Straub R E, Lehner T, Luo Y, Loth J E, Shao W, Sharpe L, Alexander J R, Das K, Simon R, Fieve R R
Department of Medical Genetics, New York State Psychiatric Institute, New York 10032.
Nat Genet. 1994 Nov;8(3):291-6. doi: 10.1038/ng1194-291.
In a preliminary genome scan of 47 bipolar disorder families, we detected in one family a lod score of 3.41 at the PFKL locus on chromosome 21q22.3. The lod score is robust to marker allele frequencies, phenocopy rates and age-dependent penetrance, and remains strongly positive with changes in affection status. Fourteen other markers in 21q22.3 were tested on this family, with largely positive lod scores. Five of the other 46 families also show positive, but modest lod scores with PFKL. When all 47 families are analysed together, there is little support for linkage to PFKL under homogeneity or heterogeneity using lod score analysis, but the model-free affected-pedigree-member method yields statistically significant results (p < 0.0003). Our results are consistent with the presence of a gene in 21q22.3 predisposing at least one family to bipolar disorder.
在对47个双相情感障碍家族进行的初步基因组扫描中,我们在一个家族中检测到位于21号染色体21q22.3上的磷酸果糖激酶L(PFKL)基因座的对数优势分数为3.41。该对数优势分数对标记等位基因频率、表型模拟率和年龄依赖性外显率具有稳健性,并且随着患病状态的变化仍保持强阳性。对该家族测试了21q22.3上的其他14个标记,对数优势分数大多为阳性。其他46个家族中的5个家族在PFKL基因座上也显示出阳性但适度的对数优势分数。当对所有47个家族进行联合分析时,使用对数优势分数分析在同质性或异质性条件下几乎没有证据支持与PFKL基因座连锁,但无模型的患病家系成员法产生了具有统计学意义的结果(p < 0.0003)。我们的结果与21q22.3中存在一个使至少一个家族易患双相情感障碍的基因一致。