Is there Progress? An Overview of Selecting Biomarker Candidates for Major Depressive Disorder

被引:59
作者
Young, Juan Joseph [1 ,2 ,3 ]
Silber, Tim
Bruno, Davide [4 ]
Galatzer-Levy, Isaac Robert [5 ]
Pomara, Nunzio [1 ,5 ,6 ]
Marmar, Charles Raymond [5 ,6 ]
机构
[1] Nathan S Kline Inst Psychiat Res, Orangeburg, NY USA
[2] Case Western Reserve Univ, Cleveland, OH 44106 USA
[3] Metrohlth Med Ctr, Cleveland, OH USA
[4] Liverpool John Moores Univ, Liverpool L3 5UX, Merseyside, England
[5] NYU, Sch Med, New York, NY USA
[6] NYU, Cohen Vet Ctr, New York, NY USA
关键词
major depression; biomarker; multiplex; assay; diagnosis; trait; state; NERVE GROWTH-FACTOR; CORTISOL AWAKENING RESPONSE; INCREASED OXIDATIVE STRESS; NEUROTROPHIC FACTOR LEVELS; SERUM-LEVELS; THYROID AUTOIMMUNITY; CEREBROSPINAL-FLUID; DNA METHYLATION; HPA AXIS; SUBCLINICAL HYPOTHYROIDISM;
D O I
10.3389/fpsyt.2016.00072
中图分类号
R749 [精神病学];
学科分类号
100205 ;
摘要
Major depressive disorder (MDD) contributes to a significant worldwide disease burden, expected to be second only to heart disease by 2050. However, accurate diagnosis has been a historical weakness in clinical psychiatry. As a result, there is a demand for diagnostic modalities with greater objectivity that could improve on current psychiatric practice that relies mainly on self-reporting of symptoms and clinical interviews. Over the past two decades, literature on a growing number of putative biomarkers for MDD increasingly suggests that MDD patients have significantly different biological profiles compared to healthy controls. However, difficulty in elucidating their exact relationships within depression pathology renders individual markers inconsistent diagnostic tools. Consequently, further biomarker research could potentially improve our understanding of MDD pathophysiology as well as aid in interpreting response to treatment, narrow differential diagnoses, and help refine current MDD criteria. Representative of this, multiplex assays using multiple sources of biomarkers are reported to be more accurate options in comparison to individual markers that exhibit lower specificity and sensitivity, and are more prone to confounding factors. In the future, more sophisticated multiplex assays may hold promise for use in screening and diagnosing depression and determining clinical severity as an advance over relying solely on current subjective diagnostic criteria. A pervasive limitation in existing research is heterogeneity inherent in MDD studies, which impacts the validity of biomarker data. Additionally, small sample sizes of most studies limit statistical power. Yet, as the RDoC project evolves to decrease these limitations, and stronger studies with more generalizable data are developed, significant advances in the next decade are expected to yield important information in the development of MDD biomarkers for use in clinical settings.
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页数:15
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共 227 条
[1]   Mass spectrometry-based proteomics [J].
Aebersold, R ;
Mann, M .
NATURE, 2003, 422 (6928) :198-207
[2]   HPA axis dysfunction in unmedicated major depressive disorder and its normalization by pharmacotherapy correlates with alteration of neural activity in prefrontal cortex and limbic/paralimbic regions [J].
Aihara, Masako ;
Ida, Itsuro ;
Yuuki, Naoya ;
Oshima, Akihiko ;
Kurnano, Hiroshi ;
Takahashi, Keisuke ;
Fukuda, Masato ;
Oriuchi, Noboru ;
Endo, Keigo ;
Matsuda, Hiroshi ;
Mikuni, Masahiko .
PSYCHIATRY RESEARCH-NEUROIMAGING, 2007, 155 (03) :245-256
[3]   Stereological analysis of the hypothalamic hypocretin/orexin neurons in an animal model of depression [J].
Allard, JS ;
Tizabi, Y ;
Shaffery, JP ;
Trouth, CO ;
Manaye, K .
NEUROPEPTIDES, 2004, 38 (05) :311-315
[4]   Endocrine and inflammatory profiles in type 2 diabetic patients with and without major depressive disorder. [J].
Alvarez A. ;
Faccioli J. ;
Guinzbourg M. ;
Castex M.M. ;
Bayón C. ;
Masson W. ;
Bluro I. ;
Kozak A. ;
Sorroche P. ;
Capurro L. ;
Grosembacher L. ;
Proietti A. ;
Finkelsztein C. ;
Costa L. ;
Day P.F. ;
Cagide A. ;
Litwak L.E. ;
Golden S.H. .
BMC Research Notes, 6 (1) :61
[5]   Angiotensin-converting enzyme gene variants are associated with both cortisol secretion and late-life depression [J].
Ancelin, M-L ;
Carriere, I. ;
Scali, J. ;
Ritchie, K. ;
Chaudieu, I. ;
Ryan, J. .
TRANSLATIONAL PSYCHIATRY, 2013, 3 :e322-e322
[6]   Interaction between 5-HT1A and BDNF genotypes increases the risk of treatment-resistant depression [J].
Anttila, S. ;
Huuhka, K. ;
Huuhka, M. ;
Rontu, R. ;
Hurme, M. ;
Leinonen, E. ;
Lehtima, T. .
JOURNAL OF NEURAL TRANSMISSION, 2007, 114 (08) :1065-1068
[7]   C-reactive protein, depressive symptoms, and risk of diabetes: Results from the English Longitudinal Study of Ageing (ELSA) [J].
Au, Bonnie ;
Smith, Kimberley J. ;
Gariepy, Genevieve ;
Schmitz, Norbert .
JOURNAL OF PSYCHOSOMATIC RESEARCH, 2014, 77 (03) :180-186
[8]   The effect of chronic antidepressant treatment on serum brain-derived neurotrophic factor levels in depressed patients: a preliminary study [J].
Aydemir, O ;
Deveci, A ;
Taneli, F .
PROGRESS IN NEURO-PSYCHOPHARMACOLOGY & BIOLOGICAL PSYCHIATRY, 2005, 29 (02) :261-265
[9]   Impaired nerve growth factor homeostasis in patients with bipolar disorder [J].
Barbosa, Izabela Guimaraes ;
Huguet, Rodrigo Barreto ;
Neves, Fernando Silva ;
Reis, Helton Jose ;
Bauer, Moises Evandro ;
Janka, Zoltan ;
Palotas, Andras ;
Teixeira, Antonio Lucio .
WORLD JOURNAL OF BIOLOGICAL PSYCHIATRY, 2011, 12 (03) :228-232
[10]  
Belmaker RH, 2008, NEW ENGL J MED, V358, P55, DOI [10.1056/NEJMra073096, 10.1038/nrdp.2016.65]