Literature DB >> 25101756

Toxocara seroprevalence among clinically healthy individuals, pregnant women and psychiatric patients and associated risk factors in Shandong Province, Eastern China.

Wei Cong1, Xiao-Xuan Zhang1, Na Zhou2, Chang-Zheng Yu3, Jia Chen4, Xiang-Yang Wang5, Bing Li6, Ai-Dong Qian7, Xing-Quan Zhu1.   

Abstract

BACKGROUND: Toxocarosis is a widespread zoonosis caused by the ascarid nematodes Toxocara canis and Toxocara cati, which primarily infect dogs and cats, respectively. Most human infections with Toxocara are asymptomatic; however, some infected individuals may develop a serious illness and even death. Nevertheless, epidemiological knowledge regarding the prevalence and risks associated with Toxocara infection is limited in China. Therefore, we performed a cross-sectional pilot study and estimated the seroprevalence of Toxocara infection in humans in Shandong Province, eastern China for the first time, from June 2011 to July 2013, involving clinically healthy individuals, pregnant women and psychiatric patients, aiming to attract public attention to Toxocara infection. METHODOLOGY/PRINCIPLE
FINDINGS: Seroprevalence of Toxocara was determined using an enzyme-linked immunosorbent assay based on a cross-sectional study conducted in Qingdao and Weihai, Shandong Province, eastern China. Factors potentially associated with Toxocara infection were identified by logistic regression analysis. The overall Toxocara seroprevalence among the study population (n = 2866) was 12.25%, and a significantly higher seroprevalence in psychiatric patients (16.40%, 73/445) than that in clinically healthy individuals (13.07%, 187/1431) and pregnant women (9.19%, 91/990) was revealed. Univariate analyses suggested that keeping dogs at home (OR = 0.06, 95% CI 0.05-0.08, P<0.001), contact with cats and dogs (OR = 0.42, 95% CI 0.33-0.53, P<0.001) and exposure with soil (OR = 0.37, 95% CI 0.28-0.49, P<0.001) were risk factors associated with Toxocara infection.
CONCLUSIONS/SIGNIFICANCE: The present study revealed, for the first time, that human infection with Toxocara is common in eastern China, posing a significant public health concern. Increasing human and dog populations, population movements and climate change all will serve to increase the importance of this zoonosis. Further studies under controlled conditions are necessary to define potential morbidity associated with Toxocara infection.

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Year:  2014        PMID: 25101756      PMCID: PMC4125144          DOI: 10.1371/journal.pntd.0003082

Source DB:  PubMed          Journal:  PLoS Negl Trop Dis        ISSN: 1935-2727


Introduction

Toxocarosis, a typical neglected and underestimated human health problem, is caused by the larval stages of Toxocara canis, the intestinal roundworms of dogs, and probably by the roundworm of cats (Toxocara cati) as well [1]–[3]. T. canis, the major cause of human toxocarosis, can reach a high prevalence owing to the large number of eggs excreted and the resistance of eggs to environmental conditions [4]. Humans can be infected by the accidental ingestion of embryonated Toxocara spp. eggs presented in contaminated soil or food, or by the ingestion of encapsulated larvae contained in the tissues of paratenic hosts [2]. Most human infections with Toxocara are asymptomatic; however, infective Toxocara larvae may migrate into internal organs via the blood and can result in a number of clinical syndromes such as visceral larva migrans (VLM), ocular larva migrans (OLM), neurotoxocarosis (NT), covert toxocarosis (CT) and eosinophilic meningoencephalitis (EME) [2]–[8]. The diagnosis of human toxocarosis is usually based on serological examinations, in combination with clinical presentations and the results of blood examinations [4]. Enzyme-Linked Immunosorbent Assay (ELISA) and Western Blotting (WB) are currently the most sensitive and reliable tools for detecting antibodies and circulating antigens [9]. However, WB is more expensive and labour-intensive than ELISA; thus alternatively, detecting reactive IgG by utilizing recombinant T. canis antigens as well as IgE antibodies in ELISA may expediently acquire convincing results [8]. Stray and domestic dogs and cats, especially from low income rural population, play a critical role in the transmission of Toxocara spp. offering environmental contamination, which extends the spreading of the infection among the human populations [10]. The growing numbers of dogs (pet and stray dogs) have resulted in closer contact between these animals and humans, enhancing the level of exposure [4]. In China, with the accelerated process of urbanization and the improvement of living standard, the number of pets raised (both in urban and rural areas) is increasing rapidly, and a series of problems are gradually emerging due to lack of quarantine and vaccination, ineffective market administration, non-standard pet hospital and environment contamination [11]. With respect to environmental characteristics, Qingdao and Weihai have a marine climate with moist air and abundant rainfall, which may contribute to become infective for the eggs [4]. Moreover, Qingdao and Weihai are important tourism and coastal open cities in eastern China, accepting a large number of tourists from home and abroad every year, and these mobility of human may introduce eggs of Toxocara spp. from other places. All of these may increase the risk of transmission of Toxocara spp. between humans and dogs and cats. Considering that toxocarosis is one of the most common helminthosis worldwide, this neglected disease has been shown through seroprevalence studies to be especially prevalent in children from socio-economically disadvantaged populations both in the tropics and sub-tropical regions as well as in many developing countries [5], [10], [12]–[18]. However, epidemiological knowledge regarding the prevalence and risks associated with Toxocara infection is limited in China [19]. Therefore, we report the seroprevalence of Toxocara infection in humans in eastern China for the first time, including clinically healthy individuals, pregnant women and psychiatric patients, aiming to attract public attention to Toxocara infection.

