Revista Brasileira de Ginecologia e Obstetrícia

Junctional Zone in Infertile Women: A Three-dimensional Ultrasound Study

DOI: 10.1055/s-0040-1708089 - volume 42 - Março 2020

Silva, Vanessa; Ramos, Flávia Fundora; Brás, Ana Filipa Matos; Santos, Ricardo Filipe Sousa; Xavier, Maria Sofia Dantas Pinto Lobo; Miguelote, Rui Filipe Oliveira

Abstract

Abstract

Objective

To analyze the interobserver and intraobserver reproducibility of the visualization and continuity of the juncional zone (JZ) by three-dimensional (3D) ultrasound in infertile women, and to evaluate the sociodemographic, hormonal, and structural factors that influence these assessments.

Methods

A prospective study conducted at the Assisted Reproductive Technology Unit of Hospital Senhora da Oliveira, in the city of Guimarães, Portugal. Transvaginal 3D ultrasonography was performed, and 2 volumes were generated per case. Two observers who were blinded to each other's work analyzed these volumes, choosing the best coronal section. Four months later, one of the observers performed the same methodology. The JZ visualization was classified as optimal, satisfactory, and unsatisfactory, and the JZ continuity, as continuous and discontinuous. The interobserver and intraobserver agreements were analyzed. The influence of hormonal, structural, and sociodemographic factors on the JZ was evaluated.

Results

In total, 65 women were included in the present study. The interobserver reproducibility was substantial for JZ visualization and continuity (k = 0.635 and 0.753 respectively), and the intraobserver reproducibility was very good for JZ visualization and continuity (k = 0.884 and 0.816 respectively). Trilaminar endometrial pattern was associated with optimal JZ visualization (p = 0.012). The increase of 1 unit in the level of serum estradiol represents a 9.9% decrease in the odds of unsatisfactory visualization of the JZ (odds ratio [OR] = 0.9; 95% confidence interval [95%CI] = 0.814–0.996; p = 0.042). Endometriosis increases the odds of unsatisfactory visualization by 24 times (OR = 23.7; 95%CI = 1.262–437.057; p = 0.034). The prevalence of discontinuous JZs was of 60%. Myomas and endometriosis were associated with discontinuous JZs (p = 0.034 and 0.016 respectively).

Conclusion

The assessment of JZ visualization and continuity by 3D ultrasound is reproducible enough to be used in the clinical practice.


Full Text

Introduction

The junctional zone (JZ) is a hormone-dependent zone that corresponds to the inner layer of the myometrium, which derives from the paramesonephric ducts. In contrast, the outer myometrium has a different embryonic origin – a mesenchymal one.1 The JZ contains myocytes as the outer myometrium, but with different morphologic characteristics. Junctional-zone myocytes have a higher nuclear-cytoplasmic ratio, reduced extracellular matrix, low content of water, and a concentric architectural arrangement.1 These characteristics enable the identification of the JZ on ultrasound.1

The JZ plays an important role in reproduction and pregnancy. Uterine contractility in non-pregnant women originated exclusively in the JZ changes in orientation, amplitude, and frequency according to the phase of the menstrual cycle.2,3 These contractions increase and take the direction of the cervix to the uterine fundus in the follicular and periovulatory phase, facilitating sperm transport.2,4,5 Peristaltic activity decreases in the luteal phase, facilitating the implantation, oxygenation, and nutrition of the blastocyst.2,6

When uterine contractility is excessive and uncoordinated, it is associated with lower pregnancy rates both in natural and assisted reproductive technology cycles.7,8 Studies2,9,10 show that a dysfunctional JZ plays an important role in the physiopathology of endometriosis, facilitating retrograde menstruation and implantation of endometrial cells in the pelvis. On the other hand, JZ characteristics observed by three-dimensional (3D) ultrasound and magnetic resonance imaging (MRI), such as increased thickness and disruption, are associated with endometriosis, but also with adenomyosis.11,12

Several studies1,13,14 suggest that the assessment of the JZ by 3D transvaginal ultrasound should be included in routine uterine ultrasound. Through the coronal plane, it is possible to delimit the JZ at the fundus and lateral walls, which is observed as a thin and regular layer with hypoechogenic characteristics between the basal layer of the endometrium and the outer myometrium.1,15 Despite growing research involving the evaluation of the JZ by 3D ultrasound, there is no universally accepted methodology.

Due to the cost-benefit ratio, convenience and availability of 3D ultrasound, and the importance of the JZ, particularly in infertile women, we aim to evaluate the interobserver and intraobserver reproducibility of the visualization and continuity of the JZ by 3D ultrasound as well as to identify the sociodemographic and physiological factors that affect the JZ.

