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Association between mitochondrial DNA levels and depression: a systematic review and meta-analysis

BMC Psychiatry volume 23, Article number: 866 (2023) Cite this article

Abstract

Background

Mitochondrial dysfunction leading to disturbances in energy metabolism has emerged as one of the risk factors in the pathogenesis of depression. Numerous studies have identified alterations in the content of mitochondrial DNA (mtDNA) in peripheral blood and cerebrospinal fluid of individuals with depression. Researchers have sought to establish a clear association between mtDNA and depression. Consequently, we conducted a comprehensive meta-analysis to assess the existing evidence regarding the impact of mtDNA on depression.

Methods

This study conducted a thorough search of the following databases up to March 13, 2023: PubMed, Embase, the Cochrane Library, the Web of Science, Wanfang Database, SINOMED, the China Science and Technology Journal Database, and China National Knowledge Infrastructure. The meta-analysis was carried out using RevMan (version 5.4) and Stata (version 16.0) software. In addition, publication bias was assessed with funnel plots, Begg’s test and Egger’s test.

Results

Our analysis included data from 10 articles, including 12 studies for further examination. A total of 1400 participants were included in this study, comprising 709 (including 300 males and 409 females) patients with depression and 691 (including 303 males and 388 females) healthy controls. The average age of depressed patients was (42.98 ± 2.55) years, and the average age of healthy people was (41.71 ± 2.6) years. The scales used to assess outcomes are Hamilton-rating scale for Depression(4 articles), Montgomery-Asberg Depression Rating Scale(3 articles), and Mini-Internatioal Neuropsychiatric Interview (1 articles). The meta-analysis revealed significantly higher levels of mtDNA in circulating blood samples and skin fibroblasts of individuals with depression in comparison to healthy controls [standardized mean difference(SMD) = 0.42, 95% confidence intervals(CI): 0.16, 0.67].

Conclusions

Our study concludes that there is a significant (p < 0.05) increase in mtDNA levels in serum, plasma, and cerebrospinal fluid in individuals with depression. These findings suggest that mtDNA could serve as a potential biomarker for diagnosing depression.

Registration number

PROSPERO CRD42023414285.

Peer Review reports

Introduction

Depression is a heterogenous disorder characterized by symptoms spanning various domains of emotion and behavior, including but not limited to, changes in mood, memory impairment, anhedonia, insomnia, fatigue, reduced appetite and libido, and in severe instances, self-harm and suicide [1]. It poses a significant threat to both mental and physical well-being and stands as the primary cause of global disability [2]. Depression is pervasive and frequently recurrent, with a worldwide prevalence of 4.4% [3]. In China, the lifetime prevalence of depression stands at 6.8%, with major depression accounting for 3.4% [4]. However, the incidence of depression continues to rise annually due to mounting societal, lifestyle, and academic pressures. A substantial proportion of patients fail to achieve remission after undergoing treatment with a selective serotonin reuptake inhibitor, with only 25–27% achieving remission following subsequent antidepressant treatments, and as many as 40% becoming treatment-resistant [5]. An impediment to effective depression care is the inaccurate diagnosis of individuals affected by the condition [6]. Presently, the assessment of depression relies on medical history, clinical symptoms, and specific evaluation scales, with a dearth of objective biomarkers for diagnostic purposes [7]. Thus, the quest for biomarkers to facilitate accurate depression diagnosis is a pressing scientific challenge.

The biological mechanisms underpinning depression remain unknown. Research into depression has expanded beyond conventional hypotheses concerning monoaminergic neurotransmitters and inflammatory mechanisms. An increasing focus has shifted towards examining the interplay between mitochondrial energy metabolism and depression. Depressed individuals often exhibit modifications in inflammatory markers, mitochondrial membrane depolarization, oxidized mtDNA, and thus increased levels of both central and peripheral reactive oxygen species (ROS) [8]. Mitochondria serve as the cellular “energy factories” of cells, preserving cellular stability by modulating calcium homeostasis, contributing to ROS and regulating apoptosis. Nonetheless, malfunctioning mitochondria lead to increased production of mitochondrial ROS (mtROS) and the release of cell-free mtDNA release [9]. MtDNA, as the genetic material of mitochondria, plays a role in mediating mitochondrial energy metabolism by encoding vital proteins required for the assembly and operation of mitochondrial respiratory complexes [10]. The mtDNA copy number can serve as an indicator of mitochondrial function and the extent of mtDNA damage [11].

Given the mounting evidence implicating mitochondrial dysfunction as a prospective molecular factor in depression, we conducted a systematic review and meta-analysis to examine the available literature that investigated the association between mtDNA and depression. To our knowledge, this represents the first study to integrate global data in elucidating the connection between mtDNA and depression.

Methods

Study registration

This systematic review and meta-analysis adhered to the Preferred Reporting Items for Systematic Reviews and Meta-Analysis (PRISMA) guidelines [12]. The review protocol was registered with PROSPERO under the registration CRD42023414285.

