the positional relationships between placenta and adenomyotic lesion. Group I: the placenta was located on the adenomyotic lesion (as shown in (a,b)). Group II: the placenta was far away from the adenomyotic lesion (c,d).\nIn order to avoid deviation, two experienced ultrasound experts who were not involved in the research re-examined the ultrasound images to confirm the diagnosis of adenomyosis and the positional relationship between placenta and adenomyotic lesion. The ultrasonic diagnostic criteria for adenomyosis were formulated according to the 2022 consensus on the revised definition of morphological ultrasound assessment (MUSA) features of adenomyosis [31].\nSummary statistics were used to characterize the study population and\ndifferences between groups were assessed using Chi-square or Fisher’s exact test\nfor categorical variables, Student’s T test for normally distributed\ncontinuous variables and Mann–Whitney U tests for non-normally distributed data.\nMultiple logistic regression analyses were used to determine the association\nbetween factors and preterm birth if the placenta was located above adenomyosis.\nCovariates in the multivariate models were selected based on a significant\nassociation at alpha\nIn this study, the patients were screened as shown in Fig. 1. The final study\nincluded 311 pregnant women with adenomyosis. The mean age was 34.39\n| Overall (n = 311) | Group I (n = 166) | Group II (n = 145) | p | ||\n| Age (mean (SD)) | 34.39 (4.53) | 34.09 (4.36) | 34.72 (4.70) | 0.22 | |\n| Age group (%) | |||||\n| 156 (50.16) | 86 (51.81) | 70 (48.28) | 0.61 | ||\n| 155 (49.84) | 80 (48.19) | 75 (51.72) | |||\n| Parity (%) | |||||\n| 0 | 123 (39.55) | 62 (37.35) | 61 (42.07) | 0.46 | |\n| 188 (60.45) | 104 (62.65) | 84 (57.93) | |||\n| ART (%) | 69 (22.19) | 40 (24.10) | 29 (20.0) | 0.47 | |\n| Adenomyosis type (%) | |||||\n| Focal | 140 (45.02) | 62 (37.35) | 78 (53.79) | 0.005 | |\n| Diffuse | 171 (54.98) | 104 (62.65) | 67 (46.21) | ||\n| Pre-pregnant hysterauxesis (%)* | 41 (18.30) | 21 (18.58) | 20 (18.02) | 1.00 | |\n| Scarred uterus (%) | 133 (42.77) | 63 (37.95) | 70 (48.28) | 0.09 | |\n| History of endometriosis (%) | 76 (24.44) | 53 (31.93) | 23 (15.86) | 0.002 |\nSD, standard deviation; ART, assisted reproductive technology.\n*Pre-pregnant uterine enlargement was defined as the volume of uterus larger than 3 months of gestation; there were 87 women without the data of pre-pregnancy uterus volume.\nAll pregnant women were divided into two groups: Group I (n = 166) indicated that the placenta was located on the adenomyotic lesion (as shown in Fig. 2a,b); Group II (n = 145) exhibited that the placenta was far away from the adenomyotic lesion (Fig. 2c,d). Compared with group II, diffuse adenomyosis was more common in group I (104 (62.65%) vs. 67 (46.21%), p = 0.01), as well as more likely to have concordant endometriosis (53 (31.93%) vs. 23 (15.86%), p = 0.002). Considering the age, parity, ART, cases with scarred uterus, history of hormone treatment and pre-pregnancy uterine size, there were no significant differences between group I and group II.\nThe pre-pregnant uterine size of patients with diffuse adenomyosis was larger than the size of patients with focal adenomyosis in both two groups (the proportion of pre-pregnant uterine size larger than three months gestation, focal vs. diffuse: group I 3 (3/62, 4.84%) vs. 18 (18/104, 17.31%), p = 0.01; group II 2 (2/78, 2.65%) vs. 18 (18/67, 26.87%)).