Uptake of Huntington disease predictive testing in a complete population

被引:69
|
作者
Morrison, P. J. [1 ,2 ]
Harding-Lester, S. [1 ]
Bradley, A. [1 ]
机构
[1] Belfast City Hosp, Reg Med Genet Ctr, Belfast BT9 7AD, Antrim, North Ireland
[2] Univ Ulster, Sch Biomed Sci, Coleraine BT52 1SA, Londonderry, North Ireland
关键词
Huntington disease; predictive testing; prevalence; uptake; EXPERIENCE; INDIVIDUALS; REPEAT; RISK;
D O I
10.1111/j.1399-0004.2010.01538.x
中图分类号
Q3 [遗传学];
学科分类号
071007 ; 090102 ;
摘要
Using the Northern Ireland Huntington disease (HD) register, the number of prospectively recorded predictive tests was analysed over a 20-year period. Two hundred and twelve patients completed predictive testing. Ninety-two (43%) received mutation-positive results and 119 (56%) mutation negative. There was one intermediate allele result. There was no significant gender difference. One hundred and eighty affected cases confirmed by molecular genetic testing were alive on 1 January 2001. The uptake of predictive testing in the entire HD 50% at-risk population in 2001 was calculated by three methods giving a range of 12.3-14.6%. Uptake after 20 years was estimated to be 14.7%. The minimum prevalence of affected HD cases was calculated as 10.6/100,000 in 2001. The total uptake of predictive testing was calculated and it suggests that a substantial number of at-risk patients do not come forward for testing until symptomatic. Pre-symptomatic testing for this late-onset condition with no present treatment, and limited management options, still presents challenges for families.
引用
收藏
页码:281 / 286
页数:6
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