Bay Biosciences provides high-quality, fresh frozen Bronchoalveolar Lavage (BAL) samples, with matched fresh frozen sera (serum), plasma, and peripheral blood mononuclear cells (PBMC) bio-fluids from patients diagnosed with idiopathic pulmonary fibrosis (IPF).

The sera (serum), plasma and PBMC bio-fluid specimens are processed from idiopathic pulmonary fibrosis (IPF) patient’s peripheral whole-blood using customized collection and processing protocols.

Fresh frozen biopsy tissue samples and matched bio-fluids are collected from unique patients diagnosed with idiopathic pulmonary fibrosis (IPF).

Idiopathic Pulmonary Fibrosis (IPF) Overview

Idiopathic pulmonary fibrosis (IPF) is a chronic and progressive lung condition. IPF causes scar tissue to build up in the lungs, leading to shortness of breath and a persistent cough.

According to the National Heart, Lung, and Blood Institute (NHLBI), IPF is a progressive condition with no known cure. However, treatment plans can help people manage the condition and improve their quality of life.

What is Idiopathic Pulmonary Fibrosis (IPF)?

Pulmonary fibrosis is a scarring of the lungs.

The NHLBI state that IPF occurs when the lung tissue that surrounds the air sacs thickens and becomes stiff, leading to permanent scarring of the lungs.

This scarring affects the function of the lungs, making it difficult to breathe.

In the past, other names for IPF included cryptogenic fibrosing alveolitis, idiopathic diffuse interstitial pulmonary fibrosis, and idiopathic fibrosing alveolitis, chronic form. Nowadays, doctors may refer to IPF as usual interstitial pneumonia.

According to the NHLBI, the symptoms of IPF develop gradually over time for some people but appear more quickly for others.

The symptoms of IPF include:

  • A dry cough that worsens and can involve bouts of uncontrollable coughing
  • Aching muscles and joints 
  • Clubbing, which is where the tips of the fingers or toes become wider and rounder
  • Fatigue
  • Feeling short of breath, which tends to occur when exercising but may worsen over time and cause people to feel out of breath when resting
  • Loss of appetite
  • Feeling unwell in general
  • Pain or tightness in the chest 
  • Unintentional weight loss over time


Types of Idiopathic Pulmonary Fibrosis (IPF)

According to the American Lung Foundation, there are more than 200 types of pulmonary fibrosis (PF), and the most common is IPF.

The Pulmonary Fibrosis Foundation state that there are five main categories for PF based on their causes:

  • Autoimmune PF: Due to autoimmune diseases, such as rheumatoid arthritis (RA) or Sjögren’s Syndrome.
  • Drug-induced PF: Due to the previous or current use of drugs that affect the lungs, such as chemotherapy, amiodarone (Pacerone), or nitrofurantoin (Macrobid). 
  • Environmental PF: Due to exposure from lung irritants, such as mold. 
  • Occupational PF: Due to exposure to dust or fumes, such as asbestos or silica.
  • Radiation-induced PF: Due to radiation treatment of the chest.

IPF differs from the other form of PF because it has no known cause.

Stages of Idiopathic Pulmonary Fibrosis (IPF)

The authors of a 2014 article state that there are no official stages of IPF but that doctors have traditionally loosely staged IPF using terms such as early or advanced, or mild, moderate, or severe.

Mild

At this stage of IPF, people may show mild symptoms of IPF and receive an initial diagnosis.

In some cases, though, people may not have any symptoms until the moderate stage of IPF.

Moderate

At this stage, there will be a large amount of scarring in the lungs, and people may need oxygen therapy.

Advanced

Symptoms are severe at this stage, and a lung transplant may be necessary.


Causes of Idiopathic Pulmonary Fibrosis (IPF)

The National Organization for Rare Disorders (NORD) suggest that most cases of IPF occur as a result of damage to the epithelial cells that line the alveoli and airways.

The NORD suggest that the body attempts to repair the damaged cells, but the response is abnormal, resulting in progressive damage and scarring to the lung tissue and alveoli.

However, researchers do not know why the initial damage that triggers the healing response occurs.

Although there is no known cause of IPF, according to the National Library of Medicine, researchers think that a mix of environmental, lifestyle, and genetic factors play a part in the disease.

The most significant risk factor appears to be a variation in the MUC5B gene, which results in high mucus production in the respiratory bronchioles.

Other risk factors for IPF include the following:

  • Age: Most people with IPF are over the age of 50 years. 
  • Being male: Approximately 75% of people with IPF are male.
  • Genetics: People with a family history of IPF have a higher risk of IPF, particularly if a first degree relative, such as a parent or sibling, has IPF. However, IPF can also occur sporadically.
  • Smoking cigarettes: About 75% of people with IPF are smokers or have previously been smokers.
  • Gastroesophageal reflux (GERD): Roughly 75% of people with IPF have acid reflux or heartburn symptoms.


