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====<big>Physiological menopause</big>====
====<big>Physiological menopause</big>====
[[Menopause]] happens normally as [[women]] age, and the main cause of the [[menopause]] is the natural shortage of the primordial follicles ([[oocytes]]) that stored in the [[ovaries]] and the decrease of the response of [[ovaries]] to [https://en.wikipedia.org/wiki/Hypothalamic%E2%80%93pituitary%E2%80%93gonadal_axis#:~:text=The%20anterior%20portion%20of%20the,gonads%20produce%20estrogen%20and%20testosterone. anterior pituitary gonads hormones] that include [[Follicle Stimulating Hormone]] (FSH) and [[Luteinizing Hormone]](LH). These [[hormones]] stimulate the [[ovaries]] to produce [[estrogen]] and [[progesterone]] hormones in a cyclic method under the control of the [[hypothalamus]] that produces the [https://www.yourhormones.info/hormones/gonadotrophin-releasing-hormone/ gonadotropin-releasing hormones] which stimulate [https://en.wikipedia.org/wiki/Hypothalamic%E2%80%93pituitary%E2%80%93gonadal_axis#:~:text=The%20anterior%20portion%20of%20the,gonads%20produce%20estrogen%20and%20testosterone. anterior pituitary gonads hormone] secretion and [[Inhibin|inhibin-B]] that plays role in the [[feedback mechanism]]. "Characteristic changes in the [https://www.glowm.com/section_view/heading/the-hypothalamic-hypophyseal-ovarian-axis-and-the-menstrual-cycle/item/282 hypothalamic-pituitary-ovarian (HPO) axis] during the [[menopause]] transition result from decreased [[ovarian]] [[feedback]] of [[inhibin]] and [[estradiol]] and are manifested primarily as elevations in [[follicle-stimulating hormone]] ([[FSH]]). [[Adrenal gland|Adrenal]] changes concurrent with the [[menopause]] transition include elevations in [[serum]] [[cortisol]] and transient elevations in [[dehydroepiandrosterone sulfate]], [[androstenediol]], and other [[adrenal]] [[Androgen|androgens]]"<ref>http://www.menopause.org/docs/default-source/2014/nams-recomm-for-clinical-care.pdf</ref>
[[Menopause]] happens normally as [[women]] age, and the main cause of the [[menopause]] is the natural shortage of the primordial follicles ([[oocytes]]) that stored in the [[ovaries]] and the decrease of the response of [[ovaries]] to [https://en.wikipedia.org/wiki/Hypothalamic%E2%80%93pituitary%E2%80%93gonadal_axis#:~:text=The%20anterior%20portion%20of%20the,gonads%20produce%20estrogen%20and%20testosterone. anterior pituitary gonads hormones] that include [[Follicle Stimulating Hormone]] (FSH) and [[Luteinizing Hormone]](LH). These [[hormones]] stimulate the [[ovaries]] to produce [[estrogen]] and [[progesterone]] hormones in a cyclic method under the control of the [[hypothalamus]] that produces the [https://www.yourhormones.info/hormones/gonadotrophin-releasing-hormone/ gonadotropin-releasing hormones] which stimulate [https://en.wikipedia.org/wiki/Hypothalamic%E2%80%93pituitary%E2%80%93gonadal_axis#:~:text=The%20anterior%20portion%20of%20the,gonads%20produce%20estrogen%20and%20testosterone. anterior pituitary gonads hormone] secretion and [[Inhibin|inhibin-B]] that plays role in the [[feedback mechanism]]. "Characteristic changes in the [https://www.glowm.com/section_view/heading/the-hypothalamic-hypophyseal-ovarian-axis-and-the-menstrual-cycle/item/282 hypothalamic-pituitary-ovarian (HPO) axis] during the [[menopause]] transition result from decreased [[ovarian]] [[feedback]] of [[inhibin]] and [[estradiol]] and are manifested primarily as elevations in [[follicle-stimulating hormone]] ([[FSH]]). [[Adrenal gland|Adrenal]] changes concurrent with the [[menopause]] transition include elevations in [[serum]] [[cortisol]] and transient elevations in [[dehydroepiandrosterone sulfate]], [[androstenediol]], and other [[adrenal]] [[Androgen|androgens]]"


