In vitro fertilisation is a form of infertility treatment where ova are removed from a woman and fertilised outside of the body by sperm. The resulting zygotes are allowed to develop for a few days before one or at most two embryos are returned to the uterus to implant and develop.
This is an inherited condition which leads to the progressive weakening and breakdown of muscles. This in turn leads to increasing levels of disability. In its most severe forms it can be fatal.
A genetic disease caused by a defective, recessive gene. It is characterised by the production of thick, sticky mucous in the lungs and pancreas which cause respiratory and digestive problems.
Controlled sequence of events that results in cell division in the body cells.
The person who receives a new healthy organ in a transplant operation
The name for a group of cells that are developing into a fetus. In humans this is from implantation to the 8th week of development
A mass of abnormal cells which keep multiplying in an uncontrolled way.
A group of cells in an organism that are specialised to work together to carry out a particular function.
A structure with a particular function which is made up of different tissues.
The person who donates an organ for a transplant operation
The development of the polymerase chain reaction has had a major impact on medicine. The ability to take a very tiny sample of DNA, even from a single cell, and amplify it to give enough material for easy analysis has opened many doors in medicine. PCR - and especially RT-PCR - has triggered the development of diagnostic techniques which would have been impossible just a few years ago.
Medical developments which have resulted or are in progress as a result of PCR include:
Amplifying the genetic material from a single bacterium or virus can provide a speedy and accurate diagnosis for serious infections such as AIDS, viral meningitis and TB, where getting the right treatment quickly can mean the difference between life and death. What is more, RT-PCR makes it possible to identify new pathogens at a speed which would have been unimaginable a few years ago. The rapid identification of the SARS virus (see Infection detection) is one example of the way PCR can help fight infections. Another example was announced in March 2017, when scientists introduced genome sequencing for pathogens in suspected cases of TB. The bacteria which cause tuberculosis take weeks to grow in culture, but genome sequencing after PCR enables them to be identified correctly in days. As a result, people with TB can be treated rapidly with the appropriate antibiotic, so they get better sooner and are less likely to spread the disease to others.
Analysing and identifying sub-strains of bacteria and viruses enables scientists and doctors to track down the source of an infection – sometimes to a specific individual or food production plant. As a result, they can prevent further spread of disease.
By identifying if a bacterial pathogen is resistant to particular antibiotics, the appropriate treatment can be given – and the risk of further resistance developing reduced. The introduction of PCR and genome sequencing of TB pathogens in 2017 enabled doctors to discover exactly which antibiotic is effective against a particular strain of TB, curing patients faster, reducing the spread of disease and minimising the development of further antibiotic resistance.
PCR makes it easier to identify individuals who carry genes which can cause problems like cystic fibrosis and muscular dystrophy. It has also made it possible to look at the genetic material taken from a single cell of a very early embryo during in vitro fertilisation, amplify it and identify potential problems relatively easily. In future, screens may even be developed for the genetic variations which give us an increased risk of developing problems such as heart disease or high blood pressure. This would allow people to alter their lifestyle to reduce their risk. Screening may also indicate whether a particular medicine is the best one for that person – this idea is called “personalised medicines.”
Cancers develop when small changes in the DNA of a cell mean that it loses the normal control of the cell cycle and grows and divides far too rapidly. Using PCR to amplify the DNA from fragments of cells in the blood gives doctors and scientists the opportunity to pick up these genetic changes in cancerous cells early in the development of the disease. The earlier cancers are detected the greater the likelihood that they can be successfully treated.
Diagnosis of bowel cancer often involves an investigation of the colon and tissue samples being taken from any areas which look suspicious. Using PCR, bowel cancer can now be detected from the DNA of cells shed in the faeces. This is an easy, quick and non-intrusive way (pleasanter for all concerned!) of making a diagnosis which gives treatment a much better chance of success.
In organ transplants, a close tissue match between the donor and the recipient reduces the chances that the new organ will be rejected. In the past, this matching has been based on blood groupings and a few other major tissue markers. As a DNA bank of all the people needing transplants can be built up, PCR will lead to increasingly sophisticated levels of tissue matching at the DNA level. PCR enables analysis of a potential donor’s tissue to be carried out quickly and effectively. This in turn should lead to more successful transplants.
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