Long term consequences of in vitro fertilization and intracytoplasmic sperm injection
July 2002
Introduction
Many thousands of children have been born from assisted reproductive
technology. In vitro fertilization (IVF) and intracytoplasmic sperm
injection (ICSI) are two techniques used. The oldest IVF baby, Louise
Brown, is now 24 years old. Most early ICSI programmes began in 1994-5,
so the eldest ICSI children are only 7-8 years old.
How safe are these procedures? Doubts have been, and continue to be,
raised about the outcomes for children who are born.1,2,3,4,5
There are few follow-up studies on outcomes after pregnancy is
established, or on long-term health consequences for mothers and
babies.6
What is currently known
IVF exposes embryos to hazards not normally encountered in a normal
pregnancy. We already know, thanks to many epidemiological studies,
that events before birth can have disease outcomes in adulthood.
7
But IVF is a relatively recent technology. It has been practiced widely
without comprehensive assessment of its efficacy and safety.
IVF has been used for many years in veterinary science. There have
been unforeseen consequences in cattle, such as the 'large offspring'
syndrome.8 IVF in animals has been associated with miscarriage, very
high birthrate, physical abnormalities and peri-natal mortality.9
Slight hormone and nutrient imbalances within the first week of
embryonic development may alter the course of development throughout
the life of IVF animals, regardless of how they appear at birth.10
In humans, IVF results in more pregnancies of multiple gestation
because usually more than one embryo is placed into the uterus. Twins
and triplets tend to have a lower birthweight than singleton
pregnancies. But babies from single IVF pregnancies also have
below-normal birth-weight.11 There is also evidence that the in vitro
environment of eggs and sperm can affect subsequent embryonic and fetal
development.12
Some examples of research suggesting the danger of IVF to children are:
- Male IVF babies had a five-fold increased risk of hypospadias.13,14
- In Finland, IVF singletons and multiples had poorer health than other infants; 25% were preterm or weighed less than 2500g.15
- In Sweden, 5680 IVF children were studied. The most common
neurological diagnosis was cerebral palsy; IVF children had increased
risk of 3.7 (singletons 2.8). Suspected developmental delay was
increased four-fold.16
ICSI is a particular IVF technique, used for severe male infertility.
ICSI bypasses natural selection of sperm (eliminates competition)
because only one sperm is used. There is no suitable animal model (an
infertile primate) available, so the safety of ICSI could not be
assessed on animal models before introduction.
17
The following concerns have arisen:18
- The risks of using sperm that potentially carry genetic
abnormalities; it is thought that males eligible for ICSI carry a
higher rate of genetic defects.
- The risks of using sperm with structural defects: although
there is no absolute evidence that a physically abnormal sperm has
abnormal genes, these sperm would not normally be able to fertilise an
egg.
- The potential for damage (eg. from the needle or the chemicals used in the procedure), especially damage to the chromosomes.
- the risk of introducing foreign material into the oocyte: some
culture media may contain heavy metals known to be toxic to sperm.
Some examples of research describing health problems for ICSI-conceived children:
- Increased prevalence of sex chromosome anomalies and a high
prevalence of structural and numerical chromosomal aberrations have
been reported.19
- Infants born after ICSI were twice as likely as naturally
conceived infants to have a major birth defect, and nearly 50% more
likely to have a minor defect. Secondary analysis (interpret with
caution) found an excess of major cardiovascular defects (odds ratio
3.99), genitourinary defects (1.33), and gastrointestinal defects
(1.84) in particular cleft palate (1.33) and diaphragmatic hernia
(7.73).20
- Infants conceived through ICSI or IVF have twice the risk of a major birth defect as naturally conceived infants.21
- ICSI offspring are at risk of also being infertile.22
Ethical analysis
Currently clinics deal with such knowledge by counselling and routinely offering prenatal genetic diagnosis.