Methods

Ethics statement

This study was approved before its commencement by the ethical committee of the Affiliated Hospital of Medical College, Qingdao University (Permit No. ECAHQU2011-006), Weihai Wendeng Central Hospital (Permit No. ECWCH2011-003), Wendeng Municipal Hospital (Permit No. ECWMH2011-008) and Wendeng People's Hospital (Permit No. ECWPH2011-002). The purpose and procedures of the study were explained to all participants, and a written informed consent was obtained from all of them. Parents/guardians provided informed consent on behalf of all child participants. The sera were collected with agreement from the volunteers or patients.

Study design and study population

A cross-sectional study was conducted in Weihai and Qingdao, China. A total of 2866 study participants were recruited between June 2011 through July 2013, including 1431 clinically healthy individuals, 990 pregnant women and 445 psychiatric patients. People who participated in health screenings in the hospitals were considered as clinically healthy individuals. The pregnant women were recruited from women visited hospitals for antenatal follow-up or medication. Inclusion criteria for the pregnant women were: 1) pregnant women in any of the three trimesters of pregnancy; 2) aged 18 years and older; and 3) who were willing to participate in this study. The psychiatric patients were hospitalized for diagnosis or treatment. Inclusion criteria for the psychiatric patients were: 1) psychiatric inpatients; 2) aged 16 years and older; and 3) who accepted to participate in this study. The capacity to consent in psychiatric patients was determined through a clinical evaluation by hospital psychiatrists. Only psychiatric patients with capacity to consent and who accepted to participate were included in the study. In addition, a written informed consent was obtained from all participants and the next-of-kin of minor participants.

Data collection

A structured questionnaire was used to assess risk factors, which included: study area, age, gender, ethnic groups, residential area, pregnancy status, stage of pregnancy, presence of cats and dogs at home, contact with cats and dogs, consumption of raw/undercooked meat, consumption of raw vegetables and fruits, source of drinking water and exposure to soil. In addition, Data of psychiatric patients were obtained from the patients, medical examination records, and informants. Classification of mental illnesses was performed according to the ICD-10 criteria [20].

Sample collection and laboratory tests

Approximately 5 mL of venous blood samples were drawn from the participants in this study. Blood samples were left overnight at room temperature to allow clotting and centrifuged at 3000 rpm for 10 min. The sera were collected in Eppendorf tubes and stored at 4°C for 24–72 h until transported in an ice box to State Key Laboratory of Veterinary Etiological Biology, Key Laboratory of Veterinary Parasitology of Gansu Province, Lanzhou Veterinary Research Institute, Chinese Academy of Agricultural Sciences, Lanzhou, Gansu Province where they were kept at −20°C until tested. Serum samples were detected for anti-Toxocara IgG antibodies using a commercially available enzyme immunoassay “Toxocara” kit (Diagnostic Automation, Inc. Calabasas, CA, USA). Absorbance reading equal to or greater than 0.3 OD units was considered to be positive. All tests were performed following the instructions of the manufacturer [5].

