Survival of Huntington’s disease patients in Serbia: longer survival in female patients

被引:0
作者
Tatjana Pekmezovic
Marina Svetel
Jelena Maric
Irena Dujmovic-Basuroski
Natasa Dragasevic
Milica Keckarevic
Stanka Romac
Vladimir S. Kostic
机构
[1] University of Belgrade,Institute of Neurology, Clinical Centre of Serbia, School of Medicine
[2] University of Belgrade,PCR Centre, School of Biology
来源
European Journal of Epidemiology | 2007年 / 22卷
关键词
Age; CAG repeat length; Female sex; Huntington’s disease; Prognosis; Survival;
D O I
暂无
中图分类号
学科分类号
摘要
The objective of this study was to estimate probability of survival of Huntington’s disease (HD) patients in Serbia as a function of CAG repeat length and selected demographic variables. This follow-up study was carried out at the Institute of Neurology, Clinical Centre of Serbia, Belgrade, 1982–2004. The study group consisted of 112 HD patients. The significant inverse correlation was found between CAG repeat length and age at onset of HD (r = −0.732, P = 0.001) and age at death (r = −0.760, P = 0.001). The cumulative probabilities of survival in a five, ten, fifteen, and twenty-years’ period were 90.9, 63.2, 10.3 and 4.5%, respectively. Higher survival probabilities were registered in female patients, as well as in those with older age at onset and lower number of CAG repeat length (≤46). The Cox regression analysis showed that significantly poorer outcome of HD in our population was related to younger age at onset (HR-hazard ratio = 1.9; P = 0.047), and larger CAG numbers (HR = 2.4; P = 0.071). The female sex was statistically significantly associated with longer survival (HR = 0.4; P = 0.007). These data might be of some importance for further exploration of natural history and prognosis of HD.
引用
收藏
页码:523 / 526
页数:3
相关论文
共 95 条
  • [1] Aylward EH(1997)Longitudinal change in basal ganglia volume in patients with Huntington s disease Neurology 48 394-7
  • [2] Li Q(1996)Trinucleotide repeat length and clinical progression in Huntington disease Neurology 46 527-31
  • [3] Stine OC(1972)Regression models and life tables J Royal Statist Soc 34 187-220
  • [4] Ranen N(1999)Correlation between triplet repeat expansion and computed tomography measures of caudate nuclei atrophy in Huntington’s disease J Neurol 246 1090-3
  • [5] Sherr M(1999)Differences in duration of Huntington’s disease based on age at onset J Neurol Neurosurg Psychiatry 66 52-6
  • [6] Barta PE(1996)Relationship between trinucleotide repeats and neuropathological changes in Huntington disease Ann Nerurol 39 132-6
  • [7] Bylsma FW(1993)A novel gene containing a trinucleotide repeat that is unstable in Huntington’s disease chromosomes Cell 72 971-83
  • [8] Pearlson GD(1994)Trinucleotide repeat length and rate of progression of Huntington’s disease Ann Neurology 36 630-5
  • [9] Ross CA(1999)Age at onset in Huntington disease: sex specific influence of apolipoprotein E genotype and normal CAG repeat length J Med Genet 36 108-11
  • [10] Brandt J(1982)Estrogen treatment of dyskinetic disorders. Neurology 32 547-9