Literature search strategy

We conducted a comprehensive search of four English electronic databases and four Chinese literature databases, spanning from their inception to March 13, 2023. The databases included PubMed, EMBASE, Cochrane Library, Web of Science, Wanfang Database, SINOMED, VIP Database, and CNKI. There were no language restrictions imposed in our search. Our search strategy employed the following keywords: (“mtDNA” OR “mitochondrial DNA”) AND (“depression” OR “depressive disorder”). To ensure comprehensive coverage, we also scrutinized the references of all the reviewed publications. Two independent reviewers (WL and YZ) were responsible for this process, and in the event of any disagreement, a third investigator (LZ) was consulted. Furthermore, we scrutinized the references of the papers included, full texts, and bibliographies of all potential articles, including relevant reviews and meta-analyses, in order to identify any additional eligible studies.

Inclusion and exclusion criteria

The inclusion criteria were established as follows: (a) the study involved individuals with depression; (b) cross-sectional, case–control or longitudinal study; (c) the studies reported mtDNA levels, including mean (M), standard deviation (SD), and sample size; (d) both individuals with depression (cases) and healthy participants (controls) were included in the studies; and (e) in cases where the same datasets were discovered during the search process, only the paper with more comprehensive findings was included in our meta-analysis.

Studies were excluded if they met any of the following criteria: (a) duplications; (b) absence of mtDNA measurement in humans; (c) absence of a healthy control group; (d) constituted case reports, review articles, systematic reviews, meta-analyses, commentaries, editorials, or meeting abstracts; or (e) were in vivo or in vitro studies.

Data extraction

We used NoteExpress software was used for literature management. Two reviewers (WL and YZ) independently extracted all data, and any disagreements were resolved through discussion, with the involvement of a third person (LZ) when necessary. We recorded pertinent study information, including the first author, publication year, participant characteristics, sample size, sample source, region, and mtDNA contents.

Quality assessment

Two authors (YC and SW) independently evaluated the risk of bias and methodological quality of the included studies using the Newcastle-Ottawa Scale (NOS), which is an evidence-based quality assessment tool designed for systematic reviews of prospective cohort studies [13]. This scale comprises eight items, and the maximum attainable score is 9 points. Studies scoring ≥ 6 points were deemed of high quality [14].

Statistical analysis

Cochrane Collaboration software (RevMan 5.4) and Stata (version 16.0) were used for all data analyses. Given the varied units of measurement for mtDNA concentrations (units/μL, copies/μL, C/μL, and some articles not specifying units) in the analyzed reports, the effect size was estimated using the Standardized Mean Difference (SMD). Heterogeneity among the studies was assessed using the I2 statistic. I2 values within the ranges of 0–25%, 26–50%, 51–75%, and 75–100% were categorized as indicating no, low, moderate, and substantial heterogeneity, respectively [15, 16]. Subgroup analyses were conducted to identify potential sources of heterogeneity, considering specimen type (plasma or non-plasma), detection method (quantitative reverse transcription polymerase chain reaction (qRT-PCR), quantitative polymerase chain reaction (qPCR), or real-time fluorescence polymerase chain reaction (rt-PCR)), and location (Asia, Europe, or North America). Sensitivity analyses were performed to ensure the reliability of the results. Furthermore, Egger’s test and Begg’s test were utilized to investigate publication bias. A z-score was employed to assess effect sizes, and a p-value of < 0.05 was considered statistically significant. All statistical tests were two-tailed, with a 95% CI, and the significance level was set at P < 0.05.

Results

Study selection

The search across the eight databases yielded a total of 1,104 articles for further assessment (11 from CNKI, 2 from Wanfang, 0 from VIP, 4 from SINOMED, 559 from PubMed, 320 from EMBASE, 203 from the Web of Science, and 5 from the Cochrane Library). After reviewing the articles, 65 were excluded due to duplications. Following the examination of titles and abstracts, 951 articles were excluded for various reasons. Ultimately, only ten studies [17,18,19,20,21,22,23,24,25,26] met our inclusion criteria after a thorough review of the full texts. The flow diagram is depicted in Fig. 1.

