Because the liver is the major site of drug metabolism, it is also the major target of drug-induced injury. Despite rigorous preclinical and clinical toxicologic studies and safety analyses in clinical trials, the frequency of drug hepatotoxicity has remained relatively unchanged during the years, and drug-induced liver injury (DILI) is still the main reason for removal of a drug from the market. Furthermore, adverse chemical reactions are not confined to pharmaceutical drugs (i.e., the drug itself and its excipients used for classic therapeutic purposes): dietary supplements and herbal medicines, often used as self-medications, also represent potential hepatotoxins. Various environmental toxins and recreational drugs, such as alcohol, illicit drugs (e.g., cocaine, heroin, ecstasy), criminal poisons, and industrial toxins (e.g., natural toxins, mushrooms, industrial chemicals, pesticides), can also give rise to hepatotoxicity. The list of putative offending drugs and toxins is extremely long and evolves with time. Although all families of therapeutic agents can potentially be involved, a small group of drugs represent the most frequently incriminated molecules ( Box 48.1 ). The circumstances of exposure to these various forms of liver toxins are listed in Box 48.2 , with the exception of alcohol injury, which is discussed in Chapter 49 .
Analgesics and antiinflammatory agents
Antituberculosis drugs: INH + RFP + PZA (F)
HAART and anti-HIV drugs (F)
Valproic acid (F)
Atrium (combination of phenobarbital, febarbamate, and difebarbamate)
Infliximab and other antibodies
Atorvastatin and other statins
Endocrine and metabolic agents
Medical herbs (germander, others) (F)
Illicit drugs: cocaine, ecstasy (F)
Aflatoxin, Amanita phalloides (F), other natural poisons
Paraquat herbicide (F)
DILI , Drug-induced liver injury; F , fatal outcome possible; HAART , highly active antiretroviral therapy; HIV , human immunodeficiency virus; INH , isoniazid; PZA , pyrazinamide; RFP , rifampicin.
Treatment: prescription medications, self-prescription
Self-poisoning, especially suicide attempts
Folk and herbal medicine
Fungal, insect, and scorpion toxins
Industrial chemicals and pesticides
Household accidents with chemical products
Self-poisoning with chemical products
Low-level chronic exposure at the workplace
Drug hepatotoxicity can be classified as either intrinsic or idiosyncratic. Intrinsic hepatotoxicity is predictable, dose dependent, and often characteristic of a particular agent when consumed in large quantities. Examples are ingestion of acetaminophen (paracetamol) and exposure to carbon tetrachloride or chloroform. Hepatotoxicity occurs in most of those who are exposed and starts shortly after some threshold for toxicity is reached. The mechanism of intrinsic injury can be direct, through damage to cells and organelles, or indirect, through conversion of a xenobiotic into an active toxin or through an immune-mediated mechanism. Idiosyncratic hepatotoxicity, by far the more frequent form of hepatotoxicity, involves unpredictable reactions that occur without warning and are unrelated to dose; they occur in particular hosts, depending on individual genetic variations in the metabolism of drugs and on environmental factors. Because the formation of reactive metabolites is a frequent mechanism of idiosyncratic reactions, the hepatotoxicity is highly dependent on the metabolic capacity of the host. In idiosyncratic toxicity, variable latency periods can be observed, from a few days to more than a year.
Diagnosis of a toxic liver injury or DILI is challenging, and it is often a diagnosis of exclusion and probability. Assessment of causality is difficult because almost all drugs and toxins are potentially hepatotoxic because of frequent idiosyncrasies and unpredictable toxicity, whereas predictable and dose-dependent liver toxins are rare. From a clinical or a pathologic point of view, any pattern of hepatic injury may be encountered and may mimic other liver diseases, and a single drug can induce different lesions in different patients. The clinical presentation is usually acute and largely reversible, but chronic disease can occur. The time of onset of liver dysfunction varies depending on the drug and the patient and can be long after the first ingestion of drug. Severe cases can occur and include mainly fulminant hepatitis: DILI is one of the major causes of acute liver failure with viral hepatitis. Significant fibrosis and cirrhosis may develop, and even hepatic tumors. In addition, hepatocytes are usually the target in DILI, but some drugs may target endothelial cells, cholangiocytes, hepatic stellate cells, and/or Kupffer cells.
The Council for International Organizations of Medical Sciences (CIOMS) has proposed consensus criteria for terminology in DILI, based on biologic tests, chronology, and availability of liver biopsy. Six categories of DILI can be defined in this system: hepatocellular injury, cholestatic injury, mixed injury, acute injury, chronic injury, and chronic liver disease ( Table 48.1 ).
|Hepatocellular injury||Isolated increase in ALT >2 × normal, or ALT/ALP ≥5|
|Cholestatic injury||Isolated increase in ALP >2 × normal, or ALT/ALP ≤2|
|Mixed injury||ALT and ALP increased and 2 < ALT/ALP <5|
|Acute injury||Above changes present for <3 mo|
|Chronic injury||Above changes present for >3 mo|
|Chronic liver disease||This term is used only after histologic confirmation|
The histologic examination of a liver biopsy specimen is not always performed, either because the toxic episode may quickly resolve or because the information provided is disappointing. Indeed, specific lesions are rare in this field. However, when analyzed by a specialist, the liver biopsy can often provide useful information for positive and differential diagnosis of DILI ( Box 48.3 ). The lesions can be classified as to pattern of injury, a topic that is discussed in detail later in this chapter.
To determine the pattern or patterns of injury
To suggest mechanisms
To confirm or suggest a drug candidate
To assess the degree of injury (grade, stage)
To exclude or find other pathologies
DILI should be included in the differential diagnosis in cases with any hepatic laboratory abnormalities or hepatic dysfunction, but the assessment of causality of a drug in liver disease is often difficult. Discussion between clinicians and pathologists is especially important in this field of hepatology.
