Alm J, Holmgren G, Larsson A, Schimpfessel L
Clin Genet. 1981 Sep;20(3):229-33.
Histidinaemia screening was included in the epidemiological survey of the Swedish neonatal screening programme, 1971-72. Dried blood samples on filter paper collected neonatally from 171,000 infants were analysed the Guthrie method. A blood histidine level above 0.96 mmol/1 (15 mg per 100 ml) was regarded as a positive test and was found in 639 infants - i.e., 1/270. No further diagnostic measures were taken until 1977 when stored dried blood samples from 273 infants with a positive screening test were analysed for urocanic acid. Four children had undetectable blood urocanic acid. They were studied and histidinaemia was confirmed in two children, and excluded in two. Both histidinaemia children had normal psychomotor development at 7 years of age, in spite of the fact that no dietary treatment was given. The incidence of histidinaemia in Sweden was estimated as 1/37,00, on the basis of neonatal screening. In addition, histidinaemia was diagnosed in four individuals who were not detected in the neonatal screening programme; of these, only one had an IQ less than 85. At present, general neonatal screening histidinaemia in Sweden does not seem justified.
1971 - 1972年,组氨酸血症筛查被纳入瑞典新生儿筛查项目的流行病学调查。采用格思里方法对从171,000名新生儿中采集的滤纸干血样进行分析。血组氨酸水平高于0.96 mmol/1(每100 ml含15 mg)被视为阳性检测结果,在639名婴儿中发现了这种情况,即1/270。直到1977年才采取进一步的诊断措施,当时对273名筛查试验阳性的婴儿的储存干血样进行尿刊酸分析。有4名儿童检测不到血中尿刊酸。对他们进行了研究,两名儿童被确诊为组氨酸血症,两名儿童被排除。尽管未进行饮食治疗,但这两名组氨酸血症儿童在7岁时精神运动发育正常。根据新生儿筛查结果,瑞典组氨酸血症的发病率估计为1/37,000。此外,在新生儿筛查项目中未被检测出的4个人被诊断为组氨酸血症;其中只有一人智商低于85。目前,瑞典对组氨酸血症进行普遍的新生儿筛查似乎没有道理。