The nomenclature of HE
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Open access peer-reviewed chapter
By Longjiang Zhang
Reviewed: January 23rd 2014Published: May 31st 2014
Hepatic encephalopathy (HE) is a neuropsychiatric syndrome that develops in patients with severe liver diseases and/or portal-systemic shunting. HE is characterized by a wide spectrum of clinical manifestations, ranging from alterations of psychometric performance to stupor and coma (Rovira et al., 2008; Cordoba J., 2011). Several non-invasive neuroimaging techniques, such as particularly magnetic resonance imaging (MRI) and magnetic resonance spectroscopy (MRS), are used for the diagnosis and prognosis of HE. These MR techniques can identify and measure the abnormal accumulation and increase of metabolite, such as glutamine and glutamate (Glx) as a result of HE in the central nervous system (CNS). Under normal circumstances, these substances are efficiently metabolized by the liver. This chapter will review the pathophysiology of HE and its conventional MRI, MRS and functional MRI findings.
Various hypotheses have been proposed to explain the complex neuropsychiatric syndrome seen in HE. Imbalance between inhibitory and excitatory neurotransmission and hyperammonemia is the primary and most widely accepted hypothesis for HE (Rovira et al., 2008; Butterth et al., 2003; Cordoba J., 2011; Cordoba & Minguczb., 2008). Downregulation of glutamate receptors and an increase in inhibitory neurotransmission result in clinical manifestations of HE. In addition, patients with liver failure or portal-systemic shunt surgery have elevated levels of circulating ammonia, which enters the brain through the blood-brain barrier, and increases the ammonia concentration in the cerebral blood up to four fold (normally in the order of two) in liver failure. Hyperammonemia disease leads to profound astrocyte changes, including astrocyte swelling in acute HE and Alzheimer type II astrocyte changes in chronic HE (Matsusue et al., 2005).
The Working Party at the 11th World Congresses of Gastroenterology, held in Vienna in 1998, recommended the nomenclature and types of HE (Table 1) (Ferenci et al., 2002). The West Haven criteria for semi-quantitative grading of HE are summarized in Table 2. HE can be classified in three main groups: episodic, chronic, and minimal, based on duration and characteristics of the clinical manifestations. Episodic HE is characterized by the development of an impaired mental state, neuromuscular abnormalities, asterixis (tremor, jerking movement of the wrist), fetor hepaticus (metcarpans pass into the lungs resulting in the presence of ammonia and ketones in the breath), and hyperventilation, which develops during a short period of time and fluctuates in severity. Chronic HE can be further classified into subgroups: relapsing HE and persistent HE. Relapsing HE manifests itself as frequent episodes of acute HE, while persistent HE refers to manifestations that do not reverse despite adequate treatment. Characteristic manifestations of severe persistent HE are dementia, Parkinsonism, or myelopathy in combination with neurologic involvement, such as ataxia, gait abnormalities, tremor (Rovira et al., 2008). Minimal HE refers to those patients HE type with cirrhosis or portal-systemic shunts who have subtly abnormal cognitive and/or neurophysiologic functions. These abnormalities cannot be detected by the standard clinical examination and can only be determined by a detailed assessment of the patient’s history and a comprehensive neurologic evaluation of cognitive performance and motor functions. The neuropsychological features of the minimal HE type include abnormalities in executive functions, particularly in selective attention and psychomotor speed (Amodio et al., 2004). However, other abnormalities, such as memory impairments, are also seen (Amodio et al., 2004). A complete psychometric assessment by a neuropsychologist is the best way to determine the extent of the attention-related cognitive impairment of a HE patient. A large number of neuropsychologic tests, such as the number connection test (NCT), the line-tracing, and inhibitory control test have been developed and are applied to describe cognitive abnormalities in patients without any clinical evidence of HE (Ferenci et al., 2002; Amodio et al., 2010). Testing across various neuropsychological domains is probably the optimal approach in order to identify cognitive and motor system abnormalities, such as attention and fine motion control. A standardized test battery, including the NCT type A and NCT type B, the line-tracing, the serial-dotting, and the digit-symbol tests (PSE-Syndrome-Test) has a high specificity for HE as compared with other metabolic encephalopathies (Ferenci et al., 2002). Changes in EEG/evoked responses and neuroimaging findings are non-specific and may not be able to provide sufficient information for the diagnosis of minimal HE.