\nThe results of comparison of perinatal outcomes are detailed in Table 2. Of the\n311 cases, 12 (3.86%) cases were diagnosed with cervical incompetence, 45\n(14.47%) cases were complicated with PIH, 60 (19.29%) cases were complicated\nwith GDM, and 15 (4.82%) cases were complicated with oligohydramnios. Twenty\nthree (7.40%) cases of FGR and 47 (15.11%) cases of premature rupture of fetal\nmembranes (PROM) were detected. There were 2 cases diagnosed with uterine rupture\nor threatened uterine rupture with both cases being in group I. The overall rate\nof preterm delivery was 25.72% (80/311), which was significantly higher in group\nI than group II (34.94% (58/166) vs. 15.17% (22/145), p\n| Overall (n = 311) | Group I (n = 166) | Group II (n = 145) | p | |\n| Cervical incompetence (%) | 12 (3.86) | 7 (4.22) | 5 (3.45) | 0.96 |\n| PIH (%) | 45 (14.47) | 20 (12.05) | 25 (17.24) | 0.26 |\n| GDM (%) | 60 (19.29) | 29 (17.45) | 31 (21.38) | 0.47 |\n| Oligohydramnios (%) | 15 (4.82) | 8 (4.82) | 7 (4.83) | 1.00 |\n| FGR | 23 (7.40) | 15 (9.04) | 8 (5.52) | 0.33 |\n| PROM (%) | 47 (15.11) | 23 (13.86) | 24 (16.55) | 0.62 |\n| Uterine rupture or threatened uterine rupture (%) | 2 (0.64) | 2 (1.20) | 0 (0.00) | 0.54 |\n| Preterm delivery (%) | 80 (25.72) | 58 (34.94) | 22 (15.17) | |\n| Fetal presentation (%) | ||||\n| Cephalic | 301 (96.78) | 159 (95.78) | 142 (97.93) | 0.45 |\n| Non-cephalic | 10 (3.22) | 7 (4.22) | 3 (2.07) | |\n| 5 min Apgar |\n11 (3.54) | 9 (5.42) | 2 (1.38) | 0.11 |\n| Delivery mode (%) | ||||\n| Vaginal delivery | 61 (19.61) | 36 (21.69) | 25 (17.24) | 0.40 |\n| Cesarean delivery | 250 (80.39) | 130 (78.31) | 120 (82.76) | |\n| Birth weight (median (IQR)) | 3090 (2580, 3400) | 3050 (2350, 3335) | 3100 (2800, 3415) | 0.02 |\n| Placenta malposition (%)* | 43 (13.83) | 33 (19.88) | 10 (6.90) | 0.002 |\n| Placental abruption (%) | 11 (3.54) | 6 (3.61) | 5 (3.45) | 1.00 |\n| Placental surface area (median (IQR)) | 324 (288, 360) | 323 (256, 360) | 342 (306, 360) | 0.004 |\n| Blood loss during delivery (median (IQR)) | 300 (200, 400) | 300 (200, 400) | 300 (200, 400) | 0.40 |\n| Postpartum hemorrhage | 23 (7.40) | 15 (9.04) | 8 (5.52) | 0.33 |\n| Composite neonatal adverse outcomes (%) | 99 (31.83) | 70 (42.17) | 29 (20.00) | |\n| Composite maternal adverse outcomes (%) | 124 (39.87) | 65 (39.16) | 59 (40.69) | 0.87 |\nPIH, pregnancy induced hypertension syndrome; GDM, gestational diabetes mellitus; FGR, fetal growth restriction; PROM, premature rupture of fetal membranes; IQR, interquartile range.\n*Placental malposition includes placenta previa or low-lying placenta.\nNeonatal adverse outcomes including: preterm delivery, FGR and 5 min Apgar\nMaternal adverse outcomes including: PIH, GDM, uterine rupture or threatened uterine rupture, placental abruption and postpartum hemorrhage.\nSpearman correlation analysis showed that the birth weight was positively associated with placental surface area.\nThere were no significant differences for cervical incompetence, PIH, GDM, oligohydramnios, FGR, PROM, uterine rupture or threatened uterine rupture, fetal presentation, fetal distress, delivery mode, placental abruption and blood loss during delivery between group I and group II.\nAs shown in Table 3, 5 variables were found to be associated with composite\nneonatal adverse outcome by multivariable logistic regression analysis. Placenta\nlocation above the uterine adenomyosis increased the risk of composite neonatal\nadverse outcome (odds ratio (OR): 3.13, 95% confidence interval (95% CI): 1.47–7.00, p = 0.004). There were 4\nother risk factors related to composite neonatal adverse outcome, including PIH\n(OR: 3.46, 95% CI: 1.39–8.70, p = 0.01), placenta malposition (OR:\n3.28, 95% CI: 1.18–9.22, p = 0.01), placenta abruption (OR: 10.14,\n95% CI: 2.26–54.44, p = 0.003) and scarred uterus (OR: 2.71, 