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Medicine » Pathology » "Liver Biopsy", book edited by Hirokazu Takahashi, ISBN 978-953-307-644-7, Published: September 6, 2011 under CC BY-NC-SA 3.0 license. © The Author(s).

Chapter 16

Noninvasive Alternatives for the Assessment of Liver Fibrosis

By Lungen Lu and Kun Zhou
DOI: 10.5772/20167

Article top

Noninvasive Alternatives for the Assessment of Liver Fibrosis

Lungen Lu 1 and Kun Zhou1

1. Introduction

Chronic liver diseases (CLD) are common and may lead to fibrosis, cirrhosis, and hepatic malignancy. Detection and staging of liver fibrosis is crucial for management of patients with CLD. At present, liver biopsy is the standard method for staging fibrosis, but biopsies are poorly tolerated because they are invasive and associated with some discomfort and complications. In addition, limitations of biopsy include intra- and inter-observer variation and sampling error1,2. In recent years, a great interest and many studies have been dedicated to the development of noninvasive tests to substitute liver biopsy for fibrosis assessment and follow-up. Unfortunately, all of them have limitations and pitfalls. To discuss their advantages and deficiencies will be helpful in scientific research and clinical practice.

2. Invasive measurements

2.1. Liver biopsy

Liver biopsy has been considered as the gold standard to confirm the clinical diagnosis, to assess the severity of necro-inflammation and fibrosis, to identify cofactors and comorbidities, and to monitor the efficacy of treatments since the first liver biopsy was performed by Paul Ehrlich in 1883 3. The procedure is particularly useful for diagnosing the earlier stages of fibrosis and identifying patients at high risk of progressing fibrosis, but it has also a number of limitations. The patient acceptance is pretty low because biopsy is expensive, invasive and associated with some discomfort and complications. Pain appears in about one fourth of patients, other complications including bleeding, biliary peritonitis, pneumothorax and a mortality rate about 0.01% 4. Sampling error of at least 24% is reported usually because of specimen fragmentation or inadequate length. Colloredo et al concluded that an optimum specimen should be at least 20 mm in length with 11 complete portal tracts1. Even with adequate-sized biopsies, the interpretation might be unreliable, because the distribution of necro-inflammation and fibrosis is not homogeneous, and liver biopsy samples only 1:50 000th of the mass of the liver.

Several semi-quantitative scoring systems have been proposed to describe and quantify the necro-inflammation, steatosis and fibrosis in the liver, particularly for chronic viral hepatitis. These include the Knodell histological activity index (HAI) first proposed in 1981, then modified to the Scheuer system, the METAVIR system and the Ishak modified HAI 5. However, all the scoring systems could only provide qualitative descriptors to stage fibrosis, and the staging of certain histopathological changes differ in different systems (Table 1). This could cause considerable intra- and inter-observer variation and difficulty in comparison 2.

Pathologic Features Knodell Scheuer METAVIR Ishak
No fibrosis0000
Enlargement of some portal tracts1111
Enlargement of most portal tracts1112
Periportal septa1212
Occasional portal-portal septa3223
Numerous septa (portal-portal and/or portal-central)3334
Occasional nodules4445
Definite cirrhosis4446

Table 1.

Scoring systems for staging fibrosis

Using computerized digital image analysis, the amount of fibrosis in liver biopsy specimens can be evaluated by a quantitative score 6-9. Though it is thought to be less reliable in determining early stage fibrosis, recent advances such as a higher resolution digital camera can improve discrimination between the varying stages of liver fibrosis, including mild fibrosis 8. It may be a more precise method than semi-quantitative histological stages for monitoring fibrosis progression or regression during clinical therapeutic trials 9. Considering the irregular shape of specimens, fractal and spectral dimension analysis can also be used to improve accuracy 10.

The detection of genes correlated with fibrosis from biopsy samples regains interest for liver biopsy. The changes in liver gene expression can indicate fibrosis progression precisely at an early stage 11. Genetic studies have identified possible genetic polymorphisms that influence the progression of liver fibrosis 12. The identification of panels of key genes correlating with differences in the progression of CLDs could lead to establishing excellent prognostic/diagnostic tools.

2.2. Hepatic venous pressure gradient

Hepatic venous pressure gradient (HVPG), as an expression of intrahepatic resistance, does not exceed 5 mmHg in absence of significant fibrotic evolution. The measurement of HVPG is a validated, safe and highly reproducible technique. It may be considered as a dynamic marker of disease progression in patients with HCV and an end point in antiviral therapy, irrespective of antiviral response 13. However, the technique is invasive, expensive, requires technical expertise, and has low patient acceptance.