In MRI exam of HE, bilateral hyperintensities at basal ganglia in T1 weighted images but without the corresponding abnormal T2 weighted signal intensity is a typical imaging feature of HE (Figure 1A).This imaging characteristic is attributed to hypermanganesemia (Gover et al., 2006; Mcphail & Taylor-Robinson., 2010).
The observed hyperintensities in bilateral basal ganglia on T1 weighted images can be reduced, or even disappear, after liver transplantation (Figure 1B and 1C) (Naegele et al., 2000; Cordoba et al., 2001; Long et al., 2009). However, no correlation between signal intensities on T2 weighted images in basal ganglia and the clinical encephalopathy or neuropsychological test performance was found, after a number of studies (Spahr et al., 2002; Thuluvath et al., 1995). Although mild brain oedema has been reported in the studies using other advanced MR sequences, no mild abnormalities can be detected in the conventional T1 and T2 weighted images, in addition to basal ganglia hyperintensity. Some studies reported high signal intensity at the centrum semiovale or corticospinal tract (along the hemispheric white matter in or around the corticospinal tract) on fast fluid attenuated inversion recovery (FLAIR) T2-weighted images (Figure 2) (Mínguez et al., 2007; Rovira et al., 2008). This is strikingly similar to signalintensity abnormalities noted in cases of amyotrophic lateral sclerosis, a neurodegenerative disease that affects motor neurons. The progressive normalization of the abnormal high signal-intensity in patients with cirrhosis can be found after the successful liver transplantation or effective treatment (Mínguez et al., 2007; Rovira et al., 2008). Therefore, observation of FLAIR white matter hyperintensities without additional imaging sequences, such as T2 weighted images cannot be used to diagnose HE.
Magnetic transfer imaging (MTI) is a singular MRI technique that has been shown to be useful in the diagnosis of HE. It is mainly based on the interaction (cross-relaxation) between protons in a relatively free environment and those in which motion is restricted (immobile water). Exchange of the saturated magnetization with free water reduces the signal intensity observed in the subsequent MR images. The degree of the signal-intensity loss depends on the attenuation of the macromolecules in a given tissue. MTI allows the measurement of magnetic transfer ratios (MTR), which reflect brain parenchymal changes that may not be visible using the standard MR techniques (Mcphail & Taylor-Robinson., 2010; Grover et al., 2006). Lower MTR can be the result of pathologies that alter the structural integrity and the relative macromolecular-water composition of brain parenchyma, such as in multiple sclerosis plaques (Rovira et al., 1999) or in end-stage cirrhosis (Rovira et al., 2001). Severe MTR decrease may be attributed to the demyelination and axonal loss, but a less severe decrease can be the result of inflammation and moderate demyelination.
All studies using MTI in HE found reduced MTR values in the examined brain regions of HE patients compared to those of controls (Miese et al., 2006; Miese et al., 2009; Poveda et al., 2010). Observed MTR decrease is mild (approximately 10%) and is not accompanied by significant abnormalities on conventional T1-and T2-weighted images, compared with the other metabolic and neurodegenerative diseases, such as experimental autoimmune encephalomyelitis, toxic demyelination, progressive multifocal leukoencephalopathy, human immunodeficiency virus encephalitis, and multiple sclerosis. The MTR reduction seems to have a temporal process in HE, an early involvement of basal ganglia and white matter has been shown (Miese et al., 2009). The MTR decrease almost returns to normal values after liver transplantation, thus supporting the hypothesis that the reduced MTR values reflect mild reversible brain edema.