95% CI:\n1.17–6.46, p = 0.02). Moreover, searman correlation analysis\ndemonstrated that the birth weight was positively associated with placental\nsurface area (R = 0.44, p\n| OR | 95% CI | p value | |||\n| (Intercept) | 0.03 | 0.01 | 0.14 | ||\n| Group | |||||\n| I (n = 166) | 3.13 | 1.47 | 7 | 0.004 | |\n| II (n = 145) | Reference | ||||\n| ART | |||||\n| yes (n = 69) | 1.44 | 0.55 | 3.67 | 0.45 | |\n| no (n = 242) | Reference | ||||\n| Age | |||||\n| 1.33 | 0.62 | 2.88 | 0.47 | ||\n| Reference | |||||\n| Parity | |||||\n| Multipara (n = 188) | 1.5 | 0.58 | 3.96 | 0.4 | |\n| Primipara (n = 123) | Reference | ||||\n| Adenomyosis type | |||||\n| Diffuse (n = 171) | 1.54 | 0.7 | 3.41 | 0.29 | |\n| Focal (n = 140) | Reference | ||||\n| Pre-pregnant enlarged uterus | |||||\n| yes (n = 41) | 0.85 | 0.31 | 2.19 | 0.74 | |\n| no (n = 270) | Reference | ||||\n| History of endometriosis | |||||\n| yes (n = 76) | 1.25 | 0.53 | 2.88 | 0.6 | |\n| no (n = 235) | Reference | ||||\n| Cervical incompetence | |||||\n| yes (n = 12) | 1.71 | 0.18 | 20.46 | 0.65 | |\n| no (n = 299) | Reference | ||||\n| PIH | |||||\n| yes (n = 45) | 3.46 | 1.39 | 8.7 | 0.01 | |\n| no (n = 266) | Reference | ||||\n| GDM | |||||\n| yes (n = 60) | 0.97 | 0.35 | 2.43 | 0.95 | |\n| no (n = 251) | Reference | ||||\n| Placenta malposition* | |||||\n| yes (n = 43) | 3.28 | 1.18 | 9.22 | 0.02 | |\n| no (n = 268) | Reference | ||||\n| Placental abruption | |||||\n| yes (n = 11) | 10.14 | 2.26 | 54.44 | 0.003 | |\n| no (n = 300) | Reference | ||||\n| Oligohydramnios | |||||\n| yes (n = 15) | 1.96 | 0.23 | 12.22 | 0.49 | |\n| no (n = 296) | Reference | ||||\n| PROM | |||||\n| yes (n = 47) | 2.41 | 0.86 | 6.52 | 0.09 | |\n| no (n = 264) | Reference | ||||\n| Delivery mode | |||||\n| Cesarean delivery (n = 250) | 0.73 | 0.25 | 2.2 | 0.56 | |\n| Vaginal delivery (n = 61) | Reference | ||||\n| Scarred uterus | |||||\n| yes (n = 133) | 2.71 | 1.17 | 6.46 | 0.02 | |\n| no (n = 178) | Reference |\nOR, Odds ratio; CI, confidence interval.\n*Placental malposition includes placenta previa or low-lying placenta.\nNeonatal adverse outcomes includes preterm delivery, FGR and 5 min Apgar\nAs shown in Table 4, placenta location above the uterine adenomyosis showed no significant effect on the risk of composite maternal adverse outcomes; however, the maternal age older than 35 years might increase the risk (OR: 2.03, 95% CI: 1.11–3.76, p = 0.02).\n| OR | 95% CI | p value | |||\n| Intercept | 0.46 | 0.15 | 1.36 | 0.17 | |\n| Group | |||||\n| I (n = 166) | 0.63 | 0.35 | 1.14 | 0.13 | |\n| II (n = 145) | Reference | ||||\n| ART | |||||\n| yes (n = 69) | 0.62 | 0.28 | 1.34 | 0.23 | |\n| no (n = 242) | Reference | ||||\n| Age | |||||\n| 2.03 | 1.11 | 3.76 | 0.02 | ||\n| Reference | |||||\n| Parity | |||||\n| Multipara (n = 188) | 1.47 | 0.7 | 3.12 | 0.31 | |\n| Primipara (n = 123) | Reference | ||||\n| Adenomyosis type | |||||\n| Diffuse (n = 171) | 1.73 | 0.91 | 3.32 | 0.1 | |\n| Focal (n = 140) | Reference | ||||\n| Pre-pregnant enlarged uterus | |||||\n| yes (n = 41) | 0.59 | 0.26 | 1.28 | 0.19 | |\n| no (n = 270) | Reference | ||||\n| History of endometriosis | |||||\n| yes (n = 76) | 0.64 | 0.3 | 1.32 | 0.23 | |\n| no (n = 235) | Reference | ||||\n| Cervical incompetence | |||||\n| yes (n = 12) | 3.34 | 0.48 | 28.61 | 0.22 | |\n| no (n = 299) | Reference | ||||\n| Placenta malposition* | |||||\n| yes (n = 43) | 2 | 0.78 | 5.27 | 0.15 | |\n| no (n = 268) | Reference | ||||\n| Oligohydramnios | |||||\n| yes (n = 15) | 0.6 | 0.08 | 3.09 | 0.56 | |\n| no (n = 296) | Reference | ||||\n| PROM | |||||\n| yes (n = 47) | 0.58 | 0.24 | 1.36 | 0.22 | |\n| no (n = 264) | Reference | ||||\n| Delivery mode | |||||\n| Cesarean delivery (n = 250) | 1.1 | 0.47 | 2.65 | 0.82 | |\n| Vaginal delivery (n = 61) | Reference | ||||\n| Scarred uterus | |||||\n| yes (n = 133) | 0.79 | 0.4 | 1.53 | 0.49 | |\n| no (n = 178) | Reference |\n*Placental malposition includes placenta previa or low-lying placenta.