Abstract
Toxoplasma gondii is an important foodborne protozoan that can be transmitted through infected blood containing tachyzoite form of the parasite. The current study aimed to evaluate the prevalence of T. gondii infection and related risk factors among healthy blood donors in Boyer-Ahmad County, southwest Iran. Blood samples were taken from 285 healthy blood donors who voluntarily agreed to participate in this study. Sera and buffy coat were isolated from the blood samples for serological and molecular evaluations. The sera were tested for anti-T. gondii antibodies (both IgG and IgM), using a commercial ELISA kit. The buffy coat of seropositive cases was evaluated for detection of T. gondii DNA by PCR. Moreover, a structured questionnaire, containing socioepidemiological data and possible risk factors, was filled out by each participant during sample collection. Anti-T. gondii antibodies were detected in sera of 48/285 (16.8%) participants. Only two of the subjects (0.7%) were seropositive for both IgG and IgM antibodies. T. gondii DNA was not detected in buffy coat of any of the seropositive cases. Risk factors such as contact with soil (OR, 9.7; 95% CI, 4.9–19.4) and consumption of semicooked meat (OR, 2.5; 95% CI, 1.2–5.03) were statistically associated with seropositivity to T. gondii. The seroprevalence rate of T. gondii antibodies in the blood donors of Boyer-Ahmad County was not high in comparison with other regions in Iran. In this study, consumption of undercooked meats, job, and contact with soil were independent risk factors associated with T. gondii infection, which can be considered as potential sources of T. gondii infection.
1. Introduction
Toxoplasma gondii is often a water and foodborne pathogen with a wide and considerable distribution which can be transmitted through blood transfusion and causes acute severe complication such as encephalitis in immunocompromised blood recipients [1, 2]. Toxoplasmosis may result in abortion or neurological abnormalities in human fetus following intrauterine transmission [1, 3]. Toxoplasmosis is an asymptomatic mild infection in most of the immunocompetent individuals, yet a number of studies have shown a significant association between latent toxoplasmosis and psychiatric disorder among immunocompetent individuals [4–6].
The main routes of T. gondii infection in human are ingesting of sporulated oocysts in contaminated water, vegetables, and fruits along with eating undercooked contaminated meat and also vertical transmission at the time of pregnancy. Moreover, the healthy human can be infected through blood transfusion or organ transplantation. Toxoplasmosis is a common infection in human and animals in all areas of Iran [2, 7–11]. Blood donors, especially those who are in the acute phase of the infection, can impose risk of T. gondii infection for the susceptible recipients [12, 13]. The mean prevalence of toxoplasmosis among Iranian blood donors varied between 12.3% and 52.8% [14]. Recent studies reported anti-T. gondii IgG antibodies in sera of 19.3% of blood donors, 8.5% of female university students, and 8.9% of pregnant women in southern Iran [2, 15, 16].
The current study was performed to assess the seroprevalence rate of T. gondii and possible associated risk factors among blood donors in Boyer-Ahmad in southwest Iran.
2. Materials and Methods
2.1. Study Area
This cross-sectional study was conducted on healthy blood donors of Boyer-Ahmad county, located in southwest Iran, from April to August 2015. Boyer-Ahmad is located in a mountainous and cold region of Iran. Snow and rainfall are plentiful in this region, especially in fall and winter seasons. The mean altitude in the area where the Boyer-Ahmad people live is 1800–2200 m above the sea level. The area has geographical coordinates between latitudes 30–9° and 31–27°N and between longitudes 49–55° and 51–42°E. Animal husbandry and gardening are common in this district. Food habits of more people are composed of meat, milk, and local vegetables. Parasitic diseases are not uncommon in this area and the area is considered as a focus of human fascioliasis as well as visceral leishmaniasis [17–21]. Also, high levels of blood-borne diseases including hepatitis C and B have been reported from the area [22, 23].
2.2. Sampling
Subjects of this study were recruited from healthy blood donors who knowingly agreed for participation in the study. All participating individuals were given a questionnaire before collection of blood sample, which provided information about their age, sex, residence area, level of education, occupation, and risk factors including the consumption of raw/undercooked meat, contact with cat, contact with soil in gardening or agricultural activities, and history of blood transfusion. Awareness about toxoplasmosis and clinical symptoms including fever, rash, and lymphadenopathy were also recorded. 5 mL of fresh blood was collected from each blood donor in plastic K2EDTA-containing tubes. Samples were centrifuged and buffy coat and sera were isolated from each sample. Collected samples were kept at −20°C until use.