Current preclinical tests for hepatotoxicity are inadequate, reflecting our limited understanding of the mechanisms of drug toxicity. In particular, “hypersensitivity” and “idiosyncratic” reactions remain poorly understood and probably affect individuals possessing a rare combination of genetic and nongenetic factors that lead to drug toxicity in a given environmental setting. Many meetings on this topic have been organized by the Center for Drug Evaluation and Research (CDER) of the U.S. Food and Drug Administration (FDA) since 2001, and collection of data in regional or national registries (e.g., Spain, France, United States) or databanks has been encouraged. The goal of the Drug-Induced Liver Injury Network (DILIN; dilin.dcri.duke.edu/ ) is to collect clinical data, genomic DNA, and liver tissues from patients who have experienced idiosyncratic drug reactions, in an effort to determine pathogeny. Recent studies from these groups have focused on the specific group of DILI cases with features of autoimmune hepatitis (AIH), which could explain recurrent DILI with different drugs in a same patient.
Despite much effort, hepatotoxicity remains a problem for many existing drugs, as well as those in development. This has a major economic impact because hepatotoxicity is the most frequent cause of postmarketing withdrawal of new medications.
This chapter reviews the main clinical features of toxin- and drug-induced disorders and describes the main pathologic patterns attributed to drugs and toxins. In the last part, some frequently prescribed hepatotoxic drugs are described more extensively to illustrate the variety of clinicopathologic presentations of liver injury.
For an extensive and detailed description of hepatotoxicity produced by a larger number of individual drugs, the reader is referred to a variety of specialized publications. Synthetic and actualized data can be obtained from specialized Web sites such as Hepatox, which was developed in France by Dr. Biour and is hosted on the Web site of the Association Française pour l’Etude du Foie ( www.afef.asso.fr/liens/Hepatox/index.phtml ), or from the Uppsala Monitoring Centre of the World Health Organization (WHO) database ( who-umc.org ).
DILI accounts for approximately 10% of cases of acute hepatitis in adults and for more than 40% of cases in individuals older than 50 years. In various series, it has accounted for 10% to 20% of cases of fulminant and subfulminant hepatitis and for 2% to 5% of patients hospitalized for jaundice. The risk of a fulminant course is much greater for DILI (20%) than for viral acute hepatitis (1%). On the other hand, drugs are less often incriminated in chronic hepatitis or cirrhosis (<1% of cases).
However, it is probable that the real incidence of DILI is much higher because of unrecognized and benign presentations. In children, DILI is less frequent, but it is also an underrecognized cause of pediatric liver disease, and large series are rare. Children could represent 5% to 8.7% of DILI patients.
A French study found an annual incidence of DILI of almost 14 cases per 100,000 population, a rate 16 times higher than that based on spontaneous reports. The most common causes of DILI are the analgesic drug acetaminophen and several antiinfectious agents such as antibiotics from different families (e.g., amoxicillin/clavulanic acid [AMC], erythromycin, minocycline), as well as antituberculosis drugs (especially isoniazid [INH]), psychotropic agents (e.g., chlorpromazine), anticonvulsants (e.g., valproic acid), anesthetics, oral contraceptives, lipid-lowering agents, antiinflammatory agents (e.g. diclofenac, disulfiram), and cardiovascular agents (e.g., amiodarone), as shown in large series (see Box 48.1 ). In children, apart from acetaminophen, antimicrobial and central nervous system agents are the most commonly implicated drug classes, representing 50% and 40% of cases, respectively, as demonstrated in the recent DILIN series. Another pediatric series from India emphasizes the role of antituberculosis drugs (e.g., INH, rifampicin [RFP], ethambutol) and anticonvulsants (phenytoin and carbamazepine), pointing out the geographic specificity for certain drug toxicities. In this Indian pediatric population, hypersensitivity features such as skin rashes, eosinophilia, fever, lymphadenopathy, and Stevens-Johnson syndrome were frequently seen (41%) and were associated with a better outcome.
The total number of drugs liable to be toxic to the liver exceeds 1100, and this long list must be frequently updated. The highest frequency of hepatotoxicity for marketed drugs has been approximately 1% (for tacrine), but for most drugs, the risk is low (1/10,000 to 1/100,000) or extremely low (1/100,000 to 1/1,000,000 for antihistaminic compounds or penicillin). However, evaluation of the accurate incidence and risk factors, as well as assessment of the causality of one or several toxic agents, remains a major problem in DILI.
In addition, overdoses of certain drugs are well known to be extremely toxic, not only in the context of a therapeutic misadventure (or with repeated doses, particularly in cases of excessive alcohol ingestion) but as a method of suicide. In the latter instance, acetaminophen is the drug most frequently used for suicidal overdose among adolescents and young adult women in the United States and Great Britain. When given in therapeutic doses for a period of 14 days, acetaminophen produced significant asymptomatic elevations in alanine aminotransferase (ALT) levels among healthy volunteers, suggesting that subclinical injury may be more common than previously believed. There was also a much lower incidence of acetaminophen toxicity as a cause of acute liver failure in children compared with adults, with almost half of all cases being indeterminate in origin. Acetaminophen toxicity is reviewed more extensively later in this chapter.
The potential hepatotoxicity of herbal remedies commonly used for self-medication (i.e., alternative or “natural” treatments) and of other botanicals (e.g., the well-known mushroom poisoning from Amanita phalloides ) should always be considered in the evaluation of pathology specimens. The list of confirmed or suspected hepatotoxic herbal components (e.g., Chinese herbs, germander ) is long, and the full extent of their toxicity remains unclear. Many alimentary supplements, including vitamins, minerals, and botanical extracts, are also recognized as possible cause of DILI, as reviewed by Navarro in 2009. For instance, many Herbalife products, used for nutrition or energy or to reduce stress, have been shown to commonly induce cytolysis, cholestasis, and even, in rare cases, acute liver failure.
Increased consumption of illicit drugs such as heroin, cocaine, and ecstasy, regardless of the route of administration (intranasally, intravenously, or by smoking), has increased the number of cases of hepatotoxicity and potentiated other factors of liver disease. For example, daily cannabis smoking is significantly associated with progression of fibrosis in patients with chronic hepatitis C virus (HCV) infection.