 

Methods

A prospective observational study was conducted with women followed at the Assisted Reproductive Technology Unit of Hospital Senhora da Oliveira, in the city of Guimarães, Portugal, from July to October of 2018. The exclusion criteria were serum follicle-stimulating hormone levels greater than 25UI/L, women older than 40 years of age, and cases with incomplete data on the ultrasound evaluation (absence of 2 volumes per case). One of the authors (VS) acquired the planes and volumes through transvaginal ultrasound (with the woman in the lithotomy position and an empty bladder), using a Samsung (Seoul, South Korea) HS50 ultrasound with a 5–9 MHz 2D/3D endocavitary probe. All evaluations were performed using a standardized methodology, as explained below.

For the uterine assessment, two-dimensional (2D) transverse and longitudinal planes were performed. The uterus was centered on the screen. In the longitudinal plane, the endometrial thickness was measured (in the double layer, in its thickest zone) parallel to the anteroposterior diameter of the uterus. In the presence of intracavitary fluid, the endometrial thickness was obtained by subtracting the thickness of the intracavitary fluid from the total thickness of the endometrial cavity.16 The anomalies observed, such as myomas or adenomyosis, were identified according to established diagnostic criteria.17 The pelvic cavity was explored for signs of endometriosis (endometriomas or deep endometriosis with the involvement of the bladder, bowel, or rectovaginal septum).18 After the 2D ultrasound, a 3D ultrasound was performed. In the longitudinal plane, the uterus was centered on the screen so that the cervical canal and the myometrium were fully visible. The 3D acquisition box was adjusted to include a margin around the uterus, which allowed delimitation of the myometrium. A maximal image quality and an acquisition angle (90°) were selected. The probe was held firmly, and the women were asked to hold their breath during acquisition to minimize the artifacts. After the acquisition, a summary evaluation of the volume was performed, and whenever it turned out to be of poor quality (a volume that did not enable the complete assessment of the uterine volume or the presence of movement artifacts), new ones were obtained. Two volumes per case were obtained from each participant, and the volumes were stored in the ultrasound memory. An analysis of the 3D volumes was performed posteriorly, using the Samsung Medison 5D Viewer software. The methodology of 3D image postprocessing and classification of JZ visualization and continuity was initially standardized between the authors (VS and FR) in a set of volumes not included in the study sample. The multiplanar image was freely adjusted for the JZ assessment to obtain a coronal plane with adequate visualization of the endometrial cavity, the external contour of the uterus, and the interstitial portions of the fallopian tube. A region of interest (ROI) box with any rendering mode combination was used to optimize the visualization of the JZ. The best reconstructed coronal image was chosen for each participant from the two volumes acquired per operator. The visualization of the JZ was classified as proposed by Naftalin et al14 (Fig. 1):

 

Fig. 1
Three-dimensional ultrasound imaging of optimal (A), satisfactory (B) and unsatisfactory (C) visualizations of the JZ in the coronal plane.

The continuity of the JZ was classified as proposed by Van den Bosch et al17 (Fig. 2):

 

Fig. 2
Three-dimensional ultrasound imaging of continuous (A) and discontinuous (B) JZ in the coronal plane. Note the discontinuous JZ on the coronal section, marked in (B) by the red circle.

Two authors (VS and FR) performed the postprocessing and analysis of the 3D volumes independently and blindly. Both authors classified the best coronal plane of the two volumes acquired per participant to determine the interobserver agreement. Four months after the first analysis, VS reassessed the volumes (two volumes per case, choosing the best reconstructed coronal image from the two volumes acquired) to determine the intraobserver agreement. The intraobserver and interobserver agreements were assessed for visualization and continuity of the JZ.

Demographic and physiological (hormonal and structural) variables, as well as gynecological antecedents were collected by consulting the participants' electronic clinical process and 2D/3D transvaginal ultrasound. Then their effects on the visualization and continuity of the JZ were evaluated.

Data analysis was performed using the Statistical Package for Social Sciences (SPSS, IBM Corp., Armonk, NY, US), version 25.0. The interobserver and intraobserver agreements were assessed using the Cohen k, which was interpreted as poor (k < 0.20), reasonable (k between 0.21 and 0.40), moderate (k between 0.41 and 0.60), good (k between 0.61 and 0.80), and very good (k between 0.81 and 1.00).19 Rejection of the null hypothesis was based on the significance level of p < 0.05. The cases of unsatisfactory visualization were excluded from the assessment of continuity of the JZ, and most cases of disagreement in the classification of visualization of the JZ (unsatisfactory versus satisfactory/optimal) were solved. The unsolved cases of disagreement were excluded from the analysis.

