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Last updated: 2026-08-10 · automatically checked, spot-checked

# Nutrition in pulmonary fibrosis (IPF)

Nutritional status and outcomes

In pulmonary fibrosis, nutritional status is an important point of attention. Research has shown that malnutrition (undernutrition) and low protein intake are associated with worse clinical outcomes and shorter survival.

ProveniIncluded in official guidelines, or approved by EMA or FDA
Poor nutritional status, measured using indices such as weight loss, low albumin levels, and low protein intake, is associated with worse survival and more complications in IPF patients.

This means that regular attention to adequate calorie and protein intake is considered important. Being underweight and loss of muscle mass are risk factors that can be medically monitored. Many centres therefore use dietitians to map weight and nutritional patterns.

Healthy eating patterns and disease progression

Recent observations suggest that following healthy dietary guidelines (the so-called "Life's Essential 8", a comprehensive health pattern) is associated with a more favourable course of lung disease, including fibrotic conditions.

ResearchediPositive results in clinical studies, not yet standard treatment
Healthy overall dietary habits (adequate vegetables, fruit, whole grains, healthy fats, limited red meat and sugar) are associated with slower disease progression and better functioning in chronic lung diseases.

This is not a proven treatment, but suggests that overall nutritional quality may play a role in how quickly the disease progresses. This supports the use of a healthy dietary pattern, but more as part of overall health than as a medicine against fibrosis itself.

Nutrition and side effects of treatment

Pirfenidone is a commonly prescribed medication for IPF. This drug can cause gastrointestinal disorders, especially nausea and reduced appetite.

ProveniIncluded in official guidelines, or approved by EMA or FDA
Olive oil appears to reduce gastrointestinal side effects of pirfenidone in some patients, although this effect does not occur in everyone.

This is not a reason to see olive oil as a "treatment", but can be a way for some patients to make eating more pleasant during pirfenidone therapy. These kinds of practical adjustments are usually discussed with your healthcare provider or dietitian, as the effect varies from person to person.

Micronutrients and inflammatory markers

Some recent studies look at the role of certain nutrients (vitamins, minerals, enzymes) in the inflammation and damage process of pulmonary fibrosis, for example the NAMPT/SIRT7 pathway involved in cell repair.

ExperimentaliOngoing in study setting, outcome still unknown
Certain micronutrients and enzymatic processes involved in cell renewal and antioxidant action are being investigated as potential starting points, but do not yet constitute a standardised nutritional intervention.

This means that research is ongoing, but it is still far too early to make claims about nutritional supplements with specific substances. Many of these are promoted online, but have no proven value in IPF. Discuss this with your healthcare provider or dietitian before adding anything yourself.

Nutrition and weight management

Weight loss is a common problem in progressive IPF. This may be due to reduced appetite (due to shortness of breath, fatigue or medication side effects), increased energy needs, or simply difficulty eating.

Maintaining healthy weight and muscle mass is important for strength, physical activity, and overall functioning. Dietitians can help with practical tips: smaller, calorie-enriched meals; food that is easier to eat; adjusted meal times around medications or oxygen use.

ProveniIncluded in official guidelines, or approved by EMA or FDA
Adequate calorie and protein intake helps prevent weight loss and muscle breakdown and contributes to better functioning.

Individual nutritional advice and guidance are therefore a standard part of multidisciplinary care for IPF.

Fluid intake and lung protection

With lung diseases, it is sometimes recommended to drink sufficient fluids to keep mucus thinner. With IPF, the role of fluid intake is less central than with other lung diseases, but adequate hydration remains important for overall health.

UnproveniNo scientific evidence that it works
Specific fluid protocols to prevent or slow down fibrosis in IPF have not been established.

Healthy drinking is simply part of daily life, but does not constitute targeted treatment against fibrosis itself.

Nutrition and medication interactions

Many medications used for IPF have no serious food interactions, but some can cause sensitivity to certain substances or work better with or without food.

ProveniIncluded in official guidelines, or approved by EMA or FDA
Some antiretroviral and immunosuppressive agents can have food interactions; this should be discussed individually with your pharmacist or doctor.

Standard advice (for example, taking pirfenidone with food, or delaying certain supplements) is medication-specific and belongs in a conversation with your own team.

Nutrition and inflammatory markers

Recent research looks at nutritional indices and inflammation markers (such as C-reactive protein and albumin levels) as possible predictors of disease progression.

ResearchediPositive results in clinical studies, not yet standard treatment
The relationship between nutritional status, inflammation markers and outcomes in IPF is being actively researched, but does not yet lead to standard nutritional interventions.

This research helps doctors better understand who is at risk, but does not immediately translate into standardised diets or supplement schedules.

Practical starting points

In practice, many IPF patients see a dietitian or nutrition specialist as part of their care team. Together you can look at:

- Maintaining healthy weight and muscle mass
- Nutrition that matches your energy and chewing level
- Managing medication side effects (nausea, reduced appetite)
- Healthy food choices that suit your preference and cultural background
- Any nutritional supplements (always ask your team first)

ProveniIncluded in official guidelines, or approved by EMA or FDA
Regular nutritional monitoring and guidance by a dietitian improves nutritional status and is recommended as part of multidisciplinary care.

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_This information never replaces a doctor's judgment. Always discuss your situation with your own healthcare provider._

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Sources used

Above each source is stated in one sentence what the research is about, so you don't have to rely on an English technical title. More studies on Idiopathic Pulmonary Fibrosis (IPF) can be found at publications and studies.

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codex.care does not provide medical advice. Always discuss symptoms, medication, and treatment choices with your own healthcare provider.