Fig. 1
figure 1

Flow diagram of study selection

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Study characteristics and quality assessment

Table 1 Characteristics of studies included in the present meta-analysis
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In total, we included 10 articles covering studies conducted from 1997 to 2023, reporting on 12 studies. These studies involved 709 individuals with depression (300 males and 409 females) and 691 healthy controls (303 males and 388 females). The average age of depressed patients was (42.98 ± 2.55) years, and the average age of healthy people was (41.71 ± 2.6) years. Four articles assessed for depression using the Hamilton-rating scale for Depression (HDRS). Three articles used the Montgomery-Asberg Depression Rating Scale (MADRS). One article used Mini-Internatioal Neuropsychiatric Interview (MINI). The other two articles did not report assessment scales. Most trials were conducted in Asia (2 in China, 1 in Japan, and 1 in Korea) and Europe (2 in Sweden, 1 in Ireland, 1 in Germany). Additionally, trials were carried out in North America (1 in the United States and 1 in Canada). The quantification of mtDNA levels was achieved using quantitative reverse transcription polymerase chain reaction (qRT-PCR), real-time fluorescence polymerase chain reaction (rt-PCR), or quantitative polymerase chain reaction (qPCR). Detailed characteristics of the included studies are presented in Table 1. For the quality evaluation of the included studies, we utilized the Newcastle-Ottawa Scale (NOS), as presented in Table 2. This assessment revealed that the quality of most articles was relatively high, with scores ranging from 5 to 7. Only one study, conducted by Kato T et al. [26], scored five due to a lack of provided information.

Table 2 Quality assessment of studies
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MtDNA levels in depression

A substantial variation in mtDNA levels was observed, favoring higher values in individuals with depression when compared to healthy controls. This difference was quantified by a SMD of 0.42 (95% CI: 0.16, 0.67) and an overall effect statistic of Z = 3.20 (P-value < 0.05). It is noteworthy that the heterogeneity was substantial (I2 = 77%). Please consult Fig. 2 for the comprehensive forest plot illustrating the outcomes of the overall meta-analysis.

Fig. 2
figure 2

Forest plot displaying the results of the meta-analysis, including all ten articles regarding mtDNA in depression, which comprises twelve comparisons

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Subgroup analysis

We conducted subgroup analyses based on specimen type (plasma or not plasma), detection method (qRT-PCR, qPCR, or rt-PCR), and geographical location (Asia, Europe, or North America). In terms of specimen type, a significant distinction between individuals with depression and healthy controls was evident in plasma specimens (SMD = 0.52, P-value < 0.05), whereas no such difference was observed in other sample types (Fig. 3A). When subgroup analysis was performed based on detection methods, a notable difference between patients with depression (SMD = 0.52, P-value < 0.05) and healthy individuals was observed when utilizing qRT-PCR (Fig. 3B). Moreover, in Europe (SMD = 0.48, P-value < 0.05) and North America (SMD = 0.69, P-value < 0.05), mtDNA levels were significantly higher in individuals with depression than in their healthy counterparts, with no statistically significant variation in Asia (Fig. 3C).

Fig. 3(A)
figure 3

Subgroup analysis categorized according to the specimen type

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Fig. 3(B)
figure 4

Subgroup analysis categorized according to the detection method

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Fig. 3(C)
figure 5

Subgroup analysis categorized according to the geographical location

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Publication bias analysis and sensitivity analysis

In our study, no evidence of publication bias was found based on the results of both Egger’s regression test (P-value = 0.518) and Begg’s continuity corrected test (P-value = 1.000). Additionally, there was no apparent asymmetry observed in the funnel plot (Fig. 4). To evaluate the stability of our results, we conducted a sensitivity analysis by systematically removing each study one by one. The results showed no significant impact on the overall findings, reinforcing the stability and reliability of our study outcomes.

Fig. 4
figure 6

Funnel plot illustrating the studies included in the meta-analysis pertaining to depression

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Discussion

Mitochondrial energy metabolism disorders are involved in depression

Depression poses a significant threat to the mental and physical well-being of individuals, making it one of the most pressing public health challenges worldwide. Alongside the typical clinical signs of depression, such as loss of pleasure and cognitive impairment, there are prominent somatic hypokinetic symptoms like fatigue, insomnia, and appetite loss [27]. Hypodynamic symptoms in depressed patients are closely linked to inadequate mitochondrial ATP production, leading some researchers to suggest that mitochondrial energy metabolism disorders are implicated in depression’s pathogenesis [28]. Mitochondria serve as the central hub for cellular energy metabolism and ROS generation, ensuring their normal function through continuous processes like biosynthesis, division, fusion, and autophagy. Mitochondrial dysfunction includes reduced ATP synthesis, respiratory chain malfunction, structural anomalies, and an excess of apoptosis [29]. Previous research has demonstrated that mitochondrial energy metabolism disruptions are common in both chronic stress animal models and depressed patients [30, 31]. In a study by Gardner et al. [32], examining muscle tissue from depressed patients, they observed a strong connection between low ATP levels and severe physical symptoms. In the hippocampus and gastrocnemius muscle of rats exposed to chronic unpredictable mild stress (CUMS), ATP content, Na/K-ATPase activity, respiratory chain complex I, III, and IV activities were all reduced, and mitochondrial ultrastructure was compromised [33]. The production of a large number of ROS through mitochondrial oxidative phosphorylation can lead to oxidative stress and subsequent mitochondrial dysfunction [34]. When Chen et al. [35] induced depression-like behavior in mice using lipopolysaccharide, they found that mitochondrial oxidative damage was associated with the development of depressive symptoms. In addition, Yuan et al. [33] found significantly more swollen mitochondria, disrupted cristae and broken mitochondrial membranes in hippocampus and gastrocnemius tissue of CUMS rats. Yuan et al. [33], in their study of CUMS rats, noted significantly more swollen mitochondria, disrupted cristae, and broken mitochondrial membranes in the hippocampus and gastrocnemius tissue. It is well-established that maintaining a normal mitochondrial membrane potential (MMP) is a prerequisite for ATP production through oxidative phosphorylation. MMP stability plays a crucial role in preserving normal cell function. Javani et al. [36] discovered a decrease in MMP in the prefrontal cortex of depressed rats, and this condition improved with mitochondrial transplantation. Li et al. [37] found that ginsenoside Rg1 reduced microglial activation and mitochondrial dysfunction, thereby alleviating depression-like behavior through the GAS5/EZH2/SOCS3/NRF2 axis. In conclusion, mitochondrial dysfunction plays a significant role in the pathogenesis of depression, offering new insights into the diagnosis and treatment of this condition.