A descriptive analysis was performed taking into account the symmetry of the distribution of the continuous variables. Based on the result of the Shapiro-Wilk test, parametric or nonparametric statistics were used according to p > 0.05 or p < 0.05. The Chi-squared (χ2) test or the Fisher exact test were used to evaluate the association between visualization or continuity of the JZ and the categorical variables. Analysis of variance (ANOVA) and t-tests were used to analyze the continuous variables with normal distribution. The continuous variables without normal distribution were compared using the Kruskall-Wallis and Mann-Whitney tests. Additionally, the effect on the visualization and continuity of the JZ was evaluated through univariate and multivariate analyses. Cases of intraobserver and interobserver disagreement were excluded from the analysis. Cases of unsatisfactory visualization were excluded to evaluate the factors that influence the continuity of the JZ.

The Health Ethics Committee of Hospital Senhora da Oliveira approved the research project. The participants signed an informed consent form to participate in the study.

Results

Sample

In total, 65 women between 23 and 40 years of age were included in the present study (mean [M] = 33.01; standard deviation [SD] = 4.27), and 24 (36.9%) had irregular cycles, 28 (43.1%) were in the follicular phase of the menstrual cycle, and 43 (66.2%) had a trilaminar endometrial pattern. No cases of adenomyosis were reported, and 15 (23.1%) of the participants had diagnosed or suspected endometriosis. The results of the remaining descriptive analysis are in Table 1.

Table 1
Descriptive analysis of the characteristics of the sample (n = 65)

Variables  
Age (years) 33.01(4.27)
Body mass index (kg/m2) 25.8(5.39)
Menarche (years) 12.66(1.66)
Parity
Nullipara 51(78.5)
Regularity of cycle
Irregular 24(36.9)
Regular 41(63.1)
Stage of the cycle
Proliferative 28(43.1)
Secretory 13(20.0)
Previous uterine surgery 3(4.6)
Follicle-stimulating hormone (IU/L) 7.20(3.77)
Luteinizing hormone (IU/L) 4.77(2.46)
Estradiol (pg/mL) 61.15(33.58)
Total testosterone (ng/dL) 26.09(10.61)
Prolactin (µg/L) 16.79(29.12)
Endometrium thickness (mm) 7.18(3.06)
Endometrium thickness (≤5 mm) 16(24.6)
Endometrial ultrasound characteristics
Trilaminar 43(66.2)
Heterogeneous 22(33.8)
Mioma 10(15.4)
Diagnosed or suspected endometriosis 16(24.6)
Adenomyosis 0(0)

Results presented as M (SD) and n(%).

Abbreviations: M, average; SD, standard deviation; n, absolute frequency; %, relative frequency; dl, deciliter; IU, international units; L, liter; pg, picogram; mL, mililiter; mm, milimeter.

Interobserver and Intraobserver Agreements Regarding JZ Visualization

Regarding the visualization of the JZ, the interobserver agreement was good, with a Cohen k of 0.635. The total agreement was of 80.0%. The highest number of disagreements occurred between cases of satisfactory and optimal visualization (17.2%). The intraobserver agreement was very good, with a Cohen k of 0.884, and the total agreement was of 93.9%. Again, the highest number of disagreements occurred between cases of satisfactory and optimal visualization (4.6%). Details of the analysis are in Tables 2 and 3.

 

Table 2
Visualization of the junctional zone and interobserver agreement (n = 65; observers: FR and VS)

  FR
VS Unsatisfactory n(%) Satisfactory n(%) Optimal n(%)
Unsatisfactory n(%) 6(9.2) 1(1.5) 0(0)
Satisfactory n(%) 2(3.1) 12(18.5) 3(4.6)
Optimal n(%) 0(0) 7(12.6) 34(52.3)
Absolute agreement Cohen k = 0.635

Table 3
Visualization of the junctional zone and intraobserver agreement (n = 65)

  2nd assessment
1st assessment Unsatisfactory n(%) Satisfactory n(%) Optimal n(%)
Unsatisfactory n(%) 7(10.8) 0(0) 0(0)
Satisfactory n(%) 1(1.5) 15(23.1) 1(1.5)
Optimal n(%) 0(0) 2(3.1) 39(60.0)
Absolute agreement Cohen k = 0.884

Interobserver and Intraobserver Agreements Regarding JZ Continuity

Regarding the continuity of the JZ, the interobserver agreement was good, with a Cohen k of 0.753. The total agreement was of 88.1%. The intraobserver agreement was very good, with a Cohen k of 0.816, and a total agreement of 91.2%. Details of the analysis are in Tables 4 and 5.