Statistical analysis

The strength of association between dependent (IgG seropositivity to Toxocara; yes/no) and independent variables 1) gender; 2) ethnic groups; 3) residence area; 4) keeping cats at home; 5) keeping dogs at home; 6) contact with cats and dogs; 7) raw vegetable consumption; 8) raw meat consumption; 9) exposure with soil; 10) source of water; was inferred by univariate logistic regression analysis using the SPSS 19.0 software package. Both dependent and independent variables were dichotomous variables. Odds ratio (OR) values were considered statistically significant if the 95% CI did not include 1. Probability (P) value<0.05 was considered as statistically significant in all the analyses.

Results

Seroprevalence among clinically healthy individuals

The clinically healthy individuals were randomly recruited from people who participated in health screenings in the hospitals. Table 1 shows the age, gender, ethnic groups, residence place and residence area distribution of clinically healthy individuals. A total of 1431 clinically healthy individuals of aged 15 to 93 years (mean 32.14 years) participated in this study. The majority (71.9%) of the clinically healthy individuals were in the age range of 20–39 years. In addition, the majority (95.6%) of their race were ethnic Han and most (70.9%) of the clinically healthy individuals lived in Weihai.
Table 1

Socio-demographic characteristics and seroprevalence of Toxocara infection among clinically healthy individuals in Shandong Province, eastern China.

CharacteristicNo. subjects testedPrevalence (%)(95%CI)OR (95%CI) P value
Age groups
19 or less13315.04 (8.96–21.11)Reference
20–2958511.45 (8.87–14.03)0.731 (0.426–1.253)0.2528
30–3944414.19 (10.94–17.44)0.934 (0.542–1.611)0.8068
40–4918110.50 (6.03–14.96)0.663 (0.338–1.298)0.2281
50–594517.78 (6.61–28.95)1.222 (0.497–3.005)0.6625
≥604323.26 (10.63–35.88)1.712 (0.730–4.016)0.2128
Gender
Male4757.16 (4.84–9.48)Reference
Female95616.00 (13.68–18.33)2.471 (1.674–3.648)<0.0001
Ethnic groups
Ethnic Han136813.23 (11.44–15.03)Reference
Ethnic Korean639.52 (2.28–16.77)0.690 (0.293–1.624)0.3933
Residence place
Qingdao41612.50 (9.32–15.68)Reference
Weihai101513.30 (11.21–15.39)1.074 (0.762–1.512)0.6833
Residence area
Urban70714.29 (11.71–16.87)Reference
Suburban or rural72411.88 (9.52–14.24)0.809 (0.594–1.101)0.1768
Anti-Toxocara IgG antibodies were detected in 187 (13.07%, 95% CI 11.32–14.81) of the 1431 clinically healthy individuals. The highest seroprevalence of Toxocara infection was detected in clinically healthy individuals aged ≥60 years old (23.26%, 95%CI 10.63–35.88) (Table 1). Moreover, statistically significant association between Toxocara seropositivity and gender was revealed in clinically healthy individuals (male: 7.16% vs female: 16.00%, OR = 2.471, 95% CI 1.674–3.648, P<0.0001).

Seroprevalence among pregnant women

A total of 990 pregnant women who visited hospitals for antenatal follow-up or medication in Qingdao (n = 445) and Weihai (n = 545) were examined for anti-Toxocara IgG antibodies. Their age, residence place, residence area and trimester of pregnancy are shown in Table 2. The mean age of the 990 pregnant women participating in the study was 28.39 years (range 18–43). Over half (52.2%) of the pregnant women were in the age range of 26–30 years. The 52.8% of the pregnant women were in their first trimester of pregnancy. In addition, nearly half of the pregnant women lived in suburban or rural areas.
Table 2

Socio-demographic characteristics and seroprevalence of Toxocara infection among pregnant women in Shandong Province, eastern China.

