Xiaohua LIU, Kaida JIANG*

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Why is diagnosing MDD challenging?

Xiaohua LIU, Kaida JIANG*

depression; diagnosis; pathogenesis; phenotype; biomarker

Depression is one of the most common mental disorders and a leading cause of years of life lost due to disability and disease burden worldwide. The global burden of disease (GBD) study in 2010 ranked depression as the second leading cause of burden. Disability-adjusted life years (DALYs) calculated by adding years lived with a disability (YLDs) and years lost because of diseasespecificpremature death (YLLs) was used to quantify the global burden attributable to depressive disorders. The 2010 GBD presented that MDD was one of the leading causes of DALYs, accounting for 2.5% of global DALYs.Also, the burden of depression was higher in women than men, and the largest proportion of YLDs from depressive disorder occurred among adults of working age. Moreover, depressive disorder was confirmed as a leading direct cause of the global disease burden and MDD also contributed to the burden allocated to suicide and ischemic heart disease.[1,2]Yet depression is widely undiagnosed. The prevalence of depression was estimated to be only 3.02% in China, which was significantly lower than that in Afghanistan (22.5%) as well as the United States (4.45%).[3]One of the reasons for this inconsistent epidemiological data might be inaccurate assessment and diagnosis.

One of the findings from the fifth edition of the Diagnostic and Statistical Manual of Mental Disorders(DSM-5) fi eld trials was frustrating due to the very poor inter-rater reliability of clinicians when diagnosing major depressive disorder (MDD). The DSM-5 fi eld trials were performed by using a test-retest reliability design with a stratified sampling method across six adult and four pediatric sites in the United States and one adult site in Canada over a 7- to 10- month period. Diagnostic interviews according to DSM-5 criteria were conducted by 279 clinicians from various mental health disciplines who received special training. Overall, 2,246 patients with various diagnoses and levels of comorbidity were recruited, and interclass kappa coefficients were calculated. The standards for the reliability coefficients for DSM-5 categorical diagnoses were set as follows:intraclass kappa of 0.8 and above were “excellent”;from 0.60 to 0.79 were “very good”; from 0.40 to 0.59 were “good”; from 0.20 to 0.39 were “questionable”;and those below 0.20 were “unacceptable”.[4]The results showed that clinician agreement about the MDD diagnosis was in the questionable range (Kappa = 0.20-0.39), and the pooled intraclass Kappa was 0.28 (95%CI 0.20-0.35) at the adult fi eld trial sites and 0.28 (95%CI 0.15-0.41) at the pediatric fi eld trial sites, respectively.[5]

How is it that difficult to recognize MDD?

The most fundamental and challenging factor may be that depression is a highly heterogeneous disease and its real pathogenesis has not been clearly elucidated.Genome-wide association studies on depression have typically failed to identify the specific genetic variants involved[6], although depression has a well-established genetic loading.[7,8]Gene-environment interactions whereby a person inherits sensitivity to environmental factors could also play a key role in MDD.[9]Again,several plausible etiological hypotheses that might be helpful for understanding the pathophysiological and therapeutic mechanisms of MDD have been proposed.Undoubtedly, depression is a multifactorial disorder and knowledge about the underlying neurobiological mechanisms is still fragmentary.[10]

As well, depression is a complex disease with many various phenotypes. Depressive symptoms could occur due to or comorbid with substance use, other psychiatric diseases or other medical conditions. Most of all, depressive symptoms are the core presentations of both unipolar depression (that is major depressive disorder) and bipolar depression. In particular, a series of important articles from the National Institute of Mental Health Collaborative Depression Study have suggested that patients with bipolar disorder are depressed for a much longer period than hypomanic or manic throughout the course of the illness.[11-13]The symptoms of hypomania tend to be more difficult to recognize, partly because the patients often consider their manic symptoms to be normal and symptoms are highly variable.[14]Therefore, these factors may potentially contribute to misdiagnosing patients with unipolar depression when in fact they have bipolar disorder. Moreover, the DSM-5 expands the scope of MDD by adding some depressive subtypes (such as disruptive mood dysregulation disorder) and specif i ers(such as “with mixed features”, “with anxious distress”,“with melancholic features”, “with atypical features”,“with peripartum onset”, “with seasonal pattern”, etc.),which may further increase the difficulty of improving the inter-rater reliability of clinicians diagnosing MDD.[15]

Finally, this is partly because of a lack of patient advocates, the stigma surrounding the condition, and inadequate mental health resources.[10]

Altogether, diagnosing MDD is challenging. Further biomarker research is still needed and may potentially improve our understanding of pathophysiology as well as antidepressant mechanisms, narrow differential diagnoses, and help to refine current diagnostic criteria. For now, the promising biomarker candidates are mainly involved in the hypothalamic-pituitaryadrenal axis system, thyroid function and antoimmunity,cytokines and inf l ammatory response, oxidative stress,neurotrophins, genetics and epigenetics, proteomics,metabolomics, and multiplex-based assays.[17]Hopefully,more sophisticated and integrated biomarkers can be discovered and applied for screening and diagnosing depression in the future as an advance over relying solely on current subjective diagnostic criteria.