 

Table 4
Continuity of the junctional zone and interobserver agreement (n = 59*; observers: VS and FR)

  FR
VS Continuous n(%) Discontinuous n(%)
Continuous n(%) 20(33.9) 2(3.4)
Discontinuous n(%) 5(8.5) 32(54.2)
Absolute agreement Cohen k = 0.753

Note:

*

Excluding cases of unsatisfactory assessment of the junctional zone (n = 6) and visualization disagreements (unsatisfactory versus satisfactory/optimal; n = 0).

Table 5
Continuity of the junctional zone and intraobserver agreement (n = 57*)

  2nd assessment
1st assessment Continuous n(%) Discontinuous n(%)
Continuous n(%) 20(35.1) 2(3.5)
Discontinuous n(%) 3(5.3) 32(56.1)
Absolute agreement Cohen k = 0.820

Note:

*

Excluding cases of unsatisfactory assessment of the junctional zone(n = 6) and visualization disagreements (unsatisfactory versus satisfactory/optimal; n = 2).

Factors Affecting JZ Visualization

We tried to identify variables that influenced the visualization of the JZ. In order to do so, cases of interobserver and intraobserver disagreement were solved. We excluded five cases without a final agreement. Regarding the visualization of the JZ among the 60 remaining cases, 65% (39/60) of the women had optimal, 25% (15/60) had satisfactory, and 10% (6/60) had unsatisfactory visualization. Serum estradiol levels, endometrial ultrasound appearance, and diagnosed or suspected endometriosis influenced the visualization of the JZ (Table 6). Higher estradiol levels were associated with better visualization of the JZ (satisfactory and optimal JZ, p = 0.016), particularly in the comparison between unsatisfactory and optimal JZ assessment (p = 0.013). On the other hand, the presence of the trilaminar endometrial pattern was associated with optimal visualization (79.5% [31/39] p = 0.012). In total, 83.3% (5/6) of the cases of diagnosed or suspected endometriosis had unsatisfactory visualization of the JZ (p < 0.001) (Table 6). Performing a univariate logistic regression model, considering the unsatisfactory assessment of the JZ as an outcome, we found that the serum estradiol levels (p = 0.016) and diagnosed or suspected endometriosis (p = 0.004) were the only factors associated with JZ visualization. The joint effect of the variables on the visualization of the JZ was evaluated by multivariate analysis. The results suggest that an increase of 1 unit in the level of serum estradiol represents a 9.9% decrease in the odds of unsatisfactory visualization (odds ratio [OR] = 0.9; 95% confidence interval [95%CI] = 0.814–0.996; p = 0.042). On the other hand, the presence of diagnosed or suspected endometriosis increases the odds of unsatisfactory visualization of the JZ by 24 times (OR = 23.7; 95%CI = 1.262–437.057; p = 0.034).

Table 6
Factors affecting the visualization of the junctional zone (n = 60#)

Factors Visualization of the junctional zone p-value
Optimal (n = 39) Satisfatory (n = 15) Unsatisfatory (n = 6)
Estradiol (pg/mL) 59.0(46.0-75.0) 50.0(42.0-84.0) 24.0(20.0-39.0) 0.016*(a)
Endometrial ultrasound characteristics       0.012*(b)
Trilaminar 31(79.5) 6(40.0) 3(50.0)  
Heterogeneous 8 (20.5) 9 (60.0) 3 (50.0)  
Diagnosed or suspected endometriosis 2 (5.1) 6 (40.0) 5 (83.3) < 0.001*(b)

Notes:

#

Excluding cases of interobserver and intraobserver disagreement in the visualization of the junctional zone (n = 5); results presented as Mdn (P25-P75) = Mdn, median; P, percentile; and n(%);

*

p < 0,05;

(a)

Kruskall-Wallis test, Dunn test with differences between unsatisfactory and optimal visualization (p = 0,013);

(b)

Chi-squared test.

Factors Affecting JZ Continuity

We tried to identify the variables that influenced the continuity of the JZ. The interobserver and intraobserver disagreements were solved, and the cases of unsatisfactory visualization were excluded. After the exclusion, 60% (33/55) of the women had a discontinuous JZ. The presence of myomas and of cases of diagnosed or suspected endometriosis are associated with discontinuous JZ (p = 0.034 and 0.016 respectively). It was not possible to determine the OR due to the absence of observed frequencies of these variables in continuous JZs (Table 7).

 

Table 7
Factors affecting the continuity of the junctional zone (n = 55#)

  JZ continuity p-value
Discontinuous n(%) Continuous n(%)
Myoma n(%) 7(21.2) 0(0) 0.034*(a)
Diagnosed or suspected endometriosis n(%) 8(24.2) 0(0) 0.016*(a)

Notes:

#

Excluding cases of unsatisfactory visualization of the junctional zone (n = 6) and interobserver and intraobserver disagreement regarding continuity of the junctional zone (n = 4); results presented as n(%);

*

p < 0,05;

(a)

Chi-squared test.