MtDNA, mitochondrial energy metabolism disorder, and depression

In addition to the aforementioned factors, including ATP synthesis, oxygen-free radical generation, and changes in MMP, the examination of mitochondrial energy metabolism at the molecular level also includes alterations in mtDNA levels. Serving as the genetic material of mitochondria, mtDNA stands out as the most frequently measured biomarker for assessing mitochondrial dysfunction [38]. However, there is no univocal explanation for variations in mtDNA levels, as both decreases and increases may indicate mitochondrial dysfunction [39]. The number of copies of mtDNA (referred to as mtDNAcn) serves as an effective indicator of a cell’s capacity to produce ATP through mitochondrial oxidative phosphorylation [40]. Consequently, measuring mtDNA levels enables us to evaluate mitochondrial function indirectly. Research suggests that higher mtDNAcn may serve as a marker of poor mitochondrial health or mitochondrial allostatic load, which could potentially account for the observed relationship between higher mtDNAcn and depression [41]. On one hand, oxidative stress can lead to changes in mitochondrial membrane permeability, resulting in increased release of mtDNA [18]. On the other hand, in cases of mitochondrial stress and defective mitophagy, mtDNAs can be released from mitochondria, potentially causing inflammation [42]. Moreover, mitochondrial dysfunction may contribute to depression by promoting oxidative stress and inflammation [43]. A study focusing on cell-free mtDNA suggests that an elevated mtDNAcn may be associated with depression and suicide attempts [44]. Pioneering research by Cai et al. [45] revealed that major depressive disorder was linked to a higher amount of mtDNA in leukocytes from saliva samples and blood. They also discovered altered mitochondrial function in tissues with increased mtDNA [45]. Hence, mtDNA emerges as a promising biomarker for further exploration of its role in depression.

Discussion of meta-analysis results

Taking into consideration the information presented above, we aimed to provide a comprehensive evaluation to enhance our understanding of altered mtDNA content in depression. In our study, we concentrated on the association between mtDNA levels and depression by conducting a systematic review and meta-analysis of 12 eligible studies, including 709 depressive patients and 691 healthy controls. Among the depressed patients, there were 409 females and 303 males, with females exhibiting a higher risk of depression than males. Gonçalves [19] et al. did not find a significant correlation between ccf-mtDNA concentration and age (r = 0.081, p = 0.56), smoking (measured by number of pack/year; rho = -0.09, p = 0.49). Chung JK [21]et al. found that gender was not associated with mtDNAcn. He [25] et al. also did not find significant differences between age and leukocyte MtDNAcn. However, more high-quality studies are needed to explore whether tobacco, age, and sex have an impact on MtDNA levels in people with depression.

Our study indicated that depressed patients had higher levels of mtDNA compared to their healthy counterparts (SMD = 0.42, 95% CI: 0.16, 0.67). Nonetheless, it is worth noting that published literature has reported conflicting findings. Four studies [17, 19, 21, 23] observed higher mtDNA levels in individuals with depression compared to healthy controls, while eight [18, 20, 22, 23, 25, 26] studies found no significant difference between depressed patients and healthy controls. However, the overall results suggested that depressed patients had higher mtDNA levels than healthy individuals. We attribute these discrepancies to various factors such as differences in age range, detection methods, tissue types, and ethnicity, among others. Heterogeneity was evident in this meta-analysis. Therefore, we conducted subgroup analyses based on specimen type, detection method, and location, as the range of mtDNAcn can be influenced by different DNA isolation and extraction techniques [46]. Moreover, mtDNA is inherently heterogeneous impacted by various environmental and genetic contexts [47]. Furthermore, different tissues or organs within individuals may require varying amounts of mtDNAcn to maintain normal function, resulting in differences in mtDNAcn levels among tissues or organst [38]. Thus, further research is needed to determine the most appropriate sample type (plasma or other samples) and the best detection method for mtDNA assessment.

