Vincent A, Clover L, Buckley C, Grimley Evans J, Rothwell P M
Department of Clinical Neurology and Weatherall Institute of Molecular Medicine, John Radcliffe Hospital, University of Oxford, Oxford OX3 9DS, UK.
J Neurol Neurosurg Psychiatry. 2003 Aug;74(8):1105-8. doi: 10.1136/jnnp.74.8.1105.
Myasthenia gravis is a potentially serious but treatable muscle disease caused by autoantibodies directed at the acetylcholine receptor (AChR) on the postsynaptic membrane of the neuromuscular junction. There is anecdotal evidence that the diagnosis is sometimes missed in older patients.
To examine the incidence and age distribution of positive AChR antibodies in samples referred to diagnostic laboratories in the UK, and the prevalence of positive AChR antibodies in samples from a cohort of older individuals.
Positive AChR antibody tests were identified from all UK centres registered for the assay with the European quality assurance scheme (EQAS) during 1997-99, and the age and sex specific incidence was calculated, based on the UK population. The prevalence of AChR antibodies in sera from a sample of 2000 individuals aged > or =60 years was determined.
3183 individuals had positive AChR antibody tests on routine screening during the years 1997 to 1999 in the UK, giving an annual incidence of 1.8/100 000. In both sexes, the age specific incidence rose steeply between the ages of 45 and 74, reaching 9.9/100 000 in men, and then fell, with a sharp decline above the age of 80. In the prevalence study, whereas only one serum from individuals aged 60-74 years was positive for AChR antibodies (0.12%), sera from eight individuals aged > or =75 years were positive (0.7%). Only one had a previous clinical diagnosis of myasthenia gravis but four others had histories of stroke or transient ischaemic attacks.
The sharp fall in the incidence of clinically recognised myasthenia gravis in people over 80 years of age in our national AChR antibody incidence study, and the high prevalence of previously unrecognised positive AChR antibodies in those > or =75 years old, suggest that myasthenia gravis may be substantially underdiagnosed in older people.
重症肌无力是一种潜在严重但可治疗的肌肉疾病,由针对神经肌肉接头突触后膜上乙酰胆碱受体(AChR)的自身抗体引起。有轶事证据表明,老年患者有时会漏诊。
研究转诊至英国诊断实验室的样本中AChR抗体阳性的发病率和年龄分布,以及一组老年个体样本中AChR抗体阳性的患病率。
从1997 - 1999年在欧洲质量保证计划(EQAS)注册进行该检测的所有英国中心中识别出AChR抗体检测阳性的情况,并根据英国人口计算年龄和性别特异性发病率。测定了2000名年龄≥60岁个体样本中AChR抗体的患病率。
1997年至1999年期间,英国有3183人在常规筛查中AChR抗体检测呈阳性,年发病率为1.8/10万。在两性中,年龄特异性发病率在45岁至74岁之间急剧上升,男性达到9.9/10万,然后下降,80岁以上急剧下降。在患病率研究中,60 - 74岁个体中只有一份血清AChR抗体呈阳性(0.12%),而75岁及以上的8名个体血清呈阳性(0.7%)。只有1人先前有重症肌无力的临床诊断,但其他4人有中风或短暂性脑缺血发作史。
在我们的全国AChR抗体发病率研究中,80岁以上人群中临床确诊的重症肌无力发病率急剧下降,以及75岁及以上人群中先前未被识别的AChR抗体阳性患病率较高,表明老年人中重症肌无力可能存在大量漏诊。