====<big>Pathological menopause</big>====
====<big>Pathological menopause</big>====
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*[[pathological]] [[disease]] in ovaries, [[premature menopause]] or [[premature ovarian failure]] termed as [https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2762081/ Primary ovarian insufficiency (POI)].(POI) is the loss of [[ovarian]] function lead to [[amenorrhea]] because of [[ovarian failure]] to respond for [https://courses.lumenlearning.com/boundless-biology/chapter/endocrine-glands/#:~:text=Endocrine%20system%3A%20gonads%20and%20their,prepare%20the%20body%20for%20childbirth. gonads hormone] ( [[FSH]], [[LH]]) and deficiency production of [[estrogen]] and [[progesterone]] hormone.
*[[pathological]] [[disease]] in ovaries, [[premature menopause]] or [[premature ovarian failure]] termed as [https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2762081/ Primary ovarian insufficiency (POI)].(POI) is the loss of [[ovarian]] function lead to [[amenorrhea]] because of [[ovarian failure]] to respond for [https://courses.lumenlearning.com/boundless-biology/chapter/endocrine-glands/#:~:text=Endocrine%20system%3A%20gonads%20and%20their,prepare%20the%20body%20for%20childbirth. gonads hormone] ( [[FSH]], [[LH]]) and deficiency production of [[estrogen]] and [[progesterone]] hormone.
*[[Premature menopause]] is a result of several [[medical condition]] such as [[Autoimmune disease]]([[Adrenal insufficiency]], Type1 [[diabetes mellitus]], [[Autoimmune thyroid diseases|Autoimmune thyroid disease]]), [[Fragile X syndrome|Fragile X Syndrome]], [[Fanconi anemia|Fanconi’s anemia]], [[Congenital adrenal hyperplasia]] due to [[17α-hydroxylase|17''α''-hydroxylase]] deficiency.<ref>https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2762081/</ref><ref>https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2762081/table/T1/</ref>
*[[Premature menopause]] is a result of several [[medical condition]] such as [[Autoimmune disease]]([[Adrenal insufficiency]], Type1 [[diabetes mellitus]], [[Autoimmune thyroid diseases|Autoimmune thyroid disease]]), [[Fragile X syndrome|Fragile X Syndrome]], [[Fanconi anemia|Fanconi’s anemia]], [[Congenital adrenal hyperplasia]] due to [[17α-hydroxylase|17''α''-hydroxylase]] deficiency.




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*[[Fragile X syndrome]] is a [[genetic disorder]] characterized by reduction of [[ovarian]] function, women that have [[Fragile X syndrome|Fragile X Syndrome]] go through early [[menopause]] an average 5 years early than other [[women]].
*[[Fragile X syndrome]] is a [[genetic disorder]] characterized by reduction of [[ovarian]] function, women that have [[Fragile X syndrome|Fragile X Syndrome]] go through early [[menopause]] an average 5 years early than other [[women]].
*[https://www.mayoclinic.org/diseases-conditions/turner-syndrome/symptoms-causes/syc-20360782#:~:text=Overview,to%20develop%20and%20heart%20defects. Turner’s syndrome]: "[[Women]] born with missing [[chromosomes]] or problems with [[chromosomes]] can go through [[menopause]] early, [[women]] are born without all or part of one [[X chromosome]], so their [[ovaries]] do not form normally at [[birth]] and their [[menstrual cycles]], including the time around [[menopause]], may not be normal"<ref>https://www.womenshealth.gov/menopause/early-or-premature-menopause</ref>
*[https://www.mayoclinic.org/diseases-conditions/turner-syndrome/symptoms-causes/syc-20360782#:~:text=Overview,to%20develop%20and%20heart%20defects. Turner’s syndrome]: "[[Women]] born with missing [[chromosomes]] or problems with [[chromosomes]] can go through [[menopause]] early, [[women]] are born without all or part of one [[X chromosome]], so their [[ovaries]] do not form normally at [[birth]] and their [[menstrual cycles]], including the time around [[menopause]], may not be normal"


