Department of Psychiatry, South Texas Psychiatric Genetics Research Center, University of Texas Health Science Center at San Antonio, 454 Soledad, Suite 200, San Antonio, TX 78205, USA.
Am J Med Genet B Neuropsychiatr Genet. 2010 Apr 5;153B(3):837-45. doi: 10.1002/ajmg.b.31047.
Chromosome 18 abnormalities are associated with a range of physical abnormalities such as short stature and hearing impairments. Psychiatric manifestations have also been observed. This study focuses on the presentations of psychiatric syndromes as they relate to specific chromosomal abnormalities of chromosome 18. Twenty-five subjects (13 with an 18q deletion, 9 with 18p tetrasomy, and 3 with an 18p deletion), were interviewed by psychiatrists (blind to specific chromosomal abnormality) using the DIGS (subjects 18 and older) or KSADS-PL (subjects under 18). A consensus best estimation diagnostic process was employed to determine psychiatric syndromes. Oligonucleotide Array Comparative Genomic Hybridization (Agilent Technologies) was utilized to define specific regions of chromosome 18 that were deleted or duplicated. These data were further analyzed to determine critical regions of the chromosome as they relate to phenotypic manifestations in these subjects. 58.3% of the chromosome 18q- deletion subjects had depressive symptoms, 58.3% had anxiety symptoms, 25% had manic symptoms, and 25% had psychotic symptoms. 66.6% of the chromosome 18p- deletion subjects had anxiety symptoms, and none had depressive, manic, or psychotic symptoms. Fifty percent of the chromosome 18p tetrasomy subjects had anxiety symptoms, 12.5% had psychotic symptoms, and 12.5% had a mood disorder. All three chromosomal disorders were associated with high anxiety rates. Psychotic, manic and depressive disorders were seen mostly in 18q- subjects and this may be helpful in narrowing regions for candidate genes for these psychiatric conditions.
18 号染色体异常与多种身体异常有关,如身材矮小和听力障碍。也观察到了精神表现。本研究侧重于与 18 号染色体特定染色体异常相关的精神综合征表现。25 名受试者(13 名 18q 缺失,9 名 18p 四倍体,3 名 18p 缺失),由精神科医生(对特定染色体异常盲)使用 DIGS(18 岁及以上)或 KSADS-PL(18 岁以下)进行访谈。采用共识最佳估计诊断过程来确定精神综合征。寡核苷酸微阵列比较基因组杂交(安捷伦科技)用于定义染色体 18 缺失或重复的特定区域。进一步分析这些数据,以确定与这些受试者表型表现相关的染色体关键区域。58.3%的 18q- 缺失受试者有抑郁症状,58.3%有焦虑症状,25%有躁狂症状,25%有精神病症状。66.6%的 18p- 缺失受试者有焦虑症状,没有抑郁、躁狂或精神病症状。50%的 18p 四倍体受试者有焦虑症状,12.5%有精神病症状,12.5%有情绪障碍。所有三种染色体疾病都与高焦虑率有关。精神病、躁狂和抑郁障碍主要见于 18q- 受试者,这可能有助于缩小这些精神疾病候选基因的区域。