Frequently, hepatotoxicity is further potentiated by the use of other drugs in combination or by alcohol intake. Therefore, when prescribing a potentially hepatotoxic drug in a patient, it is particularly important to be aware of all additional risk factors for the liver in that patient, such as alcohol, diabetes, obesity, and chronic viral hepatitis. Otherwise, the risk of DILI will increase, and also the severity of the other liver diseases can worsen. During recent decades, for example, the evolving epidemic of nonalcoholic fatty liver disease caused by metabolic syndrome has potentiated the hepatotoxic properties of certain drugs such as methotrexate—and vice versa.
Furthermore, a drug may be beneficial in the short term but harmful in the long term. For example, in individuals with human immunodeficiency virus (HIV) infection who also have hepatitis B virus (HBV) or HCV coinfection, alcohol abuse, or other hepatic risk factors, prolonged therapy with didanosine may induce chronic liver disease and may cause severe liver complications, such as variceal bleeding and portal thrombosis.
Clinical Assessment and Prediction of Hepatotoxicity
Side effects attributed to drugs and toxins in the liver are numerous and variable. Although a slight acute hepatocellular or cholestatic/mixed hepatitis is the most common presentation, DILI can mimic all forms of acute or chronic hepatitis as well as biliary or vascular hepatopathy. In addition, some liver tumors (e.g., hepatocellular adenoma, angiosarcoma) may be attributed to the long-term exposure to various drugs or toxins. Therefore, hepatologists and pathologists should consider possible drug-induced hepatotoxicity in the differential diagnosis of virtually any type of liver injury. Abnormal liver test results and nonspecific clinical signs may be present, including malaise, fatigue, abdominal discomfort, appetite loss, splenomegaly, icterus, or symptoms of acute liver failure. Signs of immunoallergic reaction, such as fever, rash, arthralgia, and eosinophilia, may be encountered but are infrequent and nonspecific. Chronologic and clinical diagnostic criteria that are useful in making the diagnosis of DILI are provided in Box 48.4 . Chronologic criteria, although usually considered essential, require an accurate clinical history, which is not always possible. Many other difficulties are frequently encountered in making the diagnosis, as shown in Box 48.5 . In some instances, clinical criteria and laboratory data help to eliminate other potential causes of hepatopathy and point to drug toxicity as the only possible differential diagnosis. Additional tests, such as seric dosage of the drug, can be helpful in some cases. Liver biopsy is not mandatory in the clinical survey, but it may provide substantial information regarding the positive and differential diagnosis of DILI (see later discussion), particularly if liver disease persists, provided that pertinent clinical information is provided and the pathologist is experienced.
Interval between beginning of treatment and onset of liver injury: 1 wk to 3 mo (shorter after readministration)
Regression of liver laboratory abnormalities after withdrawal of treatment (decrease of >50% in 1 wk)
Relapse of liver laboratory abnormalities after accidental or intentional readministration of the offending drug
Elimination of other causes (anamnesis, biologic data, or imaging data)
Previous hepatic or biliary disease
Viral hepatitis (e.g., hepatitis A, B, C, D, or E virus; cytomegalovirus; Epstein-Barr virus; herpesvirus)
Autoimmune hepatitis or cholangitis
Bacterial infection ( Listeria , Campylobacter , Salmonella )
Positive clinical criteria
Age >50 yr
Intake of many drugs
Intake of a known hepatotoxic agent
Specific serum autoantibodies: anti-M6, anti-LKM2, anti-CYP1A2, anti-CYP2E1
Drug titration in blood: acetaminophen, vitamin A
Hypersensitivity manifestations (fever, chills, skin rash, hypereosinophilia)
Liver Biopsy *
* Not necessarily required but indicated for the purposes listed.
Eliminates other causes of liver injury
Shows lesions suggestive of drug-induced hepatotoxicity
Defines lesions for new drugs
Nonspecific clinical features
Treated disease itself is responsible for liver abnormalities (e.g., bacterial infection)
Intake of several hepatotoxic drugs (e.g., combined antituberculosis agents)
Drug intake difficult to analyze
Inaccurate history or chronology
Compounds considered safe (herbal remedies)
Offending agent not considered a “drug” by the patient
Forgotten information (elderly)
Patient in coma (fulminant hepatitis)
Because of variability in both drug exposure and patient susceptibility, prediction of hepatotoxicity depends heavily on the specific type of drug used and patient characteristics ( Box 48.6 ). Some acquired factors may enhance susceptibility to one type of drug but not another. Furthermore, various genetic factors, such as deficiency in certain isoforms of cytochrome P450 (CYP450) or in other enzymatic and metabolic pathways, may contribute to drug hepatotoxicity ( Table 48.2 ). In most instances, potentially fatal idiosyncratic reactions cannot be reliably predicted. For example, troglitazone, which was an approved drug for the treatment of diabetes mellitus, is an idiosyncratic, directly hepatotoxic drug that led to an unacceptable rate of acute hepatic failure and was subsequently removed from the market.
