Conditions & Treatments

Cystic Fibrosis

Cystic fibrosis (CF) is an inherited chronic disease that affects the lungs and digestive system. CF causes the body to produce thick, sticky mucus that leads to progressive lung infection and difficulty gaining weight.

Cystic Fibrosis

Illustration of  the anatomy of the respiratory system, adult
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What is cystic fibrosis?

Cystic fibrosis (CF) is an inherited disease characterized by an abnormality in the glands that produce sweat and mucus. Due to improved treatments, people with CF, on average, live into their mid to late 30s.

Cystic fibrosis affects various organ systems in children and young adults, including the following:

  • Respiratory system

  • Digestive system

  • Reproductive system

There are about 30,000 people in the U.S. who are affected with cystic fibrosis. It occurs mainly in Caucasians of northern European ancestry, although African-Americans, Asian Americans, and Native Americans may have the disease as well.

Approximately one in 31 people in the U.S. are carriers of the cystic fibrosis gene. These people are not affected by the disease and usually do not know that they are carriers.

How does CF affect the respiratory system?

The basis for the problem with CF lies in an abnormal gene. The result of this gene defect is an atypical electrolyte transport system within the cells of the body. Electrolytes are substances in blood that are critical to cell function. The abnormal transport system in CF causes the cells in the respiratory system, especially the lungs, to absorb too much sodium and water. This causes the normal thin secretions in our lungs to become very thick and hard to remove. These thick secretions put the child with CF at risk for frequent respiratory infections.

Recurrent respiratory infections lead to progressive damage in the lungs, and eventually death of the cells in the lungs. The most common causes for infection in the lungs of the CF patient are the following bacteria:

  • Staphylococcus aureus

  • Haemophilus influenzae

  • Pseudomonas aeruginosa (PA)

PA is the most common bacteria that causes infection and can be difficult to fight with standard antibiotics.

As a result of the high rate of infection in the lower respiratory tract, people with CF may develop a chronic cough, blood in the sputum, and even have a collapsed lung. The cough is usually worse in the morning or after activity.

People with CF also experience upper respiratory tract symptoms. Some patients have nasal polyps that require surgical removal. Nasal polyps are small protrusions of tissue from the lining of the nose that can obstruct and irritate the nasal cavity. Children with CF may also have a higher rate of sinus infections.

How does CF affect the gastrointestinal (GI) system?

The organ primarily affected is the pancreas, which secretes substances that aid digestion and help control blood-glucose levels.

As a result of the abnormal electrolyte transport system in the cells, the secretions from the pancreas become thick and can lead to obstruction of the ducts of the pancreas. This obstruction may cause a decrease in the secretion of enzymes from the pancreas that normally help to digest food. A person with CF has difficulty absorbing proteins, fats, and vitamins A, D, E, and K.

The problems with the pancreas can become so severe that some of the cells in the pancreas are destroyed. This may lead to glucose intolerance and insulin-dependent diabetes. About 35 percent of CF patients develop this type of diabetes in their 20s and about 40 percent develop the disease after 30 years of age.

The symptoms that may be present due to the involvement with the GI tract include the following:

  • Bulky, greasy stools

  • Rectal prolapse. A condition in which the end part of the bowels comes out of the anus.

  • Delayed puberty

  • Fat in the stools

  • Stomach pain

  • Bloody diarrhea

The liver may also be affected. A small number of patients may actually develop liver disease. Symptoms of liver disease may include:

  • Enlarged liver

  • Swollen abdomen

  • Yellow color to the skin

  • Vomiting of blood

How does CF affect the reproductive system?

Most males with CF have obstruction of the sperm canal known as congenital bilateral absence of the vas deferens (CBAVD). This results from the abnormal electrolyte transport system in the cells, causing the secretions to become thick and may lead to obstruction and even infertility. Women also have an increase in thick cervical mucus that may lead to a decrease in fertility, although many women with CF are able to have children.

What are the symptoms of cystic fibrosis?

The following are the most common symptoms of cystic fibrosis. However, individuals may experience symptoms differently. Symptoms may include:

  • Abnormalities in the glands that produce sweat and mucus. This may cause a loss of salt. A loss of salt may cause an upset in the balance of minerals in the blood, abnormal heart rhythms, and, possibly, low blood pressure and shock.