2.3. Serologic Testing
All of the collected sera were tested for detection of anti-T. gondii IgG and IgM antibodies, using a commercial ELISA kit (ACON Biotech, Hangzhou, China), based on the manufacturer's instructions. Index value was obtained for both IgG and IgM. An index value ≤ 0.9 IU/mL was regarded as negative result, while the equivocal range was defined between 0.9 and 1.1 IU/mL and index value greater than 1.1 IU/mL was considered as positive result for both IgG and IgM.
2.4. DNA Extraction and PCR Amplification
DNA was isolated from the buffy coat of each sample, using the phenol-chloroform extraction method as previously described [2]. The conventional PCR for detection of T. gondii DNA was performed targeting a 529 bp gene, with primers TOXOF (5′- CAGGGAGGAAGACGAAAGTTG- 3′) and TOXOR (5′- CAGACACAGTGCATCTGGATT-3′) [24]. The total reaction volume was 25 μL, containing 1 unit of Taq polymerase, 12.5 μL of 2x Master Mix Red, 1.5 mM of MgCl2, 1 μL of each 20-picomole primer, 50 ng of extracted DNA, and the remaining nuclease-free water. The PCR program was set for 5 minutes at 94°C before cycling, followed by 30 cycles of denaturation at 94°C for 35 seconds, annealing at 56°C for 1 minute, extension at 72°C for 1 minute, a final extension at 72°C for 10 minutes, and final hold at 4°C for 10 minutes. Amplification was performed with negative along with positive control of T. gondii (a kind gift of Dr. Q. Asgari). The 529 bp PCR products were separated by electrophoresis in 1.5% agarose gel and stained with ethidium bromide.
2.5. Statistical Analysis
SPSS 18 software was used for all statistical analyses. The frequency of dependent variables was described, using descriptive statistics, and chi-squared and regression logistical tests (p < 0.05) were used to find out any possible association between qualitative variables and seropositivity to toxoplasmosis.
3. Results
3.1. Demographic Features of the Participants
Overall, 285 healthy blood donors were recruited in this study. The mean age of the subjects was 37 (±9.53) years. Most of the blood donors (41.8%) were in the age group of 28–37 years. The majority of the subjects were male (96.8%). Most of the subjects (36.5%) were employees.
3.2. Seroprevalence of Anti-T. gondii Antibodies
Anti-T. gondii antibodies were detected in sera of 48 out of 285 blood donors. Of these, 46 cases (16.30%) were seropositive only for IgG and 2 cases were seropositive for both IgG and IgM. Seropositivity in males and females was 16.3% and 11.1%, respectively.
3.3. Risk Factors for T. gondii Seropositivity
In the univariate analysis, three variables including contact with soil (p = 0.01), consumption of undercooked meat (as barbecue or kebab), (p = 0.007), and job (p = 0.040), were documented as associated risk factors for T. gondii seropositivity. Other risk factors and also demographic features of the blood donors were not statistically associated with the acquisition of T. gondii infection (p ≥ 0.05) (Table 1).
Table 1.