3. Serological tests

The limitations of liver biopsy led to the searching of noninvasive tests for assessment of liver fibrosis. Afdhal and Nunes et al 14 suggest the following criteria for an ideal marker of liver fibrosis: it should be liver specific; should not be influenced by alterations in liver, renal, or reticuloendothelial function; should measure one or more of the processes related to fibrosis (stage of fibrosis, activity of matrix deposition, or activity of matrix removal); and should be easy to perform.

3.1. Direct serum markers

The key step in the pathophysiology of liver fibrosis is the balance between ECM deposition and removal. Accumulation of ECM results from both increased synthesis and decreased degradation. The principal ECM constituents are synthesized by activated HSCs, while broken down by a family of enzymes known as matrix metalloproteinases (MMPs). Many studies have been dedicated to find serum ECM markers for fibrosis assessment.

Hyaluronic acid (HA), a glycosaminoglycan distributed in the connective tissue, is a component of the liver extracellular matrix, which is synthesized and degraded in the liver sinusoidal cells. The high levels of HA observed in patients with chronic liver disease, have been related with a decreased function of the endothelial sinusoidal cells. Many studies showing a close relationship between liver fibrosis and HA levels.

These similar markers of fibrosis incuding: ⑴ collagens: N-terminal peptide of type Ⅲ pro-collagen (PⅢNP), type Ⅳ collagen 7s domain(Ⅳ-7S) 15, ⑵ proteoglycans: hyaluronic acid (HA) 16, ⑶ glycoproteins: laminin (LN) 17, human cartilage glycoprotein 39 (YKL-40) 18, ⑷ collagenases and their inhibitors: MMPs, tissue inhibitor of metalloproteinases (TIMPs) 19, ⑸ cytokines: transforming growth factor β1 (TGF-β1), platelet-derived growth factor (PDGF), tumor necrosis factor β (TNF-β).

The clinical applications of such markers appear innovative, they are useful to assess the speed of liver fibrogenesis and estimate the response to anti-viral therapies or anti-fibrotic drugs. But most of them are insensitive in milder fibrosis, and it must be stressed that these markers reflect fibrogenesis and fibrolysis more than fibrosis itself. In other words, there may be a highly active fibrotic process in the liver, although fibrotic tissue has not yet been developed, or there may be heavy fibrosis in the liver but fibrotic activity is temporarily discontinued.

3.2. Serum marker panels

Since present direct markers could not satisfy the clinical need of measuring the fibrosis yet, an alternative approach turns out to be combining a number of serum markers to generate algorithms capable of evaluating fibrosis. A large number of panels have been suggested by groups worldwide 20-49 (Table 2).

These panels are mainly based on two kinds of markers, direct and indirect. Direct markers are those directly linked to the modifications in ECM metabolism, such as HA and PⅢNP. Indirect markers include a broad range of blood tests which have no direct link with liver fibrosis. They reflect liver dysfunction or other phenomena caused by fibrosis rather than fibrosis per se. Generally speaking, indexes including direct markers, such as the Fibrometer, may perform a higher accuracy, but indexes composed by only indirect markers are effective as well, and usually more useful because they are based on routine blood tests easy to be performed in a hospital general laboratory.

The diagnostic value of the models was assessed by calculating the area under the receiver operating characteristic curves (AUROC). Most studies reported an AUROC >0.80 in differentiating significant fibrosis (fibrosis spread out the portal tract with septa) from no/mild fibrosis (no fibrosis or portal fibrosis without septa), improved performance with a higher AUROC value was showed in differentiating between no cirrhosis and cirrhosis. But it must be underlined that the AUROC values in table 2 came from each different designed study and are not suitable to make a comparison.


Table 2.

Studies of serum markers panels for assessment of liver fibrosis

Chronic hepatitis B (CHB) is the most frequent infectious cause of CLD worldwide. More than 400 million people are chronically infected with HBV. The virus is responsible for more than 300,000 cases of liver cancer every year and for similar numbers of gastrointestinal haemorrhage and ascites 50. Predictive models designed specially for CHB patients have been proposed by the Shanghai Liver Fibrosis Group (SLFG) 42, Hui et al 41 and Mohamadnejad et al 45. But few of these models mentioned above has been widely validated and implemented in clinical practice. In our study of the S index 51, a simpler noninvasive model based on routine laboratory markers, we compare its diagnostic value with that of some typical models (Fig. 1), We noticed that the SLFG model and Hepascore performed better in identifying significant fibrosis than the Forns score and APRI, but the superiority was not so significant in identifying advanced fibrosis or cirrhosis. The result was similar to a validation study in CHC patients 52, indicating that such special tests might improve the sensitivity of a diagnostic model in predicting early fibrosis. But including tests unavailable in daily practice makes standardization, validation and routine bedside use difficult.


