Invasive amebic diseases caused by Entamoeba histolytica are increasing among men who have sex with men and co-infection of ameba and HIV-1 is an emerging problem in developed East Asian countries. To characterize the clinical and epidemiological features of invasive amebiasis in HIV-1 patients, the medical records of 170 co-infected cases were analyzed retrospectively, and E. histolytica genotype was assayed in 14 cases. In this series of HIV-1-infected patients, clinical presentation of invasive amebiasis was similar to that described in the normal host. High fever, leukocytosis and high CRP were associated with extraluminal amebic diseases. Two cases died from amebic colitis (resulting in intestinal perforation in one and gastrointestinal bleeding in one), and three cases died from causes unrelated to amebiasis. Treatment with metronidazole or tinidazole was successful in the other 165 cases. Luminal treatment was provided to 83 patients following metronidazole or tinidazole treatment. However, amebiasis recurred in 6 of these, a frequency similar to that seen in patients who did not receive luminal treatment. Recurrence was more frequent in HCV-antibody positive individuals and those who acquired syphilis during the follow-up period. Various genotypes of E. histolytica were identified in 14 patients but there was no correlation between genotype and clinical features. The outcome of metronidazole and tinidazole treatment of uncomplicated amebiasis was excellent even in HIV-1-infected individuals. Luminal treatment following metronidazole or tinidazole treatment does not reduce recurrence of amebiasis in high risk populations probably due to amebic re-infection.
Amebiasis is usually transmitted by ingestion of contaminated food or water in developing countries. Recently, however, increased risk for amebiasis among men who have sex with men (MSM) due to oral-anal sexual contact was reported in developed countries, resulting in growing concern on amebiasis in HIV-1-infected MSM. The recommended treatment of amebiasis is metronidazole or tinidazole, followed by a luminal agent to eliminate intestinal cyst colonization. However, the efficacy of luminal treatment in preventing recurrence has not been assessed yet. In this study, we analyzed the medical records of 170 patients with amebiasis and HIV-1 co-infection. Treatment with metronidazole or tinidazole was excellent whereas luminal treatment did not reduce the frequency of recurrence of amebiasis. Recurrence was more frequent in those MSM with signs of sexual activity such as syphilis infection. Luminal treatment following metronidazole or tinidazole treatment does not reduce recurrence of amebiasis in high risk populations.
Citation: Watanabe K, Gatanaga H, Cadiz AE-d, Tanuma J, Nozaki T, et al. (2011) Amebiasis in HIV-1-Infected Japanese Men: Clinical Features and Response to Therapy. PLoS Negl Trop Dis 5(9): e1318. doi:10.1371/journal.pntd.0001318
Editor: Judd L. Walson, University of Washington, United States of America
Received: May 10, 2011; Accepted: August 1, 2011; Published: September 13, 2011
Copyright: © 2011 Watanabe et al. This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited.
Funding: This study was supported by a grant from the National Center for Global Health and Medicine. The funder had no role in study design, data collection and analysis, decision to publish, or preparation of the manuscript.
Competing interests: The authors have declared that no competing interests exist.
Invasive amebiasis (IA) caused by Entamoeba histolytica is the second most common cause of mortality associated with parasitic infections worldwide, accounting for 40,000 to 100,000 deaths annually . Amebiasis is transmitted by ingestion of food or water containing the cyst form of E. histolytica, which is prevalent in developing countries in Central and South America, Asia, and Africa. In the developed countries, most cases arise in travelers and immigrants from such endemic areas . Recently, however, three developed East Asian countries (Japan, Taiwan, and South Korea) reported increased risk for amebiasis among men who have sex with men (MSM) due to oral-anal sexual contact –. The annual incidence of human immunodeficiency virus type 1 (HIV-1) infection is also increasing among MSM in these countries -, resulting in growing concern on IA in HIV-1-infected MSM , –, . The recommended treatment for IA is metronidazole (750 mg t. i. d. for 10 days) or tinidazole (2 g q. d. for 3 days), followed by a luminal agent (paromomycin 500 mg t. i. d. for 10 days or diloxanide furoate 500 mg t. i. d. for 10 days) to eliminate intestinal colonization , . A previous report described no difference in the response to metronidazole or tinidazole treatment between HIV-1-positive and –negative IA patients . However, the efficacy of luminal treatment in preventing recurrence, which can arise by relapse or re-infection, has not yet been assessed rigorously. In this study, we retrospectively analyzed 170 HIV-1-infected Japanese patients with IA, together with genomic typing of E. histolytica in 14 of these patients, and delineated the clinical features of IA in HIV-1-infected individuals and the efficacy of metronidazole, tinidazole and luminal treatment.
