Uterine peristalsis-induced stresses within the uterine wall may sprout adenomyosis

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A 2D model simulating intrauterine pressures found that decreasing wavelength, increasing frequency, and menstrual phase conditions produced high stress concentrations within the uterine wall, potentially causing tissue lesions and endometrial cell detachment.

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The paper studies, using a conceptual 2D finite-element model implemented in ADINA software, how uterine wall stress distributions respond to intrauterine sinusoidal pressure waves of different frequencies and wavelengths. It finds that shorter pressure-wave wavelengths produce high stress concentrations near the inner uterine cavity, that higher pressure-wave frequencies create high stress gradients, and that at the menstrual phase the highest stresses occur at the endometrial–myometrial interface. The major caveat is that this is a conceptual computational model of uterine pressure activity rather than direct experimental or clinical measurement of tissue injury. This paper is centrally about adenomyosis — it tests a “tissue injury and repair” mechanism by showing pressure-induced mechanical stresses at the endometrial–myometrial interface that could promote adenomyosis.

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Abstract

Adenomyosis is a disease in which ectopic endometrial glands and stromal cells appear in the uterine myometrium. This pathology is common among women of reproductive age, and in addition to chronic pelvic pain and heavy periods it may also cause infertility. The 'tissue injury and repair' mechanism in response to increased intrauterine pressures was proposed as the etiology for migration of fragments of basal endometrium into the myometrial wall. In order to investigate this mechanism, a conceptual two-dimensional model of the uterine wall subjected to intrauterine pressures was implemented using ADINA commercial software. The stress field within the uterine wall was examined for a variety of intrauterine sinusoidal pressure waves with varying frequencies. The results revealed that: (1) as the wavelength of the subjected pressure wave decreased, high concentration of stresses developed near the inner uterine cavity; (2) as the pressure wave frequency increased, high gradients of the stresses were obtained; (3) at menstrual phase, the highest stresses obtained at the endometrial-myometrial interface. Therefore, increased uterine activity results in high stresses which may lead to tissue lesions and detachment of endometrial cells.
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Abstract

Adenomyosis is a disease in which ectopic endometrial glands and stromal cells appear in the uterine myometrium. This pathology is common among women of reproductive age, and in addition to chronic pelvic pain and heavy periods it may also cause infertility. The ‘tissue injury and repair’ mechanism in response to increased intrauterine pressures was proposed as the etiology for migration of fragments of basal endometrium into the myometrial wall. In order to investigate this mechanism, a conceptual two-dimensional model of the uterine wall subjected to intrauterine pressures was implemented using ADINA commercial software. The stress field within the uterine wall was examined for a variety of intrauterine sinusoidal pressure waves with varying frequencies. The results revealed that: (1) as the wavelength of the subjected pressure wave decreased, high concentration of stresses developed near the inner uterine cavity; (2) as the pressure wave frequency increased, high gradients of the stresses were obtained; (3) at menstrual phase, the highest stresses obtained at the endometrial–myometrial interface. Therefore, increased uterine activity results in high stresses which may lead to tissue lesions and detachment of endometrial cells. Similar content being viewed by others

References

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Biomech Model Mechanobiol 14, 437–444 (2015). https://doi.org/10.1007/s10237-014-0614-4 Received: Accepted: Published: Issue date: DOI: https://doi.org/10.1007/s10237-014-0614-4

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Condition tags

adenomyosis

MeSH descriptors

Adenomyosis Myometrium Peristalsis Stress, Physiological Adenomyosis Female Humans Myometrium Peristalsis

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