Drug is massively absorbed in the digestive tract
Drug is metabolized by the cytochrome P450 system
Drug belongs to a family with well-documented hepatotoxicity
Drug exhibits a molecular structure predisposing to the formation of reactive metabolites
Patient Factors (Constitutional and Acquired)
>60 yr: isoniazid, nitrofurantoin
Children: valproic acid, salicylates
Women: methyldopa, nitrofurantoin
Pregnancy: acetaminophen, tetracycline
Chronic alcohol abuse: acetaminophen
Intake of other drugs
Enzyme induction: rifampicin, isoniazid
Enzyme inhibition: troleandomycin, estrogens
HIV infection: trimethoprim/sulfamethoxazole, sulfonamides
(see Table 48.2 )
|CYP2D6||Perhexiline||Enzyme deficiency: 6% of white population |
Perhexiline toxicity: 75% of patients are CYP2D6 deficient
|CYP2C19||Atrium (combination of phenobarbital, febarbamate, and difebarbamate)||Enzyme deficiency: 3% to 5% of white population |
Atrium toxicity: all patients have a complete or partial deficiency
|NAT2||Sulfonamides, dihydralazine||Transmitted as an autosomal recessive trait |
High frequency of the slow acetylation phenotype; this deficiency contributes to but is not sufficient for the toxicity
|Glutathione synthetase||Acetaminophen||Uncommon condition; deficient subjects are more susceptible to acetaminophen hepatotoxicity|
|Glutathione S -transferase type T||Tacrine||Needs to be confirmed|
|Hepatic detoxification capacity for reactive metabolites||Halothane, phenytoin, carbamazepine, amineptine, sulphonamides||Deficiencies observed in patients and some family members |
Precise defects are not identified
|Genetic variations in the immune system||Halothane, tricyclic antidepressants, chlorpromazine, others||Association between several HLA haplotypes and some hepatotoxic drugs|
Causality can be assessed with more certainty if a clear chronologic link can be demonstrated between drug intake and onset of the hepatotoxic event ( Box 48.7 ). Components of the drug signature (e.g., pattern of liver test abnormalities, duration of latency before symptomatic presentation, presence or absence of immune-mediated hypersensitivity, response to drug withdrawal), in conjunction with certain genetic and environmental risk factors, can be formulated into a clinically based scoring system that is predictive of the likelihood of liver injury. The best validated scoring system that takes into account all of these parameters is the CIOMS/Roussel-Uclaf Causality Assessment Method (RUCAM), which nonetheless has certain imperfections. The Naranjo Adverse Drug Reactions Probability Scale (NADRPS) is another simple system based on similar items. Both systems produce a numerical score, indicating that the diagnosis of DILI is definite (or probable), possible, or unlikely. However, a review of 61 case reports of DILI in the PubMed database of the National Institutes of Health over the last decade indicates that in current practice, these scores are used in no more than 25% of published cases.
Very likely (rare): Drug overdose; relapse after accidental readministration; specific features of drug hepatitis
Compatible (many cases): No specific criteria; suggestive chronology; absence of other causes
Doubtful (frequent): Missing information (chronology, clinical data); no specific criteria; frequent in fulminant hepatitis
Incompatible: Demonstration of another cause; incompatible chronology; be aware that hepatitis can occur after discontinuation of treatment (e.g., halothane, amoxicillin/clavulanic acid)
Although it is difficult to provide definitive proof of responsibility for a particular offending drug, and because readministration is ill advised, return to normal liver function after withdrawal of the drug is usually good supportive evidence of drug-induced toxicity. Additional tests may be performed on peripheral blood to identify a single causative agent. These may include drug dosing (e.g., acetaminophen), the double-locus sequence typing (DLST) method (which measures the patient’s lymphoproliferative response to growing doses of the suspected causative drug), or the leucocyte migration test (LMT). However, these tests are not simple to perform and not feasible in routine practice.
Prevention of Drug Hepatotoxicity
Assessment of toxicity in human hosts is performed before and after marketing of all drugs. During the early stages of drug development, preclinical studies in animals are mainly useful to detect dose-related predictable hepatotoxicity. Phase I safety studies in human volunteers test toxicity in few patients, after which more patients are exposed during efficacy testing in controlled clinical trials. However, almost 3000 patients need to be included to demonstrate a 1/1000 incidence of DILI, and many drugs that may induce idiosyncratic hepatotoxicity escape detection during preclinical safety assessment and clinical trials.
From a pharmaceutical research perspective, metabolite profiling is essential to rational drug design. This issue is addressed, at present, to eliminate molecules that are prone to metabolic bioactivation, based on the concept that formation of electrophilic metabolites triggers covalent protein modifications and subsequent organ toxicity. A cell-based approach for testing of cell viability, mitochondrial impairment, biliary transport, and CYP450 inhibition in the presence of a drug has become useful for the evaluation of putative hepatotoxicity. The role of mitochondria in DILI, which may be altered through direct toxicity or through immune reaction, seems central, so new drug molecules should also be screened for possible mitochondrial effects. Although such an in vitro approach is pragmatic, it has its limitations, because a linear correlation does not exist between toxicity and extent of bioactivation.
After marketing, surveillance and voluntary reporting of cases is necessary. Routine monitoring of liver enzymes does not seem useful to prevent clinically significant hepatotoxicity in the general population, but it may be interesting in high-risk patients who are taking well-known hepatotoxic drugs. At present, a few simple rules can be applied to help prevent drug hepatotoxicity ( Box 48.8 ). In the future, advances in proteomics, metabolomics, genomics, and bioinformatics may pave the way to “personalized” pharmacotherapy in which the beneficial effect of a drug in an individual is maximized and the toxicity risk minimized.
Detection of toxicity in animal or cellular models
Safety analysis in healthy volunteers and patients
Avoid readministration of the offending drug
Avoid readministration of drugs belonging to the same biochemical family
Avoid simultaneous administration of several drugs
Cytochrome P450 inhibitors: cimetidine, ketoconazole, methoxsalen, and oleandomycin may be nonselective (e.g., cimetidine) or selective for a given CYP450 isoform
Cytochrome P450 inducers: rifampicin, barbiturates, phenytoin; more selectively, omeprazole for CYP1A1 and CYP1A2
Control administration of drugs to patients with malnutrition (lack of defense against reactive metabolites) and to alcoholic patients
Be aware that elderly patients are more susceptible to drug hepatotoxicity
Be careful when administering drugs to patients with human immunodeficiency virus (HIV) infection
Coadministration of many drugs
Decreased ability to detoxify drugs (malnutrition)
Higher susceptibility to some drugs (sulfonamides)
Genetic factors: genotyping and phenotyping tests are not widely available
Follow-up of blood liver tests may be useful for detecting hepatotoxicity
Treatment and Prognosis
In most cases, no specific treatment is available for DILI, and the main element of treatment is to stop administration of the offending agent, if possible. In most cases of DILI, liver injury is mild, and biologic recovery occurs within days or weeks. However, recovery can take longer with certain drugs.
