Thursday, September 10, 2009
Wednesday, September 9, 2009
Tuesday, September 8, 2009
Wisdom of a Retiree
'I've often been asked, 'What do you old folks do now that you're retired?'
"Well..I'm fortunate to have a chemical engineering background, and one of the things I enjoy most is turning beer, wine, Scotch, and margaritas into urine."
"Well..I'm fortunate to have a chemical engineering background, and one of the things I enjoy most is turning beer, wine, Scotch, and margaritas into urine."
Monday, September 7, 2009
Sunday, September 6, 2009
Lord Winston, Labels Egg Feezing As "Expensive Confidence Trick"
Lord Winston, emeritus Professor of Fertility Studies at Imperial College London and pioneer of IVF, has criticized fertility clinics for over-hyping egg freezing services. In an interview with the Daily Mail newspaper he accuses providers of creating false optimism in the effectiveness of the procedure particularly where signing up patients for purely 'social' reasons. Before use of egg freezing grows further he calls for more research into both the effects of egg freezing on the ability to later conceive and into the long-term health implications for those born
from frozen eggs.
The comments come in response to calls, made at last week's European Society for Human Reproduction and Embryology (ESHRE) annual conference, for greater availability of egg freezing as an option for women who are postponing pregnancy until later in their lives. Lord Winston's comments partially mirror a joint statement made in February by the UK's Royal College of Obstetricians and Gynaecologists and the British Fertility
Society (BFS) which also called for women not to freeze eggs for social reasons.
Lord Winston noted that the production of six to ten eggs for freezing involves both the risk of ovarian hyperstimulation syndrome for the woman and an increased likelihood of chromosome defects in the eggs produced. Producing such a quantity of eggs he sees as dangerous yet also inadequate to ensure a viable embryo is produced. The BFS has stated that the average chance of success for any individual frozen egg is six per cent and only four children have been born from frozen eggs in the UK to date.
Additionally, the lack of data on the long term health effects - the first children conceived with frozen eggs are only now five - is provided as reason enough for adopting a cautious approach towards increasing availability of egg freezing and makes encouraging those without a pressing need (such as impending cancer treatment) all the more dubious. Lord Winston states, in unequivocal terms, 'in my view it is irresponsible [for clinics] to egg freeze until long-term animal research has been done'. The most detailed research to date is due to be published next month.
Describing the procedure as a 'quick fix', Lord Winston sees the best path forward for prolonging the ability to have a child, for social reasons, is to attempt to develop better means of postponing the menopause. Though the procedure can be justified for those with serious medical conditions it is not be encouraged as a means of delaying motherhood. The provision of egg freezing for social reasons, available for between £2,500 and £5,000 at 45 clinics in the UK, is in his view simply an 'undesirable commercial activity' and should not be encouraged.
from frozen eggs.
The comments come in response to calls, made at last week's European Society for Human Reproduction and Embryology (ESHRE) annual conference, for greater availability of egg freezing as an option for women who are postponing pregnancy until later in their lives. Lord Winston's comments partially mirror a joint statement made in February by the UK's Royal College of Obstetricians and Gynaecologists and the British Fertility
Society (BFS) which also called for women not to freeze eggs for social reasons.
Lord Winston noted that the production of six to ten eggs for freezing involves both the risk of ovarian hyperstimulation syndrome for the woman and an increased likelihood of chromosome defects in the eggs produced. Producing such a quantity of eggs he sees as dangerous yet also inadequate to ensure a viable embryo is produced. The BFS has stated that the average chance of success for any individual frozen egg is six per cent and only four children have been born from frozen eggs in the UK to date.
Additionally, the lack of data on the long term health effects - the first children conceived with frozen eggs are only now five - is provided as reason enough for adopting a cautious approach towards increasing availability of egg freezing and makes encouraging those without a pressing need (such as impending cancer treatment) all the more dubious. Lord Winston states, in unequivocal terms, 'in my view it is irresponsible [for clinics] to egg freeze until long-term animal research has been done'. The most detailed research to date is due to be published next month.
Describing the procedure as a 'quick fix', Lord Winston sees the best path forward for prolonging the ability to have a child, for social reasons, is to attempt to develop better means of postponing the menopause. Though the procedure can be justified for those with serious medical conditions it is not be encouraged as a means of delaying motherhood. The provision of egg freezing for social reasons, available for between £2,500 and £5,000 at 45 clinics in the UK, is in his view simply an 'undesirable commercial activity' and should not be encouraged.