Variables | Frequency (number) | Seropositivity (%) | Odds ratio (95% confidence interval) | p value |
---|---|---|---|---|
Blood transfusion | ||||
Yes | 8 | 37.5 | 3.09 (0.714–13.407) | 0.135 |
No | 277 | 16.2 | 1 | |
Place of residence | 0.602 | |||
City | 203 | 17.5 | 1.257 (0.618–2.559) | |
Village | 82 | 14.6 | 1 | |
Eating of semicooked meat | 0.007 | |||
Yes | 157 | 22.30 | 2.538 (1.278–5.038) | |
No | 128 | 10.15 | 1 | |
Contact with cat | 0.841 | |||
Yes | 51 | 15.6 | 0.902 (0.394–2.065) | |
No | 234 | 20.51 | ||
Taking immunosuppressive drugs | 0.199 | |||
Yes | 5 | 40 | 3.391 (.551–20.866) | |
No | 280 | 16-4 | ||
Contact with soil | 0.001 | |||
Yes | 61 | 47.5 | 9.778 (4.914–19.457) | |
No | 224 | 8.5 | ||
Job | 0.040 | |||
Employees | 112 | 25 | 1 | |
Other business | 81 | 16 | 1.744 | |
Student | 24 | 4 | 7.667 | |
Farmer and rancher | 55 | 9.09 | 3.333 | |
Unemployed | 13 | 7.70 | 4.000 | |
Educational level | 0.592 | |||
Secondary level and below | 56 | 17.86 | 1.049 (0.469–2.348) | |
High-school level | 89 | 13.5 | 1.463 (0.696–3.075) | |
University level | 140 | 18.6 | 1 | |
Blood group | 0.285 | |||
A | 88 | 13.6 | 1.715 (0.812–3.621) | |
B | 57 | 15.8 | 1.444 (0.628–3.324) | |
AB | 18 | 5.5 | 4.604 (0.585–36.226) | |
O | 122 | 21.3 | 1 | |
Washing vegetables with antiseptic materials | 0.587 | |||
Yes | 73 | 19.7 | 1 | |
No | 212 | 16.03 | 1.242 (.624–2.473) | |
Awareness about toxoplasmosis | 0.702 | |||
Yes | 10 | 10 | 0.539 (0.067–4.357) | |
No | 275 | 17.1 | 1 |
3.4. Detection of T. gondii DNA in Seropositive Subjects
None of the 48 seropositive subjects were positive for T. gondii by molecular (PCR) method.
4. Discussion
This is a cross-sectional study regarding the seroprevalence and molecular evaluation of T. gondii infection among healthy blood donors of Boyer-Ahmad County in southwest Iran. The overall seroprevalence of 16.8% for toxoplasmosis in the current study indicates a considerable rate of toxoplasmosis in the population, but the seroprevalence rate of toxoplasmosis in our study is lower than the rates reported in blood donors from most of the areas in Iran [2, 7, 25] and other regions as reported from Turkey (22.59%) [26], Czech Republic (34.23%) [27], Brazil (60%) [28], Saudi Arabia (40%) [29], Iraq (32.75%) [30], Egypt (59.6%) [31], and India (53.7%) [32]. Variations in the rate of seropositivity of T. gondii in different regions of the world or in different areas of a given country can be attributed to the differences in climate, topographical conditions, and food behavior.
Lower seroprevalence of toxoplasmosis in high altitude and cold climates has been reported, as T. gondii oocysts cannot survive for a long time in such environmental conditions. In the present study, consumption of undercooked meat was identified as a risk factor related to T. gondii seropositivity in blood donors. These findings indicate that the ingestion of undercooked meat, mainly sheep and goat, containing tissue cysts might be one of the main sources of T. gondii infection in this area [33, 34]. This notion has already been documented in other areas of Iran [8, 10]. Exposure to the soil, followed by oocysts in soil, is an important risk factor for acquisition of T. gondii. Risk factors of toxoplasmosis vary in different geographic regions. Contact with cats in Mexico and eating raw shellfish as well as exposure to domestic cats in Taiwan [35] have been counted as the main risk factors for T. gondii infection among the blood donors. In rural communities of northern Iran, consumption of undercooked sheep and goat meat and unwashed raw vegetables or fruits have been considered as the main risk factors for T. gondii infection [34], while contact with cats and consuming raw vegetables and raw milk/egg were identified as independent risk factors for T. gondii seropositivity among the healthy blood donors in the southeast of the country [36].
In the current study, there was a significant correlation between job and seropositivity with T. gondii. This fact can be justified as most of the people in the studied area live on animal husbandry and agricultural activities, which increases the chance of T. gondii infection. None of the seropositive cases were positive for T. gondii DNA. This indicates that all of the seropositive cases have been in the chronic phase of toxoplasmosis and have no risk of T. gondii infection for the recipients.
This study showed that more than 16% of the healthy blood donors in Boyer-Ahmad County in southwest Iran have anti-T. gondii antibodies in their sera and the consumption of undercooked meats, job, and contact with soil were three independent risk factors associated with T. gondii infection.
