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一项随访连锁研究支持了21号染色体长臂22区存在双相情感障碍基因座的证据。

A follow-up linkage study supports evidence for a bipolar affective disorder locus on chromosome 21q22.

作者信息

Liu J, Juo S H, Terwilliger J D, Grunn A, Tong X, Brito M, Loth J E, Kanyas K, Lerer B, Endicott J, Penchaszadeh G, Gilliam T C, Baron M

机构信息

Columbia Genome Center, Columbia University, New York, New York, USA.

出版信息

Am J Med Genet. 2001 Mar 8;105(2):189-94. doi: 10.1002/ajmg.1195.

Abstract

Evidence for linkage between bipolar affective disorder (BP) and 21q22 was first reported by our group in a single large pedigree with a lod score of 3.41 with the PFKL locus. In a subsequent study, with denser marker coverage in 40 multiplex BP pedigrees, we reported supporting evidence with a two-point lod score of 2.76 at the D21S1260 locus, about 6 cM proximal to PFKL. For cost-efficiency, the individuals genotyped in that study comprised a subset of our large pedigree sample. To augment our previous analysis, we now report a follow-up study including a larger sample set with an additional 331 typed individuals from the original 40 families, improved marker coverage, and an additional 16 pedigrees. The analysis of all 56 pedigrees (a total of 862 genotyped individuals vs. the 372 genotyped previously), the largest multigenerational BP pedigree sample reportedly analyzed to date, supports our previous results, with a two-point lod score of 3.56 with D21S1260. The 16 new pedigrees analyzed separately gave a maximum two-point lod score of 1.89 at D21S266, less than 1 cM proximal to D21S1260. Our results are consistent with a putative BP locus on 21q22.

摘要

我们小组首次报道了双相情感障碍(BP)与21q22之间的连锁证据,该证据来自一个单一的大家系,与磷酸果糖激酶L(PFKL)基因座的对数优势分数为3.41。在随后的一项研究中,对40个多重BP家系进行了更密集的标记覆盖,我们报道了在D21S1260基因座处的两点对数优势分数为2.76的支持证据,该基因座位于PFKL近端约6厘摩处。为了提高成本效益,该研究中进行基因分型的个体是我们大家系样本的一个子集。为了加强我们之前的分析,我们现在报告一项后续研究,该研究包括一个更大的样本集,其中有来自原来40个家庭的另外331名进行基因分型的个体、改进的标记覆盖,以及另外16个家系。对所有56个家系(总共862名进行基因分型的个体,与之前的372名进行基因分型的个体相比)的分析是据报道迄今为止分析的最大的多代BP家系样本,支持了我们之前的结果,D21S1260的两点对数优势分数为3.56。单独分析这16个新家系,在D21S266处的最大两点对数优势分数为1.89,该基因座位于D21S1260近端不到1厘摩处。我们的结果与21q22上一个假定的BP基因座一致。

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