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Toxoplasma gondii & Human Phenotype

Compendium of Known Effects and Ongoing Research

aging

Neurodevelopmental versus neurodegenerative model of schizophrenia and bipolar disorder: comparison with physiological brain development and aging

May 11, 2017
Buoli, M., Serati, M., Caldiroli, A., Cremaschi, L., Altamura, A.C.
Psychiatria Danubina 2017; 29: 24-27
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Available data support a contribution of both neurodevelopmental and neurodegenerative factors in the etiology of schizophrenia (SCH) and bipolar disorder (BD). Of note, one of the most important issue of the current psychiatric research is to identify the specific factors that contribute to impaired brain development and neurodegeneration in SCH and BD, and especially how these factors alter normal brain development and physiological aging process. Our hypothesis is that only specific damages, taking place in precise brain development stages, are associated with future SCH / BD onset and that neurodegeneration consists of an acceleration of brain aging after SCH / BD onset. In support of our hypothesis, the results of the present narrative mini-review shows as neurodevelopmental damages generally contribute to neuropsychiatric syndromes (e.g. hypothyroidism or treponema pallidum), but only some of them are specifically associated with adult SCH and BD (e.g. toxoplasma or substance abuse), particularly if they happen in specific stages of brain development. On the other hand, cognitive impairment and brain changes, associated with long duration of SCH / BD, look like what happens during aging: memory, executive domains and prefrontal cortex are implicated both in aging and in SCH / BD progression. Future research will explore possible validity of this etiological model for SCH and BD.

Tagged: aging, bipolar disorder (BD), neurodegeneration, neurodevelopment, schizophrenia (SCH)

Mental health

Temporal cognitive decline associated with exposure to infectious agents in a population-based, aging cohort

October 29, 2016
Nimgaonkar, V. L., Yolken, R. H., Wang, T. X., Chang, C. C. H., McClain, L., McDade, E., Snitz, B. E., Ganguli, M
Alzheimer Disease & Associated Disorders 2016; 30: 216-222
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Background:Numerous cross-sectional studies have related exposure to neurotropic infectious agents with cognitive dysfunction in older adults, however, the temporal sequence is uncertain.Methods:In a representative, well-characterized, population-based aging cohort, we determined whether the temporal trajectories of multiple cognitive domains are associated with exposure to cytomegalovirus (CMV), Herpes Simplex virus, type 1 (HSV-1), Herpes Simplex virus, type 2 (HSV-2), or Toxoplasma gondii (TOX). Complex attention, executive functions, memory, language, and visuospatial function were assessed annually for 5 years among consenting individuals. Study entry IgG antibody titers indexing exposure to each infectious agent were examined in relation to slopes of subsequent temporal cognitive decline using multiple linear regressions adjusted for potential confounders.Results:The IgG levels for HSV-2 were significantly associated with baseline cognitive domain scores (N=1022 participants). Further, the IgG levels for HSV-2, TOX, and CMV, but not HSV-1 were significantly associated with greater temporal cognitive decline that varied by type of infection.Conclusions:Exposure to CMV, HSV-2, or TOX is associated with cognitive deterioration in older individuals, independent of general age-related variables. An increased understanding of the role of infectious agents in cognitive decline may lead to new methods for its prevention and treatment.

Tagged: aging, antibodies, bipolar disorder, CMV, cognition, community, cytomegalovirus, disease, Epidemiology, herpes virus, impairment, persistent infection, Schizophrenia, simplex-virus type-1, Toxoplasma gondii, viral-infections

Cognitive functions

Temporal cognitive decline associated with exposure to infectious agents in a population-based, aging cohort

May 24, 2016
Nimgaonkar, V.L., Yolken, R.H., Wang, T.X., Chang, C-C.H., McClain, L., McDade, E., Snitz, B.E., Ganguli, M.
Alzheimer Dis. Assoc. Dis. 2016; 30: 216-222
Click for abstract
Background:Numerous cross-sectional studies have related exposure to neurotropic infectious agents with cognitive dysfunction in older adults, however, the temporal sequence is uncertain.Methods:In a representative, well-characterized, population-based aging cohort, we determined whether the temporal trajectories of multiple cognitive domains are associated with exposure to cytomegalovirus (CMV), Herpes Simplex virus, type 1 (HSV-1), Herpes Simplex virus, type 2 (HSV-2), or Toxoplasma gondii (TOX). Complex attention, executive functions, memory, language, and visuospatial function were assessed annually for 5 years among consenting individuals. Study entry IgG antibody titers indexing exposure to each infectious agent were examined in relation to slopes of subsequent temporal cognitive decline using multiple linear regressions adjusted for potential confounders.Results:The IgG levels for HSV-2 were significantly associated with baseline cognitive domain scores (N=1022 participants). Further, the IgG levels for HSV-2, TOX, and CMV, but not HSV-1 were significantly associated with greater temporal cognitive decline that varied by type of infection.Conclusions:Exposure to CMV, HSV-2, or TOX is associated with cognitive deterioration in older individuals, independent of general age-related variables. An increased understanding of the role of infectious agents in cognitive decline may lead to new methods for its prevention and treatment.