==<big>Associated Conditions</big>==
==<big>Associated Conditions</big>==
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*[[Cardiovascular disease]]: " [[Estrogen]] has a positive effect on the [[tunica intima]] of the [[Artery walls|artery wall]], helping to keep [[blood vessels]] flexible. During [[menopause]], [[estrogen]] deficiency causes [[vasoconstriction]] of the [[Blood vessel|vessel wall]] and an accelerated increase of [[Low density lipoprotein|low-density lipoprotein]] ([[LDL]]). Thus, [[menopause]] is linked to the increased risk of [[cardiovascular disease]]".
*[[Cardiovascular disease]]: " [[Estrogen]] has a positive effect on the [[tunica intima]] of the [[Artery walls|artery wall]], helping to keep [[blood vessels]] flexible. During [[menopause]], [[estrogen]] deficiency causes [[vasoconstriction]] of the [[Blood vessel|vessel wall]] and an accelerated increase of [[Low density lipoprotein|low-density lipoprotein]] ([[LDL]]). Thus, [[menopause]] is linked to the increased risk of [[cardiovascular disease]]".
*[[Osteoporosis]] is a [[disease]] of the [[bones]] that causes [[bones]] to become weak and break easily." During [[menopause]], [[estrogen]] deficiency increases [https://support.clearcorrect.com/hc/en-us/articles/203836908-Osteoclastic-and-Osteoblastic-Activity#:~:text=Osteoclastic%20activity%20refers%20to%20the,allowing%20the%20tooth%20to%20move. osteoclastic activity], such that there is an imbalance of [https://support.clearcorrect.com/hc/en-us/articles/203836908-Osteoclastic-and-Osteoblastic-Activity#:~:text=Osteoclastic%20activity%20refers%20to%20the,allowing%20the%20tooth%20to%20move. osteoclastic] and [https://www.spine-health.com/glossary/osteoblast#:~:text=An%20osteoblast%20is%20a%20cell,called%20osteoclasts%20that%20remove%20bone. osteoblastic activity]. This results in more bone being reabsorbed and overall [[bone loss]].  [[Estrogen]] deficiency leads to the release of [[cytokines]] among them RANKK ligand ([[RANKL]]), which plays a critical role in the [https://www.sciencedirect.com/topics/medicine-and-dentistry/osteoclastogenesis osteoclastogenesis] cascade. During [[menopause]], women experience an increased rate of [[bone loss]] of 3% to 5% per year for 5 to 7 years".<ref>https://www.ncbi.nlm.nih.gov/books/NBK507826/#!po=10.0000</ref>
*[[Osteoporosis]] is a [[disease]] of the [[bones]] that causes [[bones]] to become weak and break easily." During [[menopause]], [[estrogen]] deficiency increases [https://support.clearcorrect.com/hc/en-us/articles/203836908-Osteoclastic-and-Osteoblastic-Activity#:~:text=Osteoclastic%20activity%20refers%20to%20the,allowing%20the%20tooth%20to%20move. osteoclastic activity], such that there is an imbalance of [https://support.clearcorrect.com/hc/en-us/articles/203836908-Osteoclastic-and-Osteoblastic-Activity#:~:text=Osteoclastic%20activity%20refers%20to%20the,allowing%20the%20tooth%20to%20move. osteoclastic] and [https://www.spine-health.com/glossary/osteoblast#:~:text=An%20osteoblast%20is%20a%20cell,called%20osteoclasts%20that%20remove%20bone. osteoblastic activity]. This results in more bone being reabsorbed and overall [[bone loss]].  [[Estrogen]] deficiency leads to the release of [[cytokines]] among them RANKK ligand ([[RANKL]]), which plays a critical role in the [https://www.sciencedirect.com/topics/medicine-and-dentistry/osteoclastogenesis osteoclastogenesis] cascade. During [[menopause]], women experience an increased rate of [[bone loss]] of 3% to 5% per year for 5 to 7 years".




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*"The [[medulla]] develops [[stromal]] [[fibrosis]] and scars. The [[medulla]] also undergoes the [https://humpath.com/spip.php?article23415 hyalinization of vessel walls], with architectural changes of [[vessels]]".
*"The [[medulla]] develops [[stromal]] [[fibrosis]] and scars. The [[medulla]] also undergoes the [https://humpath.com/spip.php?article23415 hyalinization of vessel walls], with architectural changes of [[vessels]]".


*"There is also a significant change in the [[vagina]] during [[menopause]], the [[mucosa]] layer of the [[vagina]] begins to [[atrophy]] due to decreased [[estrogen]] that causes this [[cell]] layer to become drier and thinner. As a result, the [[vaginal]] [[mucosa]] loses its [[Elasticity (economics)|elasticity]] and becomes fragile".<ref>https://www.ncbi.nlm.nih.gov/books/NBK507826/#!po=10.0000</ref>
*"There is also a significant change in the [[vagina]] during [[menopause]], the [[mucosa]] layer of the [[vagina]] begins to [[atrophy]] due to decreased [[estrogen]] that causes this [[cell]] layer to become drier and thinner. As a result, the [[vaginal]] [[mucosa]] loses its [[Elasticity (economics)|elasticity]] and becomes fragile".




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[[Category:Menstruation]]
[[Category:Menstruation]]
[[Category:Needs content]]
[[Category:Needs content]]
<references />

Revision as of 03:11, 3 February 2021

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Editor-In-Chief: C. Michael Gibson, M.S., M.D. [1] Rahmah Al-Edresi, M.D.[2]

Overview

Menopause is natural amenorrhea that is happened without any pathological causes, but premature menopause/early menopause caused by pathological diseases, that are lead to early cessation of menses.

Pathophysiology

Physiological menopause

Menopause happens normally as women age, and the main cause of the menopause is the natural shortage of the primordial follicles (oocytes) that stored in the ovaries and the decrease of the response of ovaries to anterior pituitary gonads hormones that include Follicle Stimulating Hormone (FSH) and Luteinizing Hormone(LH). These hormones stimulate the ovaries to produce estrogen and progesterone hormones in a cyclic method under the control of the hypothalamus that produces the gonadotropin-releasing hormones which stimulate anterior pituitary gonads hormone secretion and inhibin-B that plays role in the feedback mechanism. "Characteristic changes in the hypothalamic-pituitary-ovarian (HPO) axis during the menopause transition result from decreased ovarian feedback of inhibin and estradiol and are manifested primarily as elevations in follicle-stimulating hormone (FSH). Adrenal changes concurrent with the menopause transition include elevations in serum cortisol and transient elevations in dehydroepiandrosterone sulfate, androstenediol, and other adrenal androgens"

Pathological menopause

Premature menopause/early menopause caused by:


Genetic

Associated Conditions

The most important Conditions associated with Menopause include:


Microscopic Pathology

On microscopic histopathological of menopause:






References


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