Cystic fibrosis (CF) is a genetic condition that affects the lungs, digestive system, and other organs. The body produces thick, sticky mucus that can damage or obstruct organs.
CF develops when the protein that produces mucus does not function as usual. This is what causes the mucus.
There is currently
This article explores the causes and symptoms of CF. It also looks at the treatments, risk factors, outlook, and how doctors diagnose the condition.
People with CF have a
The protein is present in
- immune system
- sweat glands
The genetic mutation mean that the CFTR protein does not function as it would in a healthy body. This malfunctioning causes the body to produce mucus that is thicker and stickier than usual. It can block the airways, causing breathing difficulties and severe lung infections.
The genetic mutation may also interfere with pancreatic function by preventing enzymes from breaking down food effectively. This can cause digestive problems that may lead to limited growth and malnutrition.
CF is a chronic condition with potentially life threatening complications. However, treatments can improve the quality and duration of life.
- shortness of breath
- persistent coughing, which may bring up blood or mucus
- other breathing difficulties
Also, in people with CF, the mucus that obstructs lung function creates optimal living conditions for pathogens. As a result, a person has an increased risk of lung infections, such as bronchitis and pneumonia.
CF symptoms can vary from person to person, depending on the affected organs. Some other possible symptoms and complications are:
- frequent sinus infections
- gastrointestinal issues, such as:
- nasal polyps, which are small, fleshy growths inside the nose
- salty skin and sweat
- night sweats
- joint and muscle pain
- low body weight
- limited growth or weight gain in children
- delayed puberty
- male infertility
- clubbed fingers and toes, due to a lack of oxygen to the extremities
Treatments can help manage symptoms and improve the quality of life. The best combination of approaches depends on a person’s symptoms. Below, we describe some treatment options.
It is crucial to loosen and clear mucus from the lungs to ease breathing and minimize the risk of infections. Airway clearance techniques can help.
Some airway clearance techniques that a person might try include:
- Postural drainage: This involves getting into certain positions so that gravity helps move mucus into the center of the airways, where it can be dislodged more easily.
- Percussion: Clapping cupped hands against the chest can help loosen mucus.
- Vibration: This involves exhaling while a therapist uses their hands to make light, repetitive movements against the chest. This vibrations help loosen the mucus.
- Breathing techniques: Specific breathing exercises can help loosen and dislodge mucus.
- Positive expiratory pressure: This involves using a device that supports airflow and helps move mucus out of the airways.
Certain medications can help alleviate CF symptoms and otherwise manage the condition. Examples include:
- Bronchodilators: These drugs help relax the muscles around the lungs, giving the airways more room to expand. Some also help clear mucus from the lungs.
- Hypertonic saline: Sterilized salt water can help clear mucus and improve lung function in people over 6 years of age.
- Ibuprofen: High doses may help slow down the decline of lung function.
- Dornase alfa: People with CF can inhale this drug to support mucus clearance.
- Antibiotics: People with CF may take antibiotics, orally or with an IV, to treat bacterial lung infections. Doctors
do not usuallyrecommend inhaled antibiotics to treat CF exacerbations due to bacterial infections.
If an infection is bacterial, antibiotics can help treat it. Also, a person may be able to
- closely following their treatment plan
- getting any vaccinations that a doctor recommends, such as a yearly flu shot and a pneumococcal vaccine
- washing their hands regularly with soap and water, especially in the following situations:
- before eating
- before taking medications or using any breathing equipment
- after using the restroom
Other treatment methods
Below are some other ways of managing CF:
Vascular access devices
These implanted devices deliver medication directly into the bloodstream, and they may be suitable for people who require long-term access to IV treatment. Having one can make managing CF more efficient and less intrusive.
The device may consist of a long, thin tube inserted into a vein in the arm and secured to the skin with stitches or adhesive. Another option is a port, a device that a surgeon implants under the skin. The port connects to an IV tube when a person needs IV medication.
Two approved CFTR modulators are ivacaftor (Kalydeco) and lumacaftor/ivacaftor (Orkambi). Kalydeco may be suitable for children 6 years and older who have an additional eight CF gene mutations. Orkambi may be suitable for those between 6 and 11 years old with a F508del genetic mutation.
Nutritional therapy for digestive symptoms
CF can affect digestive function and nutrient absorption, so receiving professional dietary guidance is key. A registered dietitian may recommend:
- Having a high fat diet: As
2021 researchhas found, having a high fat diet and taking fat-soluble vitamin supplements may help counteract nutrient malabsorption.
- Increasing the calorie intake: This can help prevent unwanted weight loss. The authors of the 2021 research report that female adults may need to consume 2,500–3,000 calories per day and male adults may need 3,000–3,700 calories per day.
- Increasing the salt intake: People with CF may need to take in more salt to counteract sweating regularly due to exercise or living in a hot climate.
- Taking pancreatic enzyme supplements: Around 80–90% of people with CF may need pancreatic enzyme supplements. This is because CF can prevent the pancreas from making the enzymes necessary to break down food. The supplements can help with:
- maintaining a healthy weight
- preventing malnutrition and vitamin deficiencies
- improving bowel movements
The CFTR gene contains codes for producing a protein that controls the flow of salt and water across cell membranes. In someone with CF, this gene does not function as usual, leading to low levels of salt and water outside the cells. The result is unusually thick, sticky mucus.
If a person has only one copy of the malfunctioning gene, they do not develop CF but they “carry” it. For a person to develop CF, both biological parents must carry the malfunctioning gene.
According to the National Organization for Rare Disorders, if two carriers have a child, there is a:
- 25% chance with each pregnancy that the child will have CF
- 50% chance with each pregnancy that the child will be a carrier but will not have it
- 25% chance that the child will not be a carrier and will not have CF
- Genetic factors: People are more likely to have CF if one or both biological parents is a carrier or has the condition. The risk also increases if people have a sibling, half-sibling, or cousin with CF.
- Race and ethnicity: CF most commonly affects people of Northern European heritage. It is less common among people who are:
- African American
- Asian American
Some symptoms of CF may appear shortly after birth. But the symptoms of mild cases may not present until adulthood. More than 1,000 people in the U.S. receive a CF diagnosis each year, with 75% receiving a diagnosis by the age of 2 years.
People can undergo screening to check if they carry the CF genetic mutation. A healthcare professional takes a blood, saliva, or cheek cell sample for DNA testing. People may have this screening
The Cystic Fibrosis Foundation reports that life expectancy and quality of life continue to improve for people with the condition.
Life expectancy varies from one person to the next and can depend on the severity of the disease.
Receiving treatment as soon as possible
Consult a doctor about any symptoms of CF.
People with CF should let a member of their healthcare team know about any significant changes in their symptoms.
- people with a family history of CF
- siblings, half-siblings, and first cousins of someone with CF
- people planning to become pregnant
CF is a genetic disorder linked to a mutation in the CFTR gene. This creates irregular proteins that cause mucus to become unusually thick and sticky.
CF primarily affects the lungs, though it can also affect the digestive system and other parts of the body.
Although there is no cure, treatments can help clear the mucus from the airways, aid digestion, and reduce the risk of complications. Continual advances in treatment improve life expectancy and the quality of life for people with CF. It is crucial to receive appropriate treatment as soon as possible.