Tagged: aging, CMV, cognition, community, Epidemiology, herpes virus, Toxoplasma gondii

Cognitive functions

Immediate rather than delayed memory impairment in older adults with latent toxoplasmosis

October 6, 2015
Mendy, A., Vieira, E. R., Albatineh, A. N., Gasana, J.
Brain Behavior and Immunity 2015; 45: 36-40
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The neurotropic parasite Toxoplasma gondii infects one third of the world population, but its effect on memory remains ambiguous. To examine a potential relationship of the infection with immediate and delayed memory, a population-based study was conducted in 4485 participants of the Third National Health and Nutrition Examination Survey aged 60 years and older. Serum anti-Toxoplasma IgG antibodies were measured by enzyme immune assay and verbal memory was assessed using the Mini-Mental State Examination and the East Boston Memory Test. The prevalence of latent toxoplasmosis was 41%; in one way analysis of variance, anti-Toxoplasma IgG antibody levels significantly differed across tertiles for immediate (P = 0.006) but not delayed memory scores (P = 0.22). In multinomial logistic regression adjusting for covariates, Toxoplasma seropositivity was associated with lower immediate memory performance (OR: 0.65, 95% CI: 0.44, 0.97 for medium tertile and OR: 0.61, 95% CI: 0.37, 0.98 for highest tertile in reference to the lowest tertile), especially in non-Hispanic Whites (OR: 0.56, 95% CI: 0.36, 0.88 for medium tertile and OR: 0.51, 95% CI: 0.30, 0.87 for highest tertile in reference to the lowest tertile). However, no relationship with delayed memory was observed. In conclusion, latent toxoplasmosis is widespread in older adults and may primarily affect immediate rather than delayed memory, particularly in White Americans.

Tagged: aging, cognition, gondii infection, memory, mice, older age, rhd molecule, risk, short-term-memory, Toxoplasma gondii, toxoplasmosis

Cognitive functions

Toxoplasma gondii impairs memory in infected seniors

October 10, 2014
Gajewski, P. D., Falkenstein, M., Hengstler, J. G., Golka, K.
Brain Behavior and Immunity 2014; 36: 193-199
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lmost 30% of humans present a Toxoplasma gondii positive antibody status and its prevalence increases with age. The central nervous system is the main target. However, little is known about the influence of asymptomatic i.e. latent Toxoplasmosis on cognitive functions in humans. To investigate neurocognitive dysfunctions in asymptomatic older adults with T. gondii positive antibody status a double-blinded neuropsychological study was conducted. The participants were classified from a population-based sample (N = 131) of healthy participants with an age of 65 years and older into two groups with 42 individuals each: Toxoplasmosis positive (T-pos; IgG > 50 IU/ml) and Toxoplasmosis negative (T-neg; IgG = 0 IU/ml). The outcome measures were a computer-based working-memory test (2-back) and several standardized psychometric tests of memory and executive cognitive functions. T-pos seniors showed an impairment of different aspects of memory. The rate of correctly detected target symbols in a 2-back task was decreased by nearly 9% (P = 0.020), corresponding to a performance reduction of about 35% in working memory relative to the T-neg group. Moreover, T-pos seniors had a lower performance in a verbal memory test, both regarding immediate recall (10% reduction; P = 0.022), delayed recognition (6%; P = 0.037) and recall from long-term memory assessed by the word fluency tests (12%; P = 0.029). In contrast, executive functions were not affected. The effects remained mostly unchanged after controlling for medication. The impairment of memory functions in T-pos seniors was accompanied by a decreased self-reported quality of life. Because of the high prevalence of asymptomatic Toxoplasmosis and an increasing population of older adults this finding is of high relevance for public health

Tagged: age, aging, behavior, challenges, cognition, Dopamine, humans, load, memory, performance, rats, task, Toxoplasma gondii, vaccines, working memory

Cognitive functions

The influence of RhD phenotype on toxoplasmosis- and age-associated changes in personality profile of blood donors

September 26, 2010
Flegr, J., Novotná, M., Fialová, A., Kolbeková, P., Gasová, Z.
Folia Parasitologica 2010; 57: 57: 143-150
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Toxoplasma gondii , a parasite infecting 20–60% of humans in various countries, influences the behaviour of infected animal and human hosts. Infected human subjects have changes in several of Cattell’s and Cloninger’s personality factors. Recently, three independent studies have shown that Rh-positive subjects are protected against the T. gondii -induced changes of reaction times and increased risk of traffic accidents. Here we searched for evidence of similar effects of RhD phenotype on toxoplasmosis- or aging-associated changes in the personality profile of about 302 blood donors. We found that Rh-positive and Rh-negative subjects responded differently to toxoplasmosis. In addition to the already known effects of toxoplasmosis on novelty seeking, self transcend - ence, superego strength and protension, we also found effects of RhD phenotype on ego strength, protension, and praxernia, as well as opposite effects of toxoplasmosis on ego strength, praxernia, ergic tension and cooperativeness in Rh-positive and Rh-negative subjects. Moreover, our results indicate that RhD phenotype might influence not only the effect of toxoplasmosis but also the effect of aging on specific personality traits.

Tagged: aging, blood group, Cattell 16PF, Cloninger TCI, manipulation., Parasite, personality, Rh factor, Rhesus factor, senescence

Personality

Topics

  • Behavior 105
  • Cognitive functions 64
  • Mental health 439
  • Morphology 6
  • Motor functions 10
  • Personality 36
  • Physical health 134
  • Reproduction 36
  • Reviews 40
  • Sensory functions 3
  • Uncategorized 2

Archives

Recent articles

  • Mortality Patterns of Toxoplasmosis and Its Comorbidities in Tanzania: A 10-Year Retrospective Hospital-Based Survey February 6, 2020
  • The role of latent toxoplasmosis in the aetiopathogenesis of schizophrenia–the risk factor or an indication of a contact with cat? February 6, 2020
  • The Association between Toxoplasma gondii Infection and Risk of Parkinson’s Disease: A Systematic Review and Meta-Analysis February 6, 2020

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