Figure 1.

ROC curves in the prediction of significant fibrosis

There are still some limitations of these marker panels to be considered. First, the design of every study differed in population characteristic, patient selection, significant fibrosis prevalence, blood test inclusion, biochemical measurement and liver histological assessment, resulted in various panels with different markers and parameters. The agreement among these indexes is poor and validation study is needed to choose a proper panel and cutoff value for clinical use. Second, none of the studies controlled for degree of necro-inflammatory activity, most of the panels include markers likely to reflect or be affected by inflammation in the liver, which is much more mobile than fibrosis stage. Third, the formulae are easy to fail because many markers included will be influenced by extrahepatic diseases or conditions such as inflammation, haemolysis, cholestasis, hypercholesterolaemia and renal failure. Finally, few of the studies include treated patients. It is not clear whether these indexes are suitable for assessing treatment response. However, a few studies by Poynard et al suggested that Fibrotest could also be used as surrogate markers of the histological impact of treatments in patients infected by HCV and HBV 53, 54.

These indexes, in their current form, are not able to give us the exact stage of fibrosis in most studies. Their main value is to reduce the need for liver biopsy by distinguishing significant fibrosis from no/mild fibrosis, and telling the presence of cirrhosis. It does not seem appropriate to completely replace liver biopsy with serum marker panels at the present time, but it can be anticipated that these indexes will become very useful in the clinical management of CLDs by offering an attractive alternative to liver biopsy, as they are noninvasive, convenient, inexpensive, and may allow dynamic assessment of fibrosis. Validation in larger cohorts of patients with different CLDs is needed before an index will be proposed for extensive clinical use.

3.3. Proteomics and glycomics

Over the last 5-6 years, it was reported that the use of proteomic patterns in serum to distinguish individual stages of fibrosis could achieve perfect diagnostic sensitivity and specificity. Using a proteome-based fingerprinting model generated by surface-enhanced laser desorption/ ionization time-of-flight (SELDI-TOF) ProteinChip arrays, Poon et al 55 achieved an AUROC of 0.93 in identifying significant fibrosis. Another proteomic index combining eight peaks established by Morra et al 56 could diagnosis advanced fibrosis with an AUROC of 0.88, significantly greater than the FibroTest AUROC of 0.81. Besides, The SELDI-TOF ProteinChip technology is useful for the early detection and prediction of HCC in patients with chronic HCV infection 57. Similar technologies were also used to generate profiles of serum N-glycan profile for identifying liver fibrosis 58, 59. Further studies identifying the altered peaks in these models to understand their origins may help to find new biomarks for fibrosis, or even improve our understanding in the mechanism of liver fibrosis.

4. Radiological tests

Since significant structural changes are present only in advanced CLDs, the routine examinations by Ultrasound (US), computed tomography (CT) and magnetic resonance imaging (MRI) could bring specific findings, but with very limited sensitivity. Thus, persistent efforts were made to search for technological developments.

4.1. Perfusion examinations

MR and Doppler US techniques are studied to find sensitive perfusion changes in the progression of fibrosis 60. For example, the circulatory changes will result in a decrease of hepatic vein transit time (HVTT), which can be measured by microbubble-enhanced US 61. Using HVTT measurements, Lim et al achieved 100% sensitivity and 80% specificity for diagnosis of cirrhosis, and 95% sensitivity and 86% specificity for differentiation of mild hepatitis from more severe liver disease 62. Progressive liver fibrosis gradually obliterates normal intrahepatic vessels and sinusoids and slows passage of blood through the parenchyma. In addition, as portal hypertension develops, portal venous flow to the liver decreases, hepatic arterial flow increases, and intrahepatic shunts form. These physiologic alterations can be detected with kinetic models of dynamic image data sets acquired rapidly after bolus intravenous injection of paramagnetic extracellular contrast agents. Several perfusion parameters can be estimated by MR perfusion imaging, a recent study applied a dual-input kinetic model for the noninvasive assessment of liver fibrosis. The dual-input approach models two sources of blood flow into the liver, via the he patic artery and portal vein, and assumes a single tissue compartment. Significant differences were found in several perfusion parameters between patients with and without advanced fibrosis 63.