Diffusion weighted imaging (DWI) is an MRI method that generates brain images based on the image contrast that is dependent on the mobility of H2O molecules in the different tissue compartments (Thoeny & De Keyzer, 2011). Water molecule motion follows the principles of Brownian motion (Provenzale et al., 2006). In a container of water, molecules undergo free, thermally agitated diffusion, which is also called isotropic (means equal in all directions). However, limited diffusion is observed since the movement of water molecules is restricted by their interactions with cell membranes and macromolecules, causing the directional specific motion of water molecules in environments, which is called anisotropic diffusion (Figure 3). DWI derives its image contrast on the basis of differences in the mobility of protons (primarily associated with water) between tissues (Thoeny & De Keyzer., 2011). Apparent diffusion coefficient (ADC) is a measurement obtained from DWI that provides estimation of water motion. DWI has a potential to locate the compartment where the increase of mobility of water molecules is more prominent. Therefore, it can be applied to differentiate cytotoxic oedema from vasogenic oedema in HE patients (Lodi et al., 2004; Mies et al., 2006; Sugimoto et al., 2008). Brain oedema refers to excess water accumulation in the intracellular and extracellular spaces of the brain. In cytotoxic oedema, there is shift of water from extracellular to intracellular compartments producing cellular swelling expressing low ADC, while in vasogenic oedema the reverse happens, producing increased ADC (Schaefer et al., 2000). Recent studies on the application of mean diffusivity measurements within normal-appearing white matter of chronic cirrhotic patients have shown significant increase in brain water diffusivity, which is more pronounced with increased severity of HE (Lodi et al., 2004). These diffusivity values correlated with neuropsychological impairment (Kumar et al., 2008) and increased venous ammonia (Lodi et al., 2004). These findings suggest an accumulation of water in the extracellular compartment and a hypothesis of cortical astrocytic swelling is not supported, but rather increased interstitial fluid or chronic demyelination (Lodi et al., 2004; Sugimoto et al., 2008; Miese et al., 2006) due to glutamine accumulation is cited as the cause of diffuse brain oedema in chronic liver failure (Lodi et al., 2004; Sugimoto et al., 2008; Miese et al., 2006).
On the other hand, the morphology and structure of tissues vary in different organs and pathologic states. Water motion occurs preferentially in some directions in certain tissues due to the presence of obstacles that limit molecular movement in some directions. Diffusion-tensor imaging (DTI) can be used to obtain anisotropy information about water diffusion in tissues when specific diffusion weighted gradients in at least six directions are applied. The most commonly used invariant indices for the measurement of anisotropic diffusions by DTI are; the relative anisotropy (RA), the fractional anisotropy (FA), and the volume ratio (VR) indices (Figure 4A). In brain imaging applications, these indices provide a quantitative measurement of the changes of white matter integrity in different brain regions that are affected by HE. Using DTI together with advanced fibre-tracking algorithms based on the obtained diffusion tensors, white matter tractography can be derived from DTI data. Therefore, it is possible to noninvasively construct 3D trajectories of neural tracts, allowing the modelling of white matter neural connectivity (Figure 4B) (Mukherjee et al., 2008a; Mukherjee et al., 2008).
FA, an index reflecting the white matter integrity, shows no significant changes in patients with chronic HE compared with normal subjects, indicating an absence of microstructural damage in these patients (Kale et al., 2006). Recently, a study by Chavarria et al. (Chavarria et al., 2010) into a rat model of acute liver failure provided experimental evidence to support the cytotoxic origin of brain oedema. Their results suggested that the metabolism of ammonia in astrocytes induces an increase of glutamine and lactate, which may mediate cortical cellular swelling. Saksena et al. (Saksena et al., 2007) also found decreased mean diffusivity values in patients with acute liver failure, suggesting an increase in the intracellular brain water content. Other studies also found decreased ADC value and high cortical signal intensity in patients with acute HE (McKinney et al., 2010; Toru et al., 2011). Therefore, it appears that two different types of brain oedema, intracellular in acute forms and probably interstitial in chronic forms, may exist in liver failure.
