Routine indexes for cirrhosis and significant fibrosis detection in patients with compensated chronic hepatitis B

Zhi-Qiao Zhang1, Li-Wen Huang2, Yong-Peng Chen2

  • 1State Key Laboratory of Organ Failure Research, Guangdong Provincial Key Laboratory of Viral Hepatitis Research, Department of Infectious Disease & Hepatology Unit, Nanfang Hospital, Southern Medical University, Guangzhou, China; Department of Infectious Diseases, Shunde Hospital, Southern Medical University, Shunde, Guangdong, China; Department of Internal Medicine, Chencun Hospital Affiliated to Shunde Hospital, Southern Medical University, Shunde, Guangdong, China.

Insights

New HeBCI and HeBFI indexes accurately detect liver fibrosis and cirrhosis in chronic hepatitis B patients. These cost-effective tools can reduce liver biopsy needs in resource-limited settings.

Area of Science:

  • Hepatology
  • Biomarker Discovery
  • Diagnostic Accuracy

Background:

  • Existing fibrosis indices like FIB-4 and APRI have limited validation in chronic hepatitis B (CHB).
  • Accurate non-invasive assessment of liver fibrosis is crucial for CHB management.
  • There is a need for validated, cost-effective tools for fibrosis staging in CHB.

Purpose of the Study:

  • To validate existing fibrosis indices (FIB-4, APRI) in CHB patients.
  • To develop and validate novel, accurate non-invasive biomarkers for liver fibrosis and cirrhosis in CHB.
  • To assess the clinical utility of new indices in resource-limited settings.

Main Methods:

  • Analysis of 1438 treatment-naïve CHB patients.
  • Development of two novel non-invasive indices: HeBCI for cirrhosis and HeBFI for significant fibrosis.
  • Validation of index performance using Area Under the Receiver Operating Characteristic Curves (AUROCs) and accuracy metrics.

Main Results:

  • HeBCI demonstrated superior AUROCs (0.841 model, 0.779 validation) for cirrhosis detection compared to FIB-4 and APRI.
  • HeBFI showed higher AUROCs (0.781 model, 0.776 validation) for significant fibrosis detection than FIB-4 and APRI.
  • HeBCI achieved 86% accuracy for cirrhosis, and HeBFI achieved 76.6% accuracy for significant fibrosis.

Conclusions:

  • The novel HeBCI and HeBFI indices show high accuracy in detecting cirrhosis and significant fibrosis in CHB patients.
  • These indices are economical and convenient, suitable for outpatient use.
  • HeBCI and HeBFI can significantly reduce the reliance on liver biopsy, particularly in resource-limited healthcare settings.
Abstract

Related Concept Videos

Dosage Compensation02:50

Dosage Compensation

In animals, gender is determined by the number and type of sex chromosome. For example, human females have two X chromosomes, and males have one X and one Y chromosome, whereas C.elegans with one X chromosome is a male, and the one with two X chromosomes is a hermaphrodite.
In addition to sexual development, the X chromosome has genes involved in autosomal functions such as brain development and the immune system. Therefore, males and females with  distinct numbers of X chromosomes will...
7.5K
Compensation Mechanisms01:28

Compensation Mechanisms

The human body employs intricate mechanisms to counteract changes in blood pH, preventing conditions like acidosis (pH < 7.35) and alkalosis (pH > 7.45). These compensatory responses aim to restore normal arterial blood pH by engaging respiratory or renal systems, depending on the source of the imbalance.
Respiratory Compensation
This mechanism addresses metabolic-induced pH imbalances by adjusting breathing rates. Respiratory compensation begins within minutes of detecting a pH...
2.1K
Cystic Fibrosis: Pathogenesis01:23

Cystic Fibrosis: Pathogenesis

Cystic fibrosis (CF), an autosomal recessive disorder, significantly affects the function of exocrine glands. This genetically inherited disease is characterized by the production of thick and sticky mucus, which can severely affect various organs and systems in the body.
CF is primarily caused by a genetic mutation in a chromosome 7 gene coding for the cystic fibrosis transmembrane conductance regulator (CFTR) protein. The most common gene mutation leading to CF is the ΔF508 mutation,...
888
Effect of Hepatic Disease on Pharmacokinetics: Dose Adjustments Due to Hepatic Impairment01:08

Effect of Hepatic Disease on Pharmacokinetics: Dose Adjustments Due to Hepatic Impairment

Hepatic impairment, characterized by decreased liver function, does not uniformly mandate adjustments in drug dosage. Whether dosage modifications are necessary depends on various factors related to the drug's metabolism and elimination pathways. If a drug is primarily excreted via the kidneys and bypasses significant hepatic processing, if it undergoes minimal metabolic transformation in the liver, or if it is volatile and primarily expelled through the lungs, dose adjustments may not be...
281
Hepatic Portal System01:21

Hepatic Portal System

The hepatic portal system, a critical part of our circulatory framework, transports nutrient-laden, deoxygenated blood from the gastrointestinal tract and spleen to the liver. This ingenious system plays an indispensable role in maintaining our body's metabolic equilibrium.
At its core, the hepatic portal vein is the result of a confluence of the superior and inferior mesenteric veins along with the splenic vein. Each of these veins has a unique role. The superior mesenteric vein is...
6.0K
Cystic Fibrosis: Management01:24

Cystic Fibrosis: Management

Cystic fibrosis (CF) is an autosomal recessive disorder that predominantly affects individuals of Northern European descent, occurring at a rate of 1 in 3500. It is caused by a genetic mutation in a gene on chromosome 7, most commonly the ΔF508 mutation, that codes for the cystic fibrosis transmembrane conductance regulator (CFTR) protein. This results in thicker mucus secretions and obstruction pathologies in multiple organs, including the lungs and sinuses.
Sinus disease and chronic...
545