Goudemand M, Goudemand J, Parquet P J, Goudemand-Joubert C, Letallec-Duytschaever F, Fontan M
J Genet Hum. 1981 Dec;29(4):419-29.
Childhood psychoses could have a genetic etiology, but early and late onset psychoses have to be separated. Genetic factors are certainly implicated in the development of late onset psychoses and appear to overlap with those of adult schizophrenia. Evidence implicating genetics in early onset psychoses is likely, as twin studies have supported this hypothesis. HLA system is a particularly suitable genetic marker. We report the results of an investigation on HLA A and B antigens we have performed on 57 psychotics (30 early onset psychotics, 27 late onset psychotics). No genetic association appears in the whole population, as well as in the early and late onset psychosis series. These results have to be compared with Golse's et al. (1977, 1980), Stebbs and Magenis' (1980) and adult schizophrenia data. Further researches with population and family pedigree are required with other major histocompatibility complex markers.
儿童期精神病可能有遗传病因,但早发性和晚发性精神病必须加以区分。遗传因素肯定与晚发性精神病的发病有关,而且似乎与成人精神分裂症的遗传因素重叠。由于双生子研究支持了这一假设,因此遗传因素与早发性精神病发病有关的证据很可能存在。HLA系统是一个特别合适的遗传标记。我们报告了对57名精神病患者(30名早发性精神病患者,27名晚发性精神病患者)进行的HLA A和B抗原调查结果。在整个人群以及早发性和晚发性精神病系列中均未发现遗传关联。这些结果必须与戈尔瑟等人(1977年、1980年)、斯特布斯和马吉尼斯(1980年)的研究结果以及成人精神分裂症的数据进行比较。需要用其他主要组织相容性复合体标记对人群和家系进行进一步研究。