Hansen T, Hemmingsen R P, Wang A G, Olsen L, Timm S, Søeby K, Jakobsen K D, Fenger M, Parnas J, Rasmussen H B, Werge T
Research Institute of Biological Psychiatry, Copenhagen University Hospital, H:S Sct. Hans Hospital, Roskilde, Denmark.
Pharmacogenomics J. 2006 Mar-Apr;6(2):120-5. doi: 10.1038/sj.tpj.6500350.
Accumulating evidence implicates deficiencies in apolipoprotein D (ApoD) function and arachidonic acid signaling in schizophrenic disorders. We addressed two hypotheses in relation to ApoD: first, polymorphisms in the ApoD gene confer susceptibility to or are markers of disease, and, second, genetic variation in the ApoD is associated with long-term clinical outcome to antipsychotic treatment. We genotyped two single-nucleotide polymorphisms in the ApoD gene in 343 chronic patients with schizophrenia spectrum disorders (ICD-10) and 346 control subjects of Danish origin. We did not find ApoD alleles, genotypes or haplotypes to be associated with disease. However, we did find that long-term clinical outcome was associated with the ApoD polymorphism rs7659 (P = 0.041) following adjustment for lifetime clinical global impression, age at first admission and gender.
越来越多的证据表明,载脂蛋白D(ApoD)功能缺陷和花生四烯酸信号传导与精神分裂症有关。我们针对ApoD提出了两个假设:第一,ApoD基因多态性是疾病易感性的指标或标志;第二,ApoD基因变异与抗精神病药物治疗的长期临床疗效相关。我们对343例患有精神分裂症谱系障碍(ICD-10)的慢性患者和346名丹麦裔对照者的ApoD基因中的两个单核苷酸多态性进行了基因分型。我们没有发现ApoD等位基因、基因型或单倍型与疾病相关。然而,在对终生临床总体印象、首次入院年龄和性别进行校正后,我们确实发现长期临床疗效与ApoD多态性rs7659相关(P = 0.041)。