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Association of mitochondrial DNA content in peripheral blood leukocyte with hepatitis B virus‐related hepatocellular carcinoma in a Chinese Han population

机译:中国汉族人群外周血白细胞线粒体DNA含量与乙型肝炎病毒相关肝细胞癌的关系

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AbstractIncreasing epidemiological evidence has indicated that inherited variations of mtDNA content could affect the genetic susceptibility of many malignancies in a tumor-specific manner. However, the association between mtDNA content and hepatocellular carcinoma (HCC) remains undetermined. In this study, mtDNA content of peripheral blood leukocytes was determined using quantitative real-time PCR in a case–control study consisting of 274 HCC cases, 126 non-cancer patient controls with chronic liver diseases (CLD), and 258 healthy controls. We found that HCC cases had a significant lower mtDNA content than CLD controls (median [range]: 0.77 [0.17–2.30] vs 0.84 [0.32–3.37]; P = 0.012) and healthy controls (0.77 [0.17–2.30] vs 0.84 [0.35–3.44]; P = 0.035). There was no difference in mtDNA content between CLD and healthy controls (0.84 [0.32–3.37] vs 0.84 [0.35–3.44]; P = 0.261). We further assessed the association between mtDNA content and HCC and found that, compared to individuals with high mtDNA content, those with low mtDNA content had a significantly increased risk of HCC when health controls (adjusted odds ratio [aOR] = 1.64, 95% confidence interval [CI] = 1.06–2.55), CLD controls (aOR = 1.57, 95% CI = 1.10–2.25) or combined controls (aOR = 1.55, 95% CI = 1.12–2.14) were used as reference. In addition, stratified analyses showed that the significant association was only evident in younger individuals, male individuals, ever-smokers, and never-drinkers. Collectively, our findings provided the first epidemiological evidence that mtDNA content in peripheral blood leukocytes is significantly associated with HCC, which warrants further validation in prospective studies. (Cancer Sci 2011; 102: 1553–1558)
机译:摘要越来越多的流行病学证据表明,mtDNA含量的遗传变异可能以肿瘤特异性方式影响许多恶性肿瘤的遗传易感性。但是,mtDNA含量与肝细胞癌(HCC)之间的关联仍不确定。在这项研究中,在一项病例对照研究中,使用定量实时PCR测定外周血白细胞的mtDNA含量,该研究包括274例HCC病例,126例慢性肝病(CLD)非癌症患者对照和258例健康对照。我们发现HCC病例的mtDNA含量显着低于CLD对照(中位[范围]:0.77 [0.17-2.30] vs 0.84 [0.32-3.37]; P = 0.012)和健康对照(0.77 [0.17-2.30] vs 0.84) [0.35-3.44]; P = 0.035)。 CLD与健康对照组之间的mtDNA含量没有差异(0.84 [0.32-3.37] vs 0.84 [0.35-3.44]; P = 0.261)。我们进一步评估了mtDNA含量与HCC之间的关联,发现与高mtDNA含量的个体相比,低mtDNA含量的个体在健康控制时的HCC风险显着增加(校正比值比[aOR] = 1.64,95%的置信度)间隔[CI] = 1.06-2.55),CLD对照(aOR = 1.57,95%CI = 1.10–2.25)或组合对照(aOR = 1.55,95%CI = 1.12–2.14)作为参考。此外,分层分析表明,这种显着相关性仅在年轻个体,男性,常吸烟者和永不饮酒者中明显。总的来说,我们的发现提供了第一个流行病学证据,即外周血白细胞中mtDNA含量与HCC显着相关,因此有必要在前瞻性研究中进一步验证。 (Cancer Sci 2011; 102:1553–1558)

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