To assess potential obvious publication bias, we examined funnel plots, Begg’s test, and Egger’s test, all of which did not suggest any noticeable bias. Additionally, our sensitivity analysis reinforced the stability and reliability of our results. It is important to note that the majority of the studies included in our analysis were cross-sectional in design. Therefore, future research should consider initiating more longitudinal studies to evaluate mtDNA levels as a predictive biomarker for depression.

Strengths and limitations

To the best of our knowledge, this is the first systematic review and meta-analysis of mtDNA levels with a specific focus on depression. Our findings indicate a significant elevation in mtDNA levels in patients with depression when compared to healthy controls, shedding light on the link between mitochondrial dysfunction and depression. Nevertheless, there are certain limitations to consider. Firstly, our results may be affected by the presence of heterogeneity, a common occurrence in many meta-analyses. Secondly, variations in biomarker units and diverse methods of analyzing the same biomarkers could potentially influence the statistical conclusions drawn from this meta-analysis. Thirdly, our study did not explore all the variables affecting mtDNA levels, such as environmental factors and concurrent illnesses. Lastly, due to insufficient numerical information in some studies, we were unable to include them, potentially impacting the results.

Conclusion

In summary, our systematic review and meta-analysis reveal that mtDNA concentrations in circulating blood samples and skin fibroblasts are elevated in depressed patients compared to healthy controls. This suggests a potential association between higher mtDNA levels and depression. The use of mtDNA as a biomarker for early diagnosis and prognosis of depression and its treatment is a promising avenue. Nonetheless, further research involving high-quality, large-scale studies is necessary for a more in-depth analysis.

Data Availability

The original contributions presented in the study are included in the article, further inquiries can be directed to the corresponding authors.

References

  1. Tartt AN, Mariani MB, Hen R, Mann JJ, Boldrini M. Dysregulation of adult hippocampal neuroplasticity in major depression: pathogenesis and therapeutic implications. Mol Psychiatry. 2022;27(6):2689–99. https://doi.org/10.1038/s41380-022-01520-y

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  2. Friedrich MJ. Depression is the leading cause of disability around the World. JAMA. 2017;317(15):1517. https://doi.org/10.1001/jama.2017.3826

    Article  PubMed  Google Scholar 

  3. Marwaha S, Palmer E, Suppes T, Cons E, Young AH, Upthegrove R. Novel and emerging treatments for major depression. Lancet. 2023;401(10371):141–53. https://doi.org/10.1016/S0140-6736(22)02080-3. Epub 2022 Dec 16.

    Article  CAS  PubMed  Google Scholar 

  4. Huang Y, Wang Y, Wang H, et al. Prevalence of mental disorders in China: a cross-sectional epidemiological study. Lancet Psychiatry. 2019;6(3):211–24. https://doi.org/10.1016/S2215-0366(18)30511-X. Epub 2019 Feb 18. Erratum in: Lancet Psychiatry. 2019;6(4):e11.

    Article  PubMed  Google Scholar 

  5. Gabriel FC, Stein AT, de Melo DO, Fontes-Mota GCH, Dos Santos IB, Rodrigues CDS, Rodrigues MC, Fráguas R, Florez ID, Correia DT, Ribeiro E. Recommendations for the pharmacological treatment of treatment-resistant depression: A systematic review protocol. PLoS One. 2022;17(4):e0267323. https://doi.org/10.1371/journal.pone.0267323. Update in: PLoS One. 2023;18(2):e0281501.

  6. Lim GY, Tam WW, Lu Y, Ho CS, Zhang MW, Ho RC. Author Correction: Prevalence of Depression in the Community from 30 Countries between 1994 and 2014. Sci Rep. 2022;12(1):14856. https://doi.org/10.1038/s41598-022-19021-x. Erratum for: Sci Rep. 2018;8(1):2861.

  7. Li W, Li X, Li Y, Chen Y, Zhu L, Guo R. Diagnostic value of MicroRNAs for depression: a systematic review and meta-analysis. J Psychiatr Res. 2023;157:132–40. Epub 2022 Nov 27.

    Article  PubMed  Google Scholar 

  8. Visentin APV, Colombo R, Scotton E, Fracasso DS, da Rosa AR, Branco CS, Salvador M. Targeting inflammatory-mitochondrial response in Major Depression: current evidence and further challenges. Oxid Med Cell Longev. 2020;2020:2972968. https://doi.org/10.1155/2020/2972968

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  9. Tripathi A, Scaini G, Barichello T, Quevedo J, Pillai A. Mitophagy in depression: pathophysiology and treatment targets. Mitochondrion. 2021;61:1–10. Epub 2021 Aug 31.

