Department of Clinical Medicine, University of Bergen, Bergen, Norway.
Mitochondrion. 2012 Nov;12(6):640-3. doi: 10.1016/j.mito.2012.08.004. Epub 2012 Aug 29.
The number of CAG repeats in the mitochondrial DNA-polymerase gamma (POLG1) gene has been associated with Parkinson disease (PD) in some populations. We sequenced the CAG tract of POLG1 in 191 Norwegian patients with PD and an equal number of controls and found an association between non-10 or 11 CAG repeats and PD in our population. While our results were significant, this trend was not maintained following correction for multiple testing. We also performed a meta-analysis of all published studies including our own that shows PD is associated with the number of CAG repeats in POLG1. The meta-analysis reveals that the rare allelic variation encompassed by non-10 CAG repeats associates significantly with PD (p=0.0017). Whether this reflects a direct influence of POLG on the pathogenesis of PD or linkage disequilibrium between POLG1 alleles and nearby, disease-influencing genetic variants remains unknown.
线粒体 DNA 聚合酶γ(POLG1)基因中的 CAG 重复次数与某些人群的帕金森病(PD)有关。我们对 191 名挪威 PD 患者和相同数量的对照组的 POLG1 的 CAG 重复序列进行了测序,发现我们人群中存在非 10 或 11 个 CAG 重复与 PD 之间的关联。虽然我们的结果具有统计学意义,但在进行多次测试校正后,这种趋势并未得到维持。我们还对包括我们自己的研究在内的所有已发表的研究进行了荟萃分析,结果表明 PD 与 POLG1 中的 CAG 重复次数有关。荟萃分析显示,非 10 个 CAG 重复所包含的罕见等位基因变异与 PD 显著相关(p=0.0017)。这是否反映了 POLG 对 PD 发病机制的直接影响,或者 POLG1 等位基因与附近影响疾病的遗传变异体之间的连锁不平衡,目前尚不清楚。