THESIS: It is the responsibility of Christians to become
informed of the ever-increasing technology of fertility drugs
and forms of technology-assisted reproduction and weigh the ethical
implications of their use before acting upon them.
Outline: Technology Assisted Reproduction
I. Introduction
II. Background
A. Infertility
B. Causes of infertility
C. Infertility Tests
II. Technological Methods of Conception
A. Artificial Insemination
B. In Vitro Fertilization
C. Gamete Intrafallopian Transfer
D. Tubal Ovum Transfer
E. Embryo Lavage
F . Surrogate Motherhood
III. Fertility Drugs
A. Hormones involved in reproduction
B. Mechanisms of drugs
C. Risks of fertility drug use
1. Multiple births and associated risks
2. Ovarian cancer
IV. Relating Faith and Technology Assisted
Reproduction
A. Cost
B. Surrogate Motherhood
C. Frozen Embryos
D. Interference with Nature
V. Conclusion
Introduction
Reproduction is fundamental for the perpetuation of a species
and therefore is a trait all species possess. Human reproduction
is usually not viewed in this context. Extinction of humans is
not considered a threat, but the ability to reproduce is an issue
of meeting social expectations. Psychologist Dr. Helen Fisher
states that society tends to pressure women into feeling that
motherhood is their sole connection to being female (Rutter,
1996). Likewise, men are influenced by society into feeling
that they need to perform their part by "planting the seed"
(Rutter, 1996). Fisher's insight may only represent
parts of the reason humans feel the need to reproduce. However,
it is evident that the ability to conceive a child is an important
issue for most married couples. Unfortunately, complications occur
when couples are infertile. Recent developments in reproductive
technology have provided alternative methods of reproduction that
can greatly enhance an infertile couple's chances of conceiving.
However, there are ethical and legal issues that accompany the
use of these reproductive technologies. It is the responsibility
of everyone, especially Christians, to become informed of the
options reproductive technology can provide as well as the legal
and ethical issues involved with their use before taking appropriate
action.
Background
Beginning at puberty, the human male makes millions of sperm a
day and continues to do so for about the next 50 years. On the
other hand, the human female is born with approximately one million
eggs, which are all that she will ever have (Infertility,
1996). The onset of menstruation during adolescence signals
the beginning of a cycle in which hormones prepare one or two
of these eggs for possible fertilization each month. These cycles
continue until menopause. Both sexes seem to be more than adequately
equipped by biology for parenthood. However, infertility affects
12% of American couples or approximately 4.5 million couples a
year (Fertility, 1998).
Infertility is technically defined as the inability to conceive
after having regular intercourse for one year without using any
form of birth control. Surprisingly, the odds against conception
are strong most of the time. A woman has just a 20-35% chance
of conceiving during each menstrual cycle, even at the peak of
fertility (Infertility, 1996). These odds decline
slightly in the women's late 20's and early 30's and more sharply
after the age 35. Male fertility also decreases with age, although
more slowly than female fertility.
Fertility is impaired in as many men as women. The problem lies
within the man a third of the time, another third of the time
within the women, and the remaining third is usually a combination
of the two (Youngkin, 1997). Health professionals
emphasize the need for infertile couples to recognize the problem
as "our" problem instead of "mine" or "your"
problem. It is less emotionally damaging this way. For these reasons,
both partners should be evaluated when a decision is made to make
an attempt at conceiving.
Common Causes of Infertility
There are many known causes of infertility. In men, low sperm
count and poor sperm motility are usually the culprits. An undescended
testicle or dilated veins in the scrotum both contribute to low
sperm count and poor sperm motility (Fertility, 1998).
Sperm becomes less viable as men become older. In addition, men
sometimes form antibodies against their sperm causing infertility
(Infertility, 1996).
