Linkage of familial schizophrenia to chromosome 13q32
Linkage of familial schizophrenia to chromosome 13q32
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DOI：
10.1086/302579
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发表时间：
1999-10-01
影响因子：
9.8
通讯作者：
Bassett, AS
中科院分区：
文献类型：
--
作者：
Brzustowicz, LM;Honer, WG;Bassett, AS
Over the past 4 years, a number of investigators have reported findings suggestive of linkage to schizophrenia, with markers on chromosomes 13q32 and 8p21, with one recent study by Blouin et al. reporting significant linkage to these regions. As part of an ongoing genome scan, we evaluated microsatellite markers spanning chromosomes 8 and 13, for linkage to schizophrenia, in 21 extended Canadian families. Families were analyzed under autosomal dominant and recessive models, with broad and narrow definitions of schizophrenia. All models produced positive LOD scores with markers on 13q, with higher scores under the recessive models. The maximum three-point LOD scores were obtained under the recessive-broad model: 3.92 at recombination fraction (theta) .1 with D13S793, under homogeneity, and 4.42 with alpha=.65 and theta=0 with D13S793, under heterogeneity. Positive LOD scores were also obtained, under all models, for markers on 8p. Although a maximum two-point LOD score of 3.49 was obtained under the dominant-narrow model with D8S136 at theta = 0.1, multipoint analysis with closely flanking markers reduced the maximum LOD score in this region to 2.13. These results provide independent significant evidence of linkage of a schizophrenia-susceptibility locus to markers on 13q32 and support the presence of a second susceptibility locus on 8p21.