Saturday, September 5, 2009
Fertility "Fingerprints"
Scientists in Ireland have discovered a group of genes that could potentially be used to predict the success of IVF treatment. The prospect of a clinical test for IVF success was raised at the annual conference of the European Society for Human Reproduction and Embryology (ESHRE), in Amsterdam.
The group, led by Dr Cathy Allen at the Rotunda Hospital, Dublin, examined the genetic profiles from blood samples taken at eight different stages during the period around conception and the early stages of the IVF cycle to analyze what differences in gene expression were seen at certain points before, during and after pregnancy. The blood samples were from five women who achieved clinical pregnancy, three women who had implantation failure and three subfertile women who conceived spontaneously.
The findings showed that activity levels of genes controlling the growth of new blood vessels, inflammation and the supply of energy to cells were different in women undergoing IVF. There was a marked difference in the expression of 200 genes at the beginning of fertility treatment between women who became pregnant and those who did not. The group concluded that this gene 'signature' was highly predictive of whether IVF worked or not, and could be used to develop a clinically useful predictive tool.
Dr Allen thinks that one of the most difficult decisions to make when undergoing IVF treatment is whether to continue with treatment after a failed attempt, as this can be emotionally and physically draining, as well as expensive. A reliable blood test could help patients and doctors with this decision.
She said: 'This work has generated a unique profile for IVF success and failure... As a practicing clinician, I think this might have a use for patients trying to decide whether they should undergo IVF or not. It's going to be a while before we have a clinical test but my gut feeling is it will be useful for identifying the unfavourable profile - those who won't get pregnant'.
Currently, advice from doctors on this decision is based upon factors such as age, lifestyle and hormone levels, but these are not often reliable. A separate team of scientists at Cardiff University has developed a questionnaire, called the FertiSTAT. Based on questions about a woman's menstrual cycle, reproductive health, lifestyle factors, age and length of time for which they have been trying for a baby, the test can be used to judge whether a woman will have fertility problems, and whether changing
their lifestyle could improve their chances of pregnancy.
Professor Luca Gianaroli, the ESHRE chairman, said of Dr Allen's findings: 'this test could save a lot of unnecessary treatment. You have to balance the cost of research and the benefits of research.'
The group, led by Dr Cathy Allen at the Rotunda Hospital, Dublin, examined the genetic profiles from blood samples taken at eight different stages during the period around conception and the early stages of the IVF cycle to analyze what differences in gene expression were seen at certain points before, during and after pregnancy. The blood samples were from five women who achieved clinical pregnancy, three women who had implantation failure and three subfertile women who conceived spontaneously.
The findings showed that activity levels of genes controlling the growth of new blood vessels, inflammation and the supply of energy to cells were different in women undergoing IVF. There was a marked difference in the expression of 200 genes at the beginning of fertility treatment between women who became pregnant and those who did not. The group concluded that this gene 'signature' was highly predictive of whether IVF worked or not, and could be used to develop a clinically useful predictive tool.
Dr Allen thinks that one of the most difficult decisions to make when undergoing IVF treatment is whether to continue with treatment after a failed attempt, as this can be emotionally and physically draining, as well as expensive. A reliable blood test could help patients and doctors with this decision.
She said: 'This work has generated a unique profile for IVF success and failure... As a practicing clinician, I think this might have a use for patients trying to decide whether they should undergo IVF or not. It's going to be a while before we have a clinical test but my gut feeling is it will be useful for identifying the unfavourable profile - those who won't get pregnant'.
Currently, advice from doctors on this decision is based upon factors such as age, lifestyle and hormone levels, but these are not often reliable. A separate team of scientists at Cardiff University has developed a questionnaire, called the FertiSTAT. Based on questions about a woman's menstrual cycle, reproductive health, lifestyle factors, age and length of time for which they have been trying for a baby, the test can be used to judge whether a woman will have fertility problems, and whether changing
their lifestyle could improve their chances of pregnancy.
Professor Luca Gianaroli, the ESHRE chairman, said of Dr Allen's findings: 'this test could save a lot of unnecessary treatment. You have to balance the cost of research and the benefits of research.'
Friday, September 4, 2009
One-stop Genetic Test For Embryos
A one-step gene mapping test for identifying genetic and chromosomal abnormalities in embryos may be available in the UK within a year. The technique, known as karyo-mapping, can screen for almost any inherited disease and is much faster than those currently available as it does not need prior knowledge of the specific gene mutation involved. The method was unveiled at the annual conference of the European Society for
Human Reproduction and Embryology (ESHRE), in Amsterdam, after researchers from the UK and US announced they had successfully screened cells taken from donated embryos that were known to have cystic fibrosis (CF).