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  10. Yan C, Duanmu X, Zeng L, Liu B, Song Z, Mitochondrial DNA. Distribution, mutations, and elimination. Cells. 2019;8(4):379. https://doi.org/10.3390/cells8040379

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  11. Ashar FN, Zhang Y, Longchamps RJ, Lane J, Moes A, Grove ML, Mychaleckyj JC, Taylor KD, Coresh J, Rotter JI, Boerwinkle E, Pankratz N, Guallar E, Arking DE. Association of mitochondrial DNA Copy Number with Cardiovascular Disease. JAMA Cardiol. 2017;2(11):1247–55. https://doi.org/10.1001/jamacardio.2017.3683

    Article  PubMed  PubMed Central  Google Scholar 

  12. Page MJ, McKenzie JE, Bossuyt PM, et al. The PRISMA 2020 statement: an updated guideline for reporting systematic reviews. BMJ. 2021;372:n71. https://doi.org/10.1136/bmj.n71

    Article  PubMed  PubMed Central  Google Scholar 

  13. Renaud-Charest O, Lui LMW, Eskander S, Ceban F, Ho R, Di Vincenzo JD, Rosenblat JD, Lee Y, Subramaniapillai M, McIntyre RS. Onset and frequency of depression in post-COVID-19 syndrome: a systematic review. J Psychiatr Res. 2021;144:129–37. Epub 2021 Sep 30.

    Article  PubMed  PubMed Central  Google Scholar 

  14. Thul TA, Corwin EJ, Carlson NS, Brennan PA, Young LJ. Oxytocin and postpartum depression: a systematic review. Psychoneuroendocrinology. 2020;120:104793. https://doi.org/10.1016/j.psyneuen.2020.104793. Epub 2020 Jul 6.

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  15. Higgins JP, Thompson SG, Deeks JJ, Altman DG. Measuring inconsistency in meta-analyses. BMJ. 2003;327(7414):557–60. https://doi.org/10.1136/bmj.327.7414.557

    Article  PubMed  PubMed Central  Google Scholar 

  16. Melamud MM, Buneva VN, Ermakov EA. Circulating cell-free DNA levels in Psychiatric Diseases: a systematic review and Meta-analysis. Int J Mol Sci. 2023;24(4):3402. https://doi.org/10.3390/ijms24043402

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  17. Ryan KM, Doody E, McLoughlin DM. Whole blood mitochondrial DNA copy number in depression and response to electroconvulsive therapy. Prog Neuropsychopharmacol Biol Psychiatry. 2023;121:110656. https://doi.org/10.1016/j.pnpbp.2022.110656. Epub 2022 Oct 7.

    Article  CAS  PubMed  Google Scholar 

  18. Ampo E, Mendes-Silva AP, Goncalves V, Bartley JM, Kuchel GA, Diniz BS. Increased levels of circulating cell-free mtDNA in the plasma of subjects with late-life Depression and Frailty: a preliminary study. Am J Geriatr Psychiatry. 2022;30(3):332–7. Epub 2021 Jul 29.

    Article  PubMed  Google Scholar 

  19. Gonçalves VF, Mendes-Silva AP, Koyama E, Vieira E, Kennedy JL, Diniz B. Increased levels of circulating cell-free mtDNA in plasma of late life depression subjects. J Psychiatr Res. 2021;139:25–9. Epub 2021 May 8.

    Article  PubMed  Google Scholar 

  20. Fernström J, Ohlsson L, Asp M, Lavant E, Holck A, Grudet C, Westrin Ã, Lindqvist D. Plasma circulating cell-free mitochondrial DNA in depressive disorders. PLoS ONE. 2021;16(11):e0259591. https://doi.org/10.1371/journal.pone.0259591

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  21. Chung JK, Lee SY, Park M, Joo EJ, Kim SA. Investigation of mitochondrial DNA copy number in patients with major depressive disorder. Psychiatry Res. 2019;282:112616. https://doi.org/10.1016/j.psychres.2019.112616. Epub 2019 Oct 14.

    Article  CAS  PubMed  Google Scholar 

  22. Kuffner K, Triebelhorn J, Meindl K, Benner C, Manook A, Sudria-Lopez D, Siebert R, Nothdurfter C, Baghai TC, Drexler K, Berneburg M, Rupprecht R, Milenkovic VM, Wetzel CH. Major Depressive Disorder Is Associated with impaired mitochondrial function in skin fibroblasts. Cells. 2020;9(4):884. https://doi.org/10.3390/cells9040884

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  23. Lindqvist D, Wolkowitz OM, Picard M, Ohlsson L, Bersani FS, Fernström J, Westrin Ã, Hough CM, Lin J, Reus VI, Epel ES, Mellon SH. Circulating cell-free mitochondrial DNA, but not leukocyte mitochondrial DNA copy number, is elevated in major depressive disorder. Neuropsychopharmacology. 2018;43(7):1557–64. https://doi.org/10.1038/s41386-017-0001-9. Epub 2018 Jan 30.

