Buscar en
Annals of Hepatology
Toda la web
Inicio Annals of Hepatology Causality imputation between herbal products and HILI: An algorithm evaluation i...
Journal Information
Vol. 25.
(November - December 2021)
Share
Share
Download PDF
More article options
Visits
2036
Vol. 25.
(November - December 2021)
Open Access
Causality imputation between herbal products and HILI: An algorithm evaluation in a systematic review
Visits
2036
Pedro Felipe Soaresa,
Corresponding author
psoares@ufba.br

Corresponding author.
, Maria Tereza Calchi Fanti Fernandesa, Andréia de Santana Souzab, Caio Medina Lopesb, Darjore Amorim Carvalho dos Santosb, Diogo Pereira Rodrigues Oliveirab, Marcela Gottschald Pereirad, Nilia Maria De Brito Lima Pradoc, Gecynalda Soares da Silva Gomese, Genário Santos Juniorf,1, Raymundo Paranáa
a School Medicine of Bahia– University Federal of Bahia, Av. Rector Miguel Calmon, S/N - Vale do Canela, 40110-100, Salvador - BA, Brazil
b Faculty of Pharmacy – University Federal of Bahia, Salvador, BA, Brazil
c Epidemiology and Collective Health Center Department, University Federal of Bahia Salvador, BA, Brazil
d Universidad Nacional de La Plata, La Plata, Argentina
e Mathematics and Statistics Institute, University Federal of Bahia, Salvador, BA, Brazil
f Sciences of Health Post Graduation Program - University Federal of Bahia, Salvador, BA, Brazil
This item has received

Under a Creative Commons license
Article information
Abstract
Full Text
Bibliography
Download PDF
Statistics
Figures (1)
Tables (3)
Table 1. Clinical and demographics characteristics of HILI cases published in literature from 1979 to 2019.
Table 2. Principal Herbs and herbal products associated with HILI cases.
Table 3. Algorithms used in the assessment of HILI causality in published cases from 1979 to 2019.
Show moreShow less
Abstract

Algorithms can have several purposes in the clinical practice. There are different scales for causality imputation in DILI (Drug-Induced Liver Injury), but the applicability and validity of these for the HILI (Herb-Induced Liver Injury) evaluation is questionable for some scales. The purpose of the study was to determine the clinical and demographic profile of the patients with HILI, and the main algorithmic scales used in its causality assessment. The methodology was a systematic review of articles in English, Spanish, or Portuguese language, from 1979 to 2019, involving humans, with descriptors related to HILI. Qualitative and quantitative statistical analysis were performed. As a result, from a total of 60 articles, 203 HILI reports were selected: 59.9% were women, similar with other studies, and the average age was 45.8 years. Jaundice was the most frequent symptom and regarding the type of lesion, the hepatocellular was the most frequent. In regard to HILI severity, 3.0% were severe and 7.6% were fatal or required liver transplantation. In 72.3% of the cases, the most used algorithm was RUCAM (Roussel Uclaf Causality Assessment Method). The conclusion of the study is that RUCAM was the most used algorithm for causality assessment in HILI. The patients were predominantly female, jaundice was the main symptom, and HILI is reversible in the majority of cases.

Keywords:
Medicinal herbs
Herbal products
HILI
Liver injury
RUCAM
Full Text
1Introduction

DILI groups include drug-induced and xenobiotic-induced hepatotoxicity [1]. The histopathology is rich and may contain several findings [2,3]. The term HILI encompasses cases of herb-induced liver injury [4]. According to WHO, 85% of the developing countries population uses these products in their primary health care [5]. Some studies on the herbs and herbal products most consumed in the West and possibly associated with liver injury indicate that green tea is the main product associated with HILI, while in the East the natural products most associated with HILI are called Traditional Chinese Medicine (TCM) [6]. The incidence of liver injury associated with herbal products is uncertain, due to the scarcity of epidemiological studies related to the subject.

Algorithms can have several purposes in the clinical practice. The most common approach for diagnosis and treatment, is a “checklist” to define conducts. An example of an algorithm used in imputation of causality in HILI is the RUCAM (Roussel Uclaf Causality Assessment Method) score, the algorithmic tool most used in current clinical practice for the evaluation of hepatotoxicity [7,8]. There are several algorithms used to evaluate HILI, however, there is still no reproducible and practical method to predict, diagnose and evaluate the risk of this kind of hepatotoxicity [9].

The aim of this study is to determine the clinical and demographic profile of the population that had HILI and the main algorithmic scales used in its causality assessment.

2Material and methods

This is a systematic literature review conducted in the Medline, Scopus, Lilacs and Web of Science databases, the MESH descriptors were: chemically-induced liver toxicity; drug-induced acute liver injury; drug-induced liver disease; drug-induced liver injury; dietary supplement; food supplementations; nutraceuticals; herbal products; herbal therapy; Chinese drugs, plant; plant extracts; medicinal plants; pharmaceutical plants; healing plants; medicinal herbs. Boolean connectors used were “AND” and “OR”. The articles in which fulltexts were not available were requested by an e-mail to the author to recover the original work.

The included articles were case reports and series cases, with full text available, published from 1979 to 2019 and involving humans. The selected articles had their titles, abstracts and methodologies read. Studies that did not use any algorithm for HILI evaluation, that did not describe HILI or that did not provide data on the cases were excluded.

To characterize the cases as HILI, the criteria by Danan et al. [10–12] were used: alanine aminotransferase (ALT) ≥ 5 x the upper limit of normal (ULN) or alkaline phosphatase (ALP) ≥ 2 x ULN. Imaging during the episode and / or histological summary, liver biopsy, serology of hepatitis caused by hepatotropic virus or other liver disease based on clinical characteristics and laboratory tests were also associated. The type of the liver injury was based on R values (ALT / ULN) / (ALP / ULN).