CharacteristicNo. subjects testedPrevalence (%)(95%CI)OR (95%CI) P value
Age groups (years)
25 or less2109.52 (5.55–13.49)Reference
26–305178.51 (6.11–10.92)0.884 (0.507–1.539)0.6621
31–3521811.01 (6.85–15.16)1.175 (0.628–2.198)0.6130
>35456.67 (0.00–13.96)0.679 (0.193–2.389)0.5437
Residence place
Qingdao4459.89 (7.11–12.66)Reference
Weihai5458.62 (6.27–10.98)0.860 (0.559–1.324)0.4936
Residence area
Urban5458.44 (6.11–10.77)Reference
Suburban or rural44510.11 (7.31–12.91)1.220 (0.793–1.879)0.3650
Trimester of pregnancy
1st trimester5239.94 (7.38–12.51)Reference
2nd trimester2207.27 (3.84–10.70)0.710 (0.396–1.274)0.2492
3rd trimester2479.31 (5.69–12.94)0.930 (0.555–1.558)0.7829
The overall seroprevalence of Toxocara infection among the pregnant women was 9.19% (91/990, 95% CI 7.39–10.99). Of these, 44 (9.89%) of 445 in Qingdao and 47 (8.62%) of 545 in Weihai were tested positive, but the difference was not statistically significant (OR = 0.860, 95% CI 0.559–1.324, P>0.05) (Table 2). The seroprevalence of Toxocara infection among the pregnant women who lived in suburban or rural areas (10.11%, 95% CI 7.31–12.91) was higher than that among those who lived in urban areas (8.44%, 95% CI 6.11–10.77) (OR = 1.220, 95% CI 0.793–1.879).

Seroprevalence among psychiatric patients

The age, gender, ethnic groups and residence area distribution of the psychiatric patients are shown in Table 3. The mean age of the 445 psychiatric patients participating in the study was 37.18 years (range 16–91). Over half (54.2%) of the psychiatric patients were in the age range of 20–39 years. The 46.5% of the population in the psychiatric patients were males (n = 207), whereas 53.5% were females (n = 238). Moreover, the majority (85.8%) of their race were ethnic Han and most (71.2%) of the psychiatric patients lived in urban areas.
Table 3

Socio-demographic characteristics and seroprevalence of Toxocara infection among psychiatric patients in Shandong Province, eastern China.

CharacteristicNo. subjects testedPrevalence (%)(95%CI)OR (95%CI) P value
Age groups
19 or less4418.18 (6.79–29.58)Reference
20–2912820.31 (13.34–27.28)1.147 (0.476–2.762)0.7595
30–3911312.39 (6.32–18.46)0.636 (0.246–1.643)0.3477
40–498010.00 (3.43–16.57)0.500 (0.173–1.441)0.1935
50–594020.00 (7.60–32.40)1.125 (0.378–3.345)0.8322
≥604022.59 (9.56–35.44)1.306 (0.450–3.796)0.6227
Gender
Male20720.29 (14.81–25.77)Reference
Female23813.03 (8.75–17.30)0.558 (0.354–0.977)0.0390
Ethnic groups
Ethnic Han38216.75 (13.01–20.50)Reference
Ethnic Korean6314.29 (5.45–22.98)0.828 (0.389–1.762)0.6240
Residence area
Urban31714.20 (10.35–18.04)Reference
Suburban or rural12821.88 (14.71–29.04)1.692 (1.002–2.860)0.0477
Table 4 shows clinical diagnosis data of the psychiatric patients based on their psychiatric disorders, which was performed according to the ICD-10 criteria. Patients suffered from organic, including symptomatic, mental disorders (F00–09) (n = 18), mental and behavioral disorders due to psychoactive substance use (F10–19) (n = 79), schizophrenia, schizotypal and delusional disorders (F20–29) (n = 34), mood (affective) disorders (F30–39) (n = 127), neurotic, stress-related and somatoform disorders (F40–49) (n = 65), mental retardation (F70–79) (n = 40), Alzheimer's disease (G30) (n = 33) and epilepsy (G40) (n = 49).
Table 4

Clinical diagnosis and seroprevalence of anti-Toxocara IgG antibodies in psychiatric patients in Shandong Province, eastern China.

Clinical DiagnosisICD-10 diagnosisPatients with anti-Toxocara IgG antibodies
No. testedNo.% (95%CI) P value*
EpilepsyG40491734.69 (21.37–48.02)<0.0001
Affective disorderF30, F391317.69 (0.00–22.18)0.5664
Somatoform disorderF4536513.89 (2.59–25.19)0.8853
SchizophreniaF2034514.71 (2.80–26.61)0.7797
Mental and behavioural disorders due to use of alcoholF10, F1853815.09 (5.46–24.73)0.6680
Mental and behavioural disorders due to use of drugF13, F15, F192627.69 (0.00–17.94)0.4188
Obsessive-compulsive disorderF4229517.24 (3.49–30.99)0.5103
Mild depressionF32.05123313.03 (0.00–26.81)0.9973
Moderate depressionF32.15152611.54 (2.86–20.22)0.7475
Major depressive disorderF32.2513937.69 (0.00–16.06)0.3235
Mental retardationF71–37, F7840717.50 (5.73–29.28)0.4139
Alzheimer's diseaseG3033721.21 (7.26–35.16)0.1725
Dementia in Alzheimer's disease with early onsetF00.018422.22 (3.02–41.43)0.2539
Total4457316.40 (12.96–19.85)0.0752

*As compared with 13.07% seroprevalence of anti-Toxocara IgG antibodies in clinically healthy individuals (187/1431).