Diagnosis of Idiopathic Pulmonary Fibrosis (IPF)

The Canadian Lung Association state that to diagnose IPF, a doctor will assess any symptoms, take a full medical history, and carry out a physical examination.

During the physical examination, they may check whether a person has:

  • Blue hands and feet
  • Clubbed toes or fingers
  • High pitched crackles coming from the lungs

A combination of tests may help a doctor confirm a diagnosis of IPF. These tests may include:

  • Breathing test: To check how well the lungs breathe air in and out and how well they oxygenate the blood.
  • Chest X-ray: To look for signs of disease and progression.
  • Blood tests: To identify other reasons for lung scarring.
  • Computerized tomography (CT) scan: To look for scarring in the lungs.
  • Lung biopsy: To confirm a diagnosis if this is not possible based on a CT scan.


Treatment of Idiopathic Pulmonary Fibrosis (IPF)

According to the NHLBI, although there is currently no cure for IPF, treatments may help slow the progression of IPF and improve quality of life.

The treatment options depend on the stage of IPF but may include:

  • Antacids: These help treat GERD if people also have this condition.
  • Kinase inhibitors: This type of medication can help slow down a loss of lung function and may prevent a sudden worsening of IPF.
  • Lung transplant: This surgery may be necessary for people with advanced IPF. 
  • Oxygen therapy: Initially, a person may need this therapy after exertion. In the later stages of IPF, they may need it continually.
  • Ventilator support: A person may need this support if their breathing problems become severe.

Other forms of treatment depend on the person’s symptoms. For example, if a person has developed a lung infection, they may require antibiotics. For a chronic cough, they may take oral codeine. Pulmonary rehabilitation may also be a part of their treatment plan.

Pulmonary rehabilitation is a program that may involve:

  • Breathing exercises
  • Counseling 
  • Education on IPF and how to manage the condition 
  • Nutritional advice
  • Physical activity to strengthen the body


Complications of Idiopathic Pulmonary Fibrosis (IPF)

Living with IPF may cause anxiety,  depression and stress. A doctor may recommend:

  • A patients support group
  • Cognitive behavioral therapy (CBT)
  • Medications, such as antidepressants

According to a 2018 article in the journal Medical Sciences, possible complications of IPF can include:

  • Difficulty sleeping
  • Lung cancer
  • Pulmonary hypertension, which is an increase of blood pressure in the blood vessels to the lungs
  • Respiratory failure, when the lungs cannot provide enough oxygen to the blood


Management of Idiopathic Pulmonary Fibrosis (IPF)

Keeping to a treatment plan can help people with IPF manage the condition and improve their quality of life.

Steps that people can take to manage IPF include:

  • Attending regular checkups 
  • Eating to support heart and lung health, such as eating smaller meals to reduce fullness, which may ease breathing 
  • Avoiding places or situations that may make breathing more difficult, such as being at high altitudes
  • Joining support groups, having counseling, and talking with family and friends can help people take care of their mental health 
  • Keeping track of symptoms and letting a healthcare professional know if they worsen 
  • Maintaining a moderate weight
  • Avoiding substances that can irritate the lungs, such as chemicals and dust
  • Refraining from smoking cigarettes and avoiding secondhand smoke
  • Staying physically active and keeping up regular, moderate exercise, such as walking or using an exercise bike


Summary

IPF is a type of pulmonary fibrosis with no known cause. Environmental, lifestyle, and genetic factors are all among the risk factors. 

If patients have any symptoms of IPF, they should see their doctor for a checkup and diagnosis.

Although there is no cure for IPF, people can work with a team of healthcare professionals to manage the condition and improve their quality of life.

Bay Biosciences is a global leader in providing researchers with high quality, clinical grade, fully characterized human tissue samples, bio-specimens, and human bio-fluid collections.

Samples available include cancer (tumor) tissue, cancer serum, cancer plasma, cancer, peripheral blood mononuclear cells (PBMC). and human tissue samples from most other therapeutic areas and diseases.

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This critical patient’s clinical data includes information relating to their past and current disease, treatment history, lifestyle choices, biomarkers, and genetic information.

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Including fresh frozen tissue samples, tumor tissue samples, formalin-fixed paraffin-embedded (FFPE), tissue slides, with matching human bio-fluids, whole blood and blood-derived products such as serum, plasma and PBMC.

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Bay Biosciences also provides human samples from normal healthy donors; volunteers, for controls and clinical research, contact us Now.

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