\nMaternal adverse outcomes includes PIH, GDM, uterine rupture or threatened uterine rupture, placental abruption and postpartum hemorrhage.\nAs shown in Table 5, 3 variables were found to be associated with placenta location above the uterine adenomyosis by multivariable logistic regression analysis. Diffuse adenomyosis (OR: 1.72, 95% CI: 1.08–2.74, p = 0.02), endometriosis history (OR: 2.07, 95% CI: 1.18–3.71, p = 0.01) and placenta malposition (OR: 2.63, 95% CI: 1.25–5.92, p = 0.01) might increase the risk of placenta implantation site overlapping the uterine adenomyosis.\n| OR | 95% CI | p value | |||\n| Intercept | 0.64 | 0.45 | 0.91 | 0.01 | |\n| Adenomyosis type | |||||\n| Diffuse (n = 171) | 1.72 | 1.08 | 2.74 | 0.02 | |\n| Focal (n = 140) | Reference | ||||\n| History of endometriosis | |||||\n| yes (n = 76) | 2.07 | 1.18 | 3.71 | 0.01 | |\n| no (n = 235) | Reference | ||||\n| Placenta malposition* | |||||\n| yes (n = 43) | 2.63 | 1.25 | 5.92 | 0.01 | |\n| no (n = 268) | Reference |\n*Placental malposition includes placenta previa or low-lying placenta.\nRecent publications have confirmed that adenomyosis was associated with increased risks of early miscarriage, second trimester miscarriage, preterm delivery, preeclampsia, FGR, placental malposition, postpartum bleeding, cesarean section rate and the incidence of pregnancy by ART [33, 34, 35]. In addition, the gestational age and neonatal birth weight at delivery were significantly lower than those of pregnant patients without adenomyosis and the placental attachment on the area of adenomyotic lesion could be associated with FGR [13, 25].\nOur study drew similar conclusions and reconfirmed the conclusion that the relationship between placental implantation site and adenomyotic lesion location had a substantial impact on pregnancy outcome of adenomyosis patients [29]. In our study, the placenta implantation site above the uterine adenomyosis had a high correlation with preterm delivery, lower birth weight and placenta malposition. However, the incidence of FGR showed no significant difference.\nAdenomyosis-associated lower neonatal birth weight and preterm delivery were thought to have a pathophysiological correlation with inflammation, free radicals and junctional zone alterations. Specifically, thickening of the myometrial junctional zone was the typical change noted in adenomyosis patients by magnetic resonance imaging (MRI). Placental dysplasia caused by impaired remodeling of spiral arteries in this area creates a hostile environment for the placenta that impedes adequate fetal exchange with the maternal blood supply, possibly through a vascular steal mechanism, leading to numerous adverse pregnancy complications [16, 36, 37, 38, 39]. Previous studies have suggested that fetuses with lower placental weight and smaller placental surface area were at higher risk of developing FGR [40, 41], a finding in accordance with the results of our study that birth weight was positively associated with placental surface area. The lower birth weight in women with placenta location overlapping adenomyosis may be related to the smaller placenta being caused by the adenomyosis.