The HILI severity were classified according to International DILI Expert Working Group as: mild (high alanine aminotransferase / alkaline phosphatase (ALT / ALP) activities meeting criteria for HILI and bilirubin concentration <2 × upper limit of normal (ULN), moderate (high ALT / ALP activities meeting criteria for HILI but bilirubin concentration ≥2 x ULN, or symptomatic hepatitis), severe (high ALT / ALP activities meeting criteria for HILI, bilirubin concentration ≥2 x ULN and any of the following: international normalized ratio ≥ 1.5; ascites and / or encephalopathy, disease duration <26 weeks and absence of underlying cirrhosis; other organ failure (considered due to HILI)) or fatal (death or transplantation caused by HILI, based on HILI severity rating).

Independent researchers conducted the data extraction. The following data were retrieved and analyzed from each article identified in the literature search: country source of the report, demographics, suspected herbal medicine, type of liver injury, biochemical parameters, histological findings, and outcome of the reaction.

Data analysis was performed qualitatively and quantitatively, using the Statistical Package for the Social Sciences (SPSS) version 21.0. Pearson's Chi Square Test was performed for categorical variables and Student's t-test for average comparisons. Statistical significance was considered p < 0.05.

3Results

A total of 60 articles were found that described cases of HILI and reported the use of at least one algorithm; of these, 203 cases were in line with Danan criteria and were included in this study (Fig. 1). The articles were from European (46.5%), Asians (31.2%), Americans (10.9%), Africans (10.9%) and Oceania (0.5%) publications. Among these, 59.9% were women, and age ranged from 1 to 82 years, with an average of 45.8 years. The percentage of elderly individuals (over 60 years) was 19.9%.

Fig. 1.

Preferred Reporting Items of Systematic Reviews (PRISMA) flow diagram.

(0.47MB).

The main natural and herbal products used were: Chelidonium majus (15.8%) [25,26], Polygonum multiflorum (12.3%) [27], Phosphagen, T-bomb II and Cell-tech (9.9%) [28], TCM (6.9%) [29] and green/black tea (6.9%) [30–36] (Table 2). About 74% of patients reported using only one hepatotoxic herbal product. The most frequent indications for use were to promote general/gastrointestinal well-being (25.2%), musculoskeletal pain (19.3%), skin and phanises lesions (4.5%), central nervous system-related complaints (4.0%). The hormonal disease/menopausal symptoms and systemic infections were 1.5% each. Sexual stimulator, antiparasitic, respiratory problems, cardiovascular disorders, diseases of the blood and hematopoietic tissue and immune system regulators were 0.5% each. About 4.0% of the cases had other non-standard indications for use; 37% of the cases omitted the indication of use.

The main symptom presented by HILI patients was jaundice (47%). Regarding the biochemical profile, AST = 893.62 U/L; ALT = 1.214.94 U/L; BT = 48.55 mg/dL; ALP = 336.38 U/L. There were no significant differences between the laboratory findings of the female and male cohort (Table 1).

Table 1.

Clinical and demographics characteristics of HILI cases published in literature from 1979 to 2019.

  Female (n = 121)  Male (n = 81)  Total (n = 203)  P value 
Age (mean, years)  49.10  41.08  45.83  <0.05 
> 60 years (%)  21.80  15.40  19.00  <0.05 
Jaundice (%)  49.60  43.00  47.00  0.366 
Type of liver injury:         
Hepatocellular (%)  81.30  47.90  66.90  <0.05 
Mixed (%)  11.50  49.30  27.80  <0.05 
Cholestatic (%)  7.30  2.70  5.30  <0.05 
AST (U/L)  1001.41  722.66  893.62  0.226 
ALT (U/L)  1260.30  1180.18  1214.94  0.140 
BilT (mg/dL)  57.33  9.00  48.55  0.352 
ALP (U/L)  325.40  313.20  336.38  0.450 
Biopsy (%)  42.90  26.60  36.40  <0.05 
Time to resolution (mean, days)  86.47  52.95  73.47  0.064 
Rechallenge (%)  4.20  3.80  4.10  0.878 
Liver Transplantation (%)  5.90  5.10  5.60  0.805 
Mortality (%)  1.70  2.50  2.00  0.677 
RUCAM used (%)  67.60  32.40  72.30  <0.05 

ALT: Aspartate Aminotransferase.; AST: Alanine Aminotransferase; BT: Total Bilirubin; ALP: Alkaline phosphatase; RUCAM: Roussel Uclaf Causality Assessment Method.

Table 2.

Principal Herbs and herbal products associated with HILI cases.

