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Research Article| Volume 71, ISSUE 6, P405-408, December 2004

No association between the PTGS2/PLA2G4A locus and schizophrenia in a Chinese population

Published:October 11, 2004DOI:https://doi.org/10.1016/j.plefa.2004.09.001

      Abstract

      The present study was undertaken to replicate an association between the PTGS2/PLA2G4A locus and schizophrenia among a Chinese population. We recruited 168 Chinese parent–offspring trios of Han descent, consisting of fathers, mothers and affected offspring with schizophrenia. Of 3 informative SNPs genotyped, no one showed allelic association with schizophrenia; the haplotype analysis also failed to capture a haplotypic association with the illness. Because the frequencies of alleles and genotypes of SNPs analyzed differ in the Chinese population as compared with a British population that initially showed the genetic association between the PTGS2/PLA2G4A locus and schizophrenia, the ethnic background may be a major reason for poor replication of the initial finding.
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      References

        • Stevens J.D.
        The distribution of phospholipid fractions in the red cell membrane of schizophrenics.
        Schizophr. Bull. 1972; 6: 60-61
        • Tolbert L.C.
        • Monti J.A.
        • O’Shields H.
        • Walter-Ryan W.
        • Meadows D.
        • Smythies J.R.
        Defects in transmethylation and membrane lipids in schizophrenia.
        Psychopharmacol. Bull. 1983; 19: 594-599
        • Hitzemann R.
        • Hirschowitz J.
        • Garver D.
        Membrane abnormalities in the psychosis and affective disorders.
        J. Psychiatr. Res. 1984; 18: 319-326
        • Keshavan M.S.
        • Mallinger A.G.
        • Pettegrew J.W.
        • Dippold C.
        Erythrocyte membrane phospholipids in psychotic patients.
        Psychiatl. Res. 1993; 49: 89-95
        • Glen A.I.
        • Glen E.M.
        • Horrobin D.F.
        • et al.
        A red cell membrane abnormality in a subgroup of schizophrenic patients.
        Evidence for two diseases. Schizophr. Res. 1994; 12: 53-61
        • Pettegrew J.W.
        • Keshavan M.S.
        • Panchalingam K.
        • et al.
        Alterations in brain high-energy phosphate and membrane phospholipid metabolism in first-episode, drug-naive schizophrenics. A pilot study of the dorsal prefrontal cortex in vivo phosphorus 31 nuclear magnetic resonance spectroscopy.
        Arch. Gen. Psychiatr. 1991; 48: 563-568
        • Fujimoto T.
        • Nakano T.
        • Takano T.
        • Hokazono Y.
        • Asakura T.
        • Tsuji T.
        Study of chronic schizophrenics using 31P magnetic resonance chemical shift imaging.
        Acta. Psychiatr. Scand. 1992; 86: 455-462
        • Stanley J.A.
        • Williamson P.C.
        • Drost D.J.
        • et al.
        Membrane phospholipid metabolism and schizophrenia, an in vivo 31P-MR spectroscopy study.
        Schizophr. Res. 1994; 13: 209-215
        • Stanley J.A.
        • Williamson P.C.
        • Drost D.J.
        • et al.
        An in vivo study of the prefrontal cortex of schizophrenic patients at different stages of illness via phosphorus magnetic resonance spectroscopy.
        Arch. Gen. Psychiatr. 1995; 52: 399-406
        • Potwarka J.J.
        • Drost D.J.
        • Williamson P.C.
        et al. A 1H-decoupled 31P chemical shift imaging study of medicated schizophrenic patients and healthy controls,.
        Biol. Psychiatr. 1999; 45: 687-693
        • Klemm S.
        • Rzanny R.
        • Riehemann S.
        • et al.
        Cerebral phosphate metabolism in first-degree relatives of patients with schizophrenia.
        Am. J. Psychiatr. 2001; 158: 958-960
        • Hudson C.J.
        • Kennedy J.L.
        • Gotowiec A.
        • et al.
        Genetic vairiant near cytosolic phospholipase A2 associated with schizophrenia.
        Schizophr. Res. 1996; 21: 111-116
        • Peet M.
        • Ramchand C.N.
        • Lee J.
        • et al.
        Association of the Ban I dimorphic site at the human cytosolic phospholipase A2 gene with schizophrenia.
        Psychiatr. Genet. 1998; 8: 191-192
        • Wei J.
        • Lee K.-H.
        • Hemmings G.P.
        Is the cPLA2 gene associated with schizophrenia?.
        Mol. Psychiatr. 1998; 3: 480-482
        • Wei J.
        • Hemmings G.P.
        A study of a genetic association between the PTGS2/PLA2G4A locus and schizophrenia.
        Prostaglandins Leukot. Essent. Fatty Acids. 2004; 70: 413-415
        • Rybakowski J.K.
        • Borkowska A.
        • Czerski P.M.
        • Dmitrzak-Weglarz M.
        • Hauser J.
        The study of cytosolic phospholipase A2 gene polymorphism in schizophrenia using eye movement disturbances as an endophenotypic marker.
        Neuropsychobiology. 2003; 47: 115-119
        • Price S.A.
        • Fox H.
        • StClair D.
        • Shaw D.J.
        Lack of association between schizophrenia and a polymorphism close to the cytosolic phospholipase A2 gene.
        Psychiatr. Genet. 1997; 7: 111-114
        • Chowdari K.V.
        • Brandstaetter B.
        • Semwal P.
        • et al.
        Association studies of cytosolic phospholipase A2 polymorphisms and schizophrenia among two independent family based samples.
        Psychiatr. Genet. 2001; 11: 207-212
        • Frieboes R.M.
        • Moises H.W.
        • Gattaz W.F.
        • et al.
        Lack of association between schizophrenia and the phospholipase-A (2) genes cPLA2 and sPLA2.
        Am. J. Med. Genet. 2001; 105: 246-249
        • Heleniak E.
        • O’Desky I.
        Histamine and prostaglandins in schizophrenia.
        Med. Hypotheses. 1999; 52: 37-42
        • Ward P.E.
        • Sutherland J.
        • Glen E.M.
        • Glen A.I.
        Niacin skin flush in schizophrenia.
        Schizophr. Res. 1998; 29: 269-274
        • Puri B.K.
        • Easton T.
        • Das I.
        • Kidanes L.
        • Richardson A.J.
        The niacin skin flush test in schizophrenia.
        Int. J. Clin. Pract. 2001; 55: 368-370
        • Puri B.K.
        • Hirsch S.R.
        • Easton T.
        • Richardson A.J.
        A volumetric biochemical niacin flush-based index that noninvasively detects fatty acid deficiency in schizophrenia.
        Prog. Neuropsychopharmacol. Biol. Psychiatr. 2002; 26: 49-52
        • Messamore E.
        • Hoffman W.F.
        • Janowsky A.
        The niacin skin flush abnormality in schizophrenia.
        Schizophr. Res. 2003; 62: 251-258
      1. The International SNP Map Working Group. A map of human genome sequence variation containing 1.42 million single nucleotide polymorphisms, Nature 409 (2001) 928–933.