Expanding the range of ZNF804A variants conferring risk of psychosis

S. Steinberg, O. Mors, A. D. Børglum, O. Gustafsson, T. Werge, P. B. Mortensen, O. A. Andreassen, E. Sigurdsson, T. E. Thorgeirsson, Y. Böttcher, P. Olason, R. A. Ophoff, S. Cichon, I. H. Gudjonsdottir, O. P.H. Pietiläinen, M. Nyegaard, A. Tuulio-Henriksson, A. Ingason, T. Hansen, L. AthanasiuJ. Suvisaari, J. Lonnqvist, T. Paunio, A. Hartmann, G. Jürgens, M. Nordentoft, D. Hougaard, B. Norgaard-Pedersen, R. Breuer, H. J. Möller, I. Giegling, B. Glenthøj, H. B. Rasmussen, M. Mattheisen, I. Bitter, J. M. Réthelyi, T. Sigmundsson, R. Fossdal, U. Thorsteinsdottir, M. Ruggeri, S. Tosato, E. Strengman, L. A. Kiemeney, I. Melle, S. Djurovic, L. Abramova, V. Kaleda, M. Walshe, E. Bramon, E. Vassos, T. Li, G. Fraser, N. Walker, T. Toulopoulou, J. Yoon, N. B. Freimer, R. M. Cantor, R. Murray, A. Kong, V. Golimbet, E. G. Jönsson, L. Terenius, I. Agartz, H. Petursson, M. M. Nöthen, M. Rietschel, L. Peltonen, D. Rujescu, D. A. Collier, H. Stefansson, D. St Clair, K. Stefansson*

*Corresponding author af dette arbejde

    Publikation: Bidrag til tidsskriftArtikelForskningpeer review

    Abstract

    A trio of genome-wide association studies recently reported sequence variants at three loci to be significantly associated with schizophrenia. No sequence polymorphism had been unequivocally (P5 × 10 8) associated with schizophrenia earlier. However, one variant, rs1344706T, had come very close. This polymorphism, located in an intron of ZNF804A, was reported to associate with schizophrenia with a P-value of 1.6 × 10 7, and with psychosis (schizophrenia plus bipolar disorder) with a P-value of 1.0 × 10 8. In this study, using 5164 schizophrenia cases and 20 709 controls, we replicated the association with schizophrenia (odds ratio OR1.08, P0.0029) and, by adding bipolar disorder patients, we also confirmed the association with psychosis (added N609, OR1.09, P0.00065). Furthermore, as it has been proposed that variants such as rs1344706Tcommon and with low relative riskmay also serve to identify regions harboring less common, higher-risk susceptibility alleles, we searched ZNF804A for large copy number variants (CNVs) in 4235 psychosis patients, 1173 patients with other psychiatric disorders and 39 481 controls. We identified two CNVs including at least part of ZNF804A in psychosis patients and no ZNF804A CNVs in controls (P0.013 for association with psychosis). In addition, we found a ZNF804A CNV in an anxiety patient (P0.0016 for association with the larger set of psychiatric disorders).

    OriginalsprogEngelsk
    Sider (fra-til)59-66
    Antal sider8
    TidsskriftMolecular Psychiatry
    Vol/bind16
    Udgave nummer1
    DOI
    StatusUdgivet - 1 jan. 2011

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