| Literature DB >> 28627421 |
Franca R Guerini1, Elisabetta Bolognesi2, Matteo Chiappedi3, Alessandro Ghezzo4, Salvatorica Manca5, Michela Zanette2, Stefano Sotgiu6, Maria Martina Mensi3, Milena Zanzottera2, Cristina Agliardi2, Andrea S Costa2, Umberto Balottin7, Mario Clerici8.
Abstract
Activating KIR-HLA-C ligand complexes and HLA-G∗14bp insertion/deletion (+/-) polymorphism were associated to Autism Spectrum Disorders (ASD) and were suggested to correlate with inflammation during fetal development. We evaluated whether HLA-G∗14bp(+/-) and KIR-HLA-C complexes are associated with cognitive and behavioral scores and EEG profile in 119 ASD children (58 from Sardinia, 61 from Peninsular Italy). KIR2DS1-C2; KIR2DS2-C1; KIR2DL1-C2; KIR2DL2-C1; KIR2DL3-C1 and HLA-G∗14bp(+/-) were molecularly genotyped by Single Specific Primer PCR and gel electrophoresis. Univariate linear model analysis adjusted for age, gender and provenience showed statistically higher scores of Childhood Autism Rating Scale (CARS) and Autistic Core Behavior in KIR2DS1-C2+/HLA-G∗14bp+ASD children (43.7±1.5, p=0.03; 3.3±0.1, p=0.03, respectively). These results suggested a synergistic polygenic association of KIR2DS1-HLAC2+/HLA-G∗14bp+ pattern with behavioral impairment in ASD children.Entities:
Keywords: Autism Spectrum Disorders; HLA-C; HLA-G14; KIR 2DS1; behavior; in utero immunology
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Year: 2017 PMID: 28627421 DOI: 10.1016/j.neuroscience.2017.06.012
Source DB: PubMed Journal: Neuroscience ISSN: 0306-4522 Impact factor: 3.590