Because of the wide spectrum of manifestations (from asymptomatic liver test abnormalities to acute liver failure), the difficulties in evaluating the course of disease, and the possibility of spontaneous return to normal liver function because of patient metabolic adaptation, it is difficult to define criteria for cessation or for possible maintenance of the suspected causative drug.
The Drug-Induced Liver Injury Network (DILIN) has developed a five-point system for grading severity based on liver tests, symptoms, jaundice, need for hospitalization, signs of hepatic failure, and death or need for liver transplantation ( livertox.nih.gov.easyaccess1.lib.cuhk.edu.hk/Severity.html ).
Various algorithms for management of DILI have been proposed, based on different biologic thresholds. For instance, jaundice and bilirubin >3 × ULN or prothrombin time/international normalized ratio (PT-INR) >1.5 × ULN should prompt discontinuation of a drug responsible for cholestatic-type injury. In hepatocellular or mixed disease, ALT >8 × ULN at any one time, or ALT >5 × ULN for >2 weeks, or ALT >3 × ULN and either bilirubin >2 × ULN or PT-INR >1.5 × ULN would lead to drug withdrawal.
The only example of a well-established specific treatment for drug-induced hepatotoxicity is prevention of severe hepatitis in patients with acetaminophen overdose by administration of N -acetylcysteine within the first 10 hours after consumption of the drug to detoxify reactive metabolites.
The usefulness of corticosteroids in immunoallergic hepatitis has not been clearly demonstrated but could be tested. In autoimmune-like drug-induced hepatitis, corticosteroids are useful.
Administration of ursodeoxycholic acid has been proposed for long-lasting chronic cholestasis and as symptomatic treatment for the relief of pruritus or as compensation for vitamin malabsorption.
In the worst-case scenario—drug- or toxin-induced fulminant hepatic failure—liver transplantation may be required.
The prognosis of drug-induced hepatotoxicity is usually excellent when the injury is acute, the cause is recognized, and the offending agent is withdrawn before the onset of severe acute or chronic injury. The term Hy’s law refers to a method of assessing a drug’s potential risk of causing serious hepatotoxicity and mortality. It is based on observations by Dr. Hy Zimmerman about the pejorative value of icteric cholestasis in DILI : Drug-induced jaundice caused by hepatocellular injury without a significant obstructive component frequently leads to a poor outcome, with a 10% to 50% rate of mortality or transplantation. This fundamental observation is based on the fact that if there is enough hepatocellular damage to impair bilirubin excretion, then there is a potential threat to life.
Clinical elements for the assessment of prognosis include age (typically worse for patients older than 50 years), sex (women being more susceptible to certain drugs), ethnicity and genetic background, nutritional status, multimedication association, and association of other general conditions (e.g., diabetes mellitus) or liver diseases (e.g., alcohol abuse, viral disease).
Because of heterogeneous reporting of biopsy findings in the literature, limited data exist on the impact of histology on the outcome of acute DILI. However, some data indicate that the extent of massive and submassive necrosis caused by toxic exposure is linked to a higher mortality rate (>85%), as also observed in other causes of acute liver failure. On the other hand, the presence of hepatic eosinophilia may be associated with a better prognosis in DILI caused by disulfiram and other drugs.
In the setting of chronic hepatitis (as is possible with amiodarone, α-methyldopa, or methotrexate), progression to fibrosis, and eventually cirrhosis, may occur during an extended period. In these circumstances, withdrawal of the drug at a later date does minimize the risk of continued progression, but reversal of fibrosis is rare. An important caveat is the risk of alcohol-induced synergistic injury. Intake of alcohol in the setting of drug-induced chronic hepatitis may exacerbate the severity of injury and cause continued progression toward cirrhosis even after the original offending drug has been withdrawn. Therefore, exclusion of alcohol and other comorbidities is part of the treatment of chronic DILI.
Pathologic Patterns of Toxic Liver Injury
Liver biopsy for adverse drug reaction is one of the most difficult and frustrating situations for the liver pathologist. Liver biopsy is not systematically done in cases of suspected DILI, and most of the time, the decision to perform a biopsy is made because of a complicated clinical situation, such as persistent abnormal liver test results after drug withdrawal, intercurrent medical conditions, multiple potential drug candidates, or a biologic context suggestive of autoimmunity. The list of drugs associated with DILI is very long, but their association with liver injury may be tenuous, and pathologic data are lacking in the literature. When available, histologic features are often nonspecific and heterogeneous among different patients and studies.
An inadequate clinical history or incomplete reporting of drug intake (e.g., nature of the drug, timing) often seriously compounds the problem for the pathologist. Only rarely is an individual histologic sign specific for a particular drug exposure; an example is fibrin-ring granuloma in allopurinol toxicity. Most of the time, a single lesion (e.g., steatosis) can be induced by various toxins. Conversely, one specific type of drug may give rise to different patterns of hepatotoxicity in different patients; for example, hepatitis, cholestasis, granulomas, or a combination of these tissue reactions can be related to phenylbutazone. Nonsteroidal antiinflammatory drugs (NSAIDs) can induce either severe hepatocellular or biliary damage, and amiodarone can produce both phospholipidosis and steatohepatitis, albeit by different mechanisms.