Herb and/or herbal product  Herbal Scientific Name  n (%) 
Greater Celandine  Chelidonium majus  32 (15.8%) [34,35
Polygonum multiflorum  Polygonum multiflorum  25 (12.3%) [17] 
Phosphagen, T-bomb II and Cell-tech  Tribulus terrestris, Eurycoma longifolia, Pueraria lobota, Avena sativa, Piper nigrum, Serenoa repens, Urtica spp., Tirgonella foenum-graecum, Trifolium pratense, Passiflora caerulea  20 (9.9%) [36] 
TCM    14 (6.9%) [37] 
Green/Black Tea  Camellia sinensis  14 (6.9%) [38–43] 
Noni  Morinda citrifolia  6 (3.0%) [44,45
Malay Jamu  Malay jamu  5 (2.5%) [37] 
Aloe vera  Aloe vera  4 (2.0%) [46,47
Flavocoxid  Flavonoids derivate  4 (2.0%) [48] 
Kava  Piper methysticum  4 (2.0%) [13,49–51
Scutellaria radix + Bombyx batryticatus + Bupleuri radix  Scutellaria radix + Bombyx batryticatus + Bupleuri radix  4 (2.0%) [52] 
Black cohosh  Cimicifuga Racemosa  3 (1.5%) [53–55] 
Innéov masa capilar®  Ribes nigrum  3 (1.5%) [56] 
Sennomotokounou  Sennomotokounou  3 (1.5%) [57] 
Ayurvedic herb    3 (1.5%) [58,59
Bupleuri radix + Polygoni multiflori radix + Psoraleae fructus  Bupleuri radix + Polygoni multiflori radix + Psoraleae fructus  3 (1.5%) [52] 
Mitragyna Speciosa  Mitragyna speciosa  2 (1.0%) [60,61
Valeriana  Valeriana officinalis  2 (1.0%) [59] 
Eucalyptus globulus  Eucalyptus globulus  2 (1.0%) [58,59
Garcinia cambogia  Garcinia cambogia  2 (1.0%) [62,63
Glycyrrhizae radix  Glycyrrhizae radix  2 (1.0%) [52] 
Hydroxycut®  Capsicum annuum  2 (1.0%) [64] 
Hypericum perforatum  Hypericum perforatum  2 (1.0%) [58,59
Meliae toonsendan fructus  Meliae toonsendan fructus  2 (1.0%) [52] 
Rhamnus purshianus  Rhamnus purshianus  2 (1.0%) [27] 
Teucrium viscidum  Teucrium viscidum  2 (1.0%) [65] 
Bodybuilder supplement    2 (1.0%) [66,67
Mass-Drol®    2 (1.0%) [68] 
Mentha piperita  Mentha piperita  2 (1.0%) [58,59
Scutellaria baicalensis + Senegalia catechu  Scutellaria baicalensis + Senegalia catechu  1 (0.5%) [69] 
Qubaibabuqi  Qubaibabuqi  1 (0.5%) [70] 
Dahanabhasma  Dahanabhasma  1 (0.5%) [71] 
Conjugated linoleic acid    1 (0.5%) [72] 
Aesculus hippocastanum  Aesculus hippocastanum  1 (0.5%) [27] 
Allium sativum  Allium sativum  1 (0.5%) [73] 
Artemisinin (Qinghaosu)    1 (0.5%) [74] 
Bakuchi, Khadin, Brahmi, Usheer    1 (0.5%) [75] 
Boldo  Peumus boldus  1 (0.5%) [76] 
Burnt clay, unknown quantities of ginger, licorice, mandarin skin, Chinese date, Inula britannica (flower), bitter orange, codonopsiz root and ‘haematitium’ (comprising zinc, tin, iron, magnesium and diferric trioxide)    1 (0.5%) [77] 
Cassiae semen  Cassiae sêmen  1 (0.5%) [52] 
Chitosan  Quitosana  1 (0.5%) [27] 
Equidimina  Symphytum officinale L.  1 (0.5%) [78] 
Equisetum arvense  Equisetum arvense  1 (0.5%) [79] 
Euforia®    1 (0.5%) [80] 
Ilicium verum  llicium verum  1 (0.5%) [79] 
Lactobacillus rhamnosus 50% Lactobacillus casei 30% Lactobacillus acidophilus 10% (Bifidobacterium longum 10% (Tonalin 1000 mg, CLA 74%–82%, PA 6%, OA 10%–20%, SA 3%, Anterior pituitary 20 mg, hypothalamus 5 mg, amino acid complex, Panax ginseng 20 mg, phylosterol complex, soyFish body oil 1000 mg, EPA 180 mg, DHA 120 mg, Vitamin D (cholecalciferol) 1000 IU    1 (0.5%) [81] 
Lesser celandine  Ranunculus ficaria  1 (0.5%) [82] 
Mistletoe/kudzu root  Viscum album, Pueraria montana  1 (0.5%) [83] 
NO Xplode®, creatine, L-carnitine, and Growth Factor ATN®    1 (0.5%) [84] 
Panax ginseng  Panax ginseng  1 (0.5%) [85] 
Pimpinella anisum  Pimpinella anisum  1 (0.5%) [79] 
Raspberry ketone, leaves, seeds, and vitamin C  Rubus idaeus  1 (0.5%) [86] 
Shen-Min    1 (0.5%) [22] 
T. Polium  T. Polium  1 (0.5%) [87] 
Cinnamon supplements    1 (0.5%) [88] 
Show-Wu-Pian    1 (0.5%) [89] 
Biosoja    1 (0.5%) [27] 

Regarding the type of liver injury, hepatocellular liver damage (66.9%) was the most frequent. The majority of patients (94.5%) were completely recovered from the liver injury; the average time to resolution was 73 days, with a median of 40 days and standard deviation equal to 129.9 days. Approximately 4.1% of the individuals were re-exposed to the culprit of HILI (Table 1).

The application of Student's t test for mean age revealed a statistically significant higher incidence of women over 60 years of age. From the analysis of the categorical variables, an association between hepatocellular lesion profile and female gender was observed. In addition, the female population had more indications for biopsy.

About severity, 9.8% were mild, 79.6% were classified as moderate, 3.0% were severe and 7.6% were fatal or required liver transplantation. Of those who died or required liver transplantation, only 36.4% underwent biopsy (Table 1). The most used algorithm for the HILI causality assessment in the collected cases was RUCAM, applied in about 72.3% of patients, predominantly among women (Table 3).

Table 3.

Algorithms used in the assessment of HILI causality in published cases from 1979 to 2019.

Algorithms (%)  Excluded  Improbable  Possible  Probable  Highly probable 
RUCAM (72.3%)  2.7%  0.7%  24.0%  41.1%  31.5% 
WHO (2.5%)  0.0%  0.0%  0.0%  60.0%  40.0% 
DILIN (2.5%)  0.0%  0.0%  0.0%  0.0%  100.0% 
Naranjo (3.0%)  0.0%  0.0%  50.0%  50.0%  0.0% 
Maria Victorino (2.5%)  0.0%  0.0%  0.0%  100.0%  0.0% 
Other's algorithms) (17.2%)  3.7%  7.4%  64.3%  21.3%  3.7% 

RUCAM: Roussel Uclaf Causality Assessment Method; WHO: World Health Organization; DILIN: Drug Induced Liver Injury Network.