In women, there is a wider range of potential causes. Endometriosis,
irregular ovulation, genital infections, and ovarian cysts are
naturally occurring causes that decrease the fertility of women
(Fertility, 1998). The use of cancer therapy
and multiple abortions also decrease fertility in women. Damaged
or missing reproductive structures are sometimes irreversible
infertile conditions, and therefore the most serious that women
can have. These conditions may either completely inhibit the reproductive
system from working or decrease its effectiveness enough for women
to be considered infertile.
Infertility Tests
There are a variety of tests that can be done to determine the
fertility of men and women. The cervical mucous test involves
both the man and woman. This test is done 2-12 hours after a couple
has had intercourse. Several samples of cervical mucous are taken
and analyzed for proper interaction between the sperm and mucous
(Infertility Tests, 1996). The mucous is also
tested to see if it contains antibodies against the sperm.
Semen analysis is usually the first test done on men to determine
the number and viability of sperm. A healthy, potent ejaculate
should contain 1.5 cubic centimeters of semen with each cc containing
approximately 70 million sperm that appear to be of normal size,
shape, and behavior (Infertility Tests, 1996).
Two special tests done on men to evaluate the potency of sperm
are the bovine mucus test and the hamster-oocyte penetration test.
In the bovine mucus test, bovine mucus is collected from the cervix
and placed in a jar. Samples of semen are then added and measurements
are made on how well the sperm can swim through the mucous (Infertility Tests, 1996). The hamster-oocyte penetration
test analyzes the sperm's ability to penetrate an egg. It requires
sperm to be added to hamster eggs cells with outer membranes removed.
Normally functioning sperm will penetrate the hamster eggs indicating
that they posses the ability to penetration human female eggs
as well (Infertility Tests, 1996).
Technological Methods of Conception
A variety of treatments are presently available for couples who
are infertile. The treatments range from simple to medically complex,
depending on the cause and degree of infertility. Some couples
require only information on sexual practices favorable to conception.
Other simple treatments include drug therapy to arrest an underlying
infection or hormone deficiency. For difficult infertility problems,
assisted reproduction technological procedures are required for
conception.
Artificial insemination is the oldest technological method of
conception and has been used for over a century (Reproductive
Tech, 1996). The technique employs the use of a catheter to
place the donor's sperm into the woman's uterus or vaginal canal.
It is performed around the time of ovulation and often needs to
be repeated over the course of four or five menstrual cycles to
obtain fertilization (Nelson, 1973). Studies
have shown that artificial insemination offers success rates between
50 % and 65 %.
Much newer than artificial insemination is in vitro fertilization
(IVF). This technique was made famous in 1978 by the birth of
Louise Brown, the world's first "test tube" baby (Reproductive Tech, 1996). IVF is an option when
various other infertility treatments have failed or are inappropriate.
It can be used in women who have a uterus and at least one ovary,
but whose fallopian tubes are damaged, missing, or diseased. First,
fertility drugs are taken by the women to prepare her eggs for
fertilization along with preparing her uterus for implantation.
Next, the eggs are removed and placed in a laboratory dish where
they are incubated with her partner's sperm for 18 hours (Reproductive Tech, 1996). After two days, several
(to increase odds of implanting) of the fertilized eggs are transferred
by instrument into the woman's uterus. Finally, a fairly new procedure
called "assisted hatching" is employed to increase the
chances of implantation. It involves opening a small slit around
the shell that covers the embryo so that content of the embryo
can be extruded in order for it to attach to the wall of the uterus
(Youngkin, 1997). A 1988 study involving 41 clinics
showed that 15.9% of women became pregnant by using IVF, but only
10.2% carried the fetus to term and delivered a living infant
(Reproductive Tech, 1996).
Technological methods of conception developed since IVF are being
used as well. Gamete intrafallopian transfer (GIFT), tubal ovum
transfer, and embryo lavage are examples of these. They each require
the use of a fertility drug in conjunction with the method itself.