However, in the absence of other causes of liver disease, the association of a certain type of necrosis, the presence of a sparse or peculiar inflammatory infiltrate, and the concomitance of steatosis and cholestasis favor the diagnosis of DILI and suggest a mechanism of toxicity ( Table 48.3 ).
|Zone 3 necrosis||Susceptibility caused by CYP450 location|
|Massive necrosis||Intrinsic or idiosyncratic toxicity|
|Necrosis + little inflammation||Intrinsic toxicity|
|Minimal portal inflammation||Intrinsic or idiosyncratic toxicity|
|Many eosinophils||Hypersensitivity reaction|
|Many neutrophils||Inflammatory response of the innate immune system to drug-induced damage of hepatocytes|
|Microvesicular steatosis||Mitochondrial injury|
|Mixed patterns||Multiple targets|
|Cholestatic hepatitis||Idiosyncratic toxin|
|Steatosis + necrosis||Indirect toxin|
Microscopic analysis of the liver benefits from knowledge of the clinical history and laboratory findings. It is based on a systematic, semiological analysis of all histologic compartments of the liver. Adverse drug reactions affect mainly hepatocytes and bile duct epithelial cells but may also damage sinusoidal cells and vessels in the liver. The spatial organization of vessels, lobules, and sinusoids is illustrated in Figure 48.1 . Individual lesions must finally be grouped to define a general and overall pattern of liver injury. The most frequent patterns of DILI are acute hepatocellular injury, predominantly cholestatic injury (of hepatocellular or biliary origin), mixed hepatocellular-cholestatic injury (i.e., cholestatic hepatitis), steatosis pattern, vascular pattern, and neoplastic pattern. These patterns are detailed in Table 48.4 , which also indicates examples of causative agents. The corresponding histology is described in the following sections. However, injury patterns are not mutually exclusive, and a mixed pattern of injury may occur in many instances of drug-related hepatotoxicity.
|Pattern of Injury||Main Drugs|
|Acute Hepatocellular Injury|
|Predominantly cytolytic (spotty, submassive, massive)||Conventional drugs: |
|New causative drugs: psychotropic and neurotropic drugs (e.g., tacrine), anti-HIV agents (e.g., didanosine, zidovudine), antimycotics (terbinafine), cytokines, growth factors (interleukins, granulocyte colony-stimulating factor), antidiabetic agents (troglitazone)|
|Herbal medicines: pyrrolizidine alkaloids ( Crotalaria, Senecio ), germander, Chinese herbal preparations|
|Illegal compounds: cocaine, ecstasy|
|Excipients: sodium saccharinate, polysorbate, propylene glycol|
|Chemical agents: carbon tetrachloride, trichloroethylene, tetrachloroethylene, toluene, dimethylformamide, vinyl chloride|
|Pure cholestasis||Oral contraceptives, estrogens, estrogens + troleandomycin or erythromycin, androgens, tamoxifen, azathioprine, cytarabine|
|Cholestasis + mild cytolysis (“cholestatic hepatitis”)||Conventional drugs: Phenothiazines, NSAIDs, macrolides, sulfonamides, β-lactam antibiotics, tricyclic antidepressants, carbamazepine, AMC, gold salts, propoxyphene|
|New drugs: |
|Mixed-pattern acute hepatitis||Numerous drugs, including AMC, aureomycin, azathioprine, cephalosporin, chemotherapeutic agents, lovastatin, meprobamate, methyldopa, nitrofurantoin, penicillamine|
|Chronic Hepatocellular Injury|
|Chronic hepatitis (with risk of cirrhosis)||Valproic acid, amiodarone, aspirin, benzarone, diclofenac, flucloxacillin, halothane, iproniazid, isoniazid, methotrexate, methyldopa, nitrofurantoin, papaverine, rampril, valproic acid; herbal medicines (germander)|
|Predominantly microvesicular||Aspirin, tetracycline, valproic acid, alcohol, NSAIDs, anti-HIV drugs, fialuridine|
|Predominantly macrovesicular||Alcohol, methotrexate, corticosteroids|
|Nonalcoholic steatohepatitis (from steatosis to cirrhosis)||DEAEH, amiodarone, perhexiline maleate, anti-HIV and antiretroviral agents, corticosteroids, tamoxifen|
|Phospholipidosis||DEAEH, amiodarone, perhexiline maleate, total parenteral nutrition|
|Hemosiderin||Excess dietary iron, alcoholism, total parenteral nutrition|
|Ground-glass changes||Phenobarbital, phenytoin, cyanamide|
|Increased mitoses||Colchicine, arsenic|
|Bile Duct Injury|
|Cholestasis + bile duct degeneration with or without inflammation||Phenothiazines, ajmaline, carbamazepine, tricyclic antidepressants, macrolides, AMC, dextropropoxyphene|
|Chronic Cholangitis ± Ductopenia|
|Primary biliary cirrhosis–like||Phenothiazines, ajmaline, arsenic derivatives, tricyclic antidepressants; macrolides, thiabendazole, tetracycline, fenofibrate; herbal medicines (germander)|
|Primary sclerosing cholangitis–like||Arterial infusion with floxuridine, formol, and hypertonic saline injection into hydatid cyst; hepatic artery embolization|
|Portal Vein Lesions|
|Hepatoportal sclerosis||Azathioprine, arsenic, Thorotrast, vinyl chloride|
|Nodular regenerative hyperplasia||Spanish toxic oil, oral contraceptives, azathioprine|
|Hepatic Artery Lesions|
|Intimal hyperplasia||Oral contraceptives|
|Hepatic Vein Lesions|
|Hepatic vein thrombosis (Budd-Chiari)||Oral contraceptives, dacarbazine, irradiation, total parenteral nutrition|
|VOD/SOS||Pyrrolizidine alkaloids, azathioprine, antineoplastic agents, alcohol, heroin|
|Sinusoidal dilation/peliosis||Oral contraceptives, estrogens, anabolic steroids, azathioprine, vitamin A, tamoxifen, danazol, heroin|
|Hepatic stellate cells|
|Hypertrophy (lipid storage) ± perisinusoidal fibrosis||Vitamin A, methotrexate, azathioprine, 6-mercaptopurine|
|Storage||Talc, polyvinyl pyrrolidone, silicone, barium|
|Sinusoidal endothelial cells||(see Hepatic Vein Lesions )|
|Epithelioid granulomas||Quinidine, hydralazine, phenytoin|
|Fibrin ring granulomas||Allopurinol|
|Granulomatous hepatitis (cytolytic ± cholestasis)||Phenylbutazone|
|Lipogranulomas||Mineral oil ingestion|
|Lipogranulomas with black pigments||Gold salts|
|Foreign body granulomas||Talc, surgical suture material|
|Hepatocellular adenoma (± intratumoral hemorrhage, subcapsular hematoma, rupture)||Oral contraceptives, anabolic/androgenic steroids, estrogens|
|Angiosarcoma||Vinyl chloride, Thorotrast|
|Hepatocellular carcinoma||Oral contraceptives, anabolic/androgenic steroids, Thorotrast|
Acute Hepatocellular Injury
Acute hepatitis accounts for 90% of drug-induced liver diseases. Essentially, this is clinically defined by ALT elevations at least 2 × the ULN, which is a marker of hepatocyte injury (cytolysis). Elevated alkaline phosphatase (AP) is an enzymatic marker of cholestasis because this enzyme is present on the apical membranes of both hepatocytes and bile duct epithelial cells. Acute hepatocellular injury may be predominantly cytolytic (ALT/AP ratio ≥5) or cholestatic (ALT/AP ≤2), or it may occur in a combined form (ALT/AP between 2 and 5).