*As compared with 13.07% seroprevalence of anti-Toxocara IgG antibodies in clinically healthy individuals (187/1431). Seventy-three (16.40%) of the 445 psychiatric patients were positive for anti-Toxocara IgG antibodies indicating latent infection with Toxocara in psychiatric patients. Table 3 shows the seroprevalences of latent Toxocara infection in the populations studied according to their socio-demographic characteristics. Table 4 shows the seroprevalences of Toxocara infection in the patients according to their psychiatric disorders. The highest prevalence of latent Toxocara infection in psychiatric patients was found in patients aged ≥60 years old (22.59%, 95% CI 9.56–35.44) (Table 3). The seroprevalence in male psychiatric patients (20.29%, 95% CI 14.81–25.77) was significantly higher than that in female psychiatric patients (13.03%, 95% CI 8.75–17.30) (OR = 0.558, 95% CI 0.354–0.977, P = 0.0390). In addition, the seroprevalence of latent Toxocara infection in psychiatric patients who lived in suburban or rural areas (21.88%, 95% CI 14.71–29.04) was significantly higher than that in urban psychiatric patients (14.20%, 95% CI 10.35–18.04) (OR = 1.692, 95% CI 1.002–2.860, P = 0.0477). With respect to clinical data, statistically significant association between Toxocara seropositivity and psychiatric diagnosis was found. The seroprevalence of latent Toxocara infection in patients with epilepsy (17/49, 34.69%, 95%CI 21.37–48.02) was significantly higher than that in clinically healthy individuals (Table 4) (P<0.0001).

Univariate logistic regression analysis

Comparing the total seropositive (351 subjects) with seronegative populations (2515 subjects), the univariate logistic regression analysis confirmed that keeping dogs at home (OR = 0.06, 95% CI 0.05–0.08, P<0.001), contact with cats and dogs (OR = 0.42, 95% CI 0.33–0.53, P<0.001) and exposure with soil (OR = 0.37, 95% CI 0.28–0.49, P<0.001) were risk factors associated with Toxocara infection. Other details are shown in Table 5.
Table 5

Odds ratio of the risk factors associated with seropositivity to Toxocara in the study population in Shandong province, eastern China.

CharacteristicNo. subjects testedPrevalence (%)(95%CI)OR (95%CI) P value
Age groups
19 or less18915.87 (10.66–21.08)Reference
20–29133111.20 (9.50–12.89)0.668 (0.436–1.023)0.0619
30–3990912.10 (9.98–14.22)0.730 (0.471–1.131)0.1572
40–4926910.04 (6.45–13.63)0.591 (0.339–1.032)0.0625
50–598518.82 (10.51–27.13)1.229 (0.629–2.400)0.5455
≥608322.89 (13.85–31.93)1.573 (0.827–2.995)0.1655
Gender
Male68211.14 (8.78–13.51)Reference
Female218412.59 (11.20–13.98)1.15 (0.88–1.51)0.3140
Ethnic groups
Ethnic Han274012.15 (10.93–13.38)Reference
Ethnic Korean12611.91 (6.25–17.56)0.98 (0.56–1.70)0.9334
Residence place
Qingdao86111.15 (9.05–13.25)Reference
Weihai200512.72 (11.26–14.18)1.16 (0.91–1.49)0.2403
Residence area
Urban156912.24 (10.62–13.86)Reference
Suburban or rural129712.26 (10.47–14.04)1.00 (0.80–1.25)0.9858
Cats at home
Yes25613.28 (9.12–17.44)Reference
No261012.15 (10.89–13.40)0.90 (0.62–1.32)0.5969
Dogs at home
Yes28856.94 (51.22–62.66)Reference
No25787.25 (6.25–8.26)0.06 (0.05–0.08)<0.001
Contact with cats and dogs
Yes131217.23 (15.18–19.27)Reference
No15548.04 (6.69–9.40)0.42 (0.33–0.53)<0.001
Raw vegetable consumption
Yes191512.59 (11.10–14.07)Reference
No95111.57 (9.53–13.60)0.91 (0.71–1.16)0.4337
Raw meat consumption
Yes199212.60 (11.14–14.06)Reference
No87411.44 (9.33–13.55)0.90 (0.70–1.15)0.3837
Exposure with soil
Yes188815.36 (13.73–16.99)Reference
No9786.24 (4.72–7.75)0.37 (0.28–0.49)<0.001
Source of water
Tap201912.28 (10.85–13.72)Reference
Well+river84712.16 (9.96–14.36)0.99 (0.77–1.26)0.9271

