Reiss A L, Freund L, Abrams M T, Boehm C, Kazazian H
Behavioral Genetics and Neuroimaging Research Center, Kennedy Krieger Institute, Baltimore, MD 21205.
Am J Hum Genet. 1993 May;52(5):884-94.
Although previous studies have suggested that the fragile X premutation (fra [X] pM) does not cause deleterious effects, methodological constraints have prevented more definitive conclusions from being reached. In this report, we describe the neuropsychiatric and cognitive-neuropsychological status of 34 adult women with the fra (X) pM, as compared with a well-matched control group of 41 mothers of fra (X)-negative children with developmental disability. The results indicate that there are no meaningful differences between adult women with the fra (X) pM and control subjects with respect to cognitive abilities or profile, neuropsychological function, psychiatric diagnoses or symptoms, and self-rated personality profile. No measure for either group showed evidence of functioning outside the normal range except for a high lifetime prevalence of major depression in both groups. Additional exploratory analyses within the fra (X) group showed no significant effect of either the size of the fra (X) insert or X chromosome inactivation pattern in leukocytes, on any measure of neurobehavioral function. These findings provide additional information to professionals providing genetic counseling to, and assessment of, fra (X) families.
尽管先前的研究表明脆性X前突变(fra [X] pM)不会产生有害影响,但方法学上的限制使得无法得出更明确的结论。在本报告中,我们描述了34名患有fra(X)pM的成年女性的神经精神和认知神经心理学状况,并与41名患有发育障碍的fra(X)阴性儿童的母亲组成的匹配良好的对照组进行了比较。结果表明,患有fra(X)pM的成年女性与对照受试者在认知能力或特征、神经心理功能、精神疾病诊断或症状以及自评人格特征方面没有有意义的差异。除了两组中重度抑郁症的终生患病率都很高外,两组的任何测量指标都没有显示出超出正常范围的功能证据。在fra(X)组内的额外探索性分析表明,fra(X)插入片段的大小或白细胞中的X染色体失活模式对任何神经行为功能测量指标均无显著影响。这些发现为向fra(X)家庭提供遗传咨询和评估的专业人员提供了更多信息。