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先天性角化不良患者的神经精神疾病:与端粒生物学有关?

Neuropsychiatric conditions among patients with dyskeratosis congenita: a link with telomere biology?

机构信息

Department of Psychiatry and Behavioral Sciences, Children's National Medical Center, Washington, DC, USA.

出版信息

Psychosomatics. 2012 May-Jun;53(3):230-5. doi: 10.1016/j.psym.2011.09.003. Epub 2012 Mar 27.

Abstract

BACKGROUND

Dyskeratosis congenita (DC), an inherited bone marrow failure syndrome (IBMFS), is caused by defects in telomere biology, which result in very short germline telomeres. Telomeres, long nucleotide repeats and a protein complex at chromosome ends, are essential for chromosomal stability. Several association studies suggest that short telomeres are associated with certain psychiatric disorders, including mood disorders and schizophrenia. There are two cases in the literature of schizophrenia and DC occurring as co-morbid conditions. We noted that many patients with DC in our cohort had neuropsychiatric conditions.

METHODS

Subjects were participants in NCI's IBMFS prospective cohort study. Psychiatric evaluation was incorporated into our clinical assessment in January 2009. Fourteen DC or DC-like patients, including six children, were evaluated in this study through in person interview by either a psychiatrist specialized in psychosomatic medicine or a child and adolescent psychiatrist.

RESULTS

Three of the six pediatric subjects and five of the eight adults had a neuropsychiatric condition such as a mood, anxiety, or adjustment disorder, intellectual disability, attention deficit hyperactivity disorder, or pervasive developmental disorders. The lifetime occurrence of any of these disorders in our study was 83% in pediatric subjects and 88% in adults. Notably, the literature reports neuropsychiatric conditions in 25% and 38% in chronically ill children and adults, respectively.

CONCLUSION

This pilot study suggests that patients with DC may have higher rates of neuropsychiatric conditions than the general population or other chronically ill individuals. This potential link between very short telomeres and neuropsychiatric conditions warrants further study.

摘要

背景

先天性角化不良(DC)是一种遗传性骨髓衰竭综合征(IBMFS),由端粒生物学缺陷引起,导致种系端粒非常短。端粒是染色体末端的长核苷酸重复序列和蛋白质复合物,对于染色体稳定性至关重要。几项关联研究表明,短端粒与某些精神疾病有关,包括心境障碍和精神分裂症。文献中有两例精神分裂症和 DC 同时发生的病例。我们注意到我们队列中的许多 DC 患者都有神经精神疾病。

方法

研究对象为 NCI 的 IBMFS 前瞻性队列研究的参与者。2009 年 1 月,我们将精神科评估纳入临床评估中。通过专门从事身心医学的精神科医生或儿童和青少年精神科医生对 14 名 DC 或类似 DC 的患者(包括 6 名儿童)进行了面对面访谈。

结果

6 名儿科患者中有 3 名,8 名成年患者中有 5 名患有神经精神疾病,如心境、焦虑或适应障碍、智力障碍、注意缺陷多动障碍或广泛性发育障碍。在我们的研究中,这些疾病在儿科患者中的终生发生率为 83%,在成年患者中的发生率为 88%。值得注意的是,文献报告慢性儿童和成年患者的神经精神疾病发生率分别为 25%和 38%。

结论

这项初步研究表明,与一般人群或其他慢性病患者相比,DC 患者可能有更高的神经精神疾病发生率。短端粒与神经精神疾病之间的这种潜在联系值得进一步研究。

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