Discussion

This pilot study investigated Toxocara seroprevalence in clinically healthy individuals, pregnant women and psychiatric patients in Shandong Province, eastern China, and potential factors associated with Toxocara infection were evaluated as well. The overall Toxocara IgG prevalence among the study population was 12.25%, which is slightly higher than that of a previous study conducted in Chengdu, China, where a 11.49% seroprevalence of Toxocara spp. infection was reported in children [19]. Such differences may due to several factors, such as geographical conditions, the type and size of population evaluated, life style of the population evaluated, as well as the specificity and sensitivity of the detection methods used. In the present study, a significantly higher seroprevalence of Toxocara seropositivity was found in psychiatric patients (16.40%) than in clinically healthy individuals (13.07%) and pregnant women (9.19%). Furthermore, seroprevalence increased along with age but not associated with gender, ethnic groups, or residence area. To the best of our knowledge, the past epidemiological knowledge regarding the prevalence and risk associated with Toxocara infection is limited in China [19], and this is the first report of Toxocara infection among clinically healthy adults, pregnant women and psychiatric patients in China. In the present study, a significantly higher seroprevalence of Toxocara seropositivity in psychiatric patients than in clinically healthy individuals and pregnant women was found. Studies of toxocarosis in psychiatric inpatients have been conducted in Mexico [5] and Italy [21]. Similarly, the highest Toxocara seroprevalence found in the psychiatric patients in our study agrees with that found in a case-control seroprevalence study in Durango, Mexico [5], where researchers found a significantly higher seroprevalence of Toxocara seropositivity in psychiatric inpatients (4.7%) as compared with control subjects (1.1%). It is not clear why psychiatric patients had an increased Toxocara seroprevalence. However, during the investigation, we found that psychiatric patients were often in poor hygiene practices and many patients have had contacted with cats and dogs, and these risk factors might have contributed to an increased Toxocara exposure. Several studies have demonstrated that contact with dogs is an important risk factor for toxocarosis [10], [22], [23]. Humans may become infected with T. canis via direct contact with dogs. Although stray dogs had a significantly higher prevalence of T. canis than domestic dogs, domestic dogs are the biggest risk for human exposure due to frequent contact with their owners [23]. T. canis eggs have been found in both the faeces and on the furs of domestic dogs in previous studies [23], [24]. Once the conditions become suitable, T. canis eggs may become embryonated in furs of domestic dogs. Therefore, direct contact with these dogs, such as petting, may increase the risk of transmission of Toxocara spp. [23], [24]. Our results revealed that the presence of dogs at home and contact with dogs and cats are risk factors for Toxocara infection in this study population. In addition, we found that female had higher seroprevalence than that in male in the present study, indicating that females are at higher risk of Toxocara infection in eastern China. This may be related to many factors. For example, females usually take more care of pet animals including dogs and cats at home, and moreover, females handle raw meat and vegetables more frequently than males because they spend more time on cooking at home. Thus it is more important to propagandize the knowledge of disease prevention in public, especially for the female groups. Moreover, our data show that Toxocara exposure is the most frequent in the aged people of more than 60 years old. Although it is different from other studies [13], [14], it may be ascribed to some typical factors in China. First, the differences in seroprevalence may due to differences in the diagnostic methods, ecological and geographical factors. In addition, life style, dietary habit, number of dogs and cats and number of sample size among the study population may contribute to the differences in Toxocara seropositivity. More importantly, with the significant socio-economic advances and an increase in living standard, pet dogs and cats are very common in Chinese family, especially in the aged, leading to frequent contact with these reservoir hosts of Toxocara and thus the increased risks [3]. Therefore, our data and other studies have emphasized again that the presence of dogs in the household and contact with dogs are considered to be the major risk factor for the presence of Toxocara seropositivity in people [25], [26], proposing that the importance of toxocarosis is likely to grow due to the rapid growth of the human and dog populations and their increasing densities in urban areas without specific control initiatives. Many studies have evaluated the consumption of raw or undercooked viscera or meat as a potential risk factor for Toxocara infection, and have shown their associations with human Toxocara seroprevalence [27]–[29]. However, in the present study no association between Toxocara seropositivity and the consumption of raw or undercooked viscera or meat was found, which may be related to the type and size of population evaluated. So, the association between toxocarosis and consumption of raw or undercooked viscera or meat warrants further research. High human Toxocara seroprevalence has been reported in areas with documented soil contamination, and the risk for transmission may be increased in proportion to the degree of environmental contamination [30], [31]. Similarly, the present study reported that there was no significant difference in the Toxocara seroprevalence between urban and suburban or rural areas (P>0.05), but humans exposed with soil was significantly relevant to positive serology (P<0.001). In conclusion, the present study revealed for the first time that human infection with Toxocara is common in eastern China, posing a significant public health concern. Increasing human and dog populations, population movements and climate change all will serve to increase the importance of this zoonosis [26]. Further studies under controlled conditions are necessary to further define potential morbidity associated with Toxocara infection. In addition, prevention efforts such as hand washing before eating and after soil contact, prevention of soil contamination in public areas by dog and cat feces, and preventive anthelmintic treatment of dogs and cats, starting at an early age, can be beneficial to minimize exposure to Toxocara spp. and help control potential morbidity associated with Toxocara infection. STROBE checklist. (DOC) Click here for additional data file.
  28 in total

