Purine metabolism is dysregulated in patients with major depressive disorder

被引:85
作者
Ali-Sisto, Toni [1 ]
Tolmunen, Tommi [1 ,2 ]
Toffol, Elena [3 ]
Viinamaki, Heimo [1 ,2 ]
Mantyselka, Pekka [5 ,6 ]
Valkonen-Korhonen, Minna [1 ,2 ]
Honkalampi, Kirsi [7 ]
Ruusunen, Anu [1 ,2 ]
Velagapudi, Vidya [3 ,4 ]
Lehto, Soili M. [1 ,2 ]
机构
[1] Univ Eastern Finland, Inst Clin Med, POB 1627, Kuopio 70211, Finland
[2] Kuopio Univ Hosp, Dept Psychiat, POB 100, Kys 70029, Finland
[3] Inst Mol Med, Metabol Unit, Helsinki, Finland
[4] Univ Helsinki, FIMM, POB 20, FI-00014 Helsinki, Finland
[5] Univ Eastern Finland, Primary Hlth Care Unit, POB 1627, Kuopio 70211, Finland
[6] Kuopio Univ Hosp, POB 1627, Kuopio 70211, Finland
[7] Univ Eastern Finland, Dept Educ & Psychol, POB 111, Joensuu 80101, Finland
关键词
Major depressive disorder; Metabolomics; Purine metabolism; Inosine; Guanosine; Xanthine; URIC-ACID LEVELS; CEREBROSPINAL-FLUID; XANTHINE-OXIDASE; ADENOSINE; INFLAMMATION; RECEPTORS; HYPOXANTHINE; ACTIVATION; SERTRALINE; INOSINE;
D O I
10.1016/j.psyneuen.2016.04.017
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Introduction: The purine cycle and altered purinergic signaling have been suggested to play a role in major depressive disorder (MDD). Nevertheless, data on this topic are scarce. Based on previous studies, we hypothesized that compared with non-depressed controls, MDD patients have distinct purine metabolite profiles. Methods: The samples comprised 99 MDD patients and 253 non-depressed controls, aged 20-71 years. Background data were collected with questionnaires. Fasting serum samples were analyzed using ultra performance liquid chromatography coupled to mass spectrometry (UPLC-MS) to determine seven purine cycle metabolites belonging to the purine cycle. We investigated the levels of these metabolites in three settings: (1) MDD patients vs. non-depressed controls and (2) remitted vs. non-remitted MDD patients, and also (3) within-group changes in metabolite levels during the follow-up period. Results: In logistic regression adjusted for age, gender, smoking, alcohol use, physical exercise, glycosylated hemoglobin, and high-density lipoprotein cholesterol, lower levels of inosine (OR 0.89, 95% CI 0.82-0.97) and guanosine (OR 0.32, 95% CI 0.17-0.59), and higher levels of xanthine (OR 2.21, 95% CI 1.30-3.75) were associated with MDD vs. the non-depressed group. Levels of several metabolites changed significantly during the follow-up period in the MDD group, but there were no differences between remitted and non-remitted groups. Conclusions: We observed altered purine metabolism in MDD patients compared with non-depressed controls. Furthermore, our observations suggest that circulating xanthine may accumulate in MDD patients. (C) 2016 Elsevier Ltd. All rights reserved.
引用
收藏
页码:25 / 32
页数:8
相关论文
共 38 条
  • [1] Abbracchio MP, 1995, MOL PHARMACOL, V48, P1038
  • [2] AGREN H, 1983, PSYCHIAT RES, V9, P179
  • [3] Babyak M., 2004, PSYCHOSOM MED
  • [4] AN INVENTORY FOR MEASURING DEPRESSION
    BECK, AT
    ERBAUGH, J
    WARD, CH
    MOCK, J
    MENDELSOHN, M
    [J]. ARCHIVES OF GENERAL PSYCHIATRY, 1961, 4 (06) : 561 - &
  • [5] Adenosine as a neuromodulator in neurological diseases
    Boison, Detlev
    [J]. CURRENT OPINION IN PHARMACOLOGY, 2008, 8 (01) : 2 - 7
  • [6] Adenosine as a modulator of brain activity
    Boison, Detlev
    [J]. DRUG NEWS & PERSPECTIVES, 2007, 20 (10) : 607 - 611
  • [7] Uric Acid as a CNS Antioxidant
    Bowman, Gene L.
    Shannon, Jackilen
    Frei, Balz
    Kaye, Jeffrey A.
    Quinn, Joseph F.
    [J]. JOURNAL OF ALZHEIMERS DISEASE, 2010, 19 (04) : 1331 - 1336
  • [8] Evaluation and interference study of hemoglobin A1c measured by turbidimetric inhibition immunoassay
    Chang, J
    Hoke, C
    Ettinger, B
    Penerian, G
    [J]. AMERICAN JOURNAL OF CLINICAL PATHOLOGY, 1998, 109 (03) : 274 - 278
  • [9] Clinical correlation of alteration of endogenous antioxidant-uric acid level in major depressive disorder
    Chaudhari K.
    Khanzode S.
    Dakhale G.
    Saoji A.
    Sarode S.
    [J]. Indian Journal of Clinical Biochemistry, 2010, 25 (1) : 77 - 81
  • [10] Neuroprotection by adenosine in the brain: From A1 receptor activation to A2A receptor blockade
    Cunha R.A.
    [J]. Purinergic Signalling, 2005, 1 (2) : 111 - 134