4.2. Liver stiffness measurement

In chronic liver disease, progressive deposition of interconnecting collagen fibers throughout the liver produces a lattice-like framework that increases parenchymal rigidity. Because liver stiffness cannot be reliably assessed with external physical palpation, an imaging approach is required. There are two main imaging methods for measuring hepatic stiffness. One is US-based transient elastography; the other is MR elastography.

The FibroScan, a new medical device based on one-dimensional transient elastography 64, which assesses fibrosis through liver stiffness measurement (LSM). A special probe generates an elastic shear wave propagating through the liver tissue, the harder the tissue, the faster the shear wave propagates. Transient elastography could accurately predict different stages of fibrosis or cirrhosis (AUROC: 0.79 for F ≥ 2, 0.91 for F ≥ 3, and 0.97 for F = 4. by the METAVIR scoring system) 65.

The major advantage of transient elastography compared with serum markers and marker panels is that it measures directly on the liver and there is no interference from extrahepatic diseases or conditions. Further more, the test is standardized and completely noninvasive. Though assessing earlier fibrosis is the common shortcoming of various noninvasive tests, Colletta et al reported that the agreement between transient elastography and liver biopsy was much better than FibroTest in normal transaminases HCV carriers with early stages of fibrosis66.

Compared to liver biopsy, transient elastography is painless, rapid, has no risk of complications, and is therefore very well accepted. Transient elastography measures liver stiffness of a volume which is 100 times bigger than the biopsy specimen. The high reproducibility (intra- and inter-observer agreement intraclass correlation coefficient was 0.98 67) and acceptance of transient elastography makes it an attractive alternative to biopsy for individual follow-up.

There are also some physical limitations of transient elastography. The signal penetrates only 25–65 mm, makes obesity (particularly the fatness of the chest wall) the most important cause of failure68. But new technological developments may overcome the limitation. Additional limitations include a narrow intercostal space and ascites. The main reason that transient elastography can not totally replace liver biopsy is that it is only a means to stage disease. It is unable to diagnose liver disease by distinguishing subtle diagnostic differences. Nor can transient elastography identify cofactors and comorbidities or grade necro-inflammation and steatosis. But it represents a totally different approach to assess fibrosis and therefore could be combined with other noninvasive modalities to better assess liver fibrosis. The combined use of transient elastography and FibroTest to evaluate liver fibrosis could avoid a biopsy procedure in most patients with chronic hepatitis C 69.

Magnetic resonance elastography (MRE) is a technique using a modified phase-contrast magnetic resonance imaging sequence to image propagating shear waves in tissue 70. The technique has been previously applied to quantitatively assess the viscoelastic properties of the breast, brain, and muscle in humans. Several recent studies showed that MRE is also a feasible method to assess the stage of liver fibrosis. Liver stiffness as measured with MR elastography increases as the stage of fibrosis advances. The differences in stiffness between patients with early stages of fibrosis (F0 vs F1 vs F2) are small and there is overlap between groups, but the differences between groups with higher stages (F2 vs F3 vs F4) are large, with little overlap between groups71. MRE has several potential advantages compared with ultrasound transient elastography. It can be performed in obesity patients. It can assess larger volumes and provide full three-dimensional information about the viscoelastic parameters of tissues. With MR techniques, a comprehensive examination of the liver can be performed, including MRE, contrast-enhanced MRI to detect hepatocellular carcinomas and perfusion MRI to assess liver function.

4.3. Real-time elastography

Real-time elastography is another ultrasound technique developed by Hitachi Medical Systems that can reveal the physical property of tissue using conventional ultrasound probes during a routine sonography examination. In the first study assessing real-time elastography for the detection of liver fibrosis 72, the AUROC was 0.75 for the diagnosis of significant fibrosis. Much higher diagnostic accuracy (AUROC = 0.93) was obtained by a mathematic combination of the elasticity score and two routine laboratory values (platelet count and GGT), which provided a more superior way to combine serological and radiological tests together.

