DeLisi, Lynn E., Shaw, Sarah H., Crow, Timothy J., Shields, Gail, Smith, Angela B., Larach, Veronica W., Wellman, Nigel, Loftus, Josephine, Nanthakumar, Betsy, Razi, Kamran, Stewart, John, Comazzi, Margherita, Vita, Antonio, Heffner, Thomas and Sherrington, Robin (2002) A genome-wide search for linkage to chromosomal regions in 382 sibling-pairs diagnosed with schizophrenia or schizoaffective disorder. American Journal of Psychiatry, 159 (5). pp. 803-812. ISSN 1535-7228

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Abstract

OBJECTIVE:
Some genome-wide scans and association studies for schizophrenia susceptibility genes have yielded significant positive findings, but there is disagreement between studies on their locations, and no mutation has yet been found in any gene. Since schizophrenia is a complex disorder, a study with sufficient power to detect a locus with a small or moderate gene effect is necessary.

METHOD:
In a genome-wide scan of 382 sibling pairs with a diagnosis of schizophrenia or schizoaffective disorder, 396 highly polymorphic markers spaced approximately 10 centimorgans apart throughout the genome were genotyped in all individuals. Multipoint nonparametric linkage analysis was performed to evaluate regions of the genome demonstrating increased allele sharing, as measured by a lod score.

RESULTS:
Two regions with multipoint maximum lod scores suggesting linkage were found. The highest lod scores occurred on chromosome 10p15-p13 (peak lod score of 3.60 at marker D10S189) and the centromeric region of chromosome 2 (peak lod score of 2.99 at marker D2S139). In addition, a maximum lod score of 2.00 was observed with marker D22S283 on chromosome 22q12, which showed evidence of an imprinting effect, whereby an excess sharing of maternal, but not paternal, alleles was present. No evidence of linkage was obtained at several locations identified in previous studies, including chromosomes 1q, 4p, 5p-q, 6p, 8p, 13q, 15p, and 18p.

CONCLUSIONS:
The findings of this large genome-wide scan emphasize the weakness and fragility of linkage reports on schizophrenia. No linkage appears to be consistently replicable across large studies. Thus, it has to be questioned whether the genetic contribution to this disorder is detectable by these strategies and the possibility raised that it may be epigenetic, i.e., related to gene expression rather than sequence variation. Nevertheless, the positive findings on chromosome 2, 10, and 22 should be pursued further.

Item Type:	Article
Identifier:	10.1176/appi.ajp.159.5.803
Keywords:	Schizophrenia; Schizoaffective disorder; Schizophrenia susceptibility genes; Association studies
Subjects:	Medicine and health > Mental health
Depositing User:	Rod Pow
Date Deposited:	02 Jul 2012 10:28
Last Modified:	06 Feb 2024 15:39
URI:	https://repository.uwl.ac.uk/id/eprint/137

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