Female Infertility

Female Infertility

Female Infertility

The successful implantation of an embryo and its healthy development into the uterus are directly dependent on the normal functioning of the following processes:

A well regulated hormonal interaction system coordinating normal ovulatory cycles, releasing genetically and structurally healthy eggs which can become fertilized by healthy spermatozoa within patent fallopian tubes and develop into early embryos that can be conceived in a uterus of optimal size and contour.

Any inherited or acquired condition which can compromise the normal processing of these mechanisms will subject a female sub-fertile or infertile.

When a female child is born and unless a genetic predisposition is present she has in her ovaries more than 2 million little follicles each containing one immature egg. At puberty (~ 12 years old), most of these eggs will be absorbed and allowed to perish depleting the cohort of the ovarian reserve to approximately 350-400 thousand. On each month it is estimated that 1000 follicles are lost through a process known as atresia while a single follicle or sometimes two will reach final maturation and release one egg each. This loss of eggs is neither dependent on the lifestyle one opts to pursue nor is limited to any hormone production, nutritional supplements or the administration of an oral contraceptive pill.

Female infertility can result due to one or more of the following reasons:

  • Genetic (Chromosomal and/or gene defects)
  • Endocrine (hormonal)
  • Mechanical and
  • Immunological

Genetic Causes

It is a fact that fertility in the female declines with advancing age and this phenomenon is attributed to two main reasons; (a) the depletion of the ovarian reserve and (b) the fragility of the chromosomal complex of the existing egg cohort. A couple is advised to visit a specialist for an initial consultation and assessment after failure to conceive following 13 months of unprotected (regular) intercourse when the female spouse is up to 34 years of age while this period is reduced to 6 months when the age is 35 or more. Over 40 the chances become substantially slimmer and eminent advice should be sought. The prevalence of chromosomal aberrations in an embryo is almost always a consequence of maternal age. This is because a female is born with the full complement of her eggs and this number will only decline over the years unlike the human male where the dynamic process of spermatogenesis produces new spermatozoa continuously.  In the process of their final maturation, both immature eggs and sperm follow a series of cellular divisions known as mitosis and meiosis. Successful fertilisation can only be achieved through the interaction of mature gametes. Chromosome abnormalities typically occur as a result of errors during these cellular divisions although environmental exposures may also be an associating factor. Derangements in the normal process of these cellular divisions result in the egg acquiring or losing one or more chromosomes and therefore its genetic contribution at fertilization will cause an imbalance resulting into early embryonic senescence or a miscarriage or the birth of a defective offspring (i.e. Dawn’s Syndrome). Similar aberrations but to a much lesser extent may be the consequence of abnormal cellular divisions post fertilization (de novo) deranging the chromosomal complement of an early developing embryo in the uterus.

While nature most often detects the chromosomal imbalance and terminates the progress of the embryo at an early stage, at times the disaggregation of the chromosomal constitution in the cells develops unidentified hence the birth of an abnormal child. The advances in laboratory medicine today allow for investigating the chromosomal constitution of embryos created in vitro therefore enabling the replacement of those with a healthy status. In this way a known or a potentially new chromosomal derangement can be screened prior to the embryo implanting into the uterus.

Endocrine (hormonal) Profiles and Normal (regular) Ovulation

Menstrual cycles are controlled by interplay of hormones associated with the hypothalamus and pituitary glands and which subsequently mediate ovarian function. At the onset of the cycle the hypothalamus triggers the release of the reproductive hormone FSH from the anterior lobe of the pituitary by secreting LHRH. The FSH acts on the ovary which recruits a number of follicles (20-50 which may be unidentified via conventional ultra sonography) from the existing cohort. One or at times two (very rarely three) of these follicles will resume growth towards final maturation. Specialized cells within the follicles namely granulosa commence active secretion of estradiol a hormone which targets the uterus aiming at its proliferative growth. As the follicle grows in size proportionate to estradiol secretion the FSH drops. At a specific concentration (~300 pmol/l) the estradiol will notify the hypophysis to release the second reproductive hormone (LH) which triggers ovulation. The collapsed follicle which delivers the egg (subsequently taken up by the fallopian tube end), seals back again (now called a corpus luteum) and starts secreting (via a different form of the granulosa cells) another hormone called progesterone which is responsible for the preparation of the uterus for embryo implantation and subsequent development.

FSH when assessed early in the menstrual cycle (normally on day 2 or day 3)  and before the estradiol rises (145 pmol/l or less) is a strong indicator of ovarian reserve while the LH index when is persistently high on the same day may be an indicator of abnormal ovarian function. While this is typically observed at menopause, when present during the reproductive years may correlate to a number of syndromes associated with ovarian dysgenesis such as Turner’s syndrome, Swyer’s syndrome, Polycystic ovarian syndrome, congenital adrenal hyperplasia or it may account for signs of premature menopause and castration (absent ovaries). On the other hand a repeatedly diminished LH secretion is most often consistent with amenorrhea (absence of menstrual period), abnormal function of the pituitary gland and/or the hypothalamus, a consequence of an eating disorder or hyperporlactinemia (increased prolactin secretion).