4.4. Double contrast material-enhanced magnetic resonance imaging

The conspicuity of gadolinium-enhanced lesions is increased in the setting of decreased signal intensity from the uninvolved liver parenchyma following superparamagnetic iron oxide (SPIO) injection. This MRI technique has been used to improve detection of focal hepatic lesion and hepatocellular carcinoma 73, 74. Recently, Aguirre et al 75 examined 101 CLD patients who underwent double-enhanced MR imaging to detect hyperintense reticulations, which are postulated to represent septal fibrosis. They achieved an accuracy of greater than 90% for the diagnosis of advanced hepatic fibrosis compared with histopathological analysis. Clinical trials are currently under way to prospectively assess fibrosis staging with this technique.

4.5. Diffusion weighted magnetic resonance imaging

Diffusion weighted magnetic resonance imaging (DWMRI) has been widely used in brain imaging for the evaluation of acute ischemic stroke. With the advent of the echo-planar MRI technique, it became possible to be applied in the abdomen for characterization of focal hepatic lesions 76. Recently, using DWMRI to measure the apparent diffusion coefficient (ADC) of water, a parameter that is dependent on the tissue structure, is introduced in the assessment of liver fibrosis 77. The ADC value is lower in livers with heavier fibrosis because of the restriction of water diffusion in fibrotic tissue. Lewin et al assessed the performance of DWMRI in 54 patients with chronic HCV infection with reference to several other noninvasive methods 78. In discriminating significant fibrosis patients, the AUC values were 0.79 for DWMRI, 0.87 for transient elastography, 0.68 for FibroTest, 0.81 for APRI, 0.72 for the Forns index, and 0.77 for hyaluronate. DWMRI performed better in discriminating patients staged F3-F4, the AUC value increased to 0.92, the same as transient elastography. But besides fibrosis, it seems that ADC values might also reflect the intensity of inflammation, necrosis and steatosis. Because technical factors lead to differences in estimated ADC, reported ADCs are variable, with considerable overlap between normal and abnormal ranges. Thus, there is a need to develop site- and technique-specific normal ranges and to standardize methods across imaging centers.

Several other MR techniques have also been introduced in the area of fibrosis assessment, such as ultrashort echo time (UTE) MRI 79 and magnetic resonance spectroscopy (MRS) 80. New MR imaging contrast agents that specifically target collagen or other extracellular matrix macromolecules may be developed. A collagen-specific MR imaging contrast agent could act as a fibrosis-imaging agent, and these agents may have higher efficacy for fibrosis assessment than the current methods 81. All such data may provide valuable information for guiding antifibrotic therapy development and monitoring patients in clinical trials.

5. Conclusion

The increasing of potentially effective managements for CLDs such as antiviral and antifibrotic therapies has led to an urgent need for a rapid, safe and repeatable tool to assess fibrosis of CLDs and to follow-up progression or regression of fibrosis during treatment. Liver biopsy has been the gold standard for the assessment of hepatic fibrosis, but the invasive procedure has considerable limitations and fails to satisfy the current needs. Many noninvasive methods have been proposed with the aim of substituting liver biopsy. The numerous advances in serological, radiological techniques and their combinations have allowed to satisfactorily identify patients without a liver biopsy. But each of them has some deficiencies and the liver biopsy will still have an important role to play. Applying new techniques for the detection of fibrosis may potentially circumvent the pitfalls and deficiencies of the existing surrogates mentioned above. These include serum proteomics, glycomics and new imaging techniques such as molecular imaging technique for the imaging of cellular biochemical processes 82, diffraction-enhanced imaging technique for the imaging of soft tissues 83, photonic imaging technique for three-dimensional whole-body images 84. However, further studies are needed to develop or validate noninvasive tests that can accurately reflect the full spectrum of hepatic fibrosis in CLDs. But an incorrigible defect in our studies will be the questionable gold standard we have to use. More errors are due to the histological staging 85. Mathematical modeling suggested that assuming either 80% or 90% diagnostic accuracy of liver biopsy, noninvasive tests cannot achieve an AUROC better than 0.9 and are likely to perform between 0.75 and 0.9 86, exactly where they are today. We may find a better surrogate for liver biopsy, but how can we prove it will be a question. Laparoscopic biopsy can decrease sampling error and increases the reliability of histopathologic assessment 87. Using automated image analysis to assess texture features and shape representation of the fibrosis structural expansion can turn the current semiquantitative methods of liver fibrosis assessment into real quantitative ones with significant reduction in variability and subjectivity 88. Validating noninvasive tests against not only histological stage scores but also digital image analysis and clinical outcomes may also be a better choice.


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