Discussion

In the present study, the interobserver and intraobserver reproducibility of the JZ visualization was substantial, with values of the Cohen k of 0.635 and 0.884 respectively. Similar results were found in other studies,14,20 which indicates that the assessment of the JZ by 3D ultrasound is reproducible enough to be used in the clinical practice. Naftalin et al14 proposed that the distinction between optimal and satisfactory visualization of the JZ is subjective. This assumption is corroborated by the present study, in which the largest discrepancies regarding JZ visualization occurred among the cases classified as optimal and satisfactory. On the other hand, the high agreement in cases of JZ visualization classified as unsatisfactory is a relevant result, because JZs with unsatisfactory visualization should not be taken into account for other qualitative or quantitative assessments. These results suggest that a JZ visualization classification system in two categories (satisfactory versus unsatisfactory) is more reproducible.

The interobserver and intraobserver reproducibility of JZ continuity were substantial with the values of Cohen k of 0.753 and 0.816 respectively. To the best of our knowledge, the present was the first study that assessed the reproducibility of this characteristic of the JZ by 3D transvaginal ultrasound. Our findings are relevant and open doors to the inclusion of this evaluation in the clinical practice and to the investigation of its relevance, as it will be discuss later.

The present study showed that estradiol levels and trilaminar endometrial pattern facilitate JZ visualization. The JZ experiences estradiol-mediated cyclic changes consistent with those occurring in the endometrium, and reaches maximal thickness around the 8th and 16th days of the menstrual cycle.3,21,22 Thus, higher estradiol levels appear to be associated with a thicker JZ, which facilitates JZ visualization. This finding needs to be proven in future studies. Additionally, estradiol influences the echogenicity of the endometrium, and its role as a confounder cannot be excluded.23 In fact, in the present study the trilaminar endometrial pattern was associated with better visualization of the JZ, perhaps because it increases the contrast between the endometrium and the myometrium, which facilitates the achievement of the ideal coronal plane for JZ visualization.

Contrary to other studies,14,24 endometrial thickness did not affect the visualization of the JZ. The prevalence of thin endometria (< 5 mm) in our study was of only 24.6%, which may have contributed to this result. As in the study by Naftalin el al,14 in the present study we were unable to demonstrate that the menstrual cycle phase affects JZ visualization. However, other studies25,26 have shown that the JZ changes between the follicular and luteal phases. One explanation for this result may be the low number of women in the luteal phase in the present study.

Previous studies12,24 show higher prevalence of abnormalities in the JZ in women with endometriosis. In the present study, most women with suspected or diagnosed endometriosis had unsatisfactory visualization of the JZ. In fact, the presence of this pathology increases the chance of unsatisfactory visualization of the JZ by ∼ 24 times. Distortions of the normal pelvic anatomy, including the uterus, associated with endometriosis make the acquisition of the ideal coronal plane for the visualization of the JZ difficult, which justifies these findings.27,28 On the other hand, the disruption of the normal architecture of the JZ associated with endometriosis makes visualization of the JZ difficult.12,24

The prevalence of discontinuous JZs was 60%. The implications of this finding in women with infertility are uncertain. According to the literature,2,9-11,27 the disruption of the normal architecture of the JZ inevitably alters the coordinated peristaltic activity of the myometrium, interferes with sperm transport and implantation, and affects fertility. Disruption of the JZ also seems to be associated with JZ hyperplasia, endometriosis, and adenomyosis-infertility-related diseases.12,27,28

In the present study, discontinuous JZs were associated with suspected or diagnosed endometriosis. Peristaltic hyperactivity of the myometrium, conditioned by JZ disruption, seems to play an important role in the pathophysiology of endometriosis, facilitating retrograde menstruation and implantation of endometrial cells in the pelvic cavity.2,9,10 On the other hand, JZ disruption may enable the penetration of endometrial glands into the myometrium and the development of adenomyosis.9,24

The prevalence of adenomyosis in women of reproductive age is heterogeneous, ranging from 16% to 66%.14,29 Different study methodologies, populations, and diagnostic criteria can explain this disparity. In the present study, the prevalence of adenomyosis was null. This prevalence draws attention to the underdiagnoses of adenomyosis in infertile women. Puente et al11 showed that only one in five infertile women had a diagnosis of adenomyosis before the ultrasound evaluation in their study, which reinforces the underdiagnosis of adenomyosis in infertile women. These results highlight the need to make physicians aware of adenomyosis in infertile women and the need to establish reproducible diagnostic ultrasound criteria.30

The pathophysiological link between adenomyosis and endometriosis seens to be a disruption of JZ.11,12,24,27,31,32 Based on this, the theory of “endometrial-subendometrial myometrium unit disruption disease” was proposed by Tocci et al.31 According to this theory, a disruption in the architecture of the JZ seems to constitute the triggering event (causing dysfunction in the uterine peristalsis), and endometriosis and adenomyosis represent phenotypes of “endomyometrial dysfunction” and not distinct pathologies.31 Efforts should be made to better describe this entity through 3D transvaginal ultrasound and to assess its impact on women's reproductive functions.