\nAdenomyosis is also an independent risk factor for impaired reproductive\nfunction [42]. These patients have a higher incidence of infertility and the\nclinical pregnancy rate of assisted reproductive technology in adenomyosis\npatients is significantly reduced [36]. In our study, 69 cases (22.19%)\nunderwent ART, with the percentage being much higher when compared with average\nwomen. Moreover, researchers have found that the adverse pregnancy outcome of\npatients whose pregnancy was complicated with adenomyosis was closely related to\nthe severity of the disease and whether it was diffuse adenomyosis [43, 44]. A\nclinical trial from Japan recruited 272 pregnant women with adenomyosis and\nreported that the rates of miscarriage (\nAlthough it is currently believed that the adverse pregnancy outcomes of\nadenomyosis patients are related to the severity and lesion type of adenomyosis\n[43, 44], the exact mechanism leading to the phenomenon is still unclear.\nThickening of the myometrium and endometrial-myometrial junction, elevated\ninflammatory cytokines, such as IL-6 and TNF-\nOur study retrospectively analyzed the clinical data of 311 pregnant patients complicated with adenomyosis. Our data demonstrated that the placental implantation site was closely related to pregnancy outcomes. If the placenta was located on or close to the adenomyotic lesion, the rate of preterm delivery and placental malposition were significantly increased, and the gestational age, neonatal birth weight and placental size were significantly decreased, which were consistent with the results reported in the literature [13, 53]. Thus, it was further confirmed that there were severe adverse pregnant outcomes in adenomyosis patients whose placenta was closely implanted to the lesion.\nOur study detected that diffuse adenomyosis, endometriosis history and placenta malposition might increase the risk of placenta implantation site overlapping the uterine adenomyosis, this pathological mechanism needs to be further explored. This indicates that patients with adenomyosis are recommended to evaluate the severity and lesion type of adenomyosis before pregnancy, and offer early intervention, especially for those women co-existing with an endometriosis history. Once the patient is pregnant, ultrasound and other imaging techniques such as MRI should be utilized to identify the relationship between the embryo implantation site and the lesion position of adenomyosis, and to check the uterine artery pulsation index, in order to closely monitor and intervene when appropriate. An early intervention is the usage of aspirin, in order to prevent early placental dysplasia, including PIH [54] and recurrent miscarriage [55]. The study of Yamanaka [56] revealed that adenomyosis had a risk of activating the blood coagulation system and increased the risk of thrombosis, suggesting that aspirin be considered to be useful in pregnancy complicated by adenomyosis.\nOur study determined that severe adverse pregnant outcomes in adenomyosis patients were closely related to the placenta implantation site if it was overlapping lesion. These conclusions are consistent with those reported by Ono et al. [29]. Due to the difficulty to distinguish junctional zone (JZ) in the pregnant uterus by ultrasound screening, it is hard for us to determine the relationship between adenomyosis lesion and JZ, as well as the exact distance between the placenta and the lesions. Thus, our recommendation is that pregnant patients complicated with adenomyosis should undergo MRI in late pregnancy to identify the relationship between placental implantation site and lesion location, uterine artery pulsation index and fetal growth.