The Institutional Review Board of National Center for Global Health and Medicine (Tokyo, Japan) approved this study. All patients who provided clinical samples for genotyping of E. histolytica gave written informed consent.
The medical records of HIV-1-infected cases diagnosed with IA at the AIDS Clinical Center, National Center for Global Health and Medicine, between April 1997 and March 2010, were reviewed. The diagnosis of IA was made when one of the following criteria was satisfied; 1) identification of and/or positive PCR (methods; see below) in clinical specimens (stool or punctuate-exudate) for erythrophagocytic trophozoites in patients with IA-related symptoms, e.g., fever and liver abscess, or tenesmus and diarrhea, 2) high serum titer (>1:100) for antibody against E. histolytica in patients with IA-related symptoms in whom microbiological cultures or histological examination of clinical specimens did not identify any pathogen, and who showed improvement of IA symptoms following metronidazole or tinidazole monotherapy –. The medical records were surveyed for patients' characteristics, presenting forms of clinical IA [e.g., colitis, amebic liver abscess (ALA), and perianal abscess], HIV-1-induced immunocompromised status, and symptoms, laboratory data and serological markers of other sexually-transmitted diseases (STD) including syphilis, hepatitis B and C viruses (HBV and HCV). After completion of treatment for IA, the medical records were followed-up until March 2010, excluding those cases found to have died or lost to follow-up.
Genotyping of E. histolytica
To determine the strains of E. histolytica among HIV-1-infected Japanese patients, genotyping of E. histolytica was performed in patients who were PCR positive. The PCR method was used for the first time in our clinic for the diagnosis of amebiasis in December 2008, and since then 14 patients had been diagnosed as IA based on a positive PCR. For the PCR, DNAs were extracted from various biological specimens (e.g., stool, colon wash and punctuate-exudate) by using QIAamp DNA stool Mini Kit (Qiagen, Valencia, CA). Polymerase chain reactions were performed with specific sets of primers designed to target each of 6 loci (D-A, S-Q, R-R, A-L, STGA-D, and N-K) of tRNA-linked polymorphic short tandem repeats (STR), as described previously . The PCR product was sequenced by ABI 3130XL Genetic Analyzer (Applied Biosystem, Foster city, CA) in both forward and reverse directions. Phylogenetic analysis and genotyping were performed as described previously .
Differences in patients' characteristics and clinical features were examined using the chi-square test or nonparametric test. The cumulative risk for recurrence was analyzed by the Kaplan-Meier method, and differences were tested by the log-rank test. The Cox proportional hazards model was used to assess the impact of luminal treatment on the recurrence rate after adjustment for other factors. The hazard ratio and 95% confidence interval were calculated. P values less than 0.05 were considered to denote statistical significance. All statistical analyses were performed using the Statistical Package for Social Sciences (SPSS Inc., Chicago, IL).