GIFT is similar to IVF except that sperm and eggs are collected
and immediately inserted into one or both fallopian tubes (Reproductive, 1996). Unlike IVF, GIFT requires that
the woman posses at least one healthy fallopian tube. However,
the success rate of GIFT is similar to IVF.
The embryo lavage method involves a third party. A fertile female
donor provides the eggs. At the proper time in her menstrual cycle,
she is artificially inseminated with the would-be father's sperm.
Upon conception, the embryo is washed out of her reproductive
tract and transferred to the uterus or fallopian tube of the woman
who is to bear the child who has additionally been treated with
fertility drugs to make her uterus receptive to the embryo (Reproductive Tech, 1996). The embryo lavage technique
allows women who have no eggs of their own to become pregnant,
provided they have a uterus.
Surrogate motherhood is an option for women who do not respond
to ovulation induction therapies, who have no ovaries, or lack
a uterus. It also may be an option for those for whom pregnancy
might be life threatening or have significant risks of transmitting
a serious genetic disorder to the child (Reproduction
Tech, 1996). First of all, a healthy, fertile woman agrees
to be artificially inseminated and also agrees to let the infertile
couple adopt the baby. In cases where the female member of the
infertile couple can safely provide eggs of her own, they can
be fertilized by the IVF process and transferred to the surrogate
woman who then carries the fetus to term. The surrogate mother
prepares her uterus by taking fertility drugs. If the female member
of the infertile couple is unable to provide eggs, the surrogate
mother's eggs are used. Surrogate motherhood is controversial
and has resulted in many court cases about custody and parentage
(Reproductive Tech, 1996).
Fertility Drugs
Hormones released from several organs in the body control the
normal female reproductive cycle. The hypothalamus gland produces
a hormone called gonadotropin-releasing hormone (GnRH). This hormone
in turn stimulates the pituitary gland. The pituitary releases
two gonadotropins, follicle-stimulating hormone (FSH) and luteinizing
hormone (LH), which are involved in reproduction. FSH and LH effect
reproduction by controlling the ovaries during the menstrual cycle.
FSH stimulates the growth of follicles. Each follicle contains
an egg and produces additional hormones. LH helps FSH to stimulate
the production of these hormones, both before and after ovulation.
About halfway through the menstrual cycle, a sudden surge of LH
and FSH causes the rupture of the dominant follicle and release
of the egg from within. At this point, LH is the most important
hormone since it enables the egg to mature and prepare for fertilization
by sperm (Reproductive Med, 1998).
Fertility drugs have been used for over 30 years and have a range
of mechanisms of action. However, the ultimate function of each
of them is increasing the level of LH and FSH (Reproductive
Med, 1998). Clomid and Serophene are specific drugs that directly
stimulate the hypothalamus while Pergonal acts by directly stimulating
the pituitary gland. Increasing the level of the gonadotropin
causes the ovaries to release multiple eggs thus increasing the
chances of pregnancy. The increased level of gonadotropins also
helps to prepare the endometrium of the uterus for the impending
implantation of the fertilized egg. The stimulation of multiple
follicular development, known as controlled ovarian hyperstimulation
(COH), is an essential step in the IVF and GIFT techniques. The
drugs used for this are mostly naturally occurring gonadotropins,
which are extracted from human urine (Reproductive
Med, 1998). Usually, a gonadotropin releasing hormone agonist
is administered beforehand to control and halt the women's natural
hormonal cycle.
Recent research has provided the technology to produce gonadotropins
via recombinant DNA technologies (Reproductive Med,
1998). This method of production results in very high purity
gonadotropins. In addition, it releases the dependence on the
collection of large amounts of urine as a source.
Risks of Fertility Drug Use
The use of fertility drugs has a number of potential risks involved.
