Understanding Inflammation and Your Immune System
Inflammation is a natural and healthy part of the body's immune response, typically triggered by injury, infection, or stress. However, when this response becomes chronic, it can be a root cause of serious conditions such as heart disease, cancer, and diabetes. Many factors influence chronic inflammation, from diet to stress levels. A growing body of research explores how fasting can help regulate the immune system and reduce chronic inflammatory markers, but the effects are highly dependent on the fasting duration and protocol.
The Anti-Inflammatory Mechanisms of Fasting
Fasting works on inflammation through several key biological pathways:
- Cellular Repair (Autophagy): Fasting gives the body a break from constant digestion, redirecting energy to cellular repair and detoxification processes. During autophagy, the body clears out damaged cells and malfunctioning components, which helps reduce the inflammatory burden. Animal studies suggest autophagy can be triggered in as little as 24-48 hours.
- Arachidonic Acid Production: A 2024 study found that fasting increases levels of arachidonic acid, a chemical that inhibits the NLRP3 inflammasome, a key driver of inflammation. This mechanism provides a clear link between fasting and reduced inflammation.
- Oxidative Stress Reduction: Fasting has been shown to enhance the body's resistance to oxidative stress, which contributes to aging and many chronic diseases.
Intermittent Fasting (IF) for Chronic Inflammation
Intermittent fasting involves cycling between periods of eating and fasting, without calorie restriction on eating days. Research consistently shows benefits for inflammation from these shorter, more frequent fasting periods.
- Time-Restricted Eating (TRE): Limiting daily eating to a specific window, such as 16 hours of fasting and an 8-hour eating window (16:8), has been shown to reduce inflammatory markers. One review of 18 studies found that intermittent fasting could significantly reduce C-reactive protein (CRP), a common marker for inflammation.
- Consistent Practice is Key: Studies on patients with inflammatory bowel disease found significant reductions in inflammation markers after eight weeks of practicing intermittent fasting (10-hour eating, 14-hour fasting). Similarly, a 30-day dawn-to-dusk intermittent fasting period (Ramadan) showed decreased TNF-α and increased adiponectin levels in overweight and obese individuals.
Prolonged Fasting: Benefits and Risks
Prolonged fasting, defined as abstaining from food for more than 24 hours, can be more complex. While some studies suggest benefits, others reveal significant risks, highlighting the importance of medical supervision.
- Potential Benefits of Shorter Prolonged Fasts (up to 48 hours): A 48-hour fast is a common prolonged fasting duration. It can induce a deeper state of autophagy and may offer metabolic benefits. A 2019 study showed an increase in metabolites linked to health benefits after 58 hours of fasting. However, a 2025 review of prolonged fasting suggests a need for caution.
- Increased Risks of Longer Fasts (48+ hours): A 2025 review in Ageing Research Reviews found that fasting for 48 hours or more might actually increase inflammatory markers in some individuals. Long-term water fasting carries significant risks, including electrolyte imbalances, dehydration, muscle breakdown, and the potentially fatal refeeding syndrome. Unsupervised prolonged fasts are not recommended.
Key Fasting Types and Their Anti-Inflammatory Potential
- 16:8 Intermittent Fasting: Daily 16-hour fasts have been linked to reduced inflammatory markers like C-reactive protein (CRP) when practiced consistently over weeks.
- 24-Hour Fast (e.g., OMAD): A single 24-hour fast has shown a drop in monocytes and an increase in anti-inflammatory chemicals.
- 30-Day Intermittent Fasting (Ramadan-style): Practicing dawn-to-dusk fasting for about a month has resulted in significant decreases in TNF-α and other inflammation markers.
- 48-Hour Fast: Research shows mixed results regarding inflammation, with some studies indicating potential benefits and others warning of increased inflammatory markers. Caution and supervision are advised.
- Extended Water-Only Fasting (5+ days): This extreme form of fasting can increase risks and may even raise certain inflammatory markers if unsupervised, potentially damaging health.
Comparison of Fasting Durations and Inflammation
| Feature | Intermittent Fasting (e.g., 16/8) | Prolonged Fasting (e.g., 48+ hours) | 
|---|---|---|
| Typical Duration | 12–24 hours daily/weekly | 48+ hours (less frequent) | 
| Inflammation Impact | Generally decreases markers like CRP, monocytes, and TNF-α over time. | Varied effects; some studies indicate increases in markers, especially after 48 hours. | 
| Key Mechanisms | Supports cellular repair (autophagy) and can reduce oxidative stress over time. | Can trigger deeper autophagy and metabolic shifts, but also carries a higher risk profile. | 
| Safety Profile | Generally considered safer for most healthy adults; fewer side effects. | Higher risk of side effects (fatigue, dehydration, electrolyte imbalance) and requires medical supervision. | 
Conclusion
There is no single answer to how many days of fasting to get rid of inflammation, as the optimal duration is a highly individual matter influenced by the specific fasting protocol and a person's overall health. While intermittent fasting protocols, ranging from 12 to 24 hours, have a strong and growing body of evidence supporting their anti-inflammatory benefits, longer fasts carry increased risks and show conflicting results in research. For most people, consistently practicing a mild to moderate intermittent fasting schedule, combined with a healthy diet and lifestyle, is a safer and more sustainable approach to reduce chronic inflammation. If considering any prolonged fasts, it is crucial to consult a healthcare professional. For those interested in evidence-based research on the topic, a case study on intermittent fasting and inflammatory response is available from the National Institutes of Health.