Since 1989, couples who are known to be at risk of having a child with a genetic disorder have had the option of screening their embryos using a technique called pre-implantation genetic diagnosis (PGD). PGD involves identifying the exact mutation causing a particular disease in a particular family, then spending many months developing a custom test. The process costs several thousand pounds and can only pick up two per cent of known genetic disorders.
Now, for a similar price, karyomapping can identify any known genetic disorder and is faster because scientists do not need to know the exact DNA mutation they are looking for. Instead they compare the DNA of affected and unaffected family members to work out which DNA section is carried only by those affected by the condition. Embryos can then be screened for this section of DNA to find out if they have inherited the mutation. In practice this involves DNA comparisons at over 300,000 locations genome-wide, but can be achieved rapidly through current microchip technology known as
'microarrays'. Another advantage is that karyomapping can simultaneously check for abnormal numbers of any of the 23 pairs of chromosomes, which can lead to conditions such as Down syndrome or trigger miscarriages.
'The hope is that clinicians will be able to test embryos for specific genetic diseases and know that, with one test, they are transferring chromosomally normal embryos. This will be a step forward from current technology that is mostly limited to choosing one test or the other,' explained karryomapping's inventor, Professor Alan Handyside of the London Bridge Fertility Gynaecology and Genetics Centre in London.
Some have argued the new technique may add to the controversy over 'designer babies' because it widens the range of genetic characteristics for which embryos can be screened and could theoretically be used to screen for non-serious conditions, or non-medical traits such as blue eyes. Professor Handyside believes this is not an issue because the relevant regulations in the UK are very strict and would remain so. 'We're not mad Frankensteins working away in our laboratories to create designer babies. We are only allowed to look for major diseases which cause handicaps,' he retorted.
Elsewhere at ESHRE scientists announced that up to 90 per cent of IVF embryos contain chromosomal abnormalities, even those produced by young, fertile couples. The surprising finding implies that current PGD techniques do nothing to improve pregnancy and live birth rates, and can potentially lead to viable embryos being discarded. This news means that the timely announcement of the new karyomapping method will be warmly welcomed by many.
Human Reproduction and Embryology (ESHRE), in Amsterdam, after researchers from the UK and US announced they had successfully screened cells taken from donated embryos that were known to have cystic fibrosis (CF).
Since 1989, couples who are known to be at risk of having a child with a genetic disorder have had the option of screening their embryos using a technique called pre-implantation genetic diagnosis (PGD). PGD involves identifying the exact mutation causing a particular disease in a particular family, then spending many months developing a custom test. The process costs several thousand pounds and can only pick up two per cent of known genetic disorders.
Now, for a similar price, karyomapping can identify any known genetic disorder and is faster because scientists do not need to know the exact DNA mutation they are looking for. Instead they compare the DNA of affected and unaffected family members to work out which DNA section is carried only by those affected by the condition. Embryos can then be screened for this section of DNA to find out if they have inherited the mutation. In practice this involves DNA comparisons at over 300,000 locations genome-wide, but can be achieved rapidly through current microchip technology known as
'microarrays'. Another advantage is that karyomapping can simultaneously check for abnormal numbers of any of the 23 pairs of chromosomes, which can lead to conditions such as Down syndrome or trigger miscarriages.
'The hope is that clinicians will be able to test embryos for specific genetic diseases and know that, with one test, they are transferring chromosomally normal embryos. This will be a step forward from current technology that is mostly limited to choosing one test or the other,' explained karryomapping's inventor, Professor Alan Handyside of the London Bridge Fertility Gynaecology and Genetics Centre in London.
Some have argued the new technique may add to the controversy over 'designer babies' because it widens the range of genetic characteristics for which embryos can be screened and could theoretically be used to screen for non-serious conditions, or non-medical traits such as blue eyes. Professor Handyside believes this is not an issue because the relevant regulations in the UK are very strict and would remain so. 'We're not mad Frankensteins working away in our laboratories to create designer babies. We are only allowed to look for major diseases which cause handicaps,' he retorted.
Elsewhere at ESHRE scientists announced that up to 90 per cent of IVF embryos contain chromosomal abnormalities, even those produced by young, fertile couples. The surprising finding implies that current PGD techniques do nothing to improve pregnancy and live birth rates, and can potentially lead to viable embryos being discarded. This news means that the timely announcement of the new karyomapping method will be warmly welcomed by many.
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