Plasma circulating cell-free mitochondrial DNA in depressive disorders

被引:27
作者
Fernstrom, Johan [1 ,2 ]
Ohlsson, Lars [3 ]
Asp, Marie [1 ,2 ]
Lavant, Eva [3 ]
Holck, Amanda [1 ,2 ]
Grudet, Cecile [1 ]
Westrin, Asa [1 ,4 ]
Lindqvist, Daniel [1 ,4 ]
机构
[1] Lund Univ, Fac Med, Dept Clin Sci Lund, Psychiat, Lund, Sweden
[2] Off Psychiat & Habilitat, Psychiat Clin Lund, Region Skane, Sweden
[3] Malmo Univ, Dept Biomed Sci, Hlth & Soc, Malmo, Sweden
[4] Off Psychiat & Habilitat, Psychiat Res Skane, Region Skane, Sweden
来源
PLOS ONE | 2021年 / 16卷 / 11期
关键词
LAMOTRIGINE; LITHIUM; RESPONSES; TRAUMA; DAMPS; ACID;
D O I
10.1371/journal.pone.0259591
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
07 ; 0710 ; 09 ;
摘要
Background Plasma circulating cell-free mitochondrial DNA (ccf-mtDNA) is an immunogenic molecule and a novel biomarker of psychiatric disorders. Some previous studies reported increased levels of ccf-mtDNA in unmedicated depression and recent suicide attempters, while other studies found unchanged or decreased ccf-mtDNA levels in depression. Inconsistent findings across studies may be explained by small sample sizes and between-study variations in somatic and psychiatric co-morbidity or medication status. Methods We measured plasma ccf-mtDNA in a cohort of 281 patients with depressive disorders and 49 healthy controls. Ninety-three percent of all patients were treated with one or several psychotropic medications. Thirty-six percent had a personality disorder, 13% bipolar disorder. All analyses involving ccf-mtDNA were a priori adjusted for age and sex. Results Mean levels in ccf-mtDNA were significantly different between patients with a current depressive episode (n = 236), remitted depressive episode (n = 45) and healthy controls (n = 49) (f = 8.3, p<0.001). Post-hoc tests revealed that both patients with current (p<0.001) and remitted (p = 0.002) depression had lower ccf-mtDNA compared to controls. Within the depressed group there was a positive correlation between ccf-mtDNA and "inflammatory depression symptoms" (r = 0.15, p = 0.02). We also found that treatment with mood stabilizers lamotrigine, valproic acid or lithium was associated with lower ccf-mtDNA (f = 8.1, p = 0.005). Discussion Decreased plasma ccf-mtDNA in difficult-to-treat depression may be partly explained by concurrent psychotropic medications and co-morbidity. Our findings suggest that ccf-mtDNA may be differentially regulated in different subtypes of depression, and this hypothesis should be pursued in future studies.
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页数:12
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