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  24. Chang CC, Jou SH, Lin TT, Lai TJ, Liu CS. Mitochondria DNA change and oxidative damage in clinically stable patients with major depressive disorder. PLoS ONE. 2015;10(5):e0125855. https://doi.org/10.1371/journal.pone.0125855

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  25. He Y, Tang J, Li Z, Li H, Liao Y, Tang Y, Tan L, Chen J, Xia K, Chen X. Leukocyte mitochondrial DNA copy number in blood is not associated with major depressive disorder in young adults. PLoS ONE. 2014;9(5):e96869. https://doi.org/10.1371/journal.pone.0096869

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  26. Kato T, Winokur G, McMahon FJ, DePaulo JR, Crowe RR. Quantitative analysis of leukocyte mitochondrial DNA deletion in affective disorders. Biol Psychiatry. 1997;42(5):311–6. https://doi.org/10.1016/S0006-3223(96)00377-0

    Article  CAS  PubMed  Google Scholar 

  27. Zhao D, Wu Z, Zhang H, Mellor D, Ding L, Wu H, Wu C, Huang J, Hong W, Peng D, Fang Y. Somatic symptoms vary in major depressive disorder in China. Compr Psychiatry. 2018;87:32–7. Epub 2018 Aug 28.

    Article  PubMed  Google Scholar 

  28. Caruso G, Benatti C, Blom JMC, Caraci F, Tascedda F. The many faces of mitochondrial dysfunction in Depression: from Pathology to Treatment. Front Pharmacol. 2019;10:995. https://doi.org/10.3389/fphar.2019.00995

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  29. Annesley SJ, Fisher PR. Mitochondria in Health and Disease. Cells. 2019;8(7):680. https://doi.org/10.3390/cells8070680

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  30. Zuccoli GS, Saia-Cereda VM, Nascimento JM, Martins-de-Souza D. The Energy Metabolism Dysfunction in Psychiatric disorders Postmortem brains: Focus on Proteomic evidence. Front Neurosci. 2017;11:493. https://doi.org/10.3389/fnins.2017.00493

    Article  PubMed  PubMed Central  Google Scholar 

  31. Lin S, Huang L, Luo ZC, Li X, Jin SY, Du ZJ, Wu DY, Xiong WC, Huang L, Luo ZY, Song YL, Wang Q, Liu XW, Ma RJ, Wang ML, Ren CR, Yang JM, Gao TM. The ATP level in the Medial Prefrontal Cortex regulates depressive-like Behavior via the Medial Prefrontal cortex-lateral habenula pathway. Biol Psychiatry. 2022;92(3):179–92. https://doi.org/10.1016/j.biopsych.2022.02.014. Epub 2022 Feb 22.

    Article  CAS  PubMed  Google Scholar 

  32. Gardner A, Boles RG. Mitochondrial energy depletion in depression with somatization. Psychother Psychosom. 2008;77(2):127–9. https://doi.org/10.1159/000112891. Epub 2008 Jan 25.

    Article  PubMed  Google Scholar 

  33. Yuan Q, Li Y, Deng X, Shi H, Zhao Z, Wang C, Feng X, Guo J, Guo R. Effects of Xingpi Kaiyu Fang on ATP, Na/K-ATPase, and respiratory chain complexes of Hippocampus and gastrocnemius muscle in depressed rats. Evid Based Complement Alternat Med. 2019;2019:6054926. https://doi.org/10.1155/2019/6054926

    Article  PubMed  PubMed Central  Google Scholar 

  34. Angelova PR, Abramov AY. Role of mitochondrial ROS in the brain: from physiology to neurodegeneration. FEBS Lett. 2018;592(5):692–702. https://doi.org/10.1002/1873-3468.12964. Epub 2018 Jan 18.

    Article  CAS  PubMed  Google Scholar 

  35. Chen WJ, Du JK, Hu X, Yu Q, Li DX, Wang CN, Zhu XY, Liu YJ. Protective effects of resveratrol on mitochondrial function in the hippocampus improves inflammation-induced depressive-like behavior. Physiol Behav. 2017;182:54–61. Epub 2017 Sep 28.

    Article  CAS  PubMed  Google Scholar 

  36. Javani G, Babri S, Farajdokht F, Ghaffari-Nasab A, Mohaddes G. Mitochondrial transplantation improves anxiety- and depression-like behaviors in aged stress-exposed rats. Mech Ageing Dev. 2022;202:111632. https://doi.org/10.1016/j.mad.2022.111632. Epub 2022 Jan 20.

    Article  CAS  PubMed  Google Scholar 

  37. Li J, Gao W, Zhao Z, Li Y, Yang L, Wei W, Ren F, Li Y, Yu Y, Duan W, Li J, Dai B, Guo R. Ginsenoside Rg1 reduced Microglial activation and mitochondrial dysfunction to Alleviate Depression-Like Behaviour Via the GAS5/EZH2/SOCS3/NRF2 Axis. Mol Neurobiol. 2022;59(5):2855–73. https://doi.org/10.1007/s12035-022-02740-7. Epub 2022 Mar 1.