Funding

This study was supported by projects from Shanghai National Science Foundation (15ZR1435400).

Conflict of interest statement

All authors declare that they have no conflicts of interest.

Authors’ contribution

Xiaohua Liu was responsible for paper writing.

Kaida Jiang was responsible for paper proof i ng.

1. Ferrari AJ, Charlson FJ, Norman RE, Patten SB, Freedman G,Murray CJ, et al. Burden of depressive disorders by country,sex, age, and year: findings from the global burden of disease study 2010. PLoS Med. 2013; 10(11): e1001547. doi:http://dx.doi.org/10.1371/journal.pmed.1001547

2. Whiteford HA, Degenhardt L, Rehm J, Baxter AJ, Ferrari AJ, Erskine HE, et al. Global burden of disease attributable to mental and substance use disorders: findings from the Global Burden of Disease Study 2010. Lancet. 2013;382(9904): 1575-1586. doi: http://dx.doi.org/10.1016/S0140-6736(13)61611-6

中午，去美食街，充了兩百元的卡。一律熟悉的各色小吃，一路走過，如若故人重逢，簡直要落淚。徘徊了又徘徊，最后，要了一碗牛肚炒面，配一碗老鴨湯。妹妹給孩子們點了牛肉炒飯，她自己要了渣肉蒸飯配赤豆酒釀。老鴨湯火候掌握得好，湯汁清澈，碧灣灣的。江南人永遠那么精致——把鴨湯燒滾，下一塊豆腐皮，下一點粉絲，最后再另給一袋小米鍋巴，反復叮嚀：不要一起放進去啊，要隨放隨吃。我點點頭，都離開了，老板娘還不忘添一句：一塊塊地泡著吃啊。端一碗老鴨湯慢慢走，旁邊的餐桌旁，有人正饕餮涼拌面，比粉絲還要細的面，春風拂面的樣子，亮汪汪的，被人麻利地嘬著，一半在嘴里，一半拖在碗里——人間至樂圖，莫非如此。

3. Smith K. Mental health: a world of depression. Nature. 2014;515(7526): 181

4. Clarke DE, Narrow WE, Regier DA, Kuramoto SJ, Kupfer DJ, Kuhl EA, et al. DSM-5 field trials in the United States and Canada, Part I: study design, sampling strategy,implementation, and analytic approaches. Am J Psychiatry.2013; 170(1): 43-58. doi: http://dx.doi.org/10.1176/appi.ajp.2012.12070998

5. Regier DA, Narrow WE, Clarke DE, Kraemer HC, Kuramoto SJ, Kuhl EA, et al. DSM-5 fi eld trials in the United States and Canada, Part II: test-retest reliability of selected categorical diagnoses. Am J Psychiatry. 2013; 170(1): 59-70. doi: http://dx.doi.org/10.1176/appi.ajp.2012.12070999

6. Major Depressive Disorder Working Group of the Psychiatric GWAS Consortium, Ripke S, Wray NR, Lewis CM, Hamilton SP, Weissman MM, Breen G, et al. A mega-analysis of genome-wide association studies for major depressive disorder. Mol Psychiatry. 2013; 18(4): 497-511. doi: http://dx.doi.org/10.1038/mp.2012.21

7. Sullivan PF, Neale MC, Kendler KS. Genetic epidemiology of major depression: review and meta-analysis. Am J Psychiatry. 2000; 157(10): 1552-1562. doi: http://dx.doi.org/10.1176/appi.ajp.157.10.1552

8. Levinson DF. The genetics of depression: a review.Biol Psychiatry. 2006; 60(2): 84-92. doi: http://dx.doi.org/10.1016/j.biopsych.2005.08.024

9. Uher R. Gene-environment interactions in common mental disorders: an update and strategy for a genome-wide search.Soc Psychiatry Psychiatr Epidemiol. 2014; 49(1): 3-14. doi:http://dx.doi.org/10.1007/s00127-013-0801-0