MRS is a non-invasive analytical method for analysing brain metabolites, often accompanied by MRI in neuroradiology practices. MR spectroscopic analysis offers a tool to interrogate the molecular process within body tissue and fluids in vivo and in vitro. In clinical application, MRS is capable of identifying and measuring the individual chemicals in the brain regions localized and sampled from MR images. 1H MRS can provide information about brain metabolites such as choline (Cho), creatine (Cr), N-acetyl aspartate (NAA), glutamine and glutamate (Glx), as well as osmolytes, such as myoinositol (mI) and taurine (Ross et al., 1994; Kreis R et al., 1992; Cordoba et al., 2002; Mcphail & Taylor-Robinson. 2010). NAA is a derivative of an amino acid found mostly in neurons; therefore, it is commonly considered as a measure of neuronal density. The peak at 3.19-3.24 ppm of MR spectra obtained in vivo represents a total Cho, including soluble membrane phospholipids: phosphorylcholine (PCho), glycerophosphocholine (GPC) and a relatively small amount of free choline. PCho is involved in the synthesis of the insoluble membrane phospholipids (Vance DE, 1996), while GPC is a product of membrane degradation and free choline is involved in synthesis of the neurotransmitter, acetylcholine, as well as of membrane synthesis (Michel et al., 2006). An increase in the total Cho peak is associated with an increase in membrane breakdown or turnover, myelination or inflammation (Astley et al., 2009). The peak of Cr spectrum is assigned at 3.02 ppm. This peak represents a combination of molecules containing creatine and phosphocreatine. When energy supply is insufficient from the Kreb’s cycle, ATP is produced from adenosine diphosphate (ADP) instead of glucose. This reaction is buffered by the phosphocreatine–creatine (PCr-Cr) system, where PCr donates a phosphate group to become Cr. It is assumed that the Cr peak reflects energy use. Glutamine and glutamate (Glx) are amino acids. Glutamate is the most abundant amino acid in the brain and is released by approximately 90% of excitatory neurons. The spectral peaks of these molecules are often grouped together as Glx in the spectra obtained at the low field, because their overlap makes it hard to resolve them separately. Two compounds become increasingly separated in the higher magnetic fields; therefore, with the increasing clinical availability of stronger magnets, there is growing importance and interests in studying these compounds. Myo-inositol (mI), a simple sugar-alcohol compound, and precursor for inositol lipid synthesis, is a putative glial cell marker because it is located primarily in glial cells and not in neurons. Astrocytes, microglia, and macrophages have been shown to increase their levels of the Na+/mI cotransporter (SMIT) in response to stress or injury and an accumulation of mI, suggesting a role of this compound in inflammation and a marker for astrogliosis and microglia activity (Gupta et al., 2010).