  • Thick mucus that accumulates in the lungs and intestines. This may cause malnutrition, poor growth, frequent respiratory infections, breathing difficulties, and chronic lung disease.

  • Other medical problems, such as:

    • Sinusitis

    • Nasal polyps

    • Clubbing of fingers and toes. A condition marked by extremely thickened fingertips and toes due to decreased oxygen in the blood.

    • Pneumothorax. Collapse of the lung often due to intense coughing.

    • Hemoptysis. Coughing up blood.

    • Cor pulmonale. Enlargement of the right side of the heart due to increased pressure in the lungs.

    • Abdominal pain

    • Excess gas in the intestines

    • Rectal prolapse

    • Liver disease

    • Diabetes

    • Pancreatitis. Inflammation of the pancreas that causes severe abdominal pain. 

    • Gallstones

    • Congenital bilateral absence of the vas deferens (CBAVD) in males

As stated above, the symptoms of CF differ for each person. Infants born with CF usually show symptoms by age two. Some children, though, may not show symptoms until later in life. The following signs are suspicious of CF, and infants having these signs may be tested for CF:

  • Diarrhea that does not go away

  • Foul-smelling stools

  • Greasy stools

  • Frequent episodes of wheezing

  • Frequent episodes of pneumonia or other lung infections

  • Persistent cough

  • Skin tastes like salt

  • Poor growth despite a good appetite

The symptoms of cystic fibrosis may resemble other conditions or medical problems. Consult a doctor for a diagnosis.

How is cystic fibrosis diagnosed?

Most cases of cystic fibrosis are now identified with newborn screening. In addition to a complete medical history and physical examination, diagnostic procedures for cystic fibrosis include a sweat test to measure the amount of sodium chloride (salt) present. Higher than normal amounts of sodium and chloride suggest cystic fibrosis. Other diagnostic procedures include:

  • Chemical tests

  • Chest X-rays

  • Lung function tests

  • Sputum cultures

  • Stool evaluations

For babies, who do not produce enough sweat, blood tests may be used.

Treatment for cystic fibrosis

Specific treatment for cystic fibrosis will be determined by your doctor based on:

  • Your age, overall health, and medical history

  • Extent of the disease

  • Expectations for the course of the disease

  • Your tolerance for specific medications, procedures, or therapies

  • Your opinion or preference

Currently, there is no cure for CF. A cure would call for gene therapy at an early age and this has not been developed yet, although research is being done in this direction. The gene that causes CF has been identified and there are hopes that this will lead to an increased understanding of the disease. Also being researched are different drug regimens to help stop CF. Goals of treatment are to ease severity of symptoms and slow the progress of the disease. Treatment may include:

  • Management of problems that cause lung obstruction, which may involve:

    • Physical therapy

    • Exercise to loosen mucus, stimulate coughing, and improve overall physical condition

    • Medications to reduce mucus and help breathing

    • Antibiotics to treat infections

    • Anti-inflammatory medications

  • Management of digestive problems, which may involve:

    • Appropriate diet

    • Pancreatic enzymes to aid digestion

    • Vitamin supplements

    • Treatments for intestinal obstructions

Newer therapies include lung transplantation for patients with end-stage lung disease. The type of transplant done is usually a heart-lung transplant, or a double lung transplant. Not everyone is a candidate for a lung transplant. Discuss this with your doctor.

The genetics of cystic fibrosis

Cystic fibrosis (CF) is a genetic disease. This means that CF is inherited. A person will be born with CF only if two CF genes are inherited--one from the mother and one from the father. A person who has only one CF gene is healthy and said to be a carrier of the disease. A carrier has an increased chance of having a child with CF. This type of inheritance is called autosomal recessive. Autosomal means that the gene is on one of the first 22 pairs of chromosomes which do not determine gender, so that the disease equally affects males and females. Recessive means that two copies of the gene, one inherited from each parent, are necessary to have the condition. Once parents have had a child with CF, there is a one in four, or 25 percent chance with each subsequent pregnancy, for another child to be born with CF. This means that there is a three out of four, or 75 percent chance, for another child to not have CF.

The birth of a child with CF is often a total surprise to a family, since most of the time (in eight out of 10 families) there is no previous family history of CF. Many autosomal recessive conditions occur this way. Since both parents are healthy, they had no prior knowledge that they carried the gene, nor that they passed the gene to their baby at the same time.