Other algorithms used for causal attribution: Clinical Diagnostic Scale (CDS); European Medicines Agency (EMEA); Drug Interaction Probability Scale (DIPS); Drug Commission of the German Medical Association (DCGMA); Bundesinstitut für Arzneimittel und Medizinprodukte (BfArM); Federal Institute for Drugs and Medicinal Products (FIDMP).

4Discussion

In this review, 60 articles and 203 cases with HILI were found. In comparison, other review studies have identified 14.029 cases of HILI [13]. This higher number can be justified by the criteria established for the selection of the cases. Using similar criteria, Becker in his review of Brazil's cases, identified only three cases of HILI, published in the literature. As for the origin of the publications in this review, data is similar, most of them were outside Europe and Asia, in which the countries with the highest number of published cases were China, Korea and Germany [13,14].

In the present study, 59.9% of the population was female, with an average age of 45.8 ± 16.2 years and a profile of predominantly hepatocellular liver injury. The clinical characteristics in HILI cases retrieved in our review was compared to those of the Spanish DILI Registry [15], US DILIN [16] and Teschke et al. [13]. According to Jung et al [17], 69.8% of the population with HILI was female, with an average age of 48.7 ± 11.3 years, and a predominantly hepatocellular lesion profile [15].

Frenzel et al. [18] revealed that green tea and black tea are among the most consumed herbal medicines in the world. In 2019 the main products associated with HILI were Greater celadine (20.8%), Teucrium racemosum (18.9%) and Teucrium polium (5.7%) [19]. Another study showed that Polygonum multiflorum was the herbal product most associated with HILI (39.2%) [20]. Similarly, among the main herbal products found in this review were: Greater Celadine (15.8%) and Polygonum multiflorum (12.3%), which matches the data published.

The mechanism for the etiology of HILI is understood. According to published studies, more than 20 different kinds of alkaloids can be found in Greater celandine, including chelerythrine, sanguinarine, berberine, chelidonine, and coptisine [21]. Cases of hepatotoxicity due to Polygonum multiflorum have been reported in China, Australia, and Italy [22]. The anthraquinones, an active ingredient of Polygonum multiflorum is considered to play a role as the potential cause of hepatotoxicity, but previous reports were nonconclusive [23–25].

As in other studies from the USA and Europe, [16] the main prescription reason for herbal products used is weight loss. According to Santos et al. [26], the main indication for the intake of natural and herbal products was weight loss (52%), followed by: relieving the symptoms of digestive disorders, constipation, hair loss, arthralgia, diabetic neuropathy, anxiety and maintaining general health. In the present study, the symptoms of digestive disorders and the musculoskeletal pain treatment were the main indications for the use of the products, according to the data found in the literature.

The most found symptom in the population was jaundice (47%), this is same with the Spanish Group [15] and Frenzel et al. [18] but the incidence higher than that in the present study. Regarding biomarkers, Lin NH et al. [19] showed that the average ALT values of HILI-related liver lesions was 1205 U/L, while the average ALP was 253.2 U/L. Compared this review, ALT and ALP were 1214 U/L and 336 U/L, respectively. The superior laboratory results found in the present study can be justified using the Danan criteria for the selection of studies. Therefore, HILI suspected cases with minimal or transitory ALT/AF elevations were excluded from the study.

In the current HILI case series, 94.5% of the patients were complete recovery. Drug-Induced Liver Injury Network (DILIN) study and García-Cortés M et al. [16,27] previously reported that HILI patients required more medical interventions and were associated with a higher risk of a severe outcome compared to DILI [23]. The time to resolution of HILI was similar with Lin et al. [19] the average was 78 days, while the time estimated in this study was 73 days. Approximately 4.1% of the individuals were re-exposed to the culprit HILI agent; according to Santos et al. [26], most patients tend to hide this information from the doctor, and it is not, in most studies, a reliable data. Regarding the degree of HILI severity, the majority was considered moderate (79.6%), according to International DILI Expert Working Group criteria. A study [28] involving 488 cases showed that HILI mortality was 4.1%. Within the study population, 36.4% underwent biopsy; 5.6% required liver transplantation and only 2.0% died. The lack of follow-up greater than 6 months by most reports and case series may have underestimated the percentage of patients who died within the sample.

Danan et al. [29,30] demonstrated that currently, RUCAM is the gold standard in the DILI/HILI assessment, with the most comprehensive validated scale available. Teschke et al. [31] revealed that 46,266 DILI cases worldwide were evaluated by RUCAM between 2014 and 2019, being the most used tool in world clinical practice. In 2019, 11,609 HILI incidents were reported by the RUCAM scale, a number much higher than that reported in previous years (about 100-1000 cases). The most used algorithm for the HILI quantification, in the collected cases, was RUCAM, applied in about 72.3% of patients. The results found in the group were: 24.0% possible, 41.1% probable and 31.5% highly probable. The WHO, Naranjo and Maria Victorino scales were the most used in the group of patients in which the RUCAM was not applied, being present mainly in the reports and series of older cases, period prior to the publication of studies that proved the good RUCAM performance in large populations and stimulating its use in the clinical management of HILI patients.

According to the recent publications on causality assessment of HILI, RUCAM is the preferred algorithm for the imputation of causal nexus in cases of liver injury and herbal products. This demonstrates the acceptance of this algorithm among experts [13,32].

In the present study, most of the selected HILI cases used the RUCAM, although it was not developed for this purpose, the validation of liver injuries by natural products requires a more precise investigation, on the suspected agent, as: information on phytochemistry that can be correlated to liver damage and the content of these active compounds. Another aspect is the presence of microbiological and physicochemical contaminants, which would require better detailing of the cases to exclude alternative causes. According to Teschke [32], HILI is a complex condition where it needs a more precise approach, especially for the time of events, and the exclusion of alternative causes is necessary.

