scholarly journals Role of interferon-γ gene polymorphisms in susceptibility to IgA nephropathy: a family-based association study

2006 ◽  
Vol 14 (4) ◽  
pp. 488-496 ◽  
Author(s):  
Francesco Paolo Schena ◽  
◽  
Giuseppina Cerullo ◽  
Diletta Domenica Torres ◽  
Francesco Scolari ◽  
...  
Author(s):  
Małgorzata Szkup ◽  
Aleksander Owczarek ◽  
Anna Lubkowska ◽  
Elżbieta Chełmecka ◽  
Karolina Skonieczna-Żydecka ◽  
...  

Metabolic syndrome (MetS) is a cluster of conditions, increasing the risk of developing diseases that can lead to premature death. Interferon γ-inducible (the production of which is dependent on the IFNγ rs2430561 polymorphism) tryptophan-kynurenine inflammatory cascade helps to understand the increased association between inflammatory process and MetS, which is why we seek the relationship between the IFNγ gene polymorphisms and serum levels of markers of interferon-gamma (IFNγ)-inducible inflammatory cascade. The study sample consisted of 416 women, including 118 (28.4%) with MetS. The research procedure involved interview, anthropometric measurements, and blood collection. Kynurenine levels were significantly higher in the group of women with MetS. In the group with MetS, the A/T genotype of the IFNγ gene was accompanied by higher kynurenine levels. A direct relationship between the IFNγ gene polymorphisms and the rest of the markers of IFNγ-inducible inflammatory cascade was not confirmed with regard to MetS in 45 to 60-year-old women. A disparity in the kynurenine level, as well as the relationship between the presence of the A/T genotype of the IFNγ gene and a higher level of kynurenine in the group of women with MetS, may indicate an association between inflammation, metabolic disorders and tryptophan-kynurenine inflammatory cascade.


PLoS ONE ◽  
2017 ◽  
Vol 12 (8) ◽  
pp. e0180488 ◽  
Author(s):  
Natalie P. Archer ◽  
Virginia Perez-Andreu ◽  
Ulrik Stoltze ◽  
Michael E. Scheurer ◽  
Anna V. Wilkinson ◽  
...  

Author(s):  
Tomasz Iwanicki ◽  
Anna Balcerzyk ◽  
Beata Kazek ◽  
Ewa Emich-Widera ◽  
Wirginia Likus ◽  
...  

AbstractThe aim of the study was to perform family-based association analysis of PRKCB1, CBLN1 and KCNMB4 gene polymorphisms and autism disorder. We comprised 206 Caucasian children with autistic spectrum disorder (ASD) and their biological parents. In transmission/disequilibrium test we observed that T-allele of the rs198198 polymorphism of the PRKCB1 gene was more often transmitted to affected children in the male subgroup (p = 0.010). Additionally, the T carrier state was significantly associated with hypotonia (p = 0.048). In the female subgroup, the T-allele carriers more often showed more mobile/vital behavior (p = 0.046). In conclusion, our study showed that the rs198198 of the PRKCB1 gene may be associated with ASD in men and with some features characteristic for the disorder.


2012 ◽  
Vol 27 (4) ◽  
pp. 345-351 ◽  
Author(s):  
Yuko Hirata ◽  
Clement C. Zai ◽  
Renan P. Souza ◽  
Jeffrey A. Lieberman ◽  
Herbert Y Meltzer ◽  
...  

2016 ◽  
Vol 68 ◽  
pp. 9-12 ◽  
Author(s):  
Dobrina Karayasheva ◽  
Maria Glushkova ◽  
Ekaterina Boteva ◽  
Vanyo Mitev ◽  
Tanya Kadiyska

Gene Reports ◽  
2018 ◽  
Vol 10 ◽  
pp. 116-122
Author(s):  
M. Vidyadhari ◽  
M. Sujatha ◽  
P. Krupa ◽  
Pratibha Nallari ◽  
A. Venkateshwari

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