scholarly journals Risk factors for Toxoplasma gondii seropositivity in the Old Order Amish

2020 ◽  
pp. 1-25
Author(s):  
A. O. Markon ◽  
K. A. Ryan ◽  
A. Wadhawan ◽  
M. Pavlovich ◽  
M.W. Groer ◽  
...  
2017 ◽  
Vol 81 (10) ◽  
pp. S84 ◽  
Author(s):  
Teodor T. Postolache ◽  
Kathleen A Ryan ◽  
Xiaoqing Peng ◽  
Mary Pavlovich ◽  
Gursharon Nijjar ◽  
...  

Pteridines ◽  
2017 ◽  
Vol 28 (3-4) ◽  
pp. 185-194 ◽  
Author(s):  
Abhishek Wadhawan ◽  
Aline Dagdag ◽  
Allyson Duffy ◽  
Melanie L. Daue ◽  
Kathy A. Ryan ◽  
...  

AbstractToxoplasma gondii (T. gondii) IgG seropositivity and serointensity have been previously associated with suicidal self-directed violence (SSDV). Although associations with unipolar depression have also been investigated, the results have been inconsistent, possibly as a consequence of high heterogeneity. We have now studied this association in a more homogeneous population, [that is (i.e.) Old Order Amish (OOA)] with previously reported high T. gondii seroprevalence. In 306 OOA with a mean age of 46.1±16.7 years, including 191 (62.4%) women in the Amish Wellness Study, we obtained both T. gondii IgG titers (by enzyme-linked immunosorbent assay [ELISA]), and depression screening questionnaires (Patient Health Questionnaire [PHQ-9] [n=280] and PHQ-2 [n=26]). Associations between T. gondii IgG and dysphoria/hopelessness and anhedonia scores on depression screening questionnaires were analyzed using multivariable linear methods with adjustment for age and sex. Serointensity was associated with both current dysphoria/hopelessness (p=0.045) and current combined anhedonia and dysphoria/hopelessness (p=0.043), while associations with simple anhedonia and past/lifelong (rather than current) phenotypes were not significant. These results indicate the need for larger longitudinal studies to corroborate the association between dysphoria/hopelessness and T. gondii IgG-titers. Current hopelessness is a known risk factor for SSDV which responds particularly well to cognitive behavioral therapy, and may be a focused treatment target for T. gondii-positive individuals at high-risk for SSDV.


2017 ◽  
Vol 81 (10) ◽  
pp. S121
Author(s):  
Abhishek Wadhawan ◽  
Aline Dagdag ◽  
Melanie Daue ◽  
Allyson Duffy ◽  
Xiaoqing Peng ◽  
...  

2017 ◽  
Vol 81 (10) ◽  
pp. S369-S370 ◽  
Author(s):  
Allyson Duffy ◽  
Jeffrey O׳Connell ◽  
Mary Pavlovich ◽  
Maureen Groer ◽  
Xiaoqing Peng ◽  
...  

2018 ◽  
Vol 83 (9) ◽  
pp. S299-S300 ◽  
Author(s):  
Abhishek Wadhawan ◽  
Melanie L. Daue ◽  
Lisa A. Brenner ◽  
Christopher A. Lowry ◽  
Aline Dagdag ◽  
...  

2018 ◽  
Vol 83 (9) ◽  
pp. S199
Author(s):  
Gurkaron Nijjar ◽  
Dolores Hill ◽  
Melanie L. Daue ◽  
Abhishek Wadhawan ◽  
Aline Dagdag ◽  
...  

SLEEP ◽  
2019 ◽  
Vol 42 (Supplement_1) ◽  
pp. A25-A26
Author(s):  
Teodor T Postolache ◽  
Cristine Corona ◽  
Zhang Man ◽  
Melanie Daue ◽  
Abhishek Wadhawan ◽  
...  

Author(s):  
Allyson R. Duffy ◽  
Jeffrey R. O’Connell ◽  
Mary Pavlovich ◽  
Kathleen A. Ryan ◽  
Christopher A. Lowry ◽  
...  

Toxoplasma gondii (T. gondii) is an intracellular parasite infecting one third of the world’s population. Latent T. gondii infection has been associated with mental illness, including schizophrenia and suicidal behavior. T. gondii IgG antibody titers were measured via ELISA. The heritability of T. gondii IgG was estimated using a mixed model that included fixed effects for age and sex and random kinship effect. Of 2017 Old Order Amish participants, 1098 had positive titers (54.4%). The heritability for T. gondii serointensity was estimated to be 0.22 (p = 1.7 × 10−8 and for seropositivity, it was estimated to be 0.28 (p = 1.9 × 10−5). Shared household environmental effects (i.e., household effects) were also determined. Household effects, modeled as a random variable, were assessed as the phenotypic covariance between any two individuals who had the same current address (i.e., contemporaneous household), and nuclear household (i.e., the phenotypic covariance between parents and children only, not other siblings or spouses). Household effects did not account for a significant proportion of variance in either T. gondii serointensity or T. gondii seropositivity. Our results suggest a significant familial aggregation of T. gondii serointensity and seropositivity with significant heritability. The shared household does not contribute significantly to family aggregation with T. gondii, suggesting that there are possible unmeasured non-household shared and non-shared environmental factors that may play a significant role. Furthermore, the small but significant heritability effects justify the exploration of genetic vulnerability to T. gondii exposure, infection, virulence, and neurotropism.


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