Clinical data and response to treatment
IA was diagnosed in 170 HIV-1-infected cases between April 1997 and March 2010 (including amebic colitis, n = 102; ALA, n = 63; and perianal abscess, n = 5, Table 1). Thirty-three patients had two of the above three clinical forms of IA. All patients were males and 164/170 (96.5%) were MSM. High rates of positive TPHA (Treponema pallidum hemagglutination assay) (71.2%) and HBV exposure (HBs antigen-positive, HBs antibody-positive, or HBc antibody-positive) (60.0%) were observed. No significant differences were seen in CD4 counts, HIV-1 loads, coexisting AIDS definite disease and the proportion of patients treated with antiretrovirals, suggesting that HIV-induced immunocompromised status did not have an impact on the clinical presentation of amebic infection, in agreement with previous data . In cases of amebic colitis (n = 102), diarrhea (69.7%) was the most common symptom followed by dysentery (55.9%) (Table 2). Fever (>37.5°C) was seen in only 20 patients (19.6%), including 5 cases with perforative peritonitis. In cases with ALA (n = 63), fever (95.2%) was the most common symptom followed by abdominal pain (55.6%). Diarrhea (46.0%) and dysentery (19.0%) were only seen in less than half of ALA cases. Single abscess (72.6%) was identified in most cases. Liver abscesses were seen more frequently in the right lobe (70.5%) than the left (9.8%). Nine patients (14.3%) had pleuritis (considered a co-existing disease), as well as abscesses in the right lobe, and 7 of these presented chest pain. Comparison of physical and laboratory data showed higher peak body temperature (BT), leukocyte count and C reactive protein (CRP) in ALA cases (Table 2) and perforative peritonitis cases (data not shown) compared with colitis cases, indicating that high fever, leukocytosis and high CRP could be the signs of extraluminal amebiasis. It is reported that high fever and leukocytosis are also common in ALA patients free of HIV-1 infection, though both parameters were unusually associated with simple amebic colitis . In ALA cases, however, leukocyte count correlated positively with CD4 count (data not shown in tables: Pearson product-moment correlation coefficient 0.36, p value 0.004) and negatively with HIV-RNA load (Pearson product-moment correlation coefficient -0.28, p value 0.03), but CRP correlated neither with CD4 count nor HIV-RNA load (CRP-CD4, p = 0.81, CRP-HIV-RNA, p = 0.32). There were also no correlations between CD4 count, HIV-RNA load, BT, leukocyte count or CRP and abscess size or number.
Table 1. Patient demographics, state of HIV, and serological markers.doi:10.1371/journal.pntd.0001318.t001
Table 2. Clinical features of amoebic colitis and ALA.doi:10.1371/journal.pntd.0001318.t002
All patients were treated with metronidazole (750 mg t. i. d. for 10 days) for IA, with the exception of two who were treated with tinidazole (2 g q. d. for 3 days). Complete remission of all IA symptoms was observed in 165 patients including the two treated with tinidazole. Five cases died within six months after diagnosis of IA; two from complications related to amebic colitis (one peritoneal perforation and one gastrointestinal bleeding), one from malignant lymphoma, one from Pneumocystis jirovecii pneumonia, and one from pulmonary thrombosis. The overall mortality rate was 3% in this study, which was comparable to those reported in non-HIV cases , .
Recurrence after treatment
Luminal agents; paromomycin and diloxanide, are not approved in Japan, and they were not always available in our facility during the study period. After completion of IA treatment with metronidazole or tinidazole, luminal agents were administered when available. Consequently, 83 cases were treated with luminal agents; 38 cases with promomycin (500 mg t. i. d. for 10 days) and 45 cases with diloxanide furoate (500 mg t. i. d. for 10 days). No significant differences were seen in patients' characteristics, including HIV-1-induced immunocompromised status, serological markers of other STD, and clinical forms and severity of amebiasis between the 83 cases with luminal treatment and 82 cases who did not receive such treatment (Table S1). The median follow-up period after completion of metronidazole or tinidazole treatment was 50 months (inter quartile range: 19–85) in those who received luminal treatment, and 43 months (inter quartile range: 23–98) in those without.
Within the 12-month post-metronidazole treatment period, recurrence of IA was noted in only two patients who did not receive luminal treatment, suggesting reactivation of residual cysts of E. histolytica (Figure 1). However, during the entire follow-up period, six in each group experienced recurrence of IA, with no significant difference in the recurrence frequency by the log-rank chi-square test. Multivariate analysis showed that recurrence did not correlate with past history of IA, CD4 count, TPHA, HBV exposure (HBs antigen-positive or HBs antibody-positive), or the presence of extraluminal IA disease (Table 3). However, a positive HCV antibody was significantly associated with IA recurrence. Recurrence also tended to occur in those who acquired new syphilis infection during the follow-up period, though the difference did not reach statistical significance.
Figure 1. Kaplan-Meier estimates of time to IA recurrence.
