López-Arlandis J M, Vílchez J J, Palau F, Sevilla T
Department of Neurology, Hospital Universitari La Fe, Valencia, Spain.
Neuroepidemiology. 1995;14(1):14-9. doi: 10.1159/000109774.
Epidemiological studies performed directly on the population show a prevalence of Friedreich's ataxia (FA) from 1 to 4.7 cases/100,000 inhabitants. An indirect epidemiological approach can be achieved using genetic methods like consanguinity studies to determine the frequency of a mutated gene and the incidence of certain diseases in the population. We obtained consanguinity data of a series of FA patients in Valencia, Spain and the figures on consanguinity in the general population that were estimated according to the Archive of Dispensations given by the Catholic church for consanguineous marriages. From these data, the frequency of the FA gene was calculated as 1/127. From these data, applying the Hardy-Weinberg principle, the frequency of the carriers was 1/64 and the incidence was 6.18/100,000 live births. Assuming a life expectancy of FA of 45 years, the prevalence was 3.83/100,000 inhabitants. These figures are in the same range as those obtained in population studies.
直接针对人群开展的流行病学研究表明,弗里德赖希共济失调(FA)的患病率为每10万居民中有1至4.7例。可采用血缘关系研究等遗传方法实现间接流行病学方法,以确定突变基因的频率以及人群中某些疾病的发病率。我们获取了西班牙巴伦西亚一系列FA患者的血缘关系数据以及根据天主教会提供的近亲婚姻豁免档案估算的普通人群中的血缘关系数据。根据这些数据,FA基因的频率计算为1/127。根据这些数据,应用哈迪-温伯格原理,携带者的频率为1/64,发病率为每10万活产中有6.18例。假设FA患者的预期寿命为45岁,患病率为每10万居民中有3.83例。这些数字与人群研究中获得的数字处于同一范围。