Introduction
The natural history of chronic liver disease is characterized by the progression to cirrhosis, first compensated, and then decompensated, which is associated with high mortality [
1]. Hepatic decompensation is defined as the development of ascites, variceal bleeding, or hepatic encephalopathy (HE) [
2]. Identification of predictors of decompensation among compensated patients is warranted because death in cirrhosis is clearly related to the development of decompensation. One of the main predictors of outcome is the stage of liver fibrosis in chronic liver disease [
3]. Liver biopsy remains the gold standard method for the assessment of liver fibrosis. However, the clinical application of liver biopsy is often limited by its invasiveness, high cost, sampling variability, interobserver variation, risk of complications, and poor patient compliance, particularly in the follow-up period [
4‐
6]. Therefore, it is desirable to develop and verify noninvasive and convenient markers to accurately evaluate liver fibrosis and inform the prognosis of liver disease.
Advances in serological and radiological tests such as serum markers, transient elastography, and their combination can achieve accurate evaluation of fibrosis and reduce the need for liver biopsy. Because hepatic fibrosis is characterized by the excessive deposition of extracellular matrix (ECM), serum markers representing ECM components are widely employed to assess the development of hepatic fibrosis [
7,
8]. Hyaluronic acid (HA), laminin (LN), collagen IV (CIV), and N-terminal propeptide of type III collagen (PIIINP) are four major serum markers for the non-invasive assessment of liver fibrosis. So far, numerous studies have shown their potential clinical value in the diagnosis of liver fibrosis and cirrhosis [
9‐
14]. Theoretically, the stage of liver fibrosis is positively correlated with the severity of liver dysfunction, which affects the survival conditions. Plevris N et al. [
15]reported that HA measurement can accurately and independently predict liver-related and all‐cause mortality in patients with liver disease. However, few studies have explored the clinical significance of HA, LN, CIV, and PIIINP in patients with liver cirrhosis. Moreover, it remains unclear whether these four serum liver fibrosis markers can predict the prognosis of patients with compensated liver cirrhosis.
Currently available survival scoring systems, such as the Child–Pugh score (CPS) and the model for end-stage liver disease (MELD) score, have been widely validated as accurate predictors of short or medium-term survival in patients with liver cirrhosis [
2]. However, their accuracy is limited in compensated cirrhosis and non‐cirrhotic liver disease because they depend on variables reflecting pathophysiological changes associated with advanced disease [
16]. Early identification of cirrhotic patients at risk for hepatic decompensation remains a major challenge. Thus, we assessed whether the HA, LN, CIV, and PIIINP levels are non-invasive predictors of hepatic decompensation in patients with compensated cirrhosis with varying etiologies.
Materials and methods
Study population
We conducted a retrospective cohort analysis of the electronic medical record database of all consecutive cases of patients diagnosed with compensated cirrhosis at the Department of Gastroenterology and Hepatology, Tianjin Second People’s Hospital, Tianjin, China, from December 2015 to December 2019. The diagnosis of cirrhosis was based on the typical imaging features, histological features, and/or presence of varices on endoscopy. Patients with previous liver decompensation (ascites, variceal bleed and HE), acute-on-chronic liver failure, or liver transplantation, patients with a known diagnosis of hepatocellular carcinoma, patients with severe extrahepatic diseases with poor short-term prognosis, or follow-up < 6 months were excluded from this study.
This study protocol was reviewed and approved by the Ethics Committee of Tianjin Second People’s Hospital, approval number [JINERRENMINLUNSHENZI (2021) NO.54], and conducted according to the principles of the Declaration of Helsinki. All patients signed a written informed consent document and gave permission for the clinical and laboratory data for study purposes.
