# Clinical characteristics and prognosis of patients with HBV-ACLF versus ALD-ACLF: a retrospective comparative study

**Authors:** Qiuyan Yao, Bohua Tang, Xiaoling Huang, Min Xiao

PMC · DOI: 10.3389/fmed.2026.1565646 · Frontiers in Medicine · 2026-02-05

## TL;DR

This study compares the clinical features and outcomes of patients with two types of liver failure caused by hepatitis B and alcohol, finding similar prognoses but different risk factors.

## Contribution

The study identifies distinct risk factors for 90-day mortality in HBV-ACLF and ALD-ACLF patients, offering insights into their clinical management.

## Key findings

- ALD-ACLF patients had higher WBC, N, and M levels but lower ALT, AST, ALB, K, and Na compared to HBV-ACLF patients.
- TBIL and PT were independent mortality risk factors in HBV-ACLF, while WBC, TBIL, and PT were linked to mortality in ALD-ACLF.
- No significant differences in overall prognosis were observed between the two groups.

## Abstract

This study aims to investigate the differences in clinical characteristics and prognosis between patients with HBV-ACLF (Hepatitis B Virus-related Acute-on-Chronic Liver Failure) and those with ALD-ACLF (Alcohol-Associated Acute-on-Chronic Liver Failure), and to identify risk factors associated with 90-day mortality in both cohorts.

This study enrolled 56 patients with HBV-ACLF and 83 patients with ALD-ACLF to compare their clinical characteristics and conduct analyses of risk factors associated with 90-day prognosis.

Compared with the HBV-ACLF cohort, the ALD-ACLF group exhibited a higher proportion of male patients and a greater prevalence of ascites. Additionally, significant differences were observed in laboratory parameters, with ALD-ACLF patients showing higher levels of WBC (white blood cells), N (neutrophils), and M (monocytes) but lower levels of ALT (alanine aminotransferase), AST (aspartate aminotransferase), ALB (albumin), K (potassium), and Na (sodium) compared to HBV-ACLF patients (p < 0.05). In terms of prognostic factors, TBIL (total bilirubin) and PT (prothrombin time) were identified as independent risk factors for 90-day mortality in HBV-ACLF patients, while WBC, TBIL, and PT were associated with 90-day mortality in ALD-ACLF patients.

Patients with ALD-ACLF typically present with a higher prevalence of comorbidities, such as ascites and infections, compared to those with HBV-ACLF. However, no significant differences in prognosis were observed between the two cohorts. For HBV-ACLF patients, elevated TBIL and prolonged PT were identified as independent risk factors for 90-day mortality. In contrast, in addition to TBIL and PT, elevated white WBC was also associated with 90-day mortality in ALD-ACLF patients. These findings warrant further validation through multicenter studies with larger sample sizes.

## Linked entities

- **Chemicals:** ALT (PubChem CID 10219674), PT (PubChem CID 23939), N (PubChem CID 223), K (PubChem CID 813), Na (PubChem CID 923)

## Full-text entities

- **Genes:** GGTLC5P (gamma-glutamyltransferase light chain 5 pseudogene) [NCBI Gene 653590] {aka GGT}, LOC102724197 (inactive glutathione hydrolase 2) [NCBI Gene 102724197] {aka GGT2}, GPT (glutamic--pyruvic transaminase) [NCBI Gene 2875] {aka AAT1, ALT, ALT1, GPT1, SGPT}, ALB (albumin) [NCBI Gene 213] {aka FDAHT, HSA, PRO0883, PRO0903, PRO1341}, SLC17A5 (solute carrier family 17 member 5) [NCBI Gene 26503] {aka AST, ISSD, NSD, SD, SIALIN, SIASD}
- **Diseases:** malignancies (MESH:D009369), SIRS (MESH:D018746), TBIL (MESH:D007647), atrophy (MESH:D001284), HBV (MESH:D006509), liver cirrhosis (MESH:D008103), hepatorenal syndrome (MESH:D006530), Cirrhosis (MESH:D005355), gut injury   inflammation (MESH:D007249), chronic liver disease (MESH:D008107), mitochondrial dysfunction (MESH:D028361), alcohol (MESH:D000437), cirrhotic (MESH:D000094724), cor pulmonale (MESH:D011660), hereditary metabolic liver disease (MESH:D030342), bleeding (MESH:D006470), esophageal or gastric varices (MESH:D004932), hypoalbuminemia (MESH:D034141), jaundice (MESH:D007565), alcoholic hepatitis (MESH:D006519), chronic renal failure (MESH:D007676), immune dysfunction (MESH:D007154), thrombocytopenia (MESH:D013921), coagulopathy (MESH:D001778), infected (MESH:D007239), coagulation factor deficiency (MESH:D020147), deterioration of liver function (MESH:D017114), toxicity (MESH:D064420), End-Stage Liver Disease (MESH:D058625), ALD-ACLF (MESH:D065290), hepatitis C virus infection (MESH:D006526), portal hypertension (MESH:D006975), Chronic infection (MESH:D000088562), ascites (MESH:D001201), ALD (MESH:D000326), hepatomegaly (MESH:D006529), necrosis (MESH:D009336), hepatocellular carcinoma (MESH:D006528), PT (MESH:D007020), autoimmune hepatitis (MESH:D019693), gastrointestinal bleeding (MESH:D006471), organ diseases (MESH:D000092124), heart failure (MESH:D006333), bacterial (MESH:D001424), ALD (MESH:D008108), lymphoma (MESH:D008223), hepatic encephalopathy (MESH:D006501), Liver Failure (MESH:D017093), Chronic Hepatitis B (MESH:D019694), hepatic injury (MESH:D056486)
- **Chemicals:** N (MESH:D009584), bilirubin (MESH:D001663), ethanol (MESH:D000431), CRRT (-), Na (MESH:D012964), K (MESH:D011188), Alcohol (MESH:D000438), ROS (MESH:D017382), pyridoxal (MESH:D011730)
- **Species:** Hepatitis B virus (no rank) [taxon 10407], Homo sapiens (human, species) [taxon 9606]

## Full text

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## Figures

8 figures with captions in the complete paper: https://tomesphere.com/paper/PMC12916582/full.md

## References

32 references — full list in the complete paper: https://tomesphere.com/paper/PMC12916582/full.md

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Source: https://tomesphere.com/paper/PMC12916582