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  38. McClintock CR, Mulholland N, Krasnodembskaya AD. Biomarkers of mitochondrial dysfunction in acute respiratory distress syndrome: a systematic review and meta-analysis. Front Med (Lausanne). 2022;9:1011819. https://doi.org/10.3389/fmed.2022.1011819

    Article  PubMed  Google Scholar 

  39. Picard M. Blood mitochondrial DNA copy number: what are we counting? Mitochondrion. 2021;60:1–11. https://doi.org/10.1016/j.mito.2021.06.010. Epub 2021 Jun 19.

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  40. St John JC. Mitochondrial DNA copy number and replication in reprogramming and differentiation. Semin Cell Dev Biol. 2016;52:93–101. https://doi.org/10.1016/j.semcdb.2016.01.028. Epub 2016 Jan 28.

    Article  CAS  PubMed  Google Scholar 

  41. Verhoeven JE, Révész D, Picard M, Epel EE, Wolkowitz OM, Matthews KA, Penninx BWJH, Puterman E. Depression, telomeres and mitochondrial DNA: between- and within-person associations from a 10-year longitudinal study. Mol Psychiatry. 2018;23(4):850–7. https://doi.org/10.1038/mp.2017.48. Epub 2017 Mar 28.

    Article  CAS  PubMed  Google Scholar 

  42. Picca A, Calvani R, Coelho-Junior HJ, Marzetti E. Cell death and inflammation: the role of Mitochondria in Health and Disease. Cells. 2021;10(3):537. https://doi.org/10.3390/cells10030537. PMID: 33802550; PMCID: PMC7998762.

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  43. Raison CL, Borisov AS, Majer M, Drake DF, Pagnoni G, Woolwine BJ, Vogt GJ, Massung B, Miller AH. Activation of central nervous system inflammatory pathways by interferon-alpha: relationship to monoamines and depression. Biol Psychiatry. 2009;65(4):296–303. Epub 2008 Sep 18.

    Article  CAS  PubMed  Google Scholar 

  44. Lindqvist D, Fernström J, Grudet C, Ljunggren L, Träskman-Bendz L, Ohlsson L, Westrin Ã. Increased plasma levels of circulating cell-free mitochondrial DNA in Suicide attempters: associations with HPA-axis hyperactivity. Transl Psychiatry. 2016;6(12):e971. https://doi.org/10.1038/tp.2016.236

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  45. Cai N, Chang S, Li Y, et al. Molecular signatures of major depression. Curr Biol. 2015;25(9):1146–56. https://doi.org/10.1016/j.cub.2015.03.008. Epub 2015 Apr 23.

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  46. Fazzini F, Schöpf B, Blatzer M, Coassin S, Hicks AA, Kronenberg F, Fendt L. Plasmid-normalized quantification of relative mitochondrial DNA copy number. Sci Rep. 2018;8(1):15347. https://doi.org/10.1038/s41598-018-33684-5

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  47. Pereira CV, Gitschlag BL, Patel MR. Cellular mechanisms of mtDNA heteroplasmy dynamics. Crit Rev Biochem Mol Biol. 2021;56(5):510–25. Epub 2021 Jun 13.

    Article  CAS  PubMed  Google Scholar 

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Acknowledgements

We thank Dr. Lingqun Zhu and Dr. Rongjuan Guo for providing professional guidance on an earlier draft of this manuscript and funding this study.

Funding

This work was supported by the National Natural Science Foundation of China (No.U21A20401).

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Authors and Affiliations

  1. Dongzhimen Hospital, Beijing University of Chinese Medicine, Beijing, 100700, China

    Wenhui Li, Yi Chen, Yudi Zhuo & Shurun Wan

  2. Key Laboratory of Chinese Internal Medicine of Ministry of Education and Beijing Key Laboratory of Dongzhimen Hospital, Beijing University of Chinese Medicine, Beijing, 100700, China

    Lingqun Zhu

  3. Dongfang Hospital, Beijing University of Chinese Medicine, Beijing, 100078, China

    Rongjuan Guo

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  1. Wenhui Li
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Contributions

WL: research design, conceptualization, writing (original draft). LZ: review and editing. YZ and YC: data management, data analysis. WL and SW: methodology, software application. RG: project administration and funding acquisition. All authors contributed to and have approved the final version of the manuscript.

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Correspondence to Lingqun Zhu or Rongjuan Guo.

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Li, W., Zhu, L., Chen, Y. et al. Association between mitochondrial DNA levels and depression: a systematic review and meta-analysis. BMC Psychiatry 23, 866 (2023). https://doi.org/10.1186/s12888-023-05358-8

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Keywords

BMC Psychiatry

ISSN: 1471-244X

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