Baseline evaluation
Patients’ demographic, clinical, and laboratory profiles at admission were recorded from the hospital electronic clinical records system. The following variables were confirmed: age, gender, etiology of liver cirrhosis, esophageal varices, received antiviral therapy, and laboratory data (alanine aminotransferase [ALT], aspartate aminotransferase [AST], alkaline phosphatase [ALP], gamma-glutamyl transpeptidase [GGT], albumin [ALB], total bilirubin [TBIL], serum creatinine [Cr], international normalised ratio [INR], and platelet count [PLT]). For all patients, blood samples were collected on the same day. Serum ALT, AST, ALP, GGT, ALB, TBIL and Cr were detected by a Hitachi 7180 Automatic Biochemical Analyser (Hitachi, Ltd, Tokyo, Japan). The MELD score, fibrosis-4 score (FIB-4) index, and AST-to-PLT ratio index (APRI) were calculated for each patient utilising laboratory data. The FIB-4 was calculated with the equation FIB-4 = [Age (years) * AST (U/L)]/[PLT (10
9/L) * ALT (U/L) ^ (1/2)] [
17]. The APRI was calculated with the equation APRI = 100 × (AST / ULN) / (PLT (×10
9/L) [
18]. Architect chemiluminescence analyzer was used to detect HBsAg and hepatitis B e antigen (HBeAg). The lower limit of quantification of quantitative HBsAg levels was 0.05 IU/mL, and that of quantitative HBeAg levels was 1.0 S/CO (≥ 1.0 S/CO indicates positive HBeAg). Serum hepatitis B virus deoxyribonucleic acid levels were assayed by automatic real-time fluorescent quantitative polymerase chain reaction technique (Cobas Taqman; Roche Diagnostics, GmbH, Mannheim, Germany), with the lowest detection limit of 20 IU/mL; the values were log transformed with units expressed in log
10 IU/mL. The coagulation tests were performed by the clotting method on the automatic coagulometer STAGO Compact (Diagnostica Stago, France). The complete blood count was measured using a Sysmex XN-2000 haematology analyser (Sysmex corporation, Kobe, Japan) according to the manufacturer’s recommendation. All cirrhotic patients underwent upper gastrointestinal endoscopy for variceal screening at baseline. Esophageal varices were graded as none, small (<5 mm diameter) or large (≥ 5 mm diameter) according to the Baveno VI guidelines [
19].
Serum liver fibrosis markers
All patients underwent baseline detection of serum liver fibrosis markers including HA, LN, CIV, and PIIINP to stage the liver disease at the discretion of their attending clinician. Blood samples drawn between 8:00 and 11:00 am after overnight fasting were used for the assays. The levels of HA, LN, CIV, and PIIINP were detected by magnetic microparticle-based chemiluminescent immunoassays using the AutoLumo A2000 Plus Fully Automated Chemiluminescence Immunoassay System (Autobio Diagnostics Co., Ltd, Zhengzhou, China). The reference values were: HA < 120 ng/mL, LN < 130 ng/mL, CIV < 95 ng/mL, and PIIINP < 15 ng/mL. The intra-assay and interassay coefficients of variation were ≤ 15.0% for the four serum liver fibrosis markers.
Follow-up and study outcomes
Usually, patients were evaluated after every 3–6 months for the presence of hepatic decompensation and for the development of hepatocellular carcinoma. The follow-up started from the inclusion of the study and ended in January 2022. The clinical outcomes were carefully recorded. The outcome of hepatic decompensation was defined as the occurrence of liver-related complications, such as ascites, variceal bleeding, or HE [
20]. Ascites was defined as the development of de novo ascites requiring initiation of diuretic therapy. Variceal bleeding was defined as portal hypertension related variceal bleeding requiring hospital admission [
19]. HE was defined as the development of grade P2 HE requiring hospital admission [
21]. Severity of liver disease was assessed by the MELD score.
The primary outcome was the nature and time of the first hepatic decompensation event. The end point was decompensation-free survival. We have combined liver decompensation and death for analysis because most deaths are attributable to decompensation in advanced liver disease. We also assessed the rate and predictors of hepatic decompensation.
Statistical analysis
Continuous variables are expressed as median with interquartile range and compared using the Mann–Whitney U test. Categorical variables are presented as frequency and percentage and were compared using Chi-square test. The number (proportion) of development of hepatic decompensation according to the tertiles of serum liver fibrosis markers were also compared using the Cochran-Armitage trend test. Outcomes were analyzed as time-to-event variables. In these analyses, the cumulative incidence function of the analyzed events was estimated. The univariate and multivariate Cox regression models were performed to investigate the influence of serum liver fibrosis markers on hepatic decompensation during follow-up. Multivariate Cox regression models were created including the variables associated with the outcome in the univariate analysis with P < 0.05. The univariate and multivariate Cox regression models were also employed to assess the hazard ratios (HR) predicting the presence of hepatic decompensation with the increasing tertile of the serum liver fibrosis markers levels. In these Cox regression models, decompensating events during follow-up were evaluated as time-dependent variables. Survival curves were compared between groups using the Kaplan–Meier method with log-rank tests. All P values were 2-tailed and values < 0.05 were considered statistically significant. Statistical analyses were performed by SPSS Statistics 26 (IBM, New York, NY, USA). The survival curve was drawn in the survival and survminer packages in R version 4.2.2 (R Foundation for Statistical Computing, Vienna, Austria) using the post-hoc Bonferroni method.