In the present study, the presence of uterine myomas was associated with the presence of discontinuous JZ. In fact, all of the myomas described were classified as type 1 to 3 myomas according to the Fédération Internationale de Gynécologie et d'Obstétrique (International Federation of Gynecology and Obstetrics, FIGO, in the French acronym) classification, which justifies the findings and implications on fertility.33

The 3D ultrasound to assess the JZ is cost-effective and noninvasive. The obtained results indicate that the assessment of the visualization and continuity of the JZ by 3D ultrasound is reproducible enough to be used in the clinical practice. The presence of disruption in the architecture of the JZ should alert the clinician to the possibility of the presence of “endometrial-subendometrial myometrium unit disruption disease” due to its association with endometriosis and adenomyosis and, consequently, its implications for women's reproductive and obstetric health.34

The assessment of visualization and continuity of the JZ can be criticized regarding its subjectivity, which is a limitation of the present study. However, the same methodology has been used in other studies14,35 to assess the reproducibility of JZ visualization, and similar results have been obtained. Another limitation consists in the small sample obtained.

To the best of our knowledge, the present is the first study aiming to assess the JZ through 3D ultrasound in infertile women in Portugal. The study raises new lines of research. One point to develop is the assessment of the impact of JZ disruption on fertility. Long-term follow-up of these women is necessary to evaluate the results of assisted reproductive technology and to relate them to our results.

Thus, due to its reproducibility, the clinical information obtained, and the cost-effectiveness, the evaluation of the JZ through 3D ultrasound should be part of the routine study of infertile women.

Conclusion

Based on the results obtained from the present study, we emphasize the reproducibility of transvaginal 3D ultrasound assessment of the JZ and the clinical benefits of its inclusion in the routine evaluation of infertile women.


Keywords

3D ultrasound; junctional zone; reproducibility; infertility; associated factors

References

  1. Saravelos SH, Jayaprakasan K, Ojha K, Li TC. Assessment of the uterus with three-dimensional ultrasound in women undergoing ART. Hum Reprod Update. 2017;23(02):188-210. Doi: 10.1093/humupd/dmw040

    » https://doi.org/10.1093/humupd/dmw040

  2. Kashgari F, Oraif A, Bajouh O. The uterine junctional zone. Life Sci J. 2015;12(12):101-106

  3. Brosens I, Derwig I, Brosens J, Fusi L, Benagiano G, Pijnenborg R. The enigmatic uterine junctional zone: the missing link between reproductive disorders and major obstetrical disorders? Hum Reprod. 2010;25(03):569-574. Doi: 10.1093/humrep/dep474

    » https://doi.org/10.1093/humrep/dep474

  4. 4

    Lesny P, Killick SR. The junctional zone of the uterus and its contractions. BJOG. 2004;111(11):1182-1189. Doi: 10.1111/j.1471-0528.2004.00350.x

    » https://doi.org/10.1111/j.1471-0528.2004.00350.x

  5. de Vries K, Lyons EA, Ballard G, Levi CS, Lindsay DJ. Contractions of the inner third of the myometrium. Am J Obstet Gynecol. 1990;162(03):679-682. Doi: 10.1016/0002-9378(90)90983-e

    » https://doi.org/10.1016/0002-9378(90)90983-e

  6. Ijland MM, Evers JL, Dunselman GA, van Katwijk C, Lo CR, Hoogland HJ. Endometrial wavelike movements during the menstrual cycle. Fertil Steril. 1996;65(04):746-749. Doi: 10.1016/s0015-0282(16)58207-7

    » https://doi.org/10.1016/s0015-0282(16)58207-7

  7. IJland MM, Evers JL, Dunselman GA, Volovics L, Hoogland HJ. Relation between endometrial wavelike activity and fecundability in spontaneous cycles. Fertil Steril. 1997;67(03):492-496. Doi: 10.1016/s0015-0282(97)80075-1

    » https://doi.org/10.1016/s0015-0282(97)80075-1

  8. Fanchin R, Righini C,Olivennes F, Taylor S, de Ziegler D, Frydman R. Uterine contractions at the time of embryo transfer alter pregnancy rates after in-vitro fertilization. HumReprod. 1998;13(07):1968-1974. Doi: 10.1093/humrep/13.7.1968