In regard to the grade found after using RUCAM in the studies, in this review, most cases were classified as possible or probable. The evaluation of retrospective cases by RUCAM, leads to low scores and lower causality classifications, due to low or negative scores, which shows weak robustness in case investigation. Randomized controlled trials are needed to establish a good benefit on the balance of risk for safe use of natural products [32].

However, Danan et al. [29,30], and Becker et al. [33] argued in their studies that RUCAM should continue to be the gold standard in the DILI/HILI evaluation and reinforced that its use to determine causality can be done retrospectively but RUCAM should better be used prospectively to collect complete data required for high causality gradings. Therefore, early application should be stimulated for the patients care with suspected HILI.

5Conclusion

The study showed that the population affected by HILI is predominantly female, with an average age of 45.8 years and a profile of hepatocellular liver injury. The main symptom presented was jaundice. RUCAM scale was the most applied in the cases of our study. There are no studies to date that compare the efficiency and superiority of scales in the DILI/HILI evaluation and quantification.AbbreviationsALT

Alanine Aminotransferase

ALP

Alkaline Phosphatase

AST

Aspartate Aminotransferase

BfArM

Bundesinstitut für Arzneimittel und Medizinprodukte

BT

Bilirubins Total

CDS

Clinical Diagnostic Scale

CIOMS

Council for International Organizations of Medical Sciences

DCGMA

Drug Commission of the German Medical Association

DILI

Drug induced liver injury

DILIN

Drug Induced Liver Injury Network

DIPS

Drug Interaction Probability Scale

EMA

European Medicines Agency

FIDMP

Federal Institute for Drugs and Medicinal Products

GGT

Gamma Glutamyl Transferase

HILI

Herb Induced Liver Injury

RUCAM

Roussel Uclaf Causality Assessment Method

SPSS

Statistical Package for the Social Sciences

TCM

Traditional Chinese Medicine

ULN

Upper Limit of Normality

WHO

World Health Organization

Funding

The present study has been supported by grants of the Maria Emilia Pedreira Freire de Carvalho Foundation, Brazil.Permission to reproduce material from other sources: None.Pedro Felipe Soares: Collected, analyzed data, and wrote manuscript.Maria Tereza Calchi Fanti Fernandes: Collected data.Andréia de Santana Souza: Collected data.Caio Medina Lopes: Collected data.Darjore Amorim Carvalho dos Santos: Collected data.Diogo Pereira Rodrigues Oliveira: Collected data.Marcela Gottschald Pereira: Collected data.Nilia Maria De Brito Lima Prado: Designed the study, revised the manuscript.Gecynalda Soares da Silva Gomes: Analysis Statistics and interpretation of data.Genário Santos: Designed the study, revised the manuscript.Raymundo Paraná: Designed the study, revised the manuscript.

