Polliack M L, Barak Y, Achiron A
Multiple Sclerosis Center, Sheba Medical Center, Tel-Hashomer, Israel.
J Am Geriatr Soc. 2001 Feb;49(2):168-71. doi: 10.1046/j.1532-5415.2001.49038.x.
The onset of multiple sclerosis (MS) after age 50 is infrequent and presents a diagnostic challenge. The purpose of the present study was to review the prevalence, presentation, and clinical characteristics of late-onset MS.
A retrospective chart review.
The Multiple Sclerosis Center at Sheba Medical Center, Israel.
640 patients with a definite diagnosis of MS.
Diagnosis of MS was established according to Poser criteria and confirmed by brain magnetic resonance imaging (MRI) using our unit's computerized database. Late-onset MS was defined as the first presentation of clinical symptoms after the age of 50 years. For each patient, age, gender, clinical presentation, disease course, neurological involvement, disease duration, neurological disability assessed, and Progression Index (PI) were analyzed. All patients were interviewed using the structured clinical interview for DSM-IV, SCID-lifetime Hebrew version.
Of 640 MS patients, 30 (4.6%) were diagnosed as suffering from late-onset MS. Mean age at onset was 53.5 +/- 3.1, range 50 to 62 years. Female to male ratio was 1.73:1. Mean disease duration was 7.6 years, range 2 to 11 years. In 50% of patients the disease course was relapsing-remitting. Motor symptoms were the most common neurological presentation at onset (63.3%). Major depressive episode was diagnosed in 6 out of 30 patients (20%) in the two years prior to the diagnosis of MS. After a mean disease duration of 7.6 years there was a marked increase in sphincteric and cerebellar involvement. In addition 7 out of 30 patients had suffered a major depressive episode within 4 years of diagnosis. Mean PI was 0.81, suggesting rapid neurological deterioration.
Late-onset MS is not rare and may present as major depression and, although neurological presentation at onset is similar to that of young adults, progression to disability is more rapid and a primary progressive course is more prevalent.
50岁后多发性硬化症(MS)的发病并不常见,且带来诊断挑战。本研究的目的是回顾迟发性MS的患病率、临床表现及临床特征。
回顾性病历审查。
以色列谢巴医疗中心的多发性硬化症中心。
640例确诊为MS的患者。
根据波泽标准确立MS诊断,并通过使用本单位的计算机数据库进行脑磁共振成像(MRI)予以确认。迟发性MS定义为50岁后首次出现临床症状。对每位患者的年龄、性别、临床表现、病程、神经受累情况、疾病持续时间、评估的神经功能残疾及进展指数(PI)进行分析。所有患者均使用DSM-IV的结构化临床访谈希伯来语终生版进行访谈。
在640例MS患者中,30例(4.6%)被诊断为迟发性MS。发病时的平均年龄为53.5±3.1岁,范围为50至62岁。女性与男性比例为1.73:1。平均病程为7.6年,范围为2至11年。50%的患者病程为复发缓解型。运动症状是发病时最常见的神经表现(63.3%)。在MS诊断前两年内,30例患者中有6例(20%)被诊断为重度抑郁发作。平均病程7.6年后,括约肌和小脑受累明显增加。此外,30例患者中有7例在诊断后4年内出现重度抑郁发作。平均PI为0.81,提示神经功能快速恶化。
迟发性MS并不罕见,可能表现为重度抑郁,尽管发病时的神经表现与年轻人相似,但进展至残疾的速度更快,且原发进展型病程更为普遍。