    » https://doi.org/10.1093/humrep/13.7.1968

  9. Leyendecker G, Kunz G, Herbertz M, Beil D, Huppert P, Mall G et al. Uterine peristaltic activity and the development of endometriosis. AnnNYAcadSci.2004;1034:338-355.Doi:10.1196/annals.1335.036

    » https://doi.org/10.1196/annals.1335.036

  10. Bulletti C, De Ziegler D, Polli V, Del Ferro E, Palini S, Flamigni C. Characteristics of uterine contractility duringmenses inwomenwith mildtomoderateendometriosis. Fertil Steril.2002;77(06):1156-1161

  11. Puente JM, Fabris A, Patel J, Patel A, Cerrillo M, Requena A et al. Adenomyosis in infertile women: prevalence and the role of 3D ultrasound as a marker of severity of the disease. Reprod Biol Endocrinol. 2016;14(01):60. Doi: 10.1186/s12958-016-0185-6

    » https://doi.org/10.1186/s12958-016-0185-6

  12. Exacoustos C, Luciano D, Corbett B, De Felice G, Di Feliciantonio M, Luciano A et al. The uterine junctional zone: a 3-dimensional ultrasound study of patients with endometriosis. Am J Obstet Gynecol. 2013;209(03):248.e1-248.e7. Doi: 10.1016/j.ajog.2013.06.006

    » https://doi.org/10.1016/j.ajog.2013.06.006

  13. Naftalin J, Jurkovic D. The endometrial-myometrial junction: a fresh look at a busy crossing. Ultrasound Obstet Gynecol. 2009;34(01):1-11. Doi: 10.1002/uog.6432

    » https://doi.org/10.1002/uog.6432

  14. Naftalin J, HooW, Nunes N, Mavrelos D, Nicks H, Jurkovic D. Interand intraobserver variability in three-dimensional ultrasound assessment of the endometrial-myometrial junction and factors affecting its visualization. Ultrasound Obstet Gynecol. 2012;39(05):587-591. Doi: 10.1002/uog.10133

    » https://doi.org/10.1002/uog.10133

  15. Maged AM, Ramzy AM, Ghar MA, El Shenoufy H, Gad Allah SH, Wahba AH et al. 3D ultrasound assessment of endometrial junctional zone anatomy as a predictor of the outcome of ICSI cycles. Eur J Obstet Gynecol Reprod Biol. 2017;212:160-165. Doi: 10.1016/j.ejogrb.2017.03.035

    » https://doi.org/10.1016/j.ejogrb.2017.03.035

  16. Lee C, Jurkovic D. Clinical presentation and investigation: the ''one-stop'' clinic, endometrial sampling, hysteroscopy, vaginal ultrasound. In: Lee C, Jurkovic D. Uterine cancer. New York, NY: Taylor and Francis; 2005:91-105

  17. Van den Bosch T, Dueholm M, Leone FP, Valentin L, Rasmussen CK, Votino A et al. Terms, definitions and measurements to describe sonographic features of myometrium and uterine masses: a consensus opinion from the Morphological Uterus Sonographic Assessment (MUSA) group. Ultrasound Obstet Gynecol. 2015;46(03):284-298. Doi: 10.1002/uog.14806

    » https://doi.org/10.1002/uog.14806

  18. Chamié LP, Blasbalg R, Pereira RM, Warmbrand G, Serafini PC. Findings of pelvic endometriosis at transvaginal US, MR imaging, and laparoscopy. Radiographics. 2011;31(04):E77-E100. Doi: 10.1148/rg.314105193

    » https://doi.org/10.1148/rg.314105193

  19. Altman DG. Practical statistics for medical research. London: Chapman and Hall; 1991. Book review of Ashby D. Stat Med. 1991;10(10):1635-1636. Doi: 10.1002/sim.4780101015

    » https://doi.org/10.1002/sim.4780101015

  20. Rasmussen CK, Glavind J, Madsen LD, Uldbjerg N, Dueholm M. Repeatability of junctionalzonemeasurements using 3-dimensional transvaginal sonography in healthy fertile women. J Ultrasound Med. 2016;35(07):1497-1508. Doi: 10.7863/ultra.15.06086

    » https://doi.org/10.7863/ultra.15.06086

  21. Hauth EA, Jaeger HJ, Libera H, Lange S, Forsting M. MR imaging of the uterus and cervix in healthywomen: determination of normal values. Eur Radiol. 2007;17(03):734-742. Doi: 10.1007/s00330- 006-0313-3