1.  Anti-Toxocara spp. antibodies in an adult healthy population: serosurvey and risk factors in Southeast Brazil.

Authors:  Elaine Cristina Negri; Vamilton Alvares Santarém; Guita Rubinsky-Elefant; Rogério Giuffrida
Journal:  Asian Pac J Trop Biomed       Date:  2013-03

2.  Anti-Toxocara antibodies detected in children attending elementary school in Vitoria, State of Espírito Santo, Brazil: prevalence and associated factors.

Authors:  Roberta Paranhos Fragoso; Mariza Buriche Macedo Monteiro; Elenice Moreira Lemos; Fausto Edmundo Lima Pereira
Journal:  Rev Soc Bras Med Trop       Date:  2011 Jul-Aug       Impact factor: 1.581

3.  Risk of Toxocara canis eggs in stray and domestic dog hair in Egypt.

Authors:  Wael F El-Tras; Hannah R Holt; Ahmed A Tayel
Journal:  Vet Parasitol       Date:  2011-01-26       Impact factor: 2.738

4.  Zoonotic risk of Toxocara canis infection through consumption of pig or poultry viscera.

Authors:  K Taira; I Saeed; A Permin; C M O Kapel
Journal:  Vet Parasitol       Date:  2004-05-07       Impact factor: 2.738

5.  Meningitis by Toxocara canis after ingestion of raw ostrich liver.

Authors:  Young Noh; Sung-Tae Hong; Ji Young Yun; Hong-Kyun Park; Jung-Hwan Oh; Young Eun Kim; Beom S Jeon
Journal:  J Korean Med Sci       Date:  2012-08-22       Impact factor: 2.153

6.  [Antibodies against Toxocara canis in human serum from western Sicily].

Authors:  M Di Fiore; A Virga; V Usticano; S Di Rosa; G B Rini
Journal:  Boll Ist Sieroter Milan       Date:  1989

7.  Transmission of Toxocara canis via ingestion of raw cow liver: a cross-sectional study in healthy adults.

Authors:  Dongil Choi; Jae Hoon Lim; Dong-Chull Choi; Kyung Soo Lee; Seung Woon Paik; Sun-Hee Kim; Yoon-Ho Choi; Sun Huh
Journal:  Korean J Parasitol       Date:  2012-03-06       Impact factor: 1.341

8.  Canine and feline parasitic zoonoses in China.

Authors:  Jia Chen; Min-Jun Xu; Dong-Hui Zhou; Hui-Qun Song; Chun-Ren Wang; Xing-Quan Zhu
Journal:  Parasit Vectors       Date:  2012-07-28       Impact factor: 3.876