An elevated prolactin in the bloodstream inhibits the pulsatile secretion of LHRH by the hypothalamus and consequently the release of FSH and LH by the hypophysis resulting in menstrual cycle disturbances or arrest. This infertility cause is easily reversed by the use of simple medication aiming at normalizing serum prolactin levels and therefore restoring normal ovarian function.

TSH another hormone produced by the hypophysis stimulates the thyroid gland to produce thyroxine (also known as T4) and then triidothyronine (T3) the two hormones which regulate the metabolism of almost every tissue in the organism. An underactive or a hyperactive thyroid (hypo and hyperthyroidism respectively) results in deranged metabolism and while a female may be able to become pregnant, the conception will not progress. An abnormal thyroid function is medically managed by the use of specific medication.

While the FSH when screened early in the follicular phase of the menstrual cycle is a denominator of an individual’s ovarian reserve the AMH affirms on the FSH value but mainly also is an indicator of the existing egg cohort potential to produce pregnancies. The higher the AMH the more optimal the fertility potential is. It is important however to acknowledge that screening AMH alone may be misleading as high levels occur in females manifesting polycystic ovarian syndrome. In this respect an objective parameter on the fertility potential can only be established following a complete hormonal profile test (FSH, LH, Estradiol and AMH) in conjunction with an internal baseline ultrasound scan (preferably between day 4-6 of menstruation) for the assessment of the ovarian status pertinent to the antral follicular count (number of existing follicles in the ovaries at the time) and ovarian volume.

Polycystic Ovaries (PCO) and Polycystic Ovarian Syndrome (PCOS)

It is important to distinguish between individuals presenting polycystic ovaries and those who manifest the syndrome associated with this condition. In essence, not everyone with ovarian cysts has PCOS. According to the Rotterdam criteria, 12 or more small follicles oriented in the periphery of an ovary should be observed (in the form of a string of pearls) to designate it as having a polycystic ovarian morphology with the volume of the ovary being at least 10 cc in size.

Normal

Polycystic

PCOS is considered the commonest endocrine disorder amongst women of reproductive age and has a diverse range of causes which are presumed to be genetically predisposed. Females with ovaries presenting this particular pattern but not manifesting the syndrome will normally achieve a pregnancy without any medical management. The syndrome has been shown to account for a large collection of symptoms most important of which are anovulation, elevated androgen hormones and insulin resistance. Anovulation results in irregular menstruation, amenorrhea and infertility while the hormonal imbalance and elevated androgen production is associated with increased hirsutism and acnes. The insulin resistance observed accounts for an increase in body weight (disproportionate to the volume of food consumption) which results to obesity.  Individuals with PCOS and who are obese are considered to be at high risk to developing diabetes type II before the onset of menopause.

Mechanical Causes

The major mechanical cause associated with female infertility is occlusion of the fallopian tubes. With this condition the normal path between the ovary and the uterus is compromised rendering sperm and egg encounter impossible. Blockage of the tubes can result from previous infection (sexually transmitted diseases i.e. Chlamydia and Gonorrhea) and surgical procedures in the pelvis ensuing in the formation of adhesions and scar tissue at the vicinity while it can also be a consequence of a congenital defect or endometriosis. Adhesions can also affect the normal functioning and mobility of the ovaries during the synergistic association they have with the fallopian tubes impairing access to the egg following ovulation. Furthermore, adhesions can form within the uterus itself negatively affecting its receptivity to embryo implantation. Finally adhesions which can form within the cervical canal most often due to previous surgical interventions will limit the normal progression of spermatozoa following ejaculation into the uterus and from there into the tubes.

While a single patent tube may suffice for a female to conceive, the structure of the counterpart may present a limiting factor. Infection of the delicate structure of the tube consistent with salpingitis can cause permanent blockage which can subsequently transform into a hydrosalpynx (when blood accumulates forming a bulge) or a pyosalpinx (when the swelling is caused by pus). Since the tube on one end is obstructed the fluid (mostly blood) which accumulates at the vicinity palidromically flows into the uterus creating a hostile environment for the embryo to implant. Certain clinicians endeavour to restore tubal patency by performing surgery but this has been proven most often a temporary solution to the problem since adhesions will reform shortly thereafter. In those cases where the presence of hydrosalpinx or pyosalpinx is diagnosed the only effective line of action is laparoscopic surgical removal.

