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Mitochondrial DNA Aberrations of Bone Marrow Cells from Patients with Aplastic Anemia

机译:再生障碍性贫血患者骨髓细胞线粒体DNA畸变

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摘要

This study was undertaken primarily to test the hypothesis that mitochondrial DNA (mtDNA) mutations may be associated with aplastic anemia. Complete mtDNA nucleotide sequence was analyzed in nine and eight bone marrow specimens from Korean patients with aplastic anemia and healthy individuals, respectively. We found a large number of polymorphisms as well as apparent new mutations in both patients and controls throughout the entire mtDNA genome; 12 mutations harbored amino acid changes in patients and none of the mutations in controls produced amino acid changes. There were heteroplasmic mutations and more nonsynonymous mtDNA changes observed in patients, so the mean number of mtDNA aberrations of bone marrow cells showed statistically significant difference overall between patients (mean=25.6) and controls (mean=12.8) (p=0.019). Our data may support an association of mtDNA aberrations with aplastic anemia.
机译:这项研究主要是为了检验线粒体DNA(mtDNA)突变可能与再生障碍性贫血有关的假设。分别从韩国再生障碍性贫血患者和健康个体的9个和8个骨髓标本中分析了完整的mtDNA核苷酸序列。我们在整个mtDNA基因组中的患者和对照中都发现了大量的多态性以及明显的新突变。患者中有12个突变具有氨基酸变化,而对照中的任何突变均未产生氨基酸变化。在患者中观察到异质性突变和更多的非同义mtDNA变化,因此骨髓细胞的mtDNA畸变平均数在患者(平均值= 25.6)和对照(平均值= 12.8)之间显示出统计学上的显着差异(p = 0.019)。我们的数据可能支持mtDNA异常与再生障碍性贫血的关联。

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