He Ying, Tang Jinsong, Li Zongchang, Li Hong, Liao Yanhui, Tang Yanqing, Tan Liwen, Chen Jindong, Xia Kun, Chen Xiaogang
Institute of Mental Health, the Second Xiangya Hospital of Central South University, Changsha, Hunan, China.
Institute of Genomic Medicine, Wenzhou Medical University, Wenzhou, Zhejiang, China.
PLoS One. 2014 May 8;9(5):e96869. doi: 10.1371/journal.pone.0096869. eCollection 2014.
Major depressive disorder (MDD) is the leading cause of disability worldwide, and has significant genetic predisposition. Mitochondria may have a role in MDD and so mitochondrial DNA (mtDNA) has been suggested as a possible biomarker for this disease. We aimed to test whether the mtDNA copy number of peripheral blood leukocytes is related to MDD in young adults.
A case-control study was conducted with 210 MDD patients and 217 healthy controls (HC). The mtDNA copy number was measured by quantitative polymerase chain reaction (qPCR) method. Depression severity was assessed by the Hamilton-17 Depression Rating Scale (HDRS-17).
We found no significant differences in mtDNA copy number between MDD patients and HC, though the power analysis showed that our sample size has enough power to detect the difference. There were also no significant correlations between mtDNA copy number and the clinical characteristics (such as age, age of onset, episodes, Hamilton Depression Rating Scale (HDRS) score and Global Assessment of Function Scale (GAF) score) in MDD patients.
Our study suggests that leukocyte mtDNA copy number is unlikely to contribute to MDD, but it doesn't mean that we can exclude the possibility of involvement of mitochondria in the disease. Further studies are required to elucidate whether mtDNA can be a biomarker of MDD.
重度抑郁症(MDD)是全球致残的主要原因,且具有显著的遗传易感性。线粒体可能在MDD中发挥作用,因此线粒体DNA(mtDNA)被认为可能是该疾病的生物标志物。我们旨在测试年轻成年人外周血白细胞的mtDNA拷贝数是否与MDD相关。
进行了一项病例对照研究,纳入210例MDD患者和217名健康对照(HC)。通过定量聚合酶链反应(qPCR)方法测量mtDNA拷贝数。采用汉密尔顿17项抑郁量表(HDRS - 17)评估抑郁严重程度。
我们发现MDD患者与HC之间的mtDNA拷贝数无显著差异,尽管功效分析表明我们的样本量有足够的能力检测到差异。MDD患者的mtDNA拷贝数与临床特征(如年龄、发病年龄、发作次数、汉密尔顿抑郁量表(HDRS)评分和功能总体评定量表(GAF)评分)之间也无显著相关性。
我们的研究表明,白细胞mtDNA拷贝数不太可能导致MDD,但这并不意味着我们可以排除线粒体参与该疾病的可能性。需要进一步研究以阐明mtDNA是否可以作为MDD的生物标志物。