Woods S W, Miller T J, Davidson L, Hawkins K A, Sernyak M J, McGlashan T H
Department of Psychiatry, Yale University School of Medicine, New Haven, CT 06519, USA.
Schizophr Res. 2001 Oct 1;52(1-2):21-7. doi: 10.1016/s0920-9964(01)00158-x.
Screening a population of relatives of current schizophrenic patients could be an efficient means to accrue a sample of early first episode or prodromal patients for a prediction study or an intervention study. The risk of new onset schizophrenia cases in any one year in a population of relatives depends on the number of schizophrenic probands and three additional factors: (1) the age of onset distribution for schizophrenia; (2) the lifetime risk of the at-risk group of relatives selected; and (3) the number of at-risk relatives per proband and their age distribution. Estimates are made for each of these parameters, and calculations are presented. The base model suggests that screening all siblings and children of patients with schizophrenia would yield approximately 19 new cases of schizophrenia per year per 10,000 relatives screened. The results of the calculation are relatively insensitive to reasonable variation of most model parameter estimates. The yield of new cases obtained by screening relatives of current patients appears to be low if the purpose is to recruit a sample for an early intervention study over a relatively short period of time.
对现患精神分裂症患者的亲属群体进行筛查,可能是为预测研究或干预研究积累早期首发或前驱期患者样本的有效手段。亲属群体中任何一年新发精神分裂症病例的风险取决于精神分裂症先证者的数量以及另外三个因素:(1)精神分裂症的发病年龄分布;(2)所选高危亲属群体的终生风险;(3)每个先证者的高危亲属数量及其年龄分布。对这些参数中的每一个都进行了估计,并给出了计算结果。基础模型表明,对精神分裂症患者的所有兄弟姐妹和子女进行筛查,每筛查10000名亲属,每年大约会产生19例新的精神分裂症病例。计算结果对大多数模型参数估计的合理变化相对不敏感。如果目的是在相对较短的时间内招募样本进行早期干预研究,那么通过筛查现患患者的亲属获得的新病例产出似乎较低。