Discussion
We conducted this large retrospective cohort study to describe the decompensation-free survival and determine the prognostic value of noninvasive serum markers including HA, LN, CIV, and PIIINP in compensated cirrhotic patients at a tertiary medical center in North China. Our results have shown that cirrhotic patients having higher serum HA, LN, CIV, and PIIINP levels have a significantly higher incidence of hepatic decompensation compared with cirrhotic patients with lower serum levels. Using Cox regression models, we have also shown that serum LN and CIV levels predict occurrence of decompensation event independent of age, etiology of cirrhosis, esophageal varices, ALP, GGT, ALB level, PLT counts, MELD score, and FIB-4 index. The associations between CIV levels and hepatic decompensation were statistically significant even after serum liver fibrosis markers were categorized according to the tertiles of serum levels in the whole series. In other words, this retrospective cohort study shows that serum liver fibrosis markers, especially in CIV, which were previously shown to be accurate markers of liver fibrosis, are also independent predictive factors for the liver decompensation that occur in cirrhotic patients with varying etiologies. Further prospective studies are required to confirm the role of serum liver fibrosis markers in these patients. To our knowledge, this is the largest study investigating the prognostic ability of serum liver fibrosis markers in a cohort of liver cirrhotic patients with varying etiologies. These findings reveal the stable prognostic role of CIV in compensated cirrhotic patients, which can identify high-risk patients early and will provide important insights into targeting ECM for the treatment of liver cirrhosis.
The etiology of cirrhosis of the patients is heterogeneous. The occurrence of decompensation differs considerably among the diseases. In addition, the triggers of decompensation are likely to differ among cirrhosis of different etiology. The heterogeneity must have caused confusion of the results. Thus, we also evaluated the predictive factors of decompensation in HBV-related cirrhosis because hepatitis B patients account for the highest proportion in this cohort. We found that after adjusting for potential confounders using a multivariable Cox regression model, higher LN and CIV levels were still found to be independently associated with hepatic decompensation. We assessed the three different decompensation events (ascites, esophageal bleeding, and HE) simultaneously [
22,
23]. The triggers of these three events are likely to differ. Thus, we also evaluated the predictive factors for ascites due to the highest proportion of patients developing ascites in this cohort. We found that after adjusting for potential confounders using a multivariable Cox regression model, higher LN and CIV levels were also independently associated with ascites.
The evaluation of fibrosis provides considerable information and is highly valuable not only for.
the diagnosis but also for the prognosis and for the therapeutic decision. In recent years, due to the increasing need to easily and accurately stage liver fibrosis before treatment and monitor the progress of the disease, non-invasive markers of liver fibrosis have been extensively investigated [
13,
24‐
27]. Biomarkers of liver fibrosis can be divided into direct and indirect markers [
28]. Direct markers are fragments of the liver matrix components produced during the fibrotic process and the molecules represent the intensity of fibrogenesis or fibrinolysis such as HA, LN, CIV, and metalloproteinases [
8]. The majority of earlier studies evaluating non-invasive fibrosis tests, were mainly cross-sectional with the aim of correlating levels of different types of simple and complex biomarkers or imaging with the stage of liver fibrosis [
12,
29‐
32]. Only a small number of studies for these markers and their combination were designed to assess disease progression [
33‐
35]. Nevertheless, these studies were performed in a low number of patients or focused on the value of HA.
