Drug Response-Related DNA Methylation Changes in Schizophrenia, Bipolar Disorder, and Major Depressive Disorder

被引:27
|
作者
Zhou, Jiaqi [1 ,2 ]
Li, Miao [1 ,2 ]
Wang, Xueying [1 ,2 ]
He, Yuwen [1 ,2 ]
Xia, Yan [1 ,2 ,3 ]
Sweeney, John A. [4 ]
Kopp, Richard F. [3 ]
Liu, Chunyu [1 ,2 ,3 ]
Chen, Chao [1 ,2 ,5 ]
机构
[1] Cent South Univ, Xiangya Hosp 2, Dept Psychiat, Ctr Med Genet, Changsha, Hunan, Peoples R China
[2] Cent South Univ, Xiangya Hosp 2, Dept Psychiat, Hunan Key Lab Med Genet,Sch Life Sci, Changsha, Hunan, Peoples R China
[3] SUNY Upstate Med Univ, Dept Psychiat, Syracuse, NY 13210 USA
[4] Univ Cincinnati, Dept Psychiat, Cincinnati, OH USA
[5] Cent South Univ, Hunan Key Lab Anim Models Human Dis, Changsha, Hunan, Peoples R China
基金
中国国家自然科学基金;
关键词
pharmacoepigenetic; DNA methylation; drug response; schizophrenia; bipolar disorder; major depressive disorder; STAR-ASTERISK-D; SEQUENCED TREATMENT ALTERNATIVES; TRANSPORTER GENE PROMOTER; GENOME-WIDE ASSOCIATION; NON-CPG METHYLATION; ANTIPSYCHOTIC TREATMENT; BRAIN; ANTIDEPRESSANT; EXPRESSION; DISEASE;
D O I
10.3389/fnins.2021.674273
中图分类号
Q189 [神经科学];
学科分类号
071006 ;
摘要
Pharmacotherapy is the most common treatment for schizophrenia (SCZ), bipolar disorder (BD), and major depressive disorder (MDD). Pharmacogenetic studies have achieved results with limited clinical utility. DNA methylation (DNAm), an epigenetic modification, has been proposed to be involved in both the pathology and drug treatment of these disorders. Emerging data indicates that DNAm could be used as a predictor of drug response for psychiatric disorders. In this study, we performed a systematic review to evaluate the reproducibility of published changes of drug response-related DNAm in SCZ, BD and MDD. A total of 37 publications were included. Since the studies involved patients of different treatment stages, we partitioned them into three groups based on their primary focuses: (1) medication-induced DNAm changes (n = 8); (2) the relationship between DNAm and clinical improvement (n = 24); and (3) comparison of DNAm status across different medications (n = 14). We found that only BDNF was consistent with the DNAm changes detected in four independent studies for MDD. It was positively correlated with clinical improvement in MDD. To develop better predictive DNAm factors for drug response, we also discussed future research strategies, including experimental, analytical procedures and statistical criteria. Our review shows promising possibilities for using BDNF DNAm as a predictor of antidepressant treatment response for MDD, while more pharmacoepigenetic studies are needed for treatments of various diseases. Future research should take advantage of a system-wide analysis with a strict and standard analytical procedure.
引用
收藏
页数:17
相关论文
共 50 条
  • [31] Genetic Susceptibility for Bipolar Disorder and Response to Antidepressants in Major Depressive Disorder
    Tansey, Katherine E.
    Guipponi, Michel
    Domenici, Enrico
    Lewis, Glyn
    Malafosse, Alain
    O'Donovan, Michael
    Wendland, Jens R.
    Lewis, Cathryn M.
    McGuffin, Peter
    Uher, Rudolf
    AMERICAN JOURNAL OF MEDICAL GENETICS PART B-NEUROPSYCHIATRIC GENETICS, 2014, 165 (01) : 77 - 83
  • [32] DNA methylation of Somatostatin in Aging and Major Depressive Disorder
    McKinney, Brandon
    Sibille, Etienne
    BIOLOGICAL PSYCHIATRY, 2014, 75 (09) : 321S - 322S
  • [33] Acute anxiety disorder, major depressive disorder, bipolar disorder and schizophrenia are related to different patterns of nigrostriatal and mesolimbic dopamine dysfunction
    Nikolaus, Susanne
    Mamlins, Eduards
    Hautzel, Hubertus
    Mueller, Hans-Wilhelm
    REVIEWS IN THE NEUROSCIENCES, 2019, 30 (04) : 381 - 426
  • [34] Shared reduction of oscillatory natural frequencies in bipolar disorder, major depressive disorder and schizophrenia
    Canali, P.
    Sarasso, S.
    Rosanova, M.
    Sferrazza-Papa, G.
    Smeraldi, E.
    Benedetti, F.
    EUROPEAN NEUROPSYCHOPHARMACOLOGY, 2015, 25 : S193 - S193
  • [35] Identifying plasma metabolic characteristics of major depressive disorder, bipolar disorder, and schizophrenia in adolescents
    Yin, Bangmin
    Cai, Yuping
    Teng, Teng
    Wang, Xiaolin
    Liu, Xueer
    Li, Xuemei
    Wang, Jie
    Wu, Hongyan
    He, Yuqian
    Ren, Fandong
    Kou, Tianzhang
    Zhu, Zheng-Jiang
    Zhou, Xinyu
    TRANSLATIONAL PSYCHIATRY, 2024, 14 (01)
  • [36] Common and Specific Functional Activity Features in Schizophrenia, Major Depressive Disorder, and Bipolar Disorder
    Yang, Yongfeng
    Liu, Shu
    Jiang, Xiaoyan
    Yu, Hongyan
    Ding, Shuang
    Lu, Yanli
    Li, Wenqiang
    Zhang, Hongxing
    Liu, Bing
    Cui, Yue
    Fan, Lingzhong
    Jiang, Tianzi
    Lv, Luxian
    FRONTIERS IN PSYCHIATRY, 2019, 10
  • [37] The role of tumour necrosis factor in the pathophysiology of major depressive disorder, bipolar disorder and schizophrenia
    Gibbons, A.
    INTERNATIONAL JOURNAL OF NEUROPSYCHOPHARMACOLOGY, 2012, 15 : 40 - 40
  • [38] Ionotropic glutamate receptor expression in the brain in schizophrenia bipolar disorder, and major depressive disorder
    Meador-Woodruff, JH
    Hogg, AJ
    Agrawal, S
    Smith, RE
    SCHIZOPHRENIA RESEARCH, 2001, 49 (1-2) : 54 - 54
  • [39] Comparison of depressive episodes in bipolar disorder and in major depressive disorder within bipolar disorder pedigrees
    Mitchell, Philip B.
    Frankland, Andrew
    Hadzi-Pavlovic, Dusan
    Roberts, Gloria
    Corry, Justine
    Wright, Adam
    Loo, Colleen K.
    Breakspear, Michael
    BRITISH JOURNAL OF PSYCHIATRY, 2011, 199 (04) : 303 - 309
  • [40] Striatal ionotropic glutamate receptor expression in schizophrenia, bipolar disorder, and major depressive disorder
    Meador-Woodruff, JH
    Hogg, AJ
    Smith, RE
    BRAIN RESEARCH BULLETIN, 2001, 55 (05) : 631 - 640