Attitudes towards assisted reproduction and preimplantation genetic diagnosis
December 17, 2008Madrid, December 15, 2008.- According to an international survey by the BBVA Foundation conducted this year, citizens in advanced societies view assisted reproduction techniques in general and in vitro fertilization in particular as firmly acceptable alternatives for people with fertility problems (over 7 points on an acceptance scale from 0 to 10 in twelve of the fifteen survey countries). However, this strong approval for in vitro fertilization dissipates in other scenarios such as using the technique to choose a baby's sex (with scores below 3 points in almost every country).
Citizens also hold contrasting views on the use of preimplantation genetic diagnosis (a genetic test that can be carried out on the embryos obtained from artificial fertilization in order to select those to be implanted in the uterus of the future mother). Its use is widely accepted in all survey countries for the purpose of selecting a healthy, compatible embryo that may help cure a sibling suffering some genetic disease (mean acceptance score of around 6.5 points across the sample of countries, with Spain's score at 7.0 on a scale from 0 to 10). Conversely, its use to choose the sex of a future baby meets with widespread rejection (mean score below 4 points).
The data that follow correspond to the "Second International Study on Biotechnology ", by the BBVA Foundation. Information was gathered by surveying a representative population sample in twelve European countries (Germany, Denmark, Spain, France, Ireland, Italy, the Netherlands, Poland, the United Kingdom, Sweden, Austria, and the Czech Republic), the United States, Japan and Israel. 1,500 face-to-face interviews were conducted in each country with subjects aged 18 and over (around 22,500 interviewees in all), with the fieldwork concluding in February 2008. The design and analysis of the survey were the work of the BBVA Foundation's Department of Social Studies and Public Opinion.
GENERAL ATTITUDES TOWARDS INFERTILITY
In order to obtain some background for attitudes towards assisted reproductive techniques, interviewees were asked what they thought would be the best option for a couple unable to have children due to problems of fertility: 1) use assisted reproduction or in vitro fertilization techniques, 2) adopt a child, or 3) accept the situation and stay childless.
In all countries, a majority chose either adoption or the use of assisted reproduction techniques, with only a small percentage most in favor of them accepting the situation.
However, we can observe highly significant differences between the countries surveyed as regards the first two options:
- Countries where the majority would opt for assisted reproduction in a case of infertility: the Netherlands, Sweden, France, Denmark, Israel, and the Czech Republic. In Spain too, this option was supported by a relative majority
- Countries where a relative majority prefer the adoption route: Germany, Austria, Italy, Poland, and the United States
- Finally, in the United Kingdom and Ireland, opinions are more evenly divided between the two alternatives.
Citizens' attitudes to in vitro fertilization are keenly differentiated depending on the specific circumstances and the goals pursued:
- The use of in vitro fertilization finds widespread acceptance in cases of 1) infertility and 2) the avoidance of genetically transmitted diseases (mean above 6 points on an acceptance scale from 0 to 10). The highest mean scores in this respect were observed in the Czech Republic, Sweden, France, Denmark and Israel
- Using the same technique so a woman aged over 45 can get pregnant meets with more divided opinions, though with rejection predominating in most societies. Mean values stood below the midpoint on the scale in all countries except Israel (where acceptance is very high), Japan and Spain, with Denmark, Germany, Austria, France and the Netherlands registering the lowest approval scores
- Finally, the use of in vitro fertilization to choose the sex of a baby provokes outright rejection in all the countries analyzed (mean score below 3 points in every case), with acceptance lowest in Denmark, Sweden, France, the Netherlands and the United Kingdom.
The application of a genetic test to the embryos obtained from artificial fertilization before they are implanted in the uterus of the future mother is another biomedical advance that brings significant medical benefits but is also a focus of moral controversy.