Acknowledgments
The study was financially supported by the office of vice-chancellor for research of Yasuj University of Medical Sciences.
Ethical Approval
The study was approved by the Ethical Committee of Yasuj University of Medical Sciences (YUMS).
Consent
Verbal informed consent for the study was obtained from all participants prior to enrolment.
Disclosure
The study was the subject of Mr. Saadat Kazemi's M.D. thesis.
Conflicts of Interest
The authors declare that they have no conflicts of interest.
Authors' Contributions
Bahador Sarkari, Abdolali Moshfe, and Ahmad Mardani conceived and designed the study. Saadat Kazemi and Nasir Arefkhah collected the samples. Nasir Arefkhah and Saadat Kazemi performed the experiments. Bahador Sarkari, Ahmad Mardani, and Nasir Arefkhah analyzed the data. Nasir Arefkhah wrote the first draft of the paper. Bahador Sarkari edited the paper. All authors read and approved the final manuscript.
References
- 1.Flegr J., Prandota J., Sovičková M., Israili Z. H. Toxoplasmosis - A global threat. Correlation of latent toxoplasmosis with specific disease burden in a set of 88 countries. PLoS ONE. 2014;9(3) doi: 10.1371/journal.pone.0090203.e90203 [DOI] [PMC free article] [PubMed] [Google Scholar]
- 2.Sarkari B., Shafiei R., Zare M., Sohrabpour S., Kasraian L. Seroprevalence and molecular diagnosis of Toxoplasma gondii infection among blood donors in southern Iran. The Journal of Infection in Developing Countries. 2014;8(4):543–547. doi: 10.3855/jidc.3831. [DOI] [PubMed] [Google Scholar]
- 3.Sarkari B., Khabisi S. A. Severe congenital toxoplasmosis: a case report and strain characterization. Case Reports in Infectious Diseases. 2015;2015:3. doi: 10.1155/2015/851085.851085 [DOI] [PMC free article] [PubMed] [Google Scholar]
- 4.Weiss L. M., Dubey J. P. Toxoplasmosis: a history of clinical observations. International Journal for Parasitology. 2009;39(8):895–901. doi: 10.1016/j.ijpara.2009.02.004. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 5.Dubey J. P., Jones J. L. Toxoplasma gondii infection in humans and animals in the United States. International Journal for Parasitology. 2008;38(11):1257–1278. doi: 10.1016/j.ijpara.2008.03.007. [DOI] [PubMed] [Google Scholar]
- 6.Rostami A., Keshavarz H., Shojaee S., Mohebali M., Meamar A. R. Frequency of Toxoplasma gondii in HIV positive patients from west of Iran by ELISA and PCR. Iranian Journal of Parasitology. 2014;9(4):474–481. [PMC free article] [PubMed] [Google Scholar]
- 7.Asgari Q., Fekri M., Monabati A. Molecular genotyping of Toxoplasma gondii in human spontaneous aborted fetuses in Shiraz, Southern Iran. Iranian Journal of Public Health. 2013;42(6):620–625. [PMC free article] [PubMed] [Google Scholar]
- 8.Asgari Q., Sarnevesht J., Kalantari M., Sadat S. J. A., Motazedian M. H., Sarkari B. Molecular survey of Toxoplasma infection in sheep and goat from Fars province, Southern Iran. Tropical Animal Health and Production. 2011;43(2):389–392. doi: 10.1007/s11250-010-9704-1. [DOI] [PubMed] [Google Scholar]
- 9.Barazesh A., Sarkari B., Mehrabi Sisakht F., Abdolahi Khabisi S., Nikbakht R., Ravanbod M. R. Seroprevalence and molecular evaluation of toxoplasmosis in patients undergoing chemotherapy for malignancies in the Bushehr Province, Southwest Iran. Jundishapur Journal of Microbiology. 2016;9(9) doi: 10.5812/jjm.35410.e35410 [DOI] [PMC free article] [PubMed] [Google Scholar]
- 10.Sarkari B., Asgari Q., Bagherian N., et al. Molecular and serological evaluation of Toxoplasma gondii infection in reared turkeys in Fars Province, Iran. Jundishapur Journal of Microbiology. 2014;7(7) doi: 10.5812/jjm.11598.e11598 [DOI] [PMC free article] [PubMed] [Google Scholar]
