Cystic Fibrosis Treatment
Cystic Fibrosis Treatment
Cystic fibrosis and Omega 3
Scientists have suggested that an imbalance of omega 3 fatty acids may cause inflammation lung patients suffering from cystic fibrosis.
Cystic fibrosis is a recessive disease affecting the lungs.
The main objective of medical research and scientific information on cystic fibrosis is to understand, treat and cure cystic fibrosis. A hereditary disease of fibrosis Living is a phenomenon that affects about 30,000 American and the disease is most common, life-shortening genetic included. Cystic fibrosis is a fatal disease caused by a defective gene that affects approximately 30,000 children in the United States.
Researchers at Beth Israel Deaconess Medical Center, University Massachusetts and Massachusetts General Hospital took tissue samples from 38 patients with cystic fibrosis.
Found at extremely levels of arachidonic acid (AA) and abnormally low levels of acid docosahexaenoic acid (DHA).
People who have no CF was not the imbalance of fatty acids.
Researchers believe that many of the symptoms cystic fibrosis, follow the same pattern: a mutant gene mutated glycoconjugates results in a defective component cell. There are about ten million asymptomatic cystic fibrosis gene defect United States.
They say that many acid and organizations very few patients in other ways "are more prone to inflammation.
The New England Journal of Medicine, suggests omega-3 found in fish, could help correct the imbalance.
Each week three young in the UK die from the disease that is caused by the defective CFTR gene.
CF causes thick, sticky mucus abnormally produced in the body, causing chronic lung inflammation causing potentially fatal infections.
The average life expectancy for a person with CF is approximately 31.
To diagnose cystic fibrosis, the laboratory conducts a test of the sweat. When the lungs and airways are blocked, the cough produces Cystic fibrosis sputum of patients and very thick. The authors concluded that the ionization of air is forced inside a natural and effective treatment for respiratory disease in patients with cystic fibrosis.
When the cystic fibrosisTR is not normal, the regulation of salt through the membrane becomes defective. In the respiratory mucosa becomes thin, thick and sticky. Since the digestive juices can not reach the intestine, because of frozen pipes in the pancreas and liver, fat and protein are not digested.
Dr. Steven Freedman of the Division of Gastroenterology at Beth Israel Deaconess Medical Center, who led the research, said: "Since 1989, we learned that the defective CFTR gene is responsible for CF.
"But I could not understand how this defective gene leads to symptoms of the disease.
"This new study sheds light on what might happen and provides a link between CFTR function and fatty acid metabolism.
He added: "We know that large amounts of AA and low amounts of DHA may be predisposed to inflammation.
"This discovery may help explain why there is an inflammatory response excess in cystic fibrosis patients.
"This is the foundation of why omega-3 fish oils in the fish cold water, and supplements, reduce inflammation and increase levels of DHA and AA to delete. "
No change in diet "
Dr Adam Jaffe, director of the Research Group in FC of London Institute of Child Health, told the BBC the research was interesting, but inconclusive.
"The patients should not alter their diet based on false associations between fatty acids and inflammation.
"But I am against them to supplement your diet."
Tom O'Connor, an expert in omega-3, shares a host of information on its website http://www.1st-Omega-3.Com
About the Author
People with cystic fibrosis have to spend much time in reviewing treatments?
or, like going to the hospital twice a week and the cold like normal people for the rest of the day?
I CF, happened about 2 hours day breathing treatments at home. I nebulizers, inhalers, antibiotics and respiratory physiotherapy. Hospital antibiotics intravenously for one or two times per year.
Cystic Fibrosis – Treatment & Life Expectancy
