Please use this identifier to cite or link to this item: https://repositorio.unifesp.br/handle/11600/56156
Title: Genome-wide investigation of schizophrenia associated plasma Ndel1 enzyme activity
Authors: Gadelha, Ary [UNIFESP]
Coleman, Jonathan
Breen, Gerome
Mazzoti, Diego Robles [UNIFESP]
Yonamine, Camila Miyagui [UNIFESP]
Pellegrino, Renata
Ota, Vanessa Kiyomi [UNIFESP]
Belangero, Sintia Iole [UNIFESP]
Glessner, Joseph
Sleiman, Patrick
Hakonarson, Hakon
Hayashi, Mirian Akemi Furuie [UNIFESP]
Bressan, Rodrigo Affonseca [UNIFESP]
Keywords: Ndel1
Schizophrenia
GWAS
Biomarker
Enzyme activity
Issue Date: 2016
Publisher: Elsevier Science Bv
Citation: Schizophrenia Research. Amsterdam, v. 172, p. 60-67, 2016.
Abstract: Ndel1 is a DISC1-interacting oligopeptidase that cleaves in vitro neuropeptides as neurotensin and bradykinin, and which has been associated with both neuronal migration and neurite outgrowth. We previously reported that plasma Ndel1 enzyme activity is lower in patients with schizophrenia (SCZ) compared to healthy controls (HCs). To our knowledge, no previous study has investigated the genetic factors associated with the plasma Ndel1 enzyme activity. In the current analyses, samples from 83 SCZ patients and 92 control subjects that were assayed for plasma Ndel1 enzyme activity were genotyped on Illumina Omni Express arrays. A genetic relationship matrix using genome-wide information was then used for ancestry correction, and association statistics were calculated genome-wide. Ndel1 enzyme activity was significantly lower in patients with SCZ (t=4.9
p < 0.001) and was found to be associated with CAMK1D, MAGI2, CCDC25, and GABGR3, at a level of suggestive significance (p < 10(-6)), independent of the clinical status. Then, we performed a model to investigate the observed differences for case/control measures. 2 SNPs at region 1p22.2 reached the p < 10(-7) level. ZFPM2 and MAD1L1 were the only two genes with more than one hit at 10-6 order of p value. Therefore, Ndel1 enzyme activity is a complex trait influenced by many different genetic variants that may contribute to SCZ physiopathology. (C) 2016 Elsevier B.V. All rights reserved.
URI: https://repositorio.unifesp.br/handle/11600/56156
ISSN: 0920-9964
Other Identifiers: http://dx.doi.org/10.1016/j.schres.2016.01.043
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