23
An abnormal result from prenatal testing is likely to culminate in
abortion. Since prenatal testing is invasive, and abortion undesirable,
a large amount of research has been conducted into preimplantation
genetic diagnosis to detect affected embryos before they are implanted
into the uterus.
But development can be affected before any defect is apparent. So
an apparently normal embryo is no guarantee that foetal development and
post-natal life will be normal.24
These concerns are a clear ethical challenge to clinics offering IVF.
What are their ethical obligations to children born from such
procedures, when doctors know there are risks involved? When IVF and
ICSI children grow up, will we see lawsuits and claims for healthcare
costs against doctors? What are the implications for informed consent?
IVF and ICSI can be described as an experiment on a large
scale, using children as subjects. While many parents may be released
from the heartbreak of infertility, the means to this end are not
ethically justified.
- Sutcliffe AG. "Intracytoplasmic sperm injection and other aspects
of new reproductive technologies" Arch Dis Child 2000; 83: 98-101
(August)
- McEvoy TG, et al "Large offspring syndrome and other
consequences of ruminant embryo culture in vitro: relevance to
blastocyst culture in human ART" Hum Fert (Camb) 2000; 3 (4): 238-246
- Boerjan ML, den Daas JH, Dieleman SJ "Embryonic origins of
health: long-term effects of IVF in human and livestock" Theriogenology
2000 January 15; 53 (2): 537-47
- ibid
- Gissler M, Malin Silverio M, Hemminki E. "In-vitro
fertilization pregnancies and perinatal health in Finland 1991-1993"
Hum Reprod 1995 July; 10 (7): 1856-61
- Corabian P, Hailey D "The efficacy and adverse effects of in
vitro fertilization and embryo transfer" Int J Technol Assess Health
Care 1999 Winter; 15 (1): 66-85
- Van der Lende T, de Loos FA, Jorna T "Postnatal health and
welfare of offspring conceived in vitro: a case for epidemiological
studies" Theriogenology 2000 January 15; 53 (2): 549-54
- McEvoy TG et al. 2000 op cit
- Rieger D "Effects of the in vitro chemical environment during
early embryogenesis on subsequent development" Arch Toxicol Suppl 1998;
20: 121-9
- Barnes FL "The effects of the early uterine environment on
the subsequent development of embryo and fetus" Theriogenology 2000
January 15; 53 (2): 649-58
- Buitendijk SE "Children after in vitro fertilization. An
overview of the literature" Int J Technol Assess Health Care 1999
Winter; 15 (1): 52-65
- Rieger D 1998 op cit
- Hypospadias: A congenital abnormality in which the male
urethra fails to reach its normal termination at the end of the penis,
emptying instead through an opening beneath the penis or in the
perineum.
- Silver RI, Rodriguez R, Chang TS, Gearhart JP "In vitro
fertilization is associated with an increased risk of hypospadias" J
Urol 1999 June; 161 (6): 1954-7
- Gissler M, Malin Silverio M, Hemminki E. 1995 op cit
- Stromberg B et al. "Neurological sequelae in children born
after in-vitro fertilisation: a population-based study" Lancet 2002
February 9; 359 (9305): 461-5
- Sutcliffe AG. 2000 op cit
- ibid
- Van der Westerlaken L. et al. "Invasive prenatal diagnosis
after intracytoplasmic sperm injection" Fert Steril June 2001, 75 (6):
1240-1241 (survey, The Netherlands)
- Kurinczuk JJ and Bower C. "Birth defects in infants conceived
by intracytoplasmic sperm injection: an alternative interpretation" BMJ
1997 November 15; 315 (7118): 1260-5
- Hansen M et al. "The risk of major birth defects after
intracytoplasmic sperm injection and in vitro fertilization" New
England Journal of Medicine March 7 2002, 346 (10): 725-730
- Meschede D et al. "Clustering of male infertility in the
families of couples treated with intracytoplasmic sperm injection" Hum
Reprod July 2000; 15 (7): 1604-1608
- Van der Westerlaken L. et al. 2001 op cit
- Rieger D 1998 op cit