Social attitudes towards preimplantation genetic testing depend strongly on the goal being pursued. Some of its main therapeutic indications - detection of genetically transmitted diseases and, more recently, the selection of a healthy, compatible embryo that can help cure a brother or sister of a genetic disease - deactivate reservations to its use, whereas its possible application in selecting the sex of the future baby activates powerful moral reservations (table 3).
A large majority of citizens are disposed to accept preimplantation genetic diagnosis:
- so a couple with serious genetic diseases can select embryos that do not carry the defective gene (mean scores above 6 points in all cases on a scale from 0 to 10, where 0 means totally unacceptable and 10 totally acceptable)
- so a couple with a child suffering some genetic disease can select embryos that are not affected by the defective gene and conceive a healthy, compatible child that can help cure its brother or sister (mean score likewise exceeding 6 points in almost every country)
- so any couple can detect whether an embryo carries a gene predisposing it to suffer some grave disease in adulthood and, in that case, select the embryos that do not carry this gene (mean acceptance ranging from 5 to 6.5 points in most countries)
The use of this application to select the baby's sex meets with the opposite response. Mean acceptance scores were below 4 points in all survey countries and extremely low (equal to or below 2 points) in Denmark, Sweden, the Netherlands and France.
USING SPERM BANKS GETS APPROVAL IN THE CASE OF COUPLES WHERE THE MALE IS INFERTILE
Finally, acceptance of the use of sperm banks to conceive a child by assisted reproduction techniques is also clearly influenced by the goal pursued:
- In all countries, a majority see using a sperm bank as acceptable in the case of couples wanting a child where the man is infertile. Acceptance scores are highest in Denmark, Sweden, and the Czech Republic.
- Conversely, the use of sperm banks to select a father who is particularly intelligent meets with widespread rejection. Within this general climate of disapproval, opinions are most hostile in France and Sweden
- The following scenarios register medium acceptance scores:
- In the case of women without a partner wishing to have a child, average acceptance exceeds the midpoint on the scale (5) in 7 out of the 15 countries, and stands below it in the rest. The most favorable opinions are expressed in the Czech Republic, Spain, and Israel, and the most unfavorable in Japan, Austria, Italy, and the United Kingdom
- With the exception of Denmark, the Netherlands, and Spain, average acceptance of the use of sperm banks by gay or lesbian couples is below the midpoint on the scale in all countries. The firmest rejection is expressed in Poland (1.1), Italy (2.4), Austria (2.9) and Japan (3.0).
- In the case of women without a partner wishing to have a child, average acceptance exceeds the midpoint on the scale (5) in 7 out of the 15 countries, and stands below it in the rest. The most favorable opinions are expressed in the Czech Republic, Spain, and Israel, and the most unfavorable in Japan, Austria, Italy, and the United Kingdom
-end-
TECHNICAL NOTESUniverse: in each country, the general population aged 18 and over.
Methods: administered face-to-face survey in the interviewee's home.
Sample size and distribution: 1,500 cases in each of the 15 countries. Multistage sample distribution stratified by region (NUTS classification or equivalent)/size of habitat, with primary units selected at random. Selection of individual respondents by the last birthday rule.
Sampling error: the sampling error estimated is 2.6%, for a confidence level of 95.5% and in the worst-case scenario (p=q=0.5). The survey was coordinated by TNS opinion. The fieldwork concluded in February 2008.
Fundación BBVA
Related Genetic Disease Articles from Brightsurf:
A novel finding on Kabuki syndrome, a rare genetic disease
It has a long time since the cause of the disease has been identified: mutations of KMT2D gene codify for MLL4, a protein involved in the regulation of chromatin, which is the complex of proteins and nucleic acids contained in the nucleus of cells.
Mystery about cause of genetic disease in horses
Warmblood fragile foal syndrome is a severe, usually fatal, genetic disease that manifests itself after birth in affected horses.
Major cause of rare genetic mitochondrial disease identified
An international study led by the Murdoch Children's Research Institute (MCRI) has given hope to families of children born with a fatal heart muscle disease caused by faulty cell machinery.