- 11.Daryani A., Sarvi S., Aarabi M., et al. Seroprevalence of Toxoplasma gondii in the Iranian general population: A systematic review and meta-analysis. Acta Tropica. 2014;137:185–194. doi: 10.1016/j.actatropica.2014.05.015. [DOI] [PubMed] [Google Scholar]
- 12.Singh G., Sehgal R. Transfusion-transmitted parasitic infections. Asian Journal of Transfusion Science. 2010;4(2):73–77. doi: 10.4103/0973-6247.67018. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 13.Foroutan-Rad M., Majidiani H., Dalvand S., et al. Toxoplasmosis in blood donors: a systematic review and meta-analysis. Transfusion Medicine Reviews. 2016;30(3):116–122. doi: 10.1016/j.tmrv.2016.03.002. [DOI] [PubMed] [Google Scholar]
- 14.Karimi G., Mardani A., Zadsar M. Prevalence of Toxoplasma gondii among Iranian blood donors: a narrative review article. Iranian Journal of Parasitology. 2016;11(1):10–18. [PMC free article] [PubMed] [Google Scholar]
- 15.Norouzi L. Y., Sarkari B., Asgari Q., Khabisi S. A. Molecular evaluation and seroprevalence of toxoplasmosis in pregnant women in Fars province, Southern Iran. Annals of Medical and Health Sciences Research. 2017;7(1):16–19. [Google Scholar]
- 16.Taghizadeh H., Shahriarirad R., Erfani A., et al. Seroepidemiological survey of toxoplasmosis among female university students in Shiraz, southern Iran. Annals of Tropical Medicine and Public Health. 2017;10(2):362–365. doi: 10.4103/1755-6783.208724. [DOI] [Google Scholar]
- 17.Sarkari B., Hosseini G., Motazedian M. H., Fararouei M., Moshfe A. Prevalence and risk factors of intestinal protozoan infections: a population-based study in rural areas of Boyer-Ahmad district, Southwestern Iran. BMC Infectious Diseases. 2016;16(1, article 703) doi: 10.1186/s12879-016-2047-4. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 18.Hosseini G., Sarkari B., Moshfe A., Motazedian M. H., Abdolahi Khabisi S. Epidemiology of human fascioliasis and intestinal helminthes in rural areas of Boyer-Ahmad Township, Southwest Iran; a population based study. Iranian Journal of Public Health. 2015;44(11):1520–1525. [PMC free article] [PubMed] [Google Scholar]
- 19.Shafiei R., Sarkari B., Sadjjadi S. M., Mowlavi G. R., Moshfe A. Molecular and morphological characterization of Fasciola spp. isolated from different host species in a newly emerging focus of human fascioliasis in Iran. Veterinary Medicine International. 2014;2014:10. doi: 10.1155/2014/405740.405740 [DOI] [PMC free article] [PubMed] [Google Scholar]
- 20.Sarkari B., Ghobakhloo N., Moshfea A. A., Eilami O. Seroprevalence of human fasciolosis in a new-emerging focus of fasciolosis in Yasuj District, Southwest of Iran. Iranian Journal of Parasitology. 2012;7(2):15–20. [PMC free article] [PubMed] [Google Scholar]
- 21.Sarkari B., Pedram N., Mohebali M., et al. Seroepidemiological study of visceral leishmaniasis in Booyerahmad district, South-West Islamic Republic of Iran. Eastern Mediterranean Health Journal. 2010;16(11):1133–1136. [PubMed] [Google Scholar]
- 22.Khosravani A., Sarkari B., Negahban H., Sharifi A., Toori M. A., Eilami O. Hepatitis B Infection among high risk population: a seroepidemiological survey in Southwest of Iran. BMC Infectious Diseases. 2012;27(12, article 378) doi: 10.1186/1471-2334-12-378. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 23.Sarkari B., Eilami O., Khosravani A., Sharifi A., Tabatabaee M., Fararouei M. High prevalence of hepatitis C infection among high risk groups in Kohgiloyeh and Boyerahmad Province, Southwest Iran. Archives of Iranian Medicine. 2012;15(5):271–274. [PubMed] [Google Scholar]
