Skibinska Maria, Hauser Joanna, Czerski Piotr M, Leszczynska-Rodziewicz Anna, Kosmowska Magdalena, Kapelski Pawel, Slopien Agnieszka, Zakrzewska Marzena, Rybakowski Janusz K
Laboratory of Psychiatric Genetics, Department of Psychiatry, University of Medical Sciences, Poznan, Poland.
World J Biol Psychiatry. 2004 Oct;5(4):215-20. doi: 10.1080/15622970410029936.
Brain-derived neurotrophic factor (BDNF) has been implicated in the pathogenesis of schizophrenia and bipolar disorder. A functional polymorphism Val66Met of BDNF gene was studied in patients with schizophrenia (n=336), bipolar affective disorder (n=352) and healthy controls (n=375). Consensus diagnosis by at least two psychiatrists, according to DSM-IV and ICD-10 criteria, was made for each patient using a structured clinical interview for DSM-IV Axis I disorders (SCID). No association was found between the studied polymorphism and schizophrenia or bipolar affective disorder either for genotype or allele distribution (for genotype: p=0.210 in schizophrenia, p=0.400 in bipolar disorder; for alleles: p=0.260 in schizophrenia, p=0.406 in bipolar disorder). Results were also not significant when analysed by gender. For males genotype distribution and allele frequency were (respectively): p=0.480 and p=0.312 in schizophrenia, p=0.819 and p=0.673 in bipolar affective disorder. Genotype distribution and allele frequency observed in the female group were: p=0.258 for genotypes, p=0.482 for alleles in schizophrenia; p=0.432 for genotypes, p=0.464 for alleles in bipolar affective disorder. A subgroup of schizophrenic (n=62) and bipolar affective patients (n=28) with early age at onset (18 years or younger) was analysed (p=0.328 for genotypes, p=0.253 for alleles in schizophrenia; p=0.032 for genotypes, p=0.858 for alleles in bipolar affective disorder).
脑源性神经营养因子(BDNF)与精神分裂症和双相情感障碍的发病机制有关。对精神分裂症患者(n = 336)、双相情感障碍患者(n = 352)和健康对照者(n = 375)进行了BDNF基因功能性多态性Val66Met的研究。根据DSM-IV和ICD-10标准,由至少两名精神科医生通过针对DSM-IV轴I障碍的结构化临床访谈(SCID)对每位患者进行共识诊断。在所研究的多态性与精神分裂症或双相情感障碍之间,无论是基因型还是等位基因分布均未发现关联(基因型:精神分裂症中p = 0.210,双相情感障碍中p = 0.400;等位基因:精神分裂症中p = 0.260,双相情感障碍中p = 0.406)。按性别分析时结果也无显著性差异。男性的基因型分布和等位基因频率分别为:精神分裂症中p = 0.480和p = 0.312,双相情感障碍中p = 0.819和p = 0.673。女性组观察到的基因型分布和等位基因频率为:精神分裂症中基因型p = 0.258,等位基因p = 0.482;双相情感障碍中基因型p = 0.432,等位基因p = 0.464。对发病年龄早(18岁或以下)的精神分裂症患者亚组(n = 62)和双相情感障碍患者亚组(n = 28)进行了分析(精神分裂症中基因型p = 0.328,等位基因p = 0.253;双相情感障碍中基因型p = 0.032,等位基因p = 0.858)。