Cumulative probability of IA recurrence after completion of metronidazole or tinidazole treatment with or without subsequent luminal treatment.doi:10.1371/journal.pntd.0001318.g001
Table 3. Multivariate analyses for factors associated with frequency of recurrence.doi:10.1371/journal.pntd.0001318.t003
Genotypes of E. histolytica
Genotyping of E. histolytica was performed in samples obtained from 14 patients between December 2009 and March 2010 (colitis, n = 8; ALA, n = 4; colitis and ALA, n = 1; and perianal abscess, n = 1; Table S2). Eleven different genotypes were recognized, including five genotypes (J8, J12, J13, J20, and J23) identified previously in Japan , and six newly recognized genotypes (J24-J29). There was no significant relation between E. histolytica genotype and clinical presentation.
In the present study, retrospective analysis of the medical records of 170 patients with HIV-1-infection and IA showed no impact for HIV-1-induced immunocompromised status on the clinical forms of amebiasis. The physical and laboratory findings showed that high fever, leukocytosis and high CRP correlated with extraluminal diseases of amebiasis. In ALA cases, however, leukocyte count correlated positively with CD4 count and negatively with HIV-RNA load, indicating that CRP is more sensitive marker for the detection of the extraluminal diseases in advanced immunocompromised patients.
Only five patients died after the diagnosis of IA; two from IA complications and three from other causes. The results indicate excellent outcome for HIV-1-infected individuals with uncomplicated amebiasis treated with metronidazole or tinidazole, in agreement with previous reports on HIV and non-HIV cases , , , , . Based on conventional wisdom and written opinion, adequate management of IA should include treatment with a luminal agent following metronidazole or tinidazole treatment, in order to eradicate residual cysts of E. histolytica due to the high rate (40–60%) of luminal colonization , –. On the other hand, the results of longitudinal observational studies indicated that asymptomatic cyst carriers rarely develop IA, and that cyst form ameba often disappears spontaneously without any treatment , . There is controversy about the need for cyst eradication following metronidazole or tinidazole treatment, especially in endemic areas where re-infection is frequent. In this study, recurrence of IA within the first year of metronidazole treatment was noted in only two patients of 82 patients who did not receive luminal therapy. Moreover, long-term follow-up indicated IA recurrence also in those who received luminal agents, and the benefits obtained from luminal treatment seemed to have disappeared. IA recurred more frequently in those with HCV infection, which was recently reported to be transmittable sexually among MSM , and in those who acquired new syphilis infection during the follow-up period, suggesting that sexually active MSM tend to experience IA recurrence due to re-acquisition of new E. histolytica infection. HBV exposure and positive TPHA at IA diagnosis did not correlate with IA recurrence probably because the high prevalence of these two parameters in this study masked the difference between recurrence and non-recurrence cases. Educational approach for safer sex may be more appropriate rather than luminal treatment to prevent IA recurrence after treatment.
Eleven genetic strains of E. histolytica were identified in this study and none of them had been reported so far from geographic areas other than Japan , , , , indicating that diverse Japan-specific isolates of E. histolytica are already prevalent among MSM in Japan. In fact, the E. histolytica seropositivity rate in HIV-1-infected MSM in our clinic was as high as 17.9% in 2009 (unpublished data), which is comparable with the seropositivity rate in Japanese MSM reported more than 20 years ago . Unfortunately, we could not compare the genotypes of E. histolytica between the incidences of the primary and recurrent IA within the same individuals due to the lack of appropriate stocked samples, which would have probably demonstrated acquisition of new infection.
Considered together, the results emphasize the difficulty of preventing IA recurrence without educational approach to prevent new amebic infection even after successful IA treatment in the high risk groups such as HIV-1-infected MSM. The spread of E. histolytica in MSM of other developed countries beyond Asia should be of great concern.
Patient demographics with and without luminal treatment.
Genotyping data of 6 STR loci in 14 clinical samples.
Conceived and designed the experiments: HG JT SO. Performed the experiments: KW AEdC TN. Analyzed the data: KW HG. Contributed reagents/materials/analysis tools: KW HG JT SO. Wrote the paper: KW HG.
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