1H MRS has been extensively used in HE studies and has consensus findings on the intracellular metabolite changes in HE. Typical 1H MRS findings of HE include: lower Cho/Cr and mI/Cr and higher Glx/Cr in all examined brain regions compared with controls (Figure 5) (Taraow et al., 2003; Weissenborn et al., 2004; Stewart et al., 2005; Mechtcheriakov et al., 2005; Miese et al., 2006; Weissenborn et al.,2007; Verma et al., 2008). Ammonia plays an important role in the series of metabolite changes in patients with cirrhosis. The increase in brain glutamine during HE increases intracellular osmolality. To maintain osmotic equilibrium, the astrocytes lose osmolytes such as mI and Cho, and a large amount of water enters the astrocyte and results in cellular swelling and impairment of cellular metabolism, further influencing neuronal and astrocyte function and the interaction between them. MRS measurable metabolite changes have been shown to correlate with improved psychometric performance (Binesh et al., 2006) following treatment (Haseler et al., 1998) and following liver transplantation (Naegele et al., 2000; Córdoba et al., 2001; Long et al., 2009). Recent pilot studies on in vitro 1H MRS of human blood or urine in acute liver failure have demonstrated significant metabolite abnormalities between survivors and nonsurvivors (Saxena et al., 2006). They found glutamine in serum and the urine glutamine: creatinine ratio was higher in non-surviving patients compared with surviving patients [serum glutamine, 3.08 (1.68-7.11) vs. 0.56 (0.34-0.99) mM, median and range; P=0.0001 and urine glutamine:creatinine ratio, 1.72 (0.24-7.76) vs. 0.39 (0.1-0.84), P=0.1], and urine urea:creatinine ratio was higher in surviving patients compared with non-surviving patients [10.83 (0.2-22.6) vs. 2.09 (0.96-4.0), P=0.002]. Their study indicated MRS had a potential use for clinical decision making about the need for advanced therapeutic intervention, such as artificial liver support or emergency liver transplantation in acute liver failure. Of these available MRS measurements, mI seems to be a more sensitive biomarker than Cho to detect HE. mI levels were negatively related to the Child-Pugh score and degree of HE (Lee et al., 1999; Zhang et al., 2010). However, values in a normal range have not been established and the diagnostic accuracy of 1H-MRS remains uncertain.
In clinical practice, accurately differentiating some metabolites, such as Glx and taurine, can be challenging with the clinical MR scanners currently available. Two-dimensional MR spectroscopy may enhance the spectral resolution to distinguish metabolites based on J coupling patterns of individual molecules. On the other hand, more sophisticated statistical techniques, such as principal components analysis (PCA), enable assessment of the variation in individual metabolites based on the data obtained from MRS measurements (Barba et al., 2008; Singhal et al., 2010). These techniques can provide quantitative information of metabolic processes and changes in the diseased tissue, and therefore can be helpful in the understanding of HE pathogenesis. Wide availability of 3 Tesla MR scanners, as well as short TE acquisition, can improve the spectral resolution and thus, allow the differentiation of Glx from NAA (Sawara et al., 2004).
Functional magnetic resonance imaging (fMRI) detects blood oxygen level-dependent (BOLD) changes in MRI signal that arise when changes in neuronal activity occur in a region of the brain after responding to a stimulus or performing a specific task (Ogawa et al., 1992). The BOLD signal is the ratio of oxy-haemoglobin to deoxy-haemoglobin during brain activation (Gore JC., 2003).
According to experimental paradigms, fMRI can be classified to task-related and resting state fMRI. In task-related fMRI design, a subject is placed in the magnet of an MRI machine, where various different kinds of stimulus are administered in a controlled fashion. Two main experimental paradigms are commonly used in task-related fMRI studies: block design and event-related paradigms (Gore JC., 2003). In resting state fMRI, the participants are required to rest in the absence of any external stimulation as well as guided to avoid reiterating any goal-directed thought pattern in their heads (Damoiseaux et al., 2006).
