A Review of Biomarkers in Mood and Psychotic Disorders: A Dissection of Clinical vs. Preclinical Correlates

被引:73
作者
Brand, Sarel J. [1 ]
Moeller, Marisa [1 ]
Harvey, Brian H. [1 ,2 ]
机构
[1] North West Univ, Div Pharmacol, Sch Pharm, Potchefstroom, South Africa
[2] North West Univ, Ctr Excellence Pharmaceut Sci, Sch Pharm, Potchefstroom, South Africa
基金
英国医学研究理事会;
关键词
Antidepressant; biomarker panel; GABA-glutamate; genomics-proteomics; immune-inflammation-redox; kynureninecytokine; neurotransmitters; nitric oxide; schizophrenia; MAJOR DEPRESSIVE DISORDER; NEUROTROPHIC FACTOR LEVELS; NITRIC-OXIDE SYNTHASE; N-ACETYL-CYSTEINE; GROWTH-FACTOR-I; CHRONIC ANTIDEPRESSANT TREATMENT; BINDING PROTEIN CREB; CHRONIC MILD STRESS; GENETIC RAT MODEL; EARLY-LIFE STRESS;
D O I
10.2174/1570159X13666150307004545
中图分类号
Q189 [神经科学];
学科分类号
071006 [神经生物学];
摘要
Despite significant research efforts aimed at understanding the neurobiological underpinnings of mood (depression, bipolar disorder) and psychotic disorders, the diagnosis and evaluation of treatment of these disorders are still based solely on relatively subjective assessment of symptoms as well as psychometric evaluations. Therefore, biological markers aimed at improving the current classification of psychotic and mood-related disorders, and that will enable patients to be stratified on a biological basis into more homogeneous clinically distinct subgroups, are urgently needed. The attainment of this goal can be facilitated by identifying biomarkers that accurately reflect pathophysiologic processes in these disorders. This review postulates that the field of psychotic and mood disorder research has advanced sufficiently to develop biochemical hypotheses of the etiopathology of the particular illness and to target the same for more effective disease modifying therapy. This implies that a "one-size fits all" paradigm in the treatment of psychotic and mood disorders is not a viable approach, but that a customized regime based on individual biological abnormalities would pave the way forward to more effective treatment. In reviewing the clinical and preclinical literature, this paper discusses the most highly regarded pathophysiologic processes in mood and psychotic disorders, thereby providing a scaffold for the selection of suitable biomarkers for future studies in this field, to develope biomarker panels, as well as to improve diagnosis and to customize treatment regimens for better therapeutic outcomes.
引用
收藏
页码:324 / 368
页数:45
相关论文
共 555 条
[1]
Safety and Efficacy of Repeated-Dose Intravenous Ketamine for Treatment-Resistant Depression [J].
aan het Rot, Marije ;
Collins, Katherine A. ;
Murrough, James W. ;
Perez, Andrew M. ;
Reich, David L. ;
Charney, Dennis S. ;
Mathew, Sanjay J. .
BIOLOGICAL PSYCHIATRY, 2010, 67 (02) :139-145
[2]
Affective lability in patients with bipolar disorders is associated with high levels of childhood trauma [J].
Aas, Monica ;
Aminoff, Sofie R. ;
Lagerberg, Trine Vik ;
Etain, Bruno ;
Agartz, Ingrid ;
Andreassen, Ole A. ;
Melle, Ingrid .
PSYCHIATRY RESEARCH, 2014, 218 (1-2) :252-255
[3]
Abi-Dargham A, 1997, J NEUROPSYCH CLIN N, V9, P1
[4]
Predisposition locus for major depression at chromosome 12q22-12q23.2 [J].
Abkevich, V ;
Camp, NJ ;
Hensel, CH ;
Neff, CD ;
Russell, DL ;
Hughes, DC ;
Plenk, AM ;
Lowry, MR ;
Richards, RL ;
Carter, C ;
Frech, GC ;
Stone, S ;
Rowe, K ;
Chau, CA ;
Cortado, K ;
Hunt, A ;
Luce, K ;
O'Neil, G ;
Poarch, J ;
Potter, J ;
Poulsen, GH ;
Saxton, H ;
Bernat-Sestak, M ;
Thompson, V ;
Gutin, A ;
Skolnick, MH ;
Shattuck, D ;
Cannon-Albright, L .
AMERICAN JOURNAL OF HUMAN GENETICS, 2003, 73 (06) :1271-1281
[5]
Serotonin model of schizophrenia: emerging role of glutamate mechanisms [J].
Aghajanian, GK ;
Marek, GJ .
BRAIN RESEARCH REVIEWS, 2000, 31 (2-3) :302-312
[6]
Antidepressant-like effects of rosiglitazone, a PPARγ agonist, in the rat forced swim and mouse tail suspension tests [J].
Ahmed, Amany Ali Eissa ;
Al-Rasheed, Nawal Mohammed ;
Al-Rasheed, Nouf Mohammed .
BEHAVIOURAL PHARMACOLOGY, 2009, 20 (07) :635-642
[7]
Evidence for decreased DARPP-32 in the prefrontal cortex of patients with schizophrenia [J].
Albert, KA ;
Hemmings, HC ;
Adamo, AIB ;
Potkin, SG ;
Akbarian, S ;
Sandman, CA ;
Cotman, CW ;
Bunney, WE ;
Greengard, P .
ARCHIVES OF GENERAL PSYCHIATRY, 2002, 59 (08) :705-712
[8]
Pharmacologic mechanisms of serotonergic regulation of dopamine neurotransmission [J].
Alex, K. D. ;
Pehek, E. A. .
PHARMACOLOGY & THERAPEUTICS, 2007, 113 (02) :296-320
[9]
Allegri Graziella, 2003, Farmaco (Lausanne), V58, P829, DOI 10.1016/S0014-827X(03)00140-X
[10]
Systematic meta-analyses and field synopsis of genetic association studies in schizophrenia: the SzGene database [J].
Allen, Nicole C. ;
Bagade, Sachin ;
McQueen, Matthew B. ;
Ioannidis, John P. A. ;
Kavvoura, Fotini K. ;
Khoury, Muin J. ;
Tanzi, Rudolph E. ;
Bertram, Lars .
NATURE GENETICS, 2008, 40 (07) :827-834