Genes are founds on structures in the cells of our body called chromosomes. There are normally 46 total, or 23 pairs of two chromosomes in each cell of our body. The seventh pair of chromosomes contains a gene called the CFTR (cystic fibrosis transmembrane regulator) gene. Mutations or errors in this gene are what cause CF. This gene is quite large and complex. Over 1,000 different mutations in this gene have been found which cause CF.

The risk for having a sporadic mutation in the gene for CF depends on your ethnic background (for persons without a family history of CF):

Ethnic background

Risk of CF mutation

Risk of child with CF

Caucasian

1 in 29

1 in 2,500-3,500

Hispanic

1 in 46

1 in 4,000-10,000

African-American

1 in 65

1 in 15,000-20,000

Asian

1 in 90

1 in 100,000

Testing for the CF gene can be done from a small blood sample or from a cheek swab, which is a brush rubbed against the inside of your cheek to obtain cells for testing. Laboratories generally test for the most common mutations.

There are many people with CF whose mutations have not been identified. In other words, all of the genetic errors that cause the disease have not been discovered. Because not all mutations are detectable, a person can still be a CF carrier even if no mutations were found by carrier testing.

Testing for the CF gene is recommended for anyone who has a family member with the disease, or whose partner is a known carrier of CF or affected with CF.

Treatment Programs


Massachusetts General Hospital understands that a variety of factors influence patients' health care decisions. That's just one reason why we're dedicated to ensuring patients understand their diagnosis and treatment options. Because a single option might not serve all patients, we offer a wide range of coordinated treatments and related services across the hospital. Patients should consult with their primary care doctor or other qualified health care provider for medical advice and diagnosis information.

Select a treatment program for more information:



Imaging

  • Adult Medicine Imaging
    The Adult Medicine Imaging Program at Massachusetts General Hospital Imaging offers a wide range of diagnostic exams and minimally invasive, image-guided treatments, all provided using leading-edge equipment and interpreted by specialty-trained radiologists.
  • Pediatric Imaging
    The Pediatric Imaging Program at Massachusetts General Hospital Imaging specializes in ensuring the safety and comfort of child patients while providing the latest technology and the expertise of specialized pediatric radiologists.
MassGeneral Hospital for Children

  • Pediatric Cystic Fibrosis Center
    The Joey O'Donnell Cystic Fibrosis Center at MassGeneral Hospital for Children is committed to providing first-class, individualized care for each patient with cystic fibrosis.
  • Pediatric Hepatobiliary and Pancreatic Program
    The Pediatric Hepatobiliary and Pancreatic Program at MassGeneral Hospital for Children diagnoses and treats infants, children and adolescents with diverse hepatic, biliary and pancreatic disorders.
  • Pediatric Endocrine Program and Diabetes Center
    The Pediatric Endocrinology Program and Diabetes Center at MassGeneral Hospital for Children is an international referral center for the management of pediatric diabetes and endocrine disorders in children and adolescents.
  • Pediatric Pulmonary Medicine
    The Division of Pediatric Pulmonary Medicine at MassGeneral Hospital for Children is a well-established clinical, training and research program. The group provides multidisciplinary comprehensive consultation, diagnostic and management services for a wide array of pulmonary conditions.
  • Pediatric Transplant Surgery
    The Pediatric Transplant Program at MassGeneral Hospital for Children is a major referral center for organ transplants for children.
Transplant Center

  • Lung Transplant Program
    The Lung Transplant Program at the Massachusetts General Hospital Transplant Center brings together state-of-the-art technology and leading-edge medical and surgical interventions to provide patients with individualized care before and after their lung transplants.
  • Transplant Psychiatry Program
    The Transplant Psychiatry Program in the Massachusetts General Hospital Transplant Center is an important part of the comprehensive and life-long care provided to transplant patients and donors.
  • Transplant Infectious Disease Program
    The Transplant Infectious Disease Program, part of the Massachusetts General Hospital Transplant Center, is a part of the life-long care provided to organ, bone marrow and stem cell transplant recipients and others with increased risk for infections.
Pulmonary and Critical Care Medicine

  • Adult Cystic Fibrosis Center
    The Massachusetts General Hospital Adult Cystic Fibrosis Program is staffed by world-class specialists who provide outstanding, comprehensive care to adults diagnosed with this uncommon and complex disease.

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