    » https://doi.org/10.1007/s00330-006-0313-3

  22. Hoad CL, Raine-Fenning NJ, Fulford J, Campbell BK, Johnson IR, Gowland PA. Uterine tissue development in healthy women during the normal menstrual cycle and investigations with magnetic resonance imaging. Am J Obstet Gynecol. 2005;192(02):648-654. Doi: 10.1016/j.ajog.2004.07.032

    » https://doi.org/10.1016/j.ajog.2004.07.032

  23. Fleischer AC, Kalemeris GC, Entman SS. Sonographic depiction of the endometrium during normal cycles. Ultrasound Med Biol. 1986;12(04):271-277. Doi: 10.1016/0301-5629(86)90336-4

    » https://doi.org/10.1016/0301-5629(86)90336-4

  24. Larsen SB, Lundorf E, Forman A, Dueholm M. Adenomyosis and junctional zone changes inpatientswith endometriosis. Eur JObstet Gynecol Reprod Biol. 2011;157(02):206-211. Doi: 10.1016/j.ejogrb.2011.03.003

    » https://doi.org/10.1016/j.ejogrb.2011.03.003

  25. Wiczyk HP, Janus CL, Richards CJ, Graf MJ, Gendal ES, Rabinowitz JG et al. Comparison of magnetic resonance imaging and ultrasound in evaluating follicular and endometrial development throughout the normal cycle. Fertil Steril. 1988;49(06):969-972. Doi: 10.1016/s0015-0282(16)59946-4

    » https://doi.org/10.1016/s0015-0282(16)59946-4

  26. McCarthy S, Tauber C, Gore J. Female pelvic anatomy: MR assessment of variations during the menstrual cycle and with use of oral contraceptives. Radiology. 1986;160(01):119-123. Doi: 10.1148/radiology.160.1.3715022

    » https://doi.org/10.1148/radiology.160.1.3715022

  27. Exacoustos C, Brienza L, Di Giovanni A, Szabolcs B, Romanini ME, Zupi E et al. Adenomyosis: three-dimensional sonographic findings of the junctional zone and correlation with histology. Ultrasound Obstet Gynecol. 2011;37(04):471-479. Doi: 10.1002/uog.8900

    » https://doi.org/10.1002/uog.8900

  28. Leyendecker G, Kunz G, Noe M, Herbertz M, Mall G. Endometriosis: a dysfunction and disease of the archimetra. Hum Reprod Update. 1998;4(05):752-762. Doi: 10.1093/humupd/4.5.752

    » https://doi.org/10.1093/humupd/4.5.752

  29. Yeniel O, Cirpan T, Ulukus M, Ozbal A, Gundem G, Ozsener S et al. Adenomyosis: prevalence, risk factors, symptoms and clinical findings. Clin Exp Obstet Gynecol. 2007;34(03):163-167

  30. Gordts S, Brosens JJ, Fusi L, Benagiano G, Brosens I. Uterine adenomyosis: a need for uniform terminology and consensus classification. Reprod Biomed Online. 2008;17(02):244-248. Doi: 10.1016/s1472-6483(10)60201-5

    » https://doi.org/10.1016/s1472-6483(10)60201-5

  31. Tocci A, Greco E, Ubaldi FM. Adenomyosis and 'endometrialsubendometrial myometrium unit disruption disease' are two different entities. Reprod Biomed Online. 2008;17(02):281-291. Doi: 10.1016/s1472-6483(10)60207-6

    » https://doi.org/10.1016/s1472-6483(10)60207-6

  32. Bazot M, Fiori O, Darai E. Adenomyosis in endometriosis-prevalence and impact on fertility. Evidence from magnetic resonance imaging. Hum Reprod. 2006;21(04):1101-1102, author reply 1102-1103. Doi: 10.1093/humrep/dei448

    » https://doi.org/10.1093/humrep/dei448

  33. Munro MG, Critchley HO, Fraser IS; FIGO Menstrual Disorders Working Group. The FIGO classification of causes of abnormal uterine bleeding in the reproductive years. Fertil Steril. 2011;95(07):2204-2208, 2208.e1-2208.e3

  34. Brosens I, Kunz G, Benagiano G. Is adenomyosis the neglected phenotype of an endomyometrial dysfunction syndrome? Gynecol Surg. 2012;9(02):131-137. Doi: 10.1007/s10397-011-0723-3

    » https://doi.org/10.1007/s10397-011-0723-3

  35. Yazbek J,Ameye L, Testa AC, Valentin L, Timmerman D, Holland TK et al. Confidence of expert ultrasound operators in making a diagnosis of adnexal tumor: effect on diagnostic accuracy and interobserver agreement. Ultrasound Obstet Gynecol. 2010;35(01):89-93. Doi: 10.1002/uog.7335

    » https://doi.org/10.1002/uog.7335