Multiple births are the most common result of using fertility
drugs and have increased dramatically since the advent of fertility
drugs. Twin births alone have increased by 42% from 1980 to 1994
(Meyer, 1997). Taking the strongest fertility
drugs results in a 15% to 30% chance of having twins (Youngkin,
1997). Twins are seven times more likely to be born smaller
than single infants leading 50% of all twins to weigh less than
5 ½ pounds compared with less than six percent of single
babies. Also, the risk of low birth weight and death increases
with multiple births--evident by the fact that more than 90% of
triplets born each year weigh less than 5 ½ pounds and
10 out of every 100 die (Meyer, 1997). However,
there are examples of success. In November 1997, Bobbi McCaughey
gave birth to the world's first set of surviving septuplets, igniting
a lot of discussion on the use of fertility drugs (Chance,
1997).
Another potential risk involved with the use of fertility drugs
is the development of ovarian cancer. However, there is no conclusive
evidence. There are data in support of an association between
fertility drugs and ovarian cancer, but there are equally convincing
data that suggest that there is no such association (Benjamin,
1996). A retrospective study from 12 published studies conducted
on white women in 1992 showed a 3-fold increase of invasive epithelial
ovarian cancer in women treated with fertility drugs over women
who were not treated. In addition, infertile women with no treatment
showed no increased risk (Benjamin, 1996). Contrary
to this study, there are additional studies with data that do
not link fertility drug use and ovarian cancer. Further studies
are needed to establish evidence for either case.
Relating Faith and Technology Assisted
Reproduction
The issues surrounding the use of technology assisted reproduction
raise difficult questions. There are many ethical, moral, and
legal questions that must be contemplated by potential users.
Even the simplest procedures may cause consequences revealing
the potential risks involved.
An issue of consideration prior to proceeding with any technology
assisted reproduction method is the cost involved. These methods
are very expensive and are usually not covered by insurance. In
fact, Massachusetts is the only state that requires insurance
companies to cover fertility procedures. As a result, the state
has five times more couples entering technology assisted reproduction
treatments (Conrad, 1997). How much money is
too much? Most treatments cost $8,000 to $10,000 for each treatment
and require at least three or four treatments for successful conception.
In the end, the cost of successfully delivering an infant by way
of technology assisted reproduction ranges from $44,000 to $212,000
(Conrad, 1997). Even if couples have the resources
to spend this much money, is it ethical to do so while many children
await adoption?
Problems also arise when one partner is unable to provide the
eggs or sperm. In these cases, the parent who did not provide
the genetic material may not feel the same bond with the child
as the other parent who is the genetic parent of the child (Lockwood, 1985). In situations where the man is
unable to produce the sperm, the woman may feel a psychological
bond with the man who donated the sperm and eventually feel distanced
from her husband. Therefore it is essential for couples planning
on taking part in such a procedure to discuss all their options
and ways to deal with these potential moral and psychological
dilemmas.
Surrogate motherhood carries the most legal implications. In addition,
the moral and psychological dilemmas can be substantial hurdles
as well. This has led some states to make it illegal to enter
a contract with a surrogate mother (Thomasma, 1996).
Five thousand legally contracted surrogate births have occurred
over the last 15 years. The surrogate mother challenged the contract
in 12 cases, but only in two cases were the sole parental rights
granted to the surrogate mother (Conrad, 1997).
The discussion of all possible consequences that may occur is
needed between the couple and the surrogate mother during the
decision process so that parental rights are successfully transferred.
Another ethical question that often arises in reproductive technology
is the issue of frozen embryos. Embryos resulting from multiple
fertilization are often frozen for later use but usually end up
being discarded (Cowley, 1995). There is legislation
that prohibits the storage of embryos for more than five years
(Biggin, 1996). A belief in life at conception
would indicate that destroying frozen embryos is morally wrong.
Additionally, many IVF's result in multiple fertilization from
the use of fertility drugs. What is done with embryos not implanted
besides storing them? Is it ethical to do so knowing that they
will be destroyed after five years?
Reproductive technology may also stir-up issues of power and control.