References
[1]
RJ Andrade, N Chalasani, ES Björnsson, A Suzuki, GA Kullak-Ublick, PB Watkins, et al.
Drug-induced liver injury.
Nat Rev Dis Primers, 5 (2019), pp. 58
[2]
D Katarey, S. Verma.
Drug-induced liver injury.
Clin Med, 16 (2016), pp. s104-s109
[3]
M Garcia-Cortes, M Robles-Diaz, C Stephens, A Ortega-Alonso, MI Lucena, RJ. Andrade.
Drug induced liver injury: an update.
Arch Toxicol, 94 (2020), pp. 3381-3407
[4]
JH Byeon, JH Kil, YC Ahn, CG. Son.
Systematic review of published data on herb induced liver injury.
J Ethnopharmacol, 233 (2019), pp. 190-196
[5]
Health Ministry of Brazil (2006). National policy of medicinal plants and herbal medicines.
[6]
J Jing, R. Teschke.
Traditional Chinese medicine and herb-induced liver injury: comparison with drug-induced liver injury.
J Clin Transl Hepatol, 6 (2018), pp. 57-68
[7]
EH Tan, EXS Low, YY Dan, BC. Tai.
Systematic review and meta-analysis of algorithms used to identify drug-induced liver injury (DILI) in health record databases.
Liver Int, 38 (2018), pp. 742-753
[8]
S. Das, SK Behera, AS Xavier, S. Velupula, SA Dkhar, S. Selvarajan.
Agreement among different scales for causality assessment in drug-induced liver injury.
Clin Drug Investig, 38 (2018), pp. 211-218
[9]
MS Barnhill, M Real, JH. Lewis.
Latest advances in diagnosing and predicting DILI: what was new in 2017?.
Expert Rev Gastroenterol Hepatol, 12 (2018), pp. 1033-1043
[10]
G Danan, C. Benichou.
Causality assessment of adverse reactions to drugs–I. A novel method based on the conclusions of international consensus meetings: application to drug-induced liver injuries.
J Clin Epidemiol, 46 (1993), pp. 1323-1330
[11]
C Benichou, G Danan, A. Flahault.
Causality assessment of adverse reactions to drugs–II. An original model for validation of drug causality assessment methods: case reports with positive rechallenge.
J Clin Epidemiol, 46 (1993), pp. 1331-1336
[12]
G Danan, R. Teschke.
RUCAM in drug and herb induced liver injury: the update.
Int J Mol Sci, 17 (2016), pp. 14
[13]
R Teschke, G. Danan.
Worldwide use of RUCAM for causality assessment in 81,856 idiosyncratic DILI and 14,029 HILI cases published 1993-Mid 2020: a comprehensive analysis.
Medicines, 7 (2020), pp. 62
[14]
CN Amadi, OE. Orisakwe.
Herb-induced liver injuries in developing nations: an update.
[15]
RJ Andrade, I Medina-Caliz, A Gonzalez-Jimenez, M Garcia-Cortes, MI. Lucena.
Hepatic damage by natural remedies.
Semin Liver Dis, 38 (2018), pp. 21-40
[16]
VJ Navarro, H Barnhart, HL Bonkovsky, T Davern, RJ Fontana, L Grant, et al.
Liver injury from herbals and dietary supplements in the U.S. Drug-Induced Liver Injury Network.
Hepatology, 60 (2014), pp. 1399-1408
[17]
KA Jung, HJ Min, SS Yoo, HJ Kim, SN Choi, CY Ha, et al.
Drug-Induced liver injury: twenty five cases of acute hepatitis following ingestion of polygonum multiflorum thunb.
Gut Liver, 5 (2011), pp. 493-499
[18]
C Frenzel, R. Teschke.
Herbal hepatotoxicity: clinical characteristics and listing compilation.
Int J Mol Sci, 17 (2016), pp. 588
[19]
NH Lin, HW Yang, YJ Su, CW. Chang.
Herb induced liver injury after using herbal medicine: a systemic review and case-control study.
Medicine, 98 (2019), pp. e14992
[20]
WJ Lee, HW Kim, HY Lee, CG. Son.
Systematic review on herb-induced liver injury in Korea.
Food Chem Toxicol, 84 (2015), pp. 47-54
[21]
ML Colombo, E. Bosisio.
Pharmacological activities of Chelidonium majus L. (Papaveraceae).
Pharmacol Res, 33 (1996), pp. 127-134
[22]
A Cárdenas, JC Restrepo, F Sierra, G. Correa.
Acute hepatitis due to shen-min: a herbal product derived from Polygonum multiflorum.
J Clin Gastroenterol, 40 (2006), pp. 629-632
[23]
PP But, B Tomlinson, KL. Lee.
Hepatitis related to the Chinese medicine Shou-wupian manufactured from Polygonum multiflorum.
Vet Hum Toxicol, 38 (1996), pp. 280-282
[24]
GJ Park, SP Mann, MC. Ngu.
Acute hepatitis induced by ShouWu-Pian, a herbal product derived from Polygonum multiflorum.
J Gastroenterol Hepatol, 16 (2001), pp. 115-117
[25]
G Mazzanti, L Batinelli, C Daniele, CM Mastroianni, M Lichtner, S Coletta, et al.
New case of acute hepatitis following the consumption of Shou Wu Pian, a Chinese herbal product derived from Polygonum multiflorum.
[26]
G Santos, J Gasca, R Parana, V Nunes, M Schinnoni, I Medina-Caliz, et al.
Profile of herbal and dietary supplements induced liver injury in Latin America: a systematic review of published reports.
Phytother Res, (2020),
[27]
M García-Cortés, Y Borraz, MI Lucena, G Peláez, J Salmerón, M Diago, et al.
Hepatotoxicidad secundaria a "productos naturales": análisis de los casos notificados al Reigstro Español de Hepatotoxicidad [Liver injury induced by "natural remedies": an analysis of cases submitted to the Spanish Liver Toxicity Registry].
Rev Esp Enferm Dig, 100 (2008), pp. 688-695
[28]
Y Zhu, M Niu, JB Wang, RL Wang, JY Li, YQ Ma, et al.
Predictors of poor outcomes in 488 patients with herb-induced liver injury.
Turk J Gastroenterol, 30 (2019), pp. 47-58
[29]
G Danan, R. Teschke.
Drug-induced liver injury: why is the Roussel Uclaf Causality Assessment Method (RUCAM) still used 25 years after its launch?.
Drug Saf, 41 (2018), pp. 735-743
[30]
G Danan, R. Teschke.
Roussel Uclaf causality assessment method for drug-induced liver injury: present and future.
Front Pharmacol, 10 (2019), pp. 853
[31]
R. Teschke, DILI Idiosyncratic.
Analysis of 46,266 cases assessed for causality by RUCAM and published from 2014 to early 2019.
Front Pharmacol, 10 (2019), pp. 730