The mechanisms involved in the development of drug-induced acute hepatitis are complex. They are rarely direct (e.g., lovastatin); usually, only massive doses of a foreign substance or extensive metabolism of a particular xenobiotic may lead to direct hepatotoxicity. Drug-induced acute hepatitis mainly results from the formation of hepatotoxic reactive metabolites, which often involve the CYP450 system. The CYP450 system, located mainly in the liver (hepatocytes) and predominantly in the centrilobular zone, metabolizes and eliminates essentially all liposoluble xenobiotics in the environment, as well as most drugs used clinically. However, several xenobiotics are transformed by the CYP450 system into stable metabolites, and many others are oxidized into unstable, chemically reactive intermediates. Reactive metabolites can attack hepatic constituents (e.g., DNA, unsaturated lipids, proteins, glutathione). The end result of this in situ reaction may be either apoptosis or cytolytic necrosis. However, for many drugs, the formation of reactive metabolites is minimal and dose dependent, so that a mild elevation of serum aminotransferases is often seen when the drug is used at therapeutic levels.
The CYP450 isoenzymes are under genetic control; therefore, the hepatic level of a given isoenzyme varies considerably among different people. Furthermore, other agents can enhance the effect of certain drugs. For instance, chronic ethanol ingestion increases a particular isoenzyme of CYP450 (i.e., CYP2E1) that activates acetaminophen.
The binding of reactive metabolites to intracellular or circulating proteins leads to a structural modification that can “mislead” the immune system into mounting an immune attack against its own hepatocytes. Halothane hepatitis is a paradigm for immune-mediated drug hepatotoxicity because of the presence of autoantibodies in the serum of affected patients. Toxic hepatitis caused only by activation of the host immune system (autoimmunity), without a contribution from direct hepatic metabolism of an exogenous drug, is uncommon. It is usually associated with hypersensitivity manifestations, such as fever, rash, and blood eosinophilia, also known as DRESS (drug rash with eosinophilia and systemic symptoms).
Genetic factors that affect hepatic drug metabolism and polymorphisms of major histocompatibility complex molecules may explain the particular susceptibility of some individuals to certain drug reactions. These factors have been clearly identified for some drugs (see Table 48.2 and the discussions of individual drugs in this chapter).
Predominantly Cytolytic Injury
The predominantly cytolytic pattern of drug-induced acute hepatitis resembles acute viral hepatitis but without further specific features. Numerous drugs can cause this pattern of liver injury, including acetaminophen, NSAIDs, psychotropic drugs, a variety of herbal medicines, cocaine, and chemical agents such as carbon tetrachloride (see Table 48.4 ). Liver damage ranges from mild hepatitis, with rapid improvement after removal of the offending drug, to severe or even fatal liver failure. Hepatocyte death results from the necrotic process or apoptosis or both. Marked lobular inflammation is typically present with toxicity from INH, monoamine oxidase inhibitors, anticonvulsants (phenytoin, valproate), and antimicrobials (sulfonamides, trimethoprim/sulfamethoxazole [co-trimoxazole], ketoconazole) but is rare or absent with toxicity from acetaminophen, cocaine, ecstasy, or carbon tetrachloride. The differential diagnosis mainly includes viral hepatitis and AIH; some data may favor DILI and may suggest a mechanism of injury ( Table 48.5 ; also see Table 48.3 ).
|AIH with DILI||Patients with known AIH; probably chance association||Usual AIH histology|
|Often advanced fibrosis|
|Drug-induced AIH (e.g., anti–TNF-α, β-interferon)||Patients with unrecognized AIH or predisposition to AIH, in whom AIH is unmasked or induced by DILI; good response to steroids; relapse after withdrawal of immunosuppression with the need to continued immunosuppressive treatment; chance association of drug intake in a patient with first presentation of AIH cannot be ruled out||Usual AIH histology|
|Centrilobular necrosis possible|
|Prominent eosinophilic infiltrates (sometimes)|
|Immune-mediated DILI (e.g., nitrofurantoin, minocycline)||Clinical and biochemical signs similar to AIH; eosinophilia and rash may be present; good response to steroids; remission is maintained after successful withdrawal of steroids||Usual AIH histology|
|Usually no advanced fibrosis|
|Centrilobular necrosis possible|
Hepatitis with Spotty Necrosis/Apoptosis.
When the mode of hepatocellular injury is predominantly cytolytic, necrosis/apoptosis can affect isolated hepatocytes in the lobule (“spotty” necrosis), resembling viral hepatitis; or, on occasion, it can take a mononucleosis-like appearance. In the former, ballooning or necrotic/apoptotic hepatocytes, scattered or in small foci, are distributed randomly in the lobule, with no or only a few inflammatory cells, leading to an acute hepatitis–like pattern or chronic lobular hepatitis ( Fig. 48.2, A and B ). INH, sulfonamides, and diclofenac and other NSAIDs can cause this pattern of injury.