\nIn our study, there was no significant difference in the incidence of FGR and PIH, regardless of the location of the placenta. Other researchers have found that PIH was a maternal complication related to an autoimmune mechanism, so it might have something to do with immune pathogenesis of adenomyosis [57]. Although other literature reported that the incidence of FGR in pregnant patients complicated with adenomyosis was mainly related to diffuse adenomyosis [52], our data showed no difference, which might due to one of the limitations of the study (the relatively small number of cases and imperfect retrospective data). There are still other limitations. The history of cesarean section and ART may be associated with the risk of maternal and neonatal outcomes but these cases were not excluded from the study. Fortunately, the patients with the history of cesarean section or ART were symmetrically distributed in two groups. Furthermore, all patients merely had ultrasound images without MRI images since our study was a retrospective approach, so the specific data of the distance between the placental implantation site and the lesion of adenomyosis could not be acquired. Obviously, it is necessary to further comprehensively apply ultrasound and MRI to classify the types of adenomyosis, measure the size of uterus, evaluate the severity of the disease, measure the distance between the placental implantation site and the lesion, and implement a multicenter prospective study with a large sample size to evaluate the adverse pregnancy outcomes of pregnant patients complicated with adenomyosis.\nPregnant women whose pregnancy is complicated by adenomyosis are associated with adverse pregnancy outcomes. When the placental implantation site overlaps the adenomyotic lesion, adverse pregnancy outcomes are more likely to occur, and include preterm delivery and lower birth weight. Women with diffuse adenomyosis, endometriosis history and placenta malposition are more likely to have placental implantation site overlapping the adenomyotic lesion. Therefore, patients with adenomyosis need detailed and thorough evaluation prior to pregnancy. Imaging examinations should be performed during the pregnant process to determine the placental implantation site, uterine artery pulsation index and fetal growth. Close monitoring and early intervention such as consultant-led care when clinically appropriate should be carried out to improve pregnancy outcomes.\nThe data and materials generated during and analyzed during the present study are available from the corresponding author upon reasonable request.\nXZ and PX designed the research study. PX, XH, YZ, YW and GZ performed the research. PX, XH, JW analyzed the data. PX, JW and XZ wrote the manuscript. All authors contributed to editorial changes in the manuscript. All authors read and approved the final manuscript. All authors have participated sufficiently in the work and agreed to be accountable for all aspects of the work.\nThis study was approved by the Ethics Committee of Women’s Hospital, School of Medicine, Zhejiang University (No. IRB-20210310-R). All patients were exempt from informed consent because this study was retrospective.\nWe appreciate the staff at the Zhejiang University, women hospital for their diligent clinical work and precise data recording in the cases we reported in this article. We thank all the participants in the study.\nThis study was funded by National Key R&D Program of China (Grant number: 2022YFC2704003) and Zhejiang Provincial Natural Science Foundation of China (grant No. LY23H040005).\nThe authors declare no conflict of interest.\nReferences\nPublisher’s Note: IMR Press stays neutral with regard to jurisdictional claims in published maps and institutional affiliations.","source_license":"CC0","license_restricted":false}