[32]
R Teschke, Y Zhu, J. Jing.
Herb-induced liver injury in asia and current role of RUCAM for causality assessment in 11,160 published cases.
J Clin Transl Hepatol, 8 (2020), pp. 200-214
[33]
MW Becker, MJM Lunardelli, CV Tovo, CR. Blatt.
Drug and herb-induced liver injury: a critical review of Brazilian cases with proposals for the improvement of causality assessment using RUCAM.
Ann Hepatol, 18 (2019), pp. 742-750
[34]
R Teschke, X Glass, J. Schulze.
Herbal hepatotoxicity by Greater Celandine (Chelidonium majus): causality assessment of 22 spontaneous reports.
Regul Toxicol Pharmacol, 61 (2011), pp. 282-291
[35]
R Teschke, X Glass, J Schulze, A. Eickhoff.
Suspected Greater Celandine hepatotoxicity: liver-specific causality evaluation of published case reports from Europe.
Eur J Gastroenterol Hepatol, 24 (2012), pp. 270-280
[36]
A Timcheh-Hariri, M Balali-Mood, E Aryan, M Sadeghi, B. Riahi-Zanjani.
Toxic hepatitis in a group of 20 male body-builders taking dietary supplements.
Food Chem Toxicol, 50 (2012), pp. 3826-3832
[37]
CT Wai, BH Tan, CL Chan, DS Sutedja, YM Lee, C Khor, et al.
Drug-induced liver injury at an Asian center: a prospective study.
[38]
EX Zheng, S Rossi, RJ Fontana, R Vuppalanchi, JH Hoofnagle, I Khan, et al.
Risk of liver injury associated with green tea extract in SLIMQUICK(®) weight loss products: results from the DILIN prospective study.
Drug Saf, 39 (2016), pp. 749-754
[39]
A Hadjipanayis, E Efstathiou, V. Papaevangelou.
Hepatotoxicity in an adolescent with black iced tea overconsumption.
Pediatr Gastroenterol Hepatol Nutr, 22 (2019), pp. 387-391
[40]
R Gloro, I Hourmand-Ollivier, B Mosquet, L Mosquet, P Rousselot, E Salamé, et al.
Fulminant hepatitis during self-medication with hydroalcoholic extract of green tea.
Eur J Gastroenterol Hepatol, 17 (2005), pp. 1135-1137
[41]
ST Lugg, D Braganza Menezes, S. Gompertz.
Chinese green tea and acute hepatitis: a rare yet recurring theme.
[42]
MH Pillukat, C Bester, A Hensel, M Lechtenberg, F Petereit, S Beckebaum, et al.
Concentrated green tea extract induces severe acute hepatitis in a 63-year-old woman–a case report with pharmaceutical analysis.
J Ethnopharmacol, 155 (2014), pp. 165-170
[43]
FJ Couturier, LJ Colemont, H Fierens, VM. Verhoeven.
Toxic hepatitis due to a food supplement: "Natural" is no synonym for "harmless".
Clin Res Hepatol Gastroenterol, 40 (2016), pp. e38-e43
[44]
A Mrzljak, I Kosuta, A Skrtic, TF Kanizaj, R. Vrhovac.
Drug-induced liver injury associated with noni (Morinda citrifolia) juice and phenobarbital.
Case Rep Gastroenterol, 7 (2013), pp. 19-24
[45]
V Stadlbauer, S Weiss, F Payer, RE. Stauber.
Herbal does not at all mean innocuous: the sixth case of hepatotoxicity associated with morinda citrifolia (noni).
Am J Gastroenterol, 103 (2008), pp. 2406-2407
[46]
HN Yang, DJ Kim, YM Kim, BH Kim, KM Sohn, MJ Choi, et al.
Aloe-induced toxic hepatitis.
J Korean Med Sci, 25 (2010), pp. 492-495
[47]
MM Bottenberg, GC Wall, RL Harvey, S. Habib.
Oral aloe vera-induced hepatitis.
Ann Pharmacother, 41 (2007), pp. 1740-1743
[48]
N Chalasani, R Vuppalanchi, V Navarro, R Fontana, H Bonkovsky, H Barnhart, et al.
Acute liver injury due to flavocoxid (Limbrel), a medical food for osteoarthritis: a case series.
[49]
SU Christl, A Seifert, D. Seeler.
Toxic hepatitis after consumption of traditional kava preparation.
J Travel Med, 16 (2009), pp. 55-56
[50]
MW Becker, EMS Lourençone, AF De Mello, A Branco, EMR Filho, CR Blatt, et al.
Liver transplantation and the use of KAVA: Case report.
Phytomedicine, 56 (2019), pp. 21-26
[51]
M Escher, J Desmeules, E Giostra, G. Mentha.
Hepatitis associated with Kava, a herbal remedy for anxiety.
[52]
D Melchart, S Hager, S Albrecht, J Dai, W Weidenhammer, R. Teschke.
Herbal traditional Chinese Medicine and suspected liver injury: a prospective study.
World J Hepatol, 9 (2017), pp. 1141-1157
[53]
SM Cohen, AM O'Connor, J Hart, NH Merel, HS. Te.
Autoimmune hepatitis associated with the use of black cohosh: a case study.
[54]
DL Franco, S Kale, DM Lam-Himlin, ME Harrison.
Black cohosh hepatotoxicity with autoimmune hepatitis presentation.
Case Rep Gastroenterol, 11 (2017), pp. 23-28
[55]
R Teschke, R Bahre, A Genthner, J Fuchs, W Schmidt-Taenzer, A. Wolff.
Suspected black cohosh hepatotoxicity–challenges and pitfalls of causality assessment.
[56]
J Fernández, C Navascués, G Albines, L Franco, M Pipa, M. Rodríguez.
Three cases of liver toxicity with a dietary supplement intended to stop hair loss.
Rev Esp Enferm Dig, 106 (2014), pp. 552-555
[57]
K Kawata, Y Takehira, Y Kobayashi, M Kitagawa, M Yamada, K Hanajima, et al.
Three cases of liver injury caused by Sennomotokounou, a Chinese dietary supplement for weight loss.
Intern Med, 42 (2003), pp. 1188-1192
[58]
M Her, Y Lee, E Jung, T Kim, D Kim.
Liver enzyme abnormalities in systemic lupus erythematosus: a focus on toxic hepatitis.
Rheumatol Int, 31 (2011), pp. 79-84
[59]
A Douros, E Bronder, F Andersohn, A Klimpel, R Kreutz, E Garbe, et al.
Herb-induced liver injury in the berlin case-control surveillance study.
Int J Mol Sci, 17 (2016), pp. 114
[60]
K Tayabali, C Bolzon, P Foster, J Patel, MO. Kalim.
Kratom: a dangerous player in the opioid crisis.
J Community Hosp Intern Med Perspect, 8 (2018), pp. 107-110
[61]
CS Osborne, AN Overstreet, DC Rockey, AD. Schreiner.
Drug-induced liver injury caused by Kratom use as an alternative pain treatment amid an ongoing opioid epidemic.
J Investig Med High Impact Case Rep, 7 (2019),
[62]