Neutrophils and eosinophils (see Fig. 48.2, C ) are often also present in the lobule and in some portal tracts. The presence of eosinophils favors a toxic rather than a viral cause of the hepatitis and suggests allergic mechanisms. The presence of prominent neutrophils in portal tracts in a cytolytic hepatitis also favors DILI to other causes. Kupffer cells are often hypertrophied and contain pigments (lipofuscin, hemosiderin), which are best seen with periodic acid–Schiff (PAS) stain, with or without diastase digestion (d-PAS). Sometimes, and especially when the delay between the cytolytic peak and the time of biopsy is great, aggregates of pigmented d-PAS–positive macrophages without any necrosis or apoptosis are the only lesions seen (“resolving hepatitis”). A prominent activation of Kupffer cells, associated with sinusoidal lymphocytosis showing lymphocytes in single files, characterizes the variant form of mononucleosis hepatitis–like injury, as typically observed in hepatotoxicity related to phenytoin (an anticonvulsant agent), paraaminosalicylate, or dapsone.
Hepatitis with Submassive Necrosis.
In cases of hepatitis with submassive necrosis, liver necrosis (whether it appears as ballooning degeneration, apoptotic bodies, or coagulative necrosis) is usually zonal and occurs mainly in the centrilobular zones, leading to dropout and loss of hepatocytes, usually with preservation of periportal hepatocytes ( Fig. 48.3 ). Extension of hepatocyte injury to the midzonal areas of the lobule may be strictly zonal and homogeneous, or it may be irregular, leading to the formation of well-demarcated, more or less confluent necrotic areas that contrast abruptly with surviving hepatocyte parenchymal regions. When necrosis is heterogeneous in distribution, it may lead to a maplike or geographic hepatitis ( Fig. 48.4 ). In areas of severe hepatocyte necrosis and collapse, the reticulin framework and endothelial cells are often preserved and are mixed with variable numbers of inflammatory cells and hypertrophied Kupffer cells or macrophages that contain a brown ceroid pigment in their cytoplasm. Significant ductular proliferation may develop around portal tracts with time, as part of a regenerative and healing process. The collapse may lead to liver atrophy, Glisson capsule retraction, and approximation of portal tracts at the microscopic level. Lesions that are heterogeneous in distribution, with irregular regeneration and collapse, can be misleading if a biopsy (usually transjugular) is performed to assess the severity of the lesions and the extent of necrosis and regeneration.
Several types of drugs may lead to this type of necroinflammatory injury, with a generally zonal coagulative pattern affecting almost exclusively the centrilobular areas. Typical examples are acetaminophen and halothane. In rare cases such as furosemide hepatotoxicity, one may see predominantly midzonal necrosis. Periportal necrosis is rare and should suggest other drugs such as cocaine ( Fig. 48.5 ), especially in combination with other toxins (e.g., halogenated hydrocarbons), as well as allylformate or albitocin.
The term massive necrosis is used to describe necrosis of almost all of the normal hepatic lobule, which usually leads to clinically fulminant hepatitis requiring liver transplantation. This type of injury can occur with most of the drugs that cause submassive centrilobular necrosis. The most common example is suicidal or accidental overdose with acetaminophen ( Fig. 48.6 ) or halothane ( Fig. 48.7 ), but other drugs also can cause this type of extensive, confluent coagulative necrosis (see Table 48.4 ). This same pattern of severe acute liver damage can result from mushroom poisoning with A. phalloides ( Fig. 48.8 ) and other environmental or illicit drugs such as ecstasy. This pattern of injury often leaves only a few remaining viable hepatocytes, usually in the periportal region, where surviving cells often exhibit microvesicular or macrovesicular steatosis (see Fig. 48.8, B ). The collapsed parenchyma is often intermingled with a prominent bile ductular reaction or proliferation and a few inflammatory cells and Kupffer cells. As a general rule, a marked contrast between the severity of parenchymal necrosis and a poorly developed (mild) inflammatory portal reaction increases the likelihood that the liver injury was caused by a drug reaction, as opposed to a viral infection. Liver atrophy is the rule.
Predominantly Cholestatic Injury
Cholestatic DILI may be caused by hepatocellular toxicity or, less frequently, by biliary lesions (see later discussion). Alterations of hepatobiliary transporters are often implicated in this type of DILI. A mixed hepatocellular-cholestatic injury (cholestatic hepatitis) occurs more frequently with drugs than a pure cholestatic hepatocellular injury does, and this type of mixed disease is also discussed later in this chapter. As mentioned earlier, severe cholestasis in DILI must be considered a pejorative prognostic factor.
The pattern of bland cholestasis is characteristic of anabolic or contraceptive steroid use. It is typified by the presence of prominent intrahepatic cholestasis, mainly in centrilobular hepatocytes, with the formation of canalicular plugs, corresponding to hepatocanalicular bilirubinostasis. On occasion, feathery degeneration of hepatocytes and liver cell rosettes may develop, especially in cases of prolonged cholestasis. Discontinuation of the offending drug is usually followed by complete recovery.
When cholestasis appears as isolated canalicular bilirubinostasis in a liver biopsy specimen, with little or no inflammation, hepatocyte necrosis, or biliary lesions, the term bland cholestasis is used. In the absence of bile duct obstruction, it suggests DILI ( Fig. 48.9 , and Table 48.3 ).
Mild hepatocyte ballooning/necrosis or apoptotic bodies, and sometimes portal inflammation, may be associated with cholestasis, in which case the injury is referred to as cholestatic hepatitis ( Fig. 48.10 and Table 48.4 ).
Mixed hepatitis combines conspicuous cytolytic injury and cholestasis ( Fig. 48.11 ) and is frequently associated with immunoallergic manifestations. Many drugs can cause either pure cholestasis (mainly steroids) or a mixed pattern of cholestatic hepatitis, including psychotropic drugs, antibiotics, antituberculosis drugs, and the NSAID diclofenac (see Table 48.4 ). In both instances, the prognosis is usually better than for drug-induced acute hepatocellular hepatitis, as described previously.