Does God approve of humans creating technology to make the process
of conception possible in cases where conception is naturally
impossible? Is it an example of humans trying to play God? Strong
opinions are present on both sides. The Roman Catholic church
condemns artificial insemination even when the husband's sperm
is being used citing that it is not acceptable to interfere with
the natural process (Bohle, 1979). Additionally,
some theologians and religious groups argue that "God intended
procreation be joined with sexual intercourse in the bonds of
marriage, and any other methods of reproduction are immoral because
they are not sanctioned by God (Conrad, 1997).
On the opposing side are those that argue that the relationship
in a marriage is to be considered above sexual intercourse. They
identify love between the husband and wife as the essential part
of a marriage, and therefore technology assisted reproduction
does not actually break the bond of marriage since the child is
conceived out of love (Bohle, 1979).
Conclusion
The technology available to us is increasing at a rapid rate.
Unfortunately, not all of the "technological advancements"
come without any ethical implications, and thus we need to be
cautious and to carefully evaluate the pros and cons of all of
it. This is especially evident in the medical field. Science has
provided many new procedures and techniques that enable us to
have significant control over many things. However, it is important
to keep in mind that we, unlike God, are simply unable to control
all things. Christians should be able to make their own decisions
based on their personal value systems on whether to employ technologically
created methods such as assisted reproduction. However, they are
responsible to become informed about these procedures and weigh
all of the possible moral and ethical implications their use might
have before using them.
Benjamin, I. (1996). "Fertility Drugs and Ovarian Cancer: What are the risks when used for Surrogacy?" OncoLink. http://www.surrogacy.com/medres/article/fertdrug.html. (September 23, 1998).
Biggin, S. M. (1996, July). "Embryo Report Opens Old Wounds."
Science. pp 177.
Bohle, B. (1979). Human life: controversies and concerns. New
York: H. W. Wilson
Company.
"A Chance at Parenthood." (1998). WB NEWS. http://broadcast.webpoint.com/wbzl/fertility/fertility_curentevents.htm. (September 24, 1998).
Conrad, D. (1997, Fall). "Assisted Reproductive Technology in the Faith Community." Biology Senior Seminar Student Papers.
Cowley, G. (1995, June). "Ethics and embryos." Newsweek. v125 n24 p66(2).
"Do Fertility Drugs Have Any Long-term Side Effects?" (1996). Home Arts. http://www.homearts.com/depts/health/57drb2.html. (September 23, 1998).
"Infertility, The Big Picture." (1996). Better Health and Medical. http://www.betterhealth.com?HK/ArticleMain/0,1349,178-496-296,00.htm. (September 23, 1998).
"Infertility Tests: Men & Women." (1996). Better Health and Medical. http://www.betterhealth.com/HK/ArticleMain/0,1349,178-496-300,00.htm. (September 23, 1998).
Lockwood, M. Ed. (1985). Moral Dilemmas in Modern Medicine. Oxford University Press.
Meyer, Tara. (1997). "Twin births soar with popularity of fertility drugs." Discovery. http://detnews.com/1997/discover/9702/20/02170076.htm. (September 24, 1998).
Nelson, J.B. (1973). Human Medicine: ethical perspectives on new medical issues. Minneapolis: Augsburg Publishing House.
"Reproductive Medicines." (1998). Organon. http://www.fertility-net.com/medicines.html. (September 23, 1998).
"Reproductive Technology." (1996). Better Health and Medical. http://www.betterhealth.com/HK/ArticleMain/0,1349,178-496-488,00.htm. (September 23, 1998).
Rutter, V. T. (1996, March). "Who stole fertility?" Psychology Today. pp. 46-49.
Thomasma, D. C. & Kushman, T. Eds. (1996). Birth to Death.
New York: Cambridge
University Press.
Youngkin, Dr. (1997). "Fertility Drugs." Texas Medical Association. http://www.texmed.org/news_events/radio_spots/ne_may0697_30.htm. (September 24, 1998).