Turner Martin R, Goldacre Raph, Talbot Kevin, Goldacre Michael J
Oxford University Nuffield Department of Clinical Neurosciences, John Radcliffe Hospital.
Oxford University Nuffield Department of Population Health, Old Road Campus, Oxford, United Kingdom.
Ann Neurol. 2016 Dec;80(6):935-938. doi: 10.1002/ana.24801. Epub 2016 Nov 14.
It is recognized that neuropsychiatric conditions are overrepresented in amyotrophic lateral sclerosis (ALS) patient kindreds and psychiatric symptoms may precede the onset of motor symptoms. Using a hospital record linkage database, hospitalization with a diagnosis of schizophrenia, bipolar disorder, depression, or anxiety was significantly associated with a first diagnosis of ALS within the following year. This is likely to specifically reflect the clinicopathological overlap of ALS with frontotemporal dementia. A diagnosis of depression was significantly associated with a first record of ALS ≥5 years later, in keeping with growing evidence for major depressive disorder as an early marker of cerebral neurodegeneration. Ann Neurol 2016;80:935-938.
人们认识到,神经精神疾病在肌萎缩侧索硬化症(ALS)患者家族中更为常见,且精神症状可能先于运动症状出现。利用医院记录链接数据库,诊断为精神分裂症、双相情感障碍、抑郁症或焦虑症的住院治疗与次年首次诊断为ALS显著相关。这可能特别反映了ALS与额颞叶痴呆的临床病理重叠。抑郁症的诊断与≥5年后首次记录的ALS显著相关,这与越来越多的证据表明重度抑郁症是脑神经元变性的早期标志物一致。《神经病学纪事》2016年;80:935 - 938。