Propping P, Friedl W, Huschka M, Schlör K H, Reimer F, Lee-Vaupel M, Conzelmann E, Sandhoff K
Hum Genet. 1986 Nov;74(3):244-8. doi: 10.1007/BF00282542.
A total of 1728 patients consecutively admitted to a neuropsychiatric hospital and 379 chronically ill inpatients were examined for activity of arylsulphatase A (ASA) in leucocytes. A further 519 healthy individuals served as controls. We did not find evidence for the involvement of low ASA activity in chronic patients. The consecutive admissions showed a slight preponderance in the lower ASA activity classes. This activity range covers persons heterozygous for ASA deficiency alleles. The data are compatible with the hypothesis that carriers of low ASA activity alleles are at a slightly higher risk for neuropsychiatric disorders.
对一家神经精神病医院连续收治的1728例患者以及379例慢性病住院患者的白细胞芳基硫酸酯酶A(ASA)活性进行了检测。另外519名健康个体作为对照。我们没有发现低ASA活性与慢性病患者有关的证据。连续收治的患者在较低ASA活性类别中略有优势。这个活性范围涵盖了ASA缺乏等位基因的杂合子个体。这些数据与低ASA活性等位基因携带者患神经精神疾病的风险略高这一假设相符。