Many behavioural studies have claimed the existence of attention alterations in cirrhotic patients without overt HE (Zhang et al., 2007a; Randolph et al., 2009; Bajaj et al., 2009). There are only a few fMRI studies into HE. Zafiris et al. (Zafiris et al., 2004) first analysed the pathologically impaired neural mechanisms of cirrhotic patients using fMRI. Nine subjects with minimal HE (MHE) and 10 controls underwent scanning while they indicated the apparent transition from a steady light to the onset of a flicker light. Judgment-related BOLD activation was decreased in MHE patients compared to controls in the right inferior parietal cortex (IPL). Impaired neural interaction between the IPL and the parietooccipital cortex (Poc), the intraparietal sulcus, the anterior cingulate cortex (ACC), the right prefrontal cortex (PFC), the medial temporal lobe, and the extrastriate cortex V5 and an enhanced coupling between IPL and the postcentral cortex were found in MHE patients. This study demonstrated an impaired and compensatory neural mechanism during visual judgment in the earliest stages of HE. Zhang et al. (Zhang et al., 2007a) used a Chinese character Stroop task as the target stimulus to investigate the neural mechanism of the cognitive control impairment in cirrhotic patients using fMRI. This study showed that simple tasks (incongruous word-reading tasks) increased the activity of the precentral and postcentral gyri in cirrhotic patients, and harder tasks (incongruous colour-naming tasks) decrease the activity of bilateral superior frontal gyrus, middle frontal gyrus, inferior frontal gyrus, medial wall frontal gyrus, ACC, temporal cortex, and parietal cortex. This study provides suggests that the abnormal anterior cingulate cortex–prefrontal cortex–parietal ‘‘fusiform’’ cortex circuit could be the neural substrarte responsible for this impaired cognitive control. However, the task-induced fMRI is better suited to the patients with low-grade or MHE who can perform the test tasks (Mcphail and Taylor-Robinson, 2010).
Recently, increasing attention has been given to detecting brain activities during resting state (Greicius et al., 2003; Greicius et al., 2004; Zhang et al., 2007b; Zhang et al., 2011). Most reported resting-state network components include; the default mode network (DMN), the sensorimotor component, the executive control component, up to three visual components, two lateralized fronto-parietal components, the auditory component and the temporoparietal component (Rosazza & Minati, 2011). As already reported, these resting-state networks consist of anatomically distinct, but functionally connected regions, which display a high level of correlated BOLD signal activity. Nowadays the DMN is the most studied network in comparison to task-induced brain networks. DMN includes the medial prefrontal cortex, rostral anterior cingulate, posterior cingulated cortex (PCC), and precuneus (Greicius et al., 2003; Greicius et al., 2004). The DMN is described by increased activity during rest, while decreased activation suppressed during cognitively demanding tasks, such as visual and auditory attention, language processing, memory, and motor activities. Abnormal default function network has been known to relate to Alzheimer disease (AD), autism, attention deficit hyperactivity disorder, schizophrenia, epilepsy, and other diseases (et al., 2005; Rombouts et al., 2005; Kennedy et al., 2006; Liang M, et al., 2006; Tian et al., 2006).
In a study by Zhang et al. (Zhang et al., 2007), the DMN of the cirrhotic patients was investigated using a block-design in which a modified Chinese Stroop task was used as the target stimulus. In this study, a subtraction method was used to study the resting-state network in patients with hepatic cirrhosis. The functional data suggest that cirrhotic patients may have a deactivated DMN. The absence of deactivation in the PCC and precuneus may be a sensitive, rather than specific, marker in patients with hepatic cirrhosis. Recently, in a resting state fMRI study (Zhang et al., 2011), a significantly reduced functional connectivity in the right middle frontal gyrus, left precuneus, and left PCC in the HE patients was observed when compared to the controls. A negative correlation was shown between left angular gyrus and left PCC activation and venous blood ammonia levels, suggesting this can be an important biomarker for HE (Figure 6).
In conclusion, HE appears as diffuse mild brain oedema, and is associated with cognition functional changes such as attention, and functional brain area changes, such as default mode brain areas. HE-associated functional and physiological abnormalities have been demonstrated by a variety of MR techniques. MRI offers a range of capabilities for investigating HE in clinical diagnosis. The recent development of fMRI and MRS expands the applications of the study of HE with the capability of assessing functional changes in brain affected by HE. These advances opens up the opportunities to better understand the pathopsychological mechanisms of HE.
We express our thanks for the grants from Natural Scientific Foundation of China (81322020, 81230032, and 81171313 to L.Z.) and the Program for New Century Excellent Talents in the University (NCET-12-0260 for L.Z.).
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