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Year : 2021  |  Volume : 34  |  Issue : 2  |  Page : 757-758

Toxoplasma gondii, Taenia solium, and adult-onset epilepsy

Department of Medicine, Federal University of Santa Maria, Santa Maria, Rio Grande do Sul, Brazil

Date of Submission03-Apr-2020
Date of Decision05-May-2020
Date of Acceptance16-May-2020
Date of Web Publication30-Jun-2021

Correspondence Address:
Jamir P Rissardo

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Source of Support: None, Conflict of Interest: None

DOI: 10.4103/mmj.mmj_117_20

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How to cite this article:
Rissardo JP, Caprara AL. Toxoplasma gondii, Taenia solium, and adult-onset epilepsy. Menoufia Med J 2021;34:757-8

How to cite this URL:
Rissardo JP, Caprara AL. Toxoplasma gondii, Taenia solium, and adult-onset epilepsy. Menoufia Med J [serial online] 2021 [cited 2023 Dec 4];34:757-8. Available from: http://www.mmj.eg.net/text.asp?2021/34/2/757/319673

We read the article entitled 'Probable relationship between Toxoplasma gondii and children with cryptogenic epilepsy' on the esteemed Menoufia Medical Journal with great interest. Khatab et al. [1] studied cryptogenic epilepsy in children, who were investigated for the seropositivity rate for antitoxoplasma immunoglobulin G antibodies. They found that the percentage of patients with chronic T. gondii infection is higher in cryptogenic epileptic patients than in individuals with known-cause epilepsy.

Herein, we would like to discuss more the relation between helminths infection and epilepsy, which is a particularly important topic in developing countries.

Some drawbacks of the study of Khatab and colleagues are that a small and selected population was studied, their percentage of cryptogenic epilepsy was higher than other general studies, and probably the association of antitoxoplasma immunoglobulin G antibodies could not directly explain the origin of epilepsy [2]. The presence of these antibodies positivity only suggests an immune memory to an infection. In this way, we believe that only larger studies assessing the epilepsy features since its beginning will probably elucidate this question [1].

However, their study contributed to the literature reinforcing the association of toxoplasmosis and cryptogenic epilepsy. Moreover, Khatab and colleagues discussed that maybe cryptogenic epileptic individuals are susceptible to the parasitic infection, for reasons unrelated to epilepsy, or owing to intrinsic immunologic differences that predispose them to epilepsy. Therefore, an explanation could be a misleading immunological response that would lead to the susceptibility of infection and epilepsy. A supporting finding of this theory is the presence of seizures caused by an abnormal inflammatory response in some infections, in which before and after the event, a marked elevation of these biomarkers was observed [3].

Another interesting point that the authors could have discussed is how much difficult was it to control the epilepsy of these patients? How many drugs were used? Were there any clinical predictors associated with drug-resistant epilepsy? Caprara et al. [4] assessed the clinical predictors associated with drug-resistant adult-onset epilepsy in Brazil during a long-term follow-up, in which more than 300 patients were followed for almost 10 years. Structural epilepsy etiology was associated with an increased chance of relapsing of 1.74 odds ratio (OR) [confidence interval (CI): 1.66–1.89], but the infectious etiology (neurocysticercosis) was positively associated with non-drug resistant (OR: 1.012, CI: 1.001–1.215). Thus, it is possible the association of neurocysticercosis as a protective factor in the development of drug-resistant epilepsy. We believe that this association should also be mentioned or analyzed by Khatab and colleagues.

A recent meta-analysis evaluating the association between T. gondii infection and risk of epilepsy in almost 800 individuals showed that cryptogenic epilepsy (OR: 2.65, CI: 1.91–3.68) and active convulsive epilepsy (OR: 1.37, CI: 1.09–1.72) were significantly associated with toxoplasmosis [5]. However, a seroepidemiological study with an Iranian population, which assessed epilepsy without subgroup analysis, revealed that the rate of T. gondii infection in epileptic patients was not higher than non-epileptic patients and healthy people in the Iranian population [6].

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  References Top

Khatab AA, Soliman MA, Abd El-Naby SA, El-Dabaa SS. Probable relationship between Toxoplasma gondii and children with cryptogenic epilepsy. Menoufia Med J 2020; 33:157.  Back to cited text no. 1
Hedman K, Lappalainen M, Seppäiä I, Mäkelä O. Recent primary toxoplasma infection indicated by a low avidity of specific IgG. J Infect Dis 1989; 159:736-740.  Back to cited text no. 2
Rissardo JP, Caprara AL, Silveira JO. Generalized convulsive status epilepticus secondary to jarisch-herxheimer reaction in neurosyphilis: a case report and literature review. Neurologist 2019; 24:29-32.  Back to cited text no. 3
Caprara ALF, Rissardo JP, Leite MT, Silveira JO, Jauris PG, Arend J, et al. Course and prognosis of adult-onset epilepsy in Brazil: a cohort study. Epilepsy Behav 2020; 105:106969.  Back to cited text no. 4
Sadeghi M, Riahi SM, Mohammadi M, Saber V, Aghamolaie S, Moghaddam SA, et al. An updated meta-analysis of the association between Toxoplasma gondii infection and risk of epilepsy. Trans R Soc Trop Med Hyg 2019; 113:453-462.  Back to cited text no. 5
Babaie J, Sayyah M, Gharagozli K, Mostafavi E, Golkar M. Seroepidemiological study of Toxoplasma gondii infection in a population of Iranian epileptic patients. EXCLI J 2017; 16:256.  Back to cited text no. 6

This article has been cited by
1 Neuropsychiatric manifestations associated with neurocysticercosis
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