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Inflammation

Blood Testing for IBD

Blood testing helps track intestinal inflammation and systemic burden in IBD, guiding assessment of activity and complications. At Superpower, we measure CRP, ESR, Albumin, FAR, and CAR. We offer in-clinic and at-home blood testing; home IBD testing is currently available in selected states. See FAQs below for more information.

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What are IBD biomarkers

IBD biomarkers are measurable signals from your immune system and gut that reveal when and how much inflammation is present in Crohn’s disease or ulcerative colitis. They translate invisible intestinal activity into objective information your care team can track, reducing guesswork and complementing symptoms and scans. Blood tests reflect whole-body inflammation and its ripple effects: a liver-made alarm protein (C-reactive protein), the rate red cells settle when inflammation is active (erythrocyte sedimentation rate), shifts in white cells and platelets (leukocytes, thrombocytes), anemia and iron status (hemoglobin, ferritin), and nutrition status (albumin). Stool testing adds a gut-specific readout from neutrophils at the bowel wall (fecal calprotectin). Together, these markers help distinguish IBD from look-alike conditions, gauge disease activity, anticipate flares, guide treatment choice and dosing, and monitor healing—often reducing the need for urgent endoscopy. Biologically, they arise from three places: liver acute-phase responses, immune-cell products, and proteins leaking from an injured intestinal barrier. Watching their patterns over time shows whether inflammation is quieting or smoldering, enabling timely, targeted care that protects the bowel.

Why is blood testing for IBD important?

  • Gauge gut inflammation and overall disease activity in IBD without invasive testing.
  • Spot active flares early by rising CRP, ESR, CAR, and FAR levels.
  • Clarify symptom cause by distinguishing inflammation from irritable bowel or noninflammatory pain.
  • Guide treatment intensity by flagging higher CAR/FAR and low albumin as severity signals.
  • Track response to therapy by following CRP, ESR, and albumin over time.
  • Flag complications risk by low albumin suggesting malnutrition or protein loss from the gut.
  • Protect fertility and pregnancy by keeping inflammation controlled and nutrition adequate.
  • Best interpreted with fecal calprotectin, hemoglobin, and your symptoms for context.

What insights will I get?

Inflammatory Bowel Disease (IBD) blood testing provides a window into how inflammation is affecting your body’s core systems—immunity, metabolism, nutrient absorption, and even energy production. Chronic inflammation in IBD can disrupt these interconnected processes, impacting everything from cardiovascular health to cognitive function. At Superpower, we measure five key biomarkers: C-reactive protein (CRP), erythrocyte sedimentation rate (ESR), albumin, fibrinogen-to-albumin ratio (FAR), and CRP-to-albumin ratio (CAR).

CRP and ESR are markers of systemic inflammation. CRP rises quickly in response to inflammation, while ESR reflects more gradual changes. Both are commonly elevated during IBD flares, signaling active immune system engagement. Albumin is a major blood protein produced by the liver; low levels can indicate inflammation, poor nutrition, or protein loss through the gut, all of which are concerns in IBD. FAR and CAR are calculated ratios that combine these markers, offering a more nuanced view of inflammation and protein status.

When these biomarkers are within healthy ranges, it suggests that inflammation is controlled, the immune system is stable, and the body’s protein reserves are adequate—key factors for maintaining gut integrity and overall resilience in IBD. Shifts outside the expected range can signal increased disease activity or complications, reflecting how well your body is coping with the demands of chronic inflammation.

Interpretation of these results depends on context. Factors like age, pregnancy, recent infections, other illnesses, medications, and even laboratory methods can influence these markers. Results should always be considered alongside your clinical history and symptoms.

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Frequently Asked Questions About

What is IBD blood testing?

It’s a blood check that tracks whole-body inflammation and protein status to understand IBD activity. Superpower tests your blood for CRP, ESR, Albumin, and the inflammation-to-protein ratios CAR (CRP/Albumin) and FAR (Fibrinogen/Albumin). CRP rises quickly with active inflammation (acute-phase response). ESR changes more slowly and reflects red cell settling in inflammatory states. Albumin often falls when inflammation is persistent or when there’s protein loss or poor intake. CAR and FAR integrate inflammatory burden against protein reserves, sharpening the picture of disease activity.

Why should I get IBD blood testing?

It quantifies inflammatory burden and protein status so you can track disease activity, gauge flare severity, and monitor response to therapy. CRP and ESR capture systemic inflammation; Albumin reflects the body’s protein reserve and negative acute-phase response; CAR and FAR combine these signals to improve risk assessment. Together, these markers help distinguish active inflammation from remission, flag complications, and complement stool tests and imaging without replacing endoscopy when needed.

Can I get a blood test at home?

Yes. With Superpower, our team member can organize a professional blood draw in your home. Your sample is collected by venipuncture, processed by accredited labs, and your CRP, ESR, Albumin, CAR, and FAR results are reported to your dashboard. It’s convenient, controlled, and designed to minimize delays between collection and analysis.

How often should I test?

Testing frequency tracks disease dynamics. During a flare, right after diagnosis, or when treatments change, testing is typically more frequent to confirm trend direction and treatment effect. In stable remission, periodic surveillance is common to confirm low inflammatory burden and adequate protein status. Trends over time are more informative than any single result, and timing should align with your clinician’s monitoring plan.

What can affect biomarker levels?

Any acute inflammation can raise CRP, ESR, CAR, and FAR, including infections, injuries, or recent surgery. Anemia, pregnancy, and age can elevate ESR independently. Albumin can fall with inflammation, liver disease, kidney protein loss, or dilution from overhydration; it can appear higher with dehydration. Obesity and smoking can raise CRP. Corticosteroids and biologics can suppress inflammatory markers even when symptoms are present.

Are there any preparations needed before the blood test for CRP, ESR, Albumin, FAR, CAR?

No special preparation is required. These are non-fasting tests. Aim for your usual routine so results reflect your baseline physiology. Stay normally hydrated. Do not stop prescribed medicines unless your clinician has told you to. If you recently had an infection, surgery, or intense exercise, tell your care team because those can shift inflammatory markers.

Can lifestyle changes affect my biomarker levels?

Yes, but disease activity is the dominant driver in IBD. Systemic inflammation (CRP, ESR, CAR, FAR) can be influenced by body weight, smoking exposure, sleep, and intercurrent infections. Albumin reflects nutritional status, inflammation, and fluid balance. While healthier patterns can lower background inflammation over time, interpretation should center on IBD activity and clinical context rather than single behaviors.

How do I interpret my results?

Higher CRP and ESR indicate more systemic inflammation; higher CAR and FAR signal a heavier inflammatory load relative to protein reserves. Lower Albumin suggests a negative acute-phase response, protein loss, or reduced synthesis. Normal values reduce the likelihood of active systemic inflammation but don’t fully exclude localized gut inflammation. Compare with prior results to see trend direction, and interpret alongside symptoms, fecal calprotectin, imaging, and endoscopy when indicated.

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UCLA Medical Professor, NYT Bestselling Author

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