Another common cause for tubal blockage and mechanically related infertility is endometriosis. This disorder develops when the specialised cells of the inner lining of the uterus migrate for reasons which are not well understood and adhere at sites outside the uterus. While the pelvic organs are more likely to be affected, endometriosis can be found in any internal organ of the female organism. The fact that the endometrial cells are under the influence of hormonal changes, they respond as if they were within the uterus causing bleeding and inflammation at the sites which they adhere. The inflammation which deteriorates with successive menstrual cycles can cause obstruction of the tubes (if these are affected) and adhesions between different organs compromising normal functionality. When endometrial cells invade the ovaries they seriously compromise the egg cytoskeleton impairing fertilisation and subsequent early embryo quality consistent with high implantation failure and early pregnancy loss. Endometriosis is classified as I and II when it has been diagnosed as superficial (subtle or typical) while III and IV classes represent cystic ovarian endometriosis with adhesions.

Ovarian Endometrioma

While symptoms can vary based on the severity of this condition, affected individuals may experience painful menstruations and coitus with extensive volume of blood discharge which can endure for several days. An elevated CA125 marker in the blood may be associated with endometriosis while a baseline ultra sound can be informative. Laparoscopy may be recommended to affirm on the condition. There is virtually no effective treatment against endometriosis other than becoming pregnant although suppression drugs to cease menstruation and/or surgery can mitigate its adverse effects.

Endometriosis can occur within the uterus itself, a condition known as adenomyosis. The uterus is comprised of three distinct layers the endometrium which is the inner part and the site of embryo implantation, the middle layer (myometrium) which is made of smooth muscle and occupies most of the volume of the uterus and the outer loose tissue membrane surrounding the uterus and separating it from the rest of the pelvic organs namely the perimetrium. By definition adenomyosis is the presence of endometrial cells and glands into the myometrium. In its simpler form the uterine muscle is completely infiltrated with endometriotic tissue which diffuses throughout without a distinct line of demarcation between the two layers (image of normal and ademomyotic uterus). Individuals presenting this condition normally manifest endometriosis too and their uteruses limit embryo implantation potential while the risks of miscarriage are considerably elevated even at later stages of the pregnancy.

The uterus can also be associated with alternative factors which can compromise embryo implantation. Conditions such as endometrial hyperplasia, endometrial polyps, endometrial fibroids, endometrial adhesions, arcuate, septate or bicornuate uterus or infection within the uterus (endometritis) adversely affect the chances of conception (images of endometrial hyperplasia, endometrial polyp).

Immunological Causes

Each organism curries a delicate immunological system whose purpose is to protect it against foreign agents ranging from simple pathogens to complex viruses. In doing so, it must be able to detect and distinguish them from the organism’s healthy tissue. For reasons which are yet to be completely elucidated the female immune system recognises and neutralizes early developing embryos as early as before implantation or shortly following their embedding into the uterus. The exact mechanisms associated with autoimmune infertility, (where the body’s same defense system reacts against and rejects an embryo from implanting as if it is a foreign threat) have been contentious and received intense scientific scrutiny. The most extensively studied group of immune cells is a type of lymphocytes (white blood cell) namely Natural Killer (NK) cells. Certain researchers fail to accept the influence which these types of cells have on the implantation embryo while criticism exists on the proposed treatments associated with counteracting their presumed inherent effects. It is however, widely accepted that following ovulation and at the onset of conception, NK cells compromise more than 80% of the white blood cell count in the endometrial cavity. NK cells are known to produce a collection of small proteins namely cytokines which have a centralized effect on the interactions between cells their communication systems and behavioural profiles. The notion exists that an imbalance in the cytokines concentration maybe an impediment to embryo implantation and ongoing developmental potential. An individual who had proven fertility in the past may raise antibodies against her embryo subsequently. What exactly causes the recognition of an embryo as hostile and why the mechanisms toward rejection were non-existent previously is yet to be elucidated.

The commonest types of antibodies which form with an elevated NK cell count are:

(i) anti-phospholipid antibodies, (ii) antithyroid antibodies and (iii) antiovarian antibodies.

What is of the essence when investigating the presence of NK cells and especially the CD69 type subgroup in females with history of early pregnancy loss or failure to conceive, is to affirm what triggered the elevated count. It must be appreciated that the human white blood cell membrane protein CD69 is an early activation marker induced not only by the NK cells but also by T lymphocytes and B cells (the major cellular components of the adaptive immune response) in response to any inflammatory stimuli. In this respect an elevated CD69 marker may not be a result of a hyperactive NK cell population. It is well documented that elevated counts of the CD69 marker during peripheral blood assessment may not predict an autoimmune related response by contrast an endometrial biopsy is a more useful diagnostic tool for establishing potential involvement of NK cells.

A second type of immune response can be encountered when a female raises antibodies in her cervical mucus creating a hostile environment for sperm survival following ejaculation. In essence anti-sperm antibodies are an immune response raised by the female where specialised white blood cells attack the sperm impairing their successful penetration into the uterus through the cervix leading to compromised fertility.