Tang S X, Yi J J, Calkins M E, Whinna D A, Kohler C G, Souders M C, McDonald-McGinn D M, Zackai E H, Emanuel B S, Gur R C, Gur R E
Department of Psychiatry, Perelman School of Medicine, University of Pennsylvania, Philadelphia, PA, USA.
Department of Child and Adolescent Psychiatry, Children's Hospital of Philadelphia, Philadelphia, PA, USA.
Psychol Med. 2014 Apr;44(6):1267-77. doi: 10.1017/S0033291713001669. Epub 2013 Sep 9.
Chromosome 22q11.2 deletion syndrome (22q11DS) is a common genetic disorder with high rates of psychosis and other psychopathologies, but few studies discuss treatment. Our aim was to characterize the prevalence and treatment of major psychiatric illnesses in a well-characterized sample of individuals with 22q11DS.
This was a cross-sectional study of 112 individuals aged 8 to 45 years with a confirmed diagnosis of 22q11DS. Each participant was administered a modified Schedule for Affective Disorders and Schizophrenia for School-Age Children (K-SADS) and the Structured Interview for Prodromal Syndromes (SIPS). Phenotypes assessed were threshold and subthreshold psychosis, depression, mania, generalized and separation anxiety, obsessions/compulsions, inattention/hyperactivity and substance use. Histories of mental health care and current psychotropic treatment were obtained.
Psychopathology was common, with 79% of individuals meeting diagnostic criteria for a disorder at the time of assessment. Diagnoses of psychosis were made in 11% of cases, attenuated positive symptom syndrome (APS) in 21%, and 47% experienced significant subthreshold symptoms. Peak occurrence of psychosis risk was during adolescence (62% of those aged 12-17 years). Criteria for a mood disorder were met by 14%, for anxiety disorder 34% and for attention deficit hyperactivity disorder (ADHD) 31%. Mental health care had been received by 63% of individuals in their lifetime, but only 40% continued therapy and 39% used psychotropics. Antipsychotics were used by 42% of participants with psychosis and none of the participants with APS. Half of those at risk for psychosis were receiving no mental health care.
Psychopathology is common in 22q11DS but is not adequately treated or clinically followed. Particular attention should be paid to subthreshold psychotic symptoms, especially in adolescents.
22q11.2缺失综合征(22q11DS)是一种常见的遗传性疾病,精神病和其他精神病理学发生率很高,但很少有研究讨论其治疗方法。我们的目的是在一个特征明确的22q11DS个体样本中,描述主要精神疾病的患病率和治疗情况。
这是一项对112名年龄在8至45岁之间、确诊为22q11DS的个体进行的横断面研究。每位参与者都接受了一份针对学龄儿童的情感障碍和精神分裂症修订版日程表(K-SADS)以及前驱综合征结构化访谈(SIPS)。评估的表型包括阈限和阈下精神病、抑郁、躁狂、广泛性和分离性焦虑、强迫观念/强迫行为、注意力不集中/多动以及物质使用。获取了心理健康护理史和当前的精神药物治疗情况。
精神病理学很常见,79%的个体在评估时符合某种疾病的诊断标准。11%的病例被诊断为精神病,21%为轻度阳性症状综合征(APS),47%有明显的阈下症状。精神病风险的高峰出现在青春期(12至17岁人群中的62%)。14%的个体符合心境障碍标准,34%符合焦虑障碍标准,31%符合注意力缺陷多动障碍(ADHD)标准。63%的个体一生中接受过心理健康护理,但只有40%继续接受治疗,39%使用精神药物。42%患有精神病的参与者使用了抗精神病药物,而患有APS的参与者无人使用。有精神病风险的个体中有一半没有接受心理健康护理。
精神病理学在22q11DS中很常见,但未得到充分治疗或临床随访。应特别关注阈下精神病症状,尤其是在青少年中。