10. Hou Z, Jiang W, Yin Y, Zhang Z, Yuan Y. The current situation on major depressive disorder in China: Research on mechanisms and clinical practice. Neurosci Bull. 2016; 32(4):389-397. doi: http://dx.doi.org/10.1007/s12264-016-0037-6

11. Judd LL, Akiskal HS, Schettler PJ, Endicott J, Maser J,Solomon DA, et al. The long-term natural history of the weekly symptomatic status of bipolar I disorder. Arch Gen Psychiatry. 2002; 59(6): 530-537

12. Judd LL, Akiskal HS, Schettler PJ, Coryell W, Endicott J, Maser JD, et al. A prospective investigation of the natural history of the long-term weekly symptomatic status of bipolar II disorder. Arch Gen Psychiatry. 2003; 60(3): 261-269

13. Judd LL, Akiskal HS, Schettler PJ, Coryell W, Maser J, Rice JA, et al. The comparative clinical phenotype and long term longitudinal episode course of bipolar I and II: a clinical spectrum or distinct disorders? J Affect Disord. 2003;73(1-2): 19-32. doi: http://dx.doi.org/10.1016/S0165-0327(02)00324-5

14. Hirschfeld RM. Bipolar depression: the real challenge. Eur Neuropsychopharmacol. 2004; 14(Suppl 2): S83-S88. doi:http://dx.doi.org/10.1016/j.euroneuro.2004.03.001

15. Liu X, Jiang K. Should major depressive disorder with mixed features be classified as a bipolar disorder? Shanghai Arch Psychiatry. 2014; 26(5): 294-296. doi: http://dx.doi.org/10.11919/j.issn.1002-0829.214146

16. Uher R, Payne JL, Pavlova B, Perlis RH. Major depressive disorder in DSM-5: implications for clinical practice and research of changes from DSM-IV. Depress Anxiety. 2014;31(6): 459-471. doi: http://dx.doi.org/10.1002/da.22217

17. Young JJ, Silber T, Bruno D, Galatzer-Levy IR, Pomara N,Marmar CR. Is there progress? An overview of selecting biomarker candidates for major depressive disorder. Front Psychiatry. 2016; 7: 72. doi: http://dx.doi.org/10.3389/fpsyt.2016.00072

Dr. Xiaohua Liu graduated and obtained a doctoral degree in Psychiatry and Mental Health from the Shanghai Medical College at Fudan University in 2006. She has been working at the Shanghai Mental Health Center, Shanghai Jiao Tong University School of Medicine since 2006. As a visiting scholar, Dr. Liu studied in the department of Psychiatry at the University of California, San Diego from 2012 to 2014. Now she is working as an attending doctor in the Mood Disorders Unit at the Shanghai Mental Health Center, Shanghai Jiao Tong University School of Medicine. Her research interests include the genetics of psychiatric disorders, especially mood disorders.

為什么診斷抑郁癥是一個挑戰(zhàn)？

劉曉華，江開達

抑郁癥、診斷、發(fā)病機制、表型、生物標志物

Depression is highly prevalent and one of the major contributors to disability worldwide.However, one of the findings from the DSM-5 fi eld trials was that inter-rater reliability for diagnosing major depressive disorder was very poor. Why is diagnosing MDD so challenging? This article attempts to explain why undefined pathogenesis and complicated phenotypes complicate the diagnosis of MDD. However,further biomarker and translational research is still necessary to help clinicians screen and diagnose depression in the future rather than relying solely on current subjective diagnostic criteria.

[Shanghai Arch Psychiatry. 2016; 28(6): 343-345.

http://dx.doi.org/10.11919/j.issn.1002-0829.216073]

Division of Mood Disorders, Department of Psychiatry, Shanghai Mental Health Center, Shanghai Jiao Tong University School of Medicine, Shanghai, PR China

*correspondence: Professor Kaida Jiang. Mailing address: 600 South Wanping RD, Xuhui District, Shanghai, China. Postcode: 200030. E-Mail:

jiangkaida163@163.com

概述：抑郁癥非常普遍，也是全球范圍導致殘疾的主要原因之一。然而，DSM-5現(xiàn)場測試發(fā)現(xiàn)診斷抑郁癥（major depressive disorder, MDD）的評估者間信度是很差的。為什么診斷MDD如此具有挑戰(zhàn)性？本文嘗試闡明為什么抑郁癥發(fā)病機制的不確定性和表現(xiàn)形式的復雜性會使診斷變得困難。然而，將來仍然需要其他的生物標志物和轉(zhuǎn)化醫(yī)學研究來幫助臨床醫(yī)生篩選和診斷抑郁癥，而不是單純依靠目前的主觀性診斷標準。