MN Yousaf, FS Chaudhary, SM Hodanazari, CD. Sittambalam.
Hepatotoxicity associated with Garcinia cambogia: a case report.
World J Hepatol, 11 (2019), pp. 735-742
[63]
A Sharma, E Akagi, A Njie, S Goyal, C Arsene, G Krishnamoorthy, et al.
Acute hepatitis due to garcinia cambogia extract, an herbal weight loss supplement.
Case Rep Gastrointest Med, 2018 (2018),
[64]
L Dara, J Hewett, JK. Lim.
Hydroxycut hepatotoxicity: a case series and review of liver toxicity from herbal weight loss supplements.
World J Gastroenterol, 14 (2008), pp. 6999-7004
[65]
WT Poon, TL Chau, CK Lai, KY Tse, YC Chan, KS Leung, et al.
Hepatitis induced by Teucrium viscidum.
Clin Toxicol, 46 (2008), pp. 819-822
[66]
C El Rahi, N Thompson-Moore, P Mejia, P. De Hoyos.
Successful use of N-acetylcysteine to treat severe hepatic injury caused by a dietary fitness supplement.
Pharmacotherapy, 35 (2015), pp. e96-e101
[67]
A Stolz, V Navarro, PH Hayashi, RJ Fontana, HX Barnhart, J Gu, et al.
Severe and protracted cholestasis in 44 young men taking bodybuilding supplements: assessment of genetic, clinical and chemical risk factors.
Aliment Pharmacol Ther, 49 (2019), pp. 1195-1204
[68]
Y El Sherrif, JR Potts, MR Howard, A Barnardo, S Cairns, AS Knisely, et al.
Hepatotoxicity from anabolic androgenic steroids marketed as dietary supplements: contribution from ATP8B1/ABCB11 mutations?.
Liver Int, 33 (2013), pp. 1266-1270
[69]
L Yang, A Aronsohn, J Hart, D. Jensen.
Herbal hepatoxicity from Chinese skullcap: a case report.
World J Hepatol, 4 (2012), pp. 231-233
[70]
A Li, M Gao, N Zhao, P Li, J Zhu, W. Li.
Acute liver failure associated with Fructus Psoraleae: a case report and literature review.
BMC Complement Altern Med, 19 (2019), pp. 84
[71]
CA Philips, R Paramaguru, P. Augustine.
Ayurveda metallic-mineral 'Bhasma'-associated severe liver injury.
[72]
R Nortadas, J. Barata.
Fulminant hepatitis during self-medication with conjugated linoleic acid.
Ann Hepatol, 11 (2012), pp. 265-267
[73]
SA Shaikh, S Tischer, EK Choi, RJ. Fontana.
Good for the lung but bad for the liver? Garlic-induced hepatotoxicity following liver transplantation.
J Clin Pharm Ther, 42 (2017), pp. 646-648
[74]
S. Kumar.
Cholestatic liver injury secondary to artemisinin.
Hepatology, 62 (2015 Sep), pp. 973-974
[75]
R Teschke, R. Bahre.
Severe hepatotoxicity by Indian Ayurvedic herbal products: a structured causality assessment.
Ann Hepatol, 8 (2009), pp. 258-266
[76]
F Piscaglia, S Leoni, A Venturi, F Graziella, G Donati, L. Bolondi.
Caution in the use of boldo in herbal laxatives: a case of hepatotoxicity.
Scand J Gastroenterol, 40 (2005), pp. 236-239
[77]
A N Webb, W Hardikar, NE Cranswick, GR. Somers.
Probable herbal medication induced fulminant hepatic failure.
J Paediatr Child Health, 41 (2005), pp. 530-531
[78]
V Rollason, L Spahr, M. Escher.
Severe liver injury due to a homemade flower pollen preparation in a patient with high CYP3A enzyme activity: a case report.
Eur J Clin Pharmacol, 72 (2016), pp. 507-508
[79]
E Ocete-Hita, MJ Sameron-Fernández, JM González Gómez, E Urrutia Maldonado, M Salmerón Ruiz, A Ruiz-Extremera, et al.
Hepatotoxicidad y consumo de productos de herboristería en la población pediátrica [Hepatotoxicity from the consumption of herbalist products by a paediatric population].
Nutr Hosp, 32 (2015), pp. 652-655
[80]
E Jiménez-Encarnación, G Ríos, A Muñoz-Mirabal, LM. Vilá.
Euforia-induced acute hepatitis in a patient with scleroderma.
[81]
K Cvijovic, H Boon, W Jaeger, S Vohra, SONAR group.
Polypharmacy, multiple natural health products and hepatotoxicity.
CMAJ, 183 (2011), pp. E1085-E1089
[82]
B Yilmaz, B Yilmaz, B Aktaş, O Unlu, EC. Roach.
Lesser celandine (pilewort) induced acute toxic liver injury: the first case report worldwide.
World J Hepatol, 7 (2015), pp. 285-288
[83]
HJ Kim, H Kim, JH Ahn, HJ. Suk.
Liver injury induced by herbal extracts containing mistletoe and kudzu.
J Altern Complement Med, 21 (2015), pp. 180-185
[84]
G Avelar-Escobar, J Méndez-Navarro, NX Ortiz-Olvera, G Castellanos, R Ramos, VE Gallardo-Cabrera, et al.
Hepatotoxicity associated with dietary energy supplements: use and abuse by young athletes.
Ann Hepatol, 11 (2012), pp. 564-569
[85]
N Bilgi, K Bell, AN Ananthakrishnan, E. Atallah.
Imatinib and Panax ginseng: a potential interaction resulting in liver toxicity.
Ann Pharmacother, 44 (2010), pp. 926-928
[86]
T Sohda, H Shiga, H Nakane, S Nishizawa, M Yoshikane, A Anan, et al.
Rapid-onset primary biliary cirrhosis resembling drug-induced liver injury.
Intern Med, 44 (2005), pp. 1051-1054
[87]
I Starakis, D Siagris, L Leonidou, E Mazokopakis, A Tsamandas, C. Karatza.
Hepatitis caused by the herbal remedy Teucrium polium L.
Eur J Gastroenterol Hepatol, 18 (2006), pp. 681-683
[88]
D Brancheau, B Patel, M. Zughaib.
Do cinnamon supplements cause acute hepatitis?.
Am J Case Rep, 16 (2015), pp. 250-254
[89]
M Furukawa, S Kasajima, Y Nakamura, M Shouzushima, N Nagatani, A Takinishi, et al.
Toxic hepatitis induced by show-wu-pian, a Chinese herbal preparation.
Intern Med, 49 (2010), pp. 1537-1540

Acknowledgements: We gratefully acknowledge the Instituto D'Or de Pesquisa e Ensino (IDOR), Salvador, Brazil.

Copyright © 2021. Fundación Clínica Médica Sur, A.C.
Article options
Tools
es en pt

¿Es usted profesional sanitario apto para prescribir o dispensar medicamentos?

Are you a health professional able to prescribe or dispense drugs?

Você é um profissional de saúde habilitado a prescrever ou dispensar medicamentos