Reproductive ethics Flashcards

1
Q

New reproductive
technologies

A

 Human embryonic stem cells
 Somatic nuclear transfer
 patient-specific embryonic stem cells
 human-animals hybrid embryos

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2
Q

Eugenics

A

 “Good genes” or “good birth”
 The use of genetics to improve the health of a
population

Negative selection: Don’t allow “bad genes” to
be reproduced
 Forced sterilization or abortion
 Marriage restrictions
 “Euthanasia”

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3
Q

Definitions

A

Embryo

-> human organism during first 56 days of its development following fertilization/creation,excluding time during which its development has been suspended

 Foetus

-> human organism from 57th day following fertilization/creation until birth

 Human reproductive material

->sperm, ovum or other human cell or human gene, and includes a part of any of them

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4
Q

Rights Based Ethics

A

*What becomes of the idea that everyone is created equal if you
start designing children?

*Loss of autonomy because of a necessity to be competitive in
society

*Inherently discriminatory; makes assumptions about quality of life

“Most people with disabilities rate their quality of life as much
higher than other people think. People make the decision [to
reject embryos] based on a prejudice that having a disability
means having a low quality of life.“ (Zitner 2002)

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5
Q

Utilitarianism

A

The greatest good for the greatest number suggests that…

The alleviation of suffering for many is important.

 IVF helps many infertile couples achieve a life-long dream of having a child.

 PGD helps those same couples reach their goal of a disease free child.

 Is a disease free society is preferable for all members
of society?

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6
Q

Peter Singer (Preference
Utilitarian)

A

 We already allow this kind of treatment. It has
benefited many people.
 Individuals should be free to make their own
choices on this issue as it is a private matter
harming no-one else.
 Many children have been born as a result of this
technology. It hasn’t harmed any of them or
society so we should conclude that it is
acceptable.
22

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7
Q

Pre-implantation Genetic Diagnosis (PGD)

A

Genetic analysis of a single cell from an eight-cell
embryo done in conjunction with in vitro
fertilization (IVF) to improve the chances of a
“normal” pregnancy

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8
Q

Why consider PGD in addition to IVF?

A

1.recurrent miscarriages
2.one child already affected with a genetic disease
3.family history of inherited disease
4.maternal age older than 38
5.prior failure with IVF
6.family “balancing” for sex

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9
Q

The Methods of Preimplantation Genetic
Diagnosis

A
  1. Remove a single cell from the 6-8-cell embryo
    using a fine glass needle to puncture the zona pellucida and aspirate the cell
  • In skilled hands, this generally does not harm the developing embryo.
  • Each cell is called a blastomere.
  1. Prepare a metaphase spread of chromosomes to assess karyotype (number and integrity of each chromosome)
  2. Two types of assessment techniques are common:

a. chromosome “painting” (or FISH) using fluorescent
probes specific for each chromosome. These allow
number and size of each chromosome to be checked.
* useful for identifying aneuploidies (incorrect
chromosome numbers) and translocations

  • procedure destroys the tested cell
  • limited number of chromosomes can be checked
    simultaneously; some abnormalites undetectable
  1. Two types of assessment techniques are common:
    a. chromosome “painting” (or FISH)
    b. genetic testing for specific disease loci (PCR or gene
    chips)
    Polymerase chain reaction (PCR)
    - amplification of DNA specific to a gene of interest (family
    history guides choice of genes)
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10
Q

Risks of IVF to the mother/couple:

A
  • Multiple pregnancies (20-30%)
  • Ectopic pregnancy
  • Cancellation (over- or under-response to ovarian induction)
  • Ovarian hyperstimulation syndrome (fluid build-up in pelvic
    cavity due to ovarian enlargement; clotting problems)
  • Mechanical injury to bowel, bladder, ureters, or blood vessels during egg retrieval
  • Greater risk of premature delivery and delivery by Caesarean section
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11
Q

Risks to the child conceived via IVF/PGD:

A
  • Low birth weight; premature birth
  • Developmental delays
  • Cognitive problems (ADHD)
  • Urogenital problems
  • Cerebral palsy
  • Certain cancers (e.g., Beckwith-Weidemann syndrome, which
    may be related to ICSI)

(Note: The vast majority of children born of IVF appear normal. Low birth weight, cognitive delays, and cerebral palsy are more common for any multiple-birth situation. Very few controlled, longitudinal studies have compare IVF to natural.)

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12
Q

Proposed AHR Act –
Prohibited Activities

A

 The proposed legislation would ban:
 creating a human clone for any purpose (i.e.
reproductive or therapeutic);
 creating an in vitro embryo for any purpose other
than creating a human being, or improving
assisted reproduction procedures;
 creating an embryo from an embryo or fetus for
the purpose of reproduction;
 maintaining an embryo outside a woman’s body
beyond the 14th day of its development;

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13
Q

Germ-Line Alteration?

A

 The act forbids altering “the genome of a cell of
a human being or in vitro embryo such that the
alteration is capable of being transmitted to
descendants;”

 But why not, e.g., allow permanent removal of
the gene for sickle-cell anemia from a particular
family line?

distinguish 2 kinds
 negative = correcting or avoiding ‘defects‘
 positive = making ‘improvements‘
 Strongest arguments are for negative genetic
engineering

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14
Q

Objection 1: Playing
God / Unnaturalness

A

‘To engage in germ-line alteration is playing
God.’

 Ethically a need to explore how this instance is different than other apparently morally OK
“acting unnaturally”

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15
Q

Uncertainty about Effects

A

Our knowledge of what exactly the alteration will do is incomplete.

 This objection’s force will decrease with time.

 We should be careful of identifying particular
traits as definitively problematic, e.g., in some
contexts, the gene for sickle-cell anemia
confers an advantage (i.e., protection from
malaria)

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16
Q

Commodification

A

For many people, there is a fundamental flaw at
the heart of genetic engineering which it shares with eugenics

 This alleged flaw is that genetic engineering involves seeing those who are engineered as
things or commodities, not as things with intrinsic value.

 ‘Commercialization’ is generally seen as a clear instance of commodification, although not the only such instance

17
Q

When is a Thing Being
Commodified?

A

 To treat an embryo as a thing to be bought,
sold or redesigned is generally claimed to
involve treating it as a mere means to an end
(i.e., as a commodity)
 Can we contrast genetic engineering with good
nutrition, exercise, education, self development?
When is the line crossed and why?

Effectively, the worry is the same here.
 “payment for human gametes is inappropriate, as it would
constitute commercialization of human reproductive
material”
 Is commercializing parts of a human body is to
commercializing humans themselves?
 Treating bodies as property

18
Q

Ethical issues from IVF

A

IVF
 Family structure, surrogacy

Cryopreservation
 Posthumous baby

Preimplantation genetic diagnosis
 Desinger baby
 Selection of embryos for HLA

19
Q
A