Ozer Suzan, Ulusoy Semra, Okur Hamza, Göğüş Ahmet, Akarsu Nurten A, Uluşahin Aylin
Oğr, Gör., Psikiyatri AD., Pediyatrik Hematoloji Unitesi, Gen Haritalama Laboratuvari, Ankara.
Turk Psikiyatri Derg. 2003 Spring;14(1):7-19.
It is a long-standing debate whether schizophrenia and bipolar disorder are separate clinical entities or different poles on a spectrum. In this paper we present a family overloaded with schizophrenia, and schizoaffective, bipolar and unipolar disorders. Common loci for bipolar affective disorder and schizophrenia were tested by linkage analysis.
The pedigree of an index family which had been followed by our department for nearly 20 years was extended. The index family members were diagnosed by two psychiatrists with two distinct structured interview schedules (SCID-I and SADS-L). A field visit was undertaken for the evaluation of the extended family (n= 40) and SADS-L was used for psychiatric assessment. Blood samples were collected for molecular studies. A linkage study has been performed for overlapping susceptibility regions for schizophrenia and affective disorders (10p13-p12, 13q32, 18p and 22q11-q13) and a locus (20p11.2-q13) to which a linkage had been shown in a bipolar family who lived in the same region. Both autosomal recessive and dominant mode of inheritance were assumed in the analysis.
The pedigree consisted of 108 individuals of whom 23 are affected. All affected subjects presented psychotic features except for 5 unipolar patients. The pedigree was reconstructed with respect to psychosis phenotype. Further linkage and haplotype analysis excluded all five loci on chromosomes 10, 13, 18, 20 and 22 under both autosomal dominant and recessive modes of inheritance assumption.
A potential linkage between the psychosis gene and reported susceptibility loci overlapping in bipolar affective disorder and schizophrenia was not demonstrated Genome-wide analysis should be performed.
精神分裂症和双相情感障碍是独立的临床实体还是同一谱系的不同两极,这一争论由来已久。在本文中,我们展示了一个患有精神分裂症、分裂情感性障碍、双相情感障碍和单相情感障碍的家族。通过连锁分析检测双相情感障碍和精神分裂症的共同基因座。
对我科随访近20年的一个索引家族的谱系进行扩展。由两名精神科医生使用两种不同的结构化访谈量表(SCID-I和SADS-L)对索引家族成员进行诊断。对扩展家族(n = 40)进行实地访视以进行评估,并使用SADS-L进行精神科评估。采集血样用于分子研究。对精神分裂症和情感障碍的重叠易感区域(10p13-p12、13q32、18p和22q11-q13)以及在同一地区居住的一个双相情感障碍家族中显示有连锁关系的一个基因座(20p11.2-q13)进行了连锁研究。分析中假定了常染色体隐性和显性遗传模式。
该谱系由108人组成,其中23人患病。除5名单相情感障碍患者外,所有患病个体均有精神病性特征。根据精神病表型重建了谱系。在常染色体显性和隐性遗传模式假定下,进一步的连锁和单倍型分析排除了染色体10、13、18、20和22上的所有五个基因座。
未证实精神病基因与双相情感障碍和精神分裂症中报道的重叠易感基因座之间存在潜在连锁关系。应进行全基因组分析。