9.  Toxocara seropositivity, atopy and wheezing in children living in poor neighbourhoods in urban Latin American.

Authors:  Lívia Ribeiro Mendonça; Rafael Valente Veiga; Vitor Camilo Cavalcante Dattoli; Camila Alexandrina Figueiredo; Rosemeire Fiaccone; Jackson Santos; Álvaro Augusto Cruz; Laura Cunha Rodrigues; Philip John Cooper; Lain Carlos Pontes-de-Carvalho; Maurício Lima Barreto; Neuza Maria Alcantara-Neves
Journal:  PLoS Negl Trop Dis       Date:  2012-11-01

10.  Toxocariasis: America's most common neglected infection of poverty and a helminthiasis of global importance?

Authors:  Peter J Hotez; Patricia P Wilkins
Journal:  PLoS Negl Trop Dis       Date:  2009-03-31
View more
  15 in total

Review 1.  Cerebral Toxocariasis: Silent Progression to Neurodegenerative Disorders?

Authors:  Chia-Kwung Fan; Celia V Holland; Karen Loxton; Ursula Barghouth
Journal:  Clin Microbiol Rev       Date:  2015-07       Impact factor: 26.132

2.  T oxocara canis prevalence in soil, dog stool, and human serum samples from a rural village in Los Baños, Laguna, Philippines.

Authors:  Moses Edric G Abadilla; Vachel Gay V Paller
Journal:  J Parasit Dis       Date:  2022-06-30

3.  Lack of Association between Toxocara Exposure and Suicide Attempts in Psychiatric Patients.

Authors:  Cosme Alvarado-Esquivel; Jesús Hernández-Tinoco; Luis Francisco Sánchez-Anguiano
Journal:  J Parasitol Res       Date:  2015-09-21

4.  The Seropositivity of Toxocara spp. Antibodies in Pregnant Women Attented at the University Hospital in Southern Brazil and the Factors Associated with Infection.

Authors:  Paula Costa Santos; Lis Maurente Lehmann; Carolina Lorenzi; Carolina Hirsch; Paula Lima Telmo; Gabriela Torres Mattos; Priscila Silva Cadore; Gabriel Baracy Klafke; Maria Elisabeth Aires Berne; Carla Vitola Gonçalves; Carlos James Scaini
Journal:  PLoS One       Date:  2015-07-06       Impact factor: 3.240

5.  Prevalence and Risk Factors of Intestinal Parasites in Cats from China.

Authors:  Yurong Yang; Hongde Liang
Journal:  Biomed Res Int       Date:  2015-05-11       Impact factor: 3.411

6.  MicroRNAs of Toxocara canis and their predicted functional roles.

Authors:  Guangxu Ma; Yongfang Luo; Honghong Zhu; Yongli Luo; Pasi K Korhonen; Neil D Young; Robin B Gasser; Rongqiong Zhou
Journal:  Parasit Vectors       Date:  2016-04-23       Impact factor: 3.876

7.  Seroepidemiological Study of Toxocariasis among Volunteers Animal Husbandry Workers and Veterinary in Southern Anatolia in Turkey in 2014.

Authors:  Hamdi Sozen; Burak E Citil; Selmin Caylak; Aysegul A Gokmen; Selçuk Kaya; Mustafa Demirci; Metin Korkmaz; Cem Sahin; Ismail Kirli
Journal:  Iran J Parasitol       Date:  2015 Jul-Sep       Impact factor: 1.012

8.  Global toxocariasis research trends from 1932 to 2015: a bibliometric analysis.

Authors:  Sa'ed H Zyoud
Journal:  Health Res Policy Syst       Date:  2017-02-23

9.  Seroprevalence and associated risk factors of Toxocara infection in Korean, Manchu, Mongol, and Han ethnic groups in northern China.

Authors:  G-L Yang; X-X Zhang; C-W Shi; W-T Yang; Y-L Jiang; Z-T Wei; C-F Wang; Q Zhao
Journal:  Epidemiol Infect       Date:  2016-07-26       Impact factor: 4.434

10.  Eosinophilic Myocarditis due to Toxocariasis: Not a Rare Cause.

Authors:  Shunichi Shibazaki; Shunsuke Eguchi; Takashi Endo; Tadamasa Wakabayashi; Makoto Araki; Yoshiaki Gu; Taku Imai; Kouji Asano; Norihide Taniuchi
Journal:  Case Rep Cardiol       Date:  2016-03-31
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