Patients in the present study, who developed decompensation during follow-up had higher serum levels of HA, LN and CIV at baseline. It is well known that determination of ECM components may identify fibrosis of patients. Therefore, it is not surprising that higher HA, LN and CIV levels do indicate a more advanced fibrosis stage of the liver, which may logically have a higher likelihood of producing hepatic decompensation, which carry a poor prognosis. Our findings are in keeping with that of a previous study, which has shown that serum LN and HA, especially in LN, can be used as prognostic markers in addition to the CPS criteria in liver cirrhosis [
35]. Nevertheless, the study was performed in a low number of patients and did not provide information on the value of CIV. HA is a glucosamine glycan existing in connective tissue, which is synthesized by mesenchymal cells and almost completely cleared by hepatic sinusoidal endothelial cells (about 1% is excreted through the kidney) [
15]. HA has been extensively investigated as a simple non-invasive marker of fibrosis, with studies showing that it correlates with the degree of liver fibrosis [
14,
35‐
37]. LN is synthesized by hepatocytes and sinusoidal cells, and is one of the main glycoproteins of basement membrane [
38]. It has been reported that the serum fibrosis indices including LN can reflect the activity of liver fibrosis to a certain extent [
39,
40]. CIV is an important component of normal ECM. Unlike type I and III collagen (partly processed proteolytically), CIV remains intact in the matrix and therefore serum components of CIV are considered to mainly reflect matrix degradation [
41]. Serum CIV levels have previously been shown to correlate positively with the degree of hepatic fibrosis [
12,
30,
31,
42]. Qi et al. suggested that CIV, LN, and HA levels were significantly associated with the severity of liver dysfunction, but might be inappropriate for the prognostic assessment of liver cirrhosis [
43], which was inconsistent with our study. This may be due to the differences of the number of cases and the characteristics of patients.
Assessment of the risk of severe complications of cirrhotic patients has important clinical and therapeutical significance. The most widely used prognostic assessment in patients with liver cirrhosis is based on CPS and MELD score [
2,
16]. The advantage of our study is the well-defined patient population of compensated cirrhosis with low MELD score. It is not easy to classify and identify patients who are likely to decompensate early. Therefore, defining predictors of decompensation is important for this group of patients. Moreover, the distribution range of the CPS and MELD score in compensated patients are much narrower than in decompensated patients because these patients often have normal TBIL, ALB, PT, INR, and Cr levels, and their increases only in presence of decompensation, whereas the LN and CIV levels, especially CIV, provide more information independent of MELD score for predicting liver decompensation due to their wider distribution. An important observation of our study was that patients with similar baseline MELD score had significant differences in LN and CIV levels. However, the trend for LN was not significant when it was categorized according to the tertiles of serum levels. In view of the results of our study, CIV appeared to be reliable biomarkers of disease progression and liver decompensation in patients with cirrhosis.
Our study argues for the fact that higher serum liver fibrosis markers levels should be recognized as major contributors which affects the occurrence of liver-related complications in patients with compensated cirrhosis. We do propose that patients with compensated cirrhosis should have a baseline tests of serum liver fibrosis markers and those with higher levels should be followed up more rigorously. Serum liver fibrosis markers are valuable, low-cost and easily available non-invasive predictors of liver decompensation in cirrhotic patients with varying etiologies. The implementation of the serum liver fibrosis markers tests in clinical routine could open up new strategies and allow individualized patient care. We also demonstrated that etiology of alcoholic cirrhosis, esophageal varices, older age, higher GGT, and lower PLT counts were independently associated with an increase in decompensation, which corroborate several prior publications [
15,
44‐
47]. Therefore, we think that patients with alcoholic cirrhosis, esophageal varices, older age, higher GGT, and lower PLT counts at baseline were more likely to develop liver-related complications.
We recognized several limitations of our study. A potential limitation of the current study is that this was a retrospective analysis although all data was prospectively collected. Moreover, repeat data of serum liver fibrosis markers were not available in this cohort of patients, which reduced our ability to reliably determine the influence of changes in their levels on hepatic decompensation. This may require a large-scale prospective study with a series of measurements of serum liver fibrosis markers. Finally, patients from a longer distance do often miss their follow-up because they think they are keeping relatively well. Despite these limitations, as far as we know, this is the largest study investigating the prognostic ability of serum liver fibrosis markers in a cohort of cirrhotic patients with varying etiologies.
Publisher’s Note
Springer Nature remains neutral with regard to jurisdictional claims in published maps and institutional affiliations.