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Trending Topics in Gastroenterology

Explore current gastroenterology questions, clinical answers, and emerging research by topic.

81

Efficacy of TDF, TAF, TMF, and TDF-to-TAF switch in chronic hepatitis B:

The efficacy of TDF, TAF, TMF, and the TDF-to-TAF switch in treating chronic hepatitis B (CHB) has been extensively studied to identify the most effective regimen for individualized...

82

Gut mycobiome

The gut mycobiome refers to the fungal community residing within the human gastrointestinal system. While the gut microbiome (bacteria) has been extensively studied, the mycobiome remains underexplored, despite...

83

The prognostic value of the direct bilirubin to albumin ratio

The direct bilirubin-to-albumin ratio (DBAR) has emerged as a reliable prognostic marker for assessing 28-day mortality in critically ill patients with cirrhosis, as demonstrated by a study utilizing...

84

Immune Dysfunction and Infection Risk in Advanced Liver Disease

Immune dysfunction and infection risk are critical and interlinked concerns in patients with advanced liver disease, including cirrhosis and acute-on-chronic liver failure (ACLF). The immune system undergoes profound...

85

PPAR Vs UDCA in PBC

Primary biliary cholangitis (PBC) is a chronic autoimmune liver disease characterized by progressive destruction of bile ducts, leading to cholestasis and liver damage. Ursodeoxycholic acid (UDCA) is the...

86

Bezafibrate, PBC and Transplant-free survival

Bezafibrate has emerged as a significant therapeutic agent for improving transplant-free survival in patients with primary biliary cholangitis (PBC) when used in combination with ursodeoxycholic acid (UDCA). PBC...

87

Fibrates for Itch (FITCH) in Fibrosing Cholangiopathies

The FITCH trial investigated the efficacy of bezafibrate, a broad peroxisome proliferator-activated receptor (PPAR) agonist, in alleviating moderate to severe pruritus in patients with fibrosing cholangiopathies, including primary...

88

RESPONSE Trial and PBC

The RESPONSE trial was a pivotal phase 3 study designed to evaluate the efficacy and safety of seladelpar, a selective peroxisome proliferator–activated receptor delta (PPARδ) agonist, in patients...

89

ELATIVE and PBC

The ELATIVE trial was a clinical study designed to evaluate the efficacy and safety of elafibranor, a dual PPAR-α/δ agonist, as a potential second-line treatment for primary biliary...

90

POISE Study

The POISE study is a phase 3 clinical trial designed to evaluate the efficacy and safety of obeticholic acid (OCA), a farnesoid X receptor (FXR) agonist, in patients...

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