Curing genetic disease in human cells
Scientists from the groups of Hans Clevers (Hubrecht Institute) and Jeffrey Beekman (UMC Utrecht) show for the first time that a newer type of CRISPR, called base-editing, can safely cure cystic fibrosis in stem cells derived from patients.
Genetic variants reduce risk of Alzheimer's disease
A DNA study of over 10,000 people by UCL scientists has identified a class of gene variants that appear to protect against Alzheimer's disease.
The claw disease tyloma is primarily genetic in cows
Scientists at Martin Luther University Halle-Wittenberg (MLU) and Georg August University Göttingen have succeeded in proving that a claw disease in cows is primarily genetic.
Cardiac genetic mutation may not always predict heart disease
One in 10 people with this condition were born with a mutation in the TTN gene, but -- until now -- it has been unclear whether everyone with these mutations will inevitably develop dilated cardiomyopathy.
How a zebrafish could help solve the mysteries of genetic brain disease
A close look at the rapidly developing zebrafish embryo is helping neuroscientists better understand the potential underpinnings of brain disorders, including autism and schizophrenia.
First genetic clue for elusive pediatric liver disease
A nationwide consortium of researchers has identified the first genetic defect linked to biliary atresia, a mysterious liver disease that is the leading cause for liver transplantation in children.
Unveiling disease-causing genetic changes in chromosome 17
Extensive single Watson-Crick base pair mutations can occur in addition to duplication or deletion of an entire group of genes on chromosomal region 17p11.2.
Read More: Genetic Disease News and Genetic Disease Current Events
It has a long time since the cause of the disease has been identified: mutations of KMT2D gene codify for MLL4, a protein involved in the regulation of chromatin, which is the complex of proteins and nucleic acids contained in the nucleus of cells.
Mystery about cause of genetic disease in horses
Warmblood fragile foal syndrome is a severe, usually fatal, genetic disease that manifests itself after birth in affected horses.
Major cause of rare genetic mitochondrial disease identified
An international study led by the Murdoch Children's Research Institute (MCRI) has given hope to families of children born with a fatal heart muscle disease caused by faulty cell machinery.
Curing genetic disease in human cells
Scientists from the groups of Hans Clevers (Hubrecht Institute) and Jeffrey Beekman (UMC Utrecht) show for the first time that a newer type of CRISPR, called base-editing, can safely cure cystic fibrosis in stem cells derived from patients.
Genetic variants reduce risk of Alzheimer's disease
A DNA study of over 10,000 people by UCL scientists has identified a class of gene variants that appear to protect against Alzheimer's disease.
The claw disease tyloma is primarily genetic in cows
Scientists at Martin Luther University Halle-Wittenberg (MLU) and Georg August University Göttingen have succeeded in proving that a claw disease in cows is primarily genetic.
Cardiac genetic mutation may not always predict heart disease
One in 10 people with this condition were born with a mutation in the TTN gene, but -- until now -- it has been unclear whether everyone with these mutations will inevitably develop dilated cardiomyopathy.
How a zebrafish could help solve the mysteries of genetic brain disease
A close look at the rapidly developing zebrafish embryo is helping neuroscientists better understand the potential underpinnings of brain disorders, including autism and schizophrenia.
First genetic clue for elusive pediatric liver disease
A nationwide consortium of researchers has identified the first genetic defect linked to biliary atresia, a mysterious liver disease that is the leading cause for liver transplantation in children.
Unveiling disease-causing genetic changes in chromosome 17
Extensive single Watson-Crick base pair mutations can occur in addition to duplication or deletion of an entire group of genes on chromosomal region 17p11.2.
Read More: Genetic Disease News and Genetic Disease Current Events
Brightsurf.com is a participant in the Amazon Services LLC Associates Program, an affiliate advertising program designed to provide a means for sites to earn advertising fees by advertising and linking to Amazon.com.