- 24.Edvinsson B., Jalal S., Nord C. E., Pedersen B. S., Evengård B. DNA extraction and PCR assays for detection of Toxoplasma gondii. APMIS-Acta Pathologica, Microbiologica et Immunologica Scandinavica. 2004;112(6):342–348. doi: 10.1111/j.1600-0463.2004.apm1120604.x. [DOI] [PubMed] [Google Scholar]
- 25.Mansouri A., Adhami Mojarad M. R., Badfar G., et al. Epidemiology of Toxoplasma gondii among blood donors in Iran: a systematic review and meta-analysis. Transfusion and Apheresis Science. 2017;56(3):404–409. doi: 10.1016/j.transci.2017.03.011. [DOI] [PubMed] [Google Scholar]
- 26.Eser B., Yay M. Prevalence of anti-toxoplasma gondii antibodies in Turkish blood donors. Ethiopian Medical Journal. 2006;44(3):257–261. [PubMed] [Google Scholar]
- 27.Svobodová V., Literák I. Prevalence of IgM and IgG antibodies to Toxoplasma gondii in blood donors in the Czech Republic. European Journal of Epidemiology. 1998;14(8):803–805. doi: 10.1023/a:1007589422080. [DOI] [PubMed] [Google Scholar]
- 28.Vaz R. S., Guimarães A. T. B., Bonanato L. D., Thomaz-Soccol V. Technical evaluation of serological screening tests for anti-Toxoplasma gondii antibodies to prevent unnecessary transfusion risks. Revista Brasileira de Hematologia e Hemoterapia. 2008;30(4):277–280. doi: 10.1590/S1516-84842008000400009. [DOI] [Google Scholar]
- 29.Makki S. M., Abdel-Tawab A. H. Anti-Toxoplasma gondii antibodies among volunteer blood donors in eastern Saudi Arabia. Journal of the Egyptian Society of Parasitology. 2010;40(2):401–412. [PubMed] [Google Scholar]
- 30.Zghair K. H., AL-Qadhi B. N., Mahmood S. H. The effect of toxoplasmosis on the level of some sex hormones in males blood donors in Baghdad. Journal of Parasitic Diseases. 2015;39(3):393–400. doi: 10.1007/s12639-013-0382-6. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 31.Elsheikha H. M., Azab M. S., Abousamra N. K., Rahbar M. H., Elghannam D. M., Raafat D. Seroprevalence of and risk factors for Toxoplasma gondii antibodies among asymptomatic blood donors in Egypt. Parasitology Research. 2009;104(6):1471–1476. doi: 10.1007/s00436-009-1350-z. [DOI] [PubMed] [Google Scholar]
- 32.Elhence P., Agarwal P., Prasad K. N., Chaudhary R. K. Seroprevalence of Toxoplasma gondii antibodies in North Indian blood donors: implications for transfusion transmissible toxoplasmosis. Transfusion and Apheresis Science. 2010;43(1):37–40. doi: 10.1016/j.transci.2010.05.004. [DOI] [PubMed] [Google Scholar]
- 33.Cook A. J. C., Gilbert R. E., Buffolano W., et al. Sources of toxoplasma infection in pregnant women: European multicentre case-control study. British Medical Journal. 2000;321(7254):142–147. doi: 10.1136/bmj.321.7254.142. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 34.Rostami A., Seyyedtabaei S. J., Aghamolaie S., et al. Seroprevalence and risk factors associated with toxoplasma gondii infection among rural communities in northern Iran. Revista do Instituto de Medicina Tropical de São Paulo. 2016;58 doi: 10.1590/S1678-9946201658070. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 35.Chiang T.-Y., Kuo M.-C., Chen C.-H., et al. Risk factors for acute toxoplasma gondiidiseases in Taiwan: a population-based case-control study. PLoS ONE. 2014;9(3) doi: 10.1371/journal.pone.0090880.e90880 [DOI] [PMC free article] [PubMed] [Google Scholar]
- 36.Mahmoudvand H., Dezaki E. S., Soleimani S., et al. Seroprevalence and risk factors of Toxoplasma gondii infection among healthy blood donors in south-east of Iran. Parasite Immunology. 2015;37(7):362–367. doi: 10.1111/pim.12198. [DOI] [PubMed] [Google Scholar]