Genetic Relationships Between Schizophrenia, Bipolar Disorder, and Schizoaffective Disorder

被引:199
作者
Cardno, Alastair G. [1 ]
Owen, Michael J. [2 ,3 ]
机构
[1] Univ Leeds, Acad Unit Psychiat & Behav Sci, Leeds LS2 9LJ, W Yorkshire, England
[2] Cardiff Univ, MRC Ctr Neuropsychiat Genet & Genom, Cardiff CF10 3AX, S Glam, Wales
[3] Cardiff Univ, Neurosci & Mental Hlth Res Inst, Cardiff CF10 3AX, S Glam, Wales
基金
英国医学研究理事会;
关键词
family studies; twin; adoption; GWAS; copy number variants; GENOME-WIDE ASSOCIATION; RARE CHROMOSOMAL DELETIONS; DSM-III; PSYCHIATRIC-DISORDERS; ROSCOMMON FAMILY; COMMON VARIANTS; INCREASE RISK; TWIN; PSYCHOSES; ETIOLOGY;
D O I
10.1093/schbul/sbu016
中图分类号
R749 [精神病学];
学科分类号
100205 ;
摘要
There is substantial evidence for partial overlap of genetic influences on schizophrenia and bipolar disorder, with family, twin, and adoption studies showing a genetic correlation between the disorders of around 0.6. Results of genome-wide association studies are consistent with commonly occurring genetic risk variants, contributing to both the shared and nonshared aspects, while studies of large, rare chromosomal structural variants, particularly copy number variants, show a stronger influence on schizophrenia than bipolar disorder to date. Schizoaffective disorder has been less investigated but shows substantial familial overlap with both schizophrenia and bipolar disorder. A twin analysis is consistent with genetic influences on schizoaffective episodes being entirely shared with genetic influences on schizophrenic and manic episodes, while association studies suggest the possibility of some relatively specific genetic influences on broadly defined schizoaffective disorder, bipolar subtype. Further insights into genetic relationships between these disorders are expected as studies continue to increase in sample size and in technical and analytical sophistication, information on phenotypes beyond clinical diagnoses are increasingly incorporated, and approaches such as next-generation sequencing identify additional types of genetic risk variant.
引用
收藏
页码:504 / 515
页数:12
相关论文
共 143 条
[1]   Boosting the Power of Schizophrenia Genetics by Leveraging New Statistical Tools [J].
Andreassen, Ole A. ;
Thompson, Wesley K. ;
Dale, Anders M. .
SCHIZOPHRENIA BULLETIN, 2014, 40 (01) :13-17
[2]   Improved Detection of Common Variants Associated with Schizophrenia and Bipolar Disorder Using Pleiotropy-Informed Conditional False Discovery Rate [J].
Andreassen, Ole A. ;
Thompson, Wesley K. ;
Schork, Andrew J. ;
Ripke, Stephan ;
Mattingsdal, Morten ;
Kelsoe, John R. ;
Kendler, Kenneth S. ;
O'Donovan, Michael C. ;
Rujescu, Dan ;
Werge, Thomas ;
Sklar, Pamela ;
Roddey, J. Cooper ;
Chen, Chi-Hua ;
McEvoy, Linda ;
Desikan, Rahul S. ;
Djurovic, Srdjan ;
Dale, Anders M. .
PLOS GENETICS, 2013, 9 (04)
[3]  
[Anonymous], 1972, MAUDSLEY MONOGRAPH
[4]  
[Anonymous], 1896, The clinical roots of the schizophrenia concepts
[5]  
[Anonymous], TLS TIMES LIT S 0114
[6]  
[Anonymous], 1982, SCHIZOPHRENIA EPIGEN
[7]  
[Anonymous], COMPANION PSYCHIAT S
[8]  
[Anonymous], 2004, PSYCHIAT GENETICS GE
[9]  
Bassett AS, 2000, AM J MED GENET, V97, P45, DOI 10.1002/(SICI)1096-8628(200021)97:1<45::AID-AJMG6>3.0.CO
[10]  
2-9