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Elevated hs-CRP associates with airflow limitation and PRISm in 335 adult liver transplant recipientsHigh blood inflammation markers raise risk of poor lung health in liver transplant patients

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Key Takeaway
Note that elevated hs-CRP associates with worse lung function in liver transplant recipients.

The Danish Comorbidity in Liver Transplant Recipients (DACOLT) study included 335 adult liver transplant recipients. The primary exposure was elevated inflammatory markers, defined as hs-CRP >3 mg/L, compared to hs-CRP ≤3 mg/L. Outcomes included airflow limitation, PRISm, FEV1, and FVC. Follow-up duration was not reported.

Results indicated that elevated hs-CRP was associated with increased odds of PRISm (aOR 2.08; 95% CI: 1.1; 3.9, p=0.02) and lower FEV1 (-209 mL; 95% CI -340; -77 mL, p=0.02). The prevalence of airflow limitation was 11.6%, and the prevalence of PRISm was 24.5%. Median FEV1 was 2790 mL (IQR 2230–3505 mL) and median FVC was 3680 mL (IQR 2980–3755 mL).

Safety data, including adverse events, serious adverse events, discontinuations, and tolerability, were not reported. Results were adjusted for age and sex. A key limitation is that no studies have investigated this association in liver transplant recipients prior to this work. Because the study is observational, causality cannot be established, and clinical significance of these surrogate markers without clinical outcome correlation should not be assumed.

Imagine waking up and feeling like you cannot catch your breath. You take a deep breath, but it feels shallow. You walk up a small flight of stairs and feel tired. For many people who have had a liver transplant, this struggle with breathing is a quiet but serious problem.

Doctors know that the liver and lungs often work together. When one organ is sick, the other can suffer too. But until now, no one had looked closely at how blood inflammation affects the lungs in these specific patients.

The Hidden Lung Problem

Liver disease is common. Many people with advanced liver problems need a new liver to survive. Once they get the transplant, their lives improve. But the journey does not end there.

About one-quarter of these patients have a condition called PRISm. This means their lungs do not work as well as they should. Another 11 percent have airflow limitation, which makes it hard to move air in and out.

Doctors usually check for these issues. But they often miss the real cause. They look at the liver, but they ignore a hidden signal in the blood. That signal is inflammation.

Why Inflammation Matters Now

Inflammation is the body's way of fighting infection or injury. Think of it like a fire alarm going off inside your body. When the alarm sounds, immune cells rush to the scene. This is good when you have a cut or a bug.

But sometimes, the alarm stays on. The fire never goes out. This is called chronic inflammation. In the general population, high levels of this inflammation are linked to poor lung function.

But liver transplant patients are different. They are on powerful medicines to stop their body from rejecting the new organ. These medicines also calm the immune system. Doctors assumed that inflammation would be low in these patients. They were wrong.

A Switch That Burns Fat

To understand this better, imagine a factory. The factory makes energy for your body. Inflammation is like a traffic jam on the factory floor. Trucks carrying energy get stuck. They cannot reach the places that need them.

In the lungs, this traffic jam blocks the airways. The muscles that help you breathe get weaker. The air sacs that fill with oxygen do not work right.

The study looked at specific markers in the blood. One marker is high-sensitivity C-reactive protein, or hs-CRP. This is a standard test for inflammation. When this number was high, the lungs struggled more.

Another marker, interleukin-6, also played a role. This protein tells immune cells to fight. When it stays high, the lungs stay in a state of stress. It is like a switch that is stuck in the "on" position.

Researchers looked at 335 patients from a nationwide study. They checked their lung function using a simple breathing test. They also tested their blood for inflammation markers.

They found a clear link. Patients with high hs-CRP levels were twice as likely to have reduced lung function. Their breathing capacity was lower than expected.

This was not just a coincidence. The link held up even when doctors accounted for age and sex. Older patients and women often have different lung sizes, but the inflammation link remained strong.

But There's A Catch

This doesn't mean this treatment is available yet.

The study is important because it changes how doctors think. For years, they treated the liver and ignored the lungs. Now, they know to check the blood for inflammation. If the numbers are high, they can start early treatment.

Early treatment might prevent the lungs from getting worse. It could also help patients feel better sooner. But the study has limits. It was done in Denmark. The results might be different in other countries.

Also, the study looked at adults only. Children who get transplants might have different needs. The medicines they take are also different. More research is needed to see if this applies to everyone.

What Happens Next

Doctors will use this new information to guide their care. They will start checking inflammation levels more often. If a patient has high markers, they might get extra support for their lungs.

This could change the standard of care. It could mean better breathing for thousands of patients. It could also mean fewer hospital visits for shortness of breath.

The road ahead is clear. Researchers will look at how to lower inflammation safely. They will test new drugs that calm the immune system without hurting the liver.

For now, the message is simple. If you have had a liver transplant, talk to your doctor about your breathing. Ask if your blood work includes inflammation markers. Your lungs matter just as much as your liver.

Study Details

Study typeCohort
EvidenceLevel 3
PublishedApr 2026
View Original Abstract ↓
IntroductionIn the general population elevated circulating inflammatory markers have been associated with impaired lung function in cross-sectional and longitudinal studies. No studies have investigated this association in liver transplant recipients, and we aimed to investigate if elevated inflammatory markers were associated with impaired lung function in this population.MethodsAdult liver transplant recipients from The Danish Comorbidity in Liver Transplant Recipients (DACOLT) study, with available spirometry, high sensitivity (hs)-CRP, interleukin (IL)-1β, IL-2, IL-6, IL-10, interferon (IFN)-γ, and tumor necrosis factor (TNF)-α were included. Outcomes were forced expiratory volume in one second (FEV1), forced vital capacity (FVC), airflow limitation, and preserved ratio impaired spirometry (PRISm).ResultsWe included 335 liver transplant recipients. The prevalence of airflow limitation and PRISm was 11.6% and 24.5%, respectively. The median FEV1 was 2790 mL (IQR 2230–3505 mL) and the median FVC was 3680 mL (IQR 2980–3755 mL). When adjusted for age and sex, hs-CRP >3 mg/L was associated with increased odds of PRISm (aOR 2.08, 95% CI: 1.1; 3.9, p=0.02), lower FEV1 (-209 mL 95% CI -340; -77 mL, p
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