McMonagle P, Webb S, Hutchinson M
Department of Neurology, St Vincent's University Hospital, Elm Park, Dublin 4, Ireland.
J Neurol Neurosurg Psychiatry. 2002 Jan;72(1):43-6. doi: 10.1136/jnnp.72.1.43.
Hereditary spastic paraparesis (HSP) is clinically and genetically heterogeneous. "Pure" autosomal dominant (AD) HSP is most common and eight genetic loci are identified to date. Previous studies have included autosomal recessive and sporadic cases in prevalence calculations. This study aimed to determine the prevalence and features of pure ADHSP in the island of Ireland.
Index cases were identified from a 5 year survey of all adult and paediatric neurologists, clinical geneticists, hospital records, and hospital inpatient enquiry system data in Ireland, north and south. Families were examined by two neurologists and classified as affected or unaffected according to specific criteria. The prevalence date was set at 1 June 2000 and the midyear population estimate for the previous year was 5.436 million.
Eighty two patients with pure ADHSP and a further 12 obligate carriers from 19 families were identified. In total 69 patients with pure ADHSP were alive and resident in Ireland at the prevalence date. Twenty nine per cent of these were asymptomatic but with signs of paraparesis.
The prevalence of ADHSP in Ireland to estimated to be 1.27/100 000 population. The high proportion of asymptomatic cases and obligate carriers means that this condition is likely to be underdiagnosed.
遗传性痉挛性截瘫(HSP)在临床和遗传方面具有异质性。“纯合”常染色体显性(AD)HSP最为常见,迄今为止已确定了8个基因位点。以往的研究在患病率计算中纳入了常染色体隐性和散发病例。本研究旨在确定爱尔兰岛纯合ADHSP的患病率及特征。
通过对爱尔兰南北地区所有成人及儿科神经科医生、临床遗传学家、医院记录及医院住院查询系统数据进行为期5年的调查,确定索引病例。由两名神经科医生对家庭进行检查,并根据特定标准将其分类为患病或未患病。患病率日期设定为2000年6月1日,上一年年中人口估计数为543.6万。
共确定了来自19个家庭的82例纯合ADHSP患者以及另外12名必然携带者。在患病率日期,共有69例纯合ADHSP患者在世并居住在爱尔兰。其中29%无症状,但有截瘫体征。
据估计,爱尔兰ADHSP的患病率为1.27/10万人口。无症状病例和必然携带者的高比例意味着这种疾病可能未得到充分诊断。