Effectiveness of pharmacogenomics on the response and remission of treatment-resistant depression: a meta-analysis of randomised controlled trials

被引:1
作者
Cheng, Yu [1 ]
Liu, Hongmei [1 ]
Yuan, Ruixue [1 ]
Yuan, Kai [1 ]
Yu, Shunying [1 ]
机构
[1] Shanghai Jiao Tong Univ, Sch Med, Shanghai Mental Hlth Ctr, Shanghai, Peoples R China
关键词
Depressive Disorder; Treatment-Resistant; Randomized Controlled Trials as Topic; Meta-Analysis as Topic; CYP2C19; GENOTYPES; MAJOR DEPRESSION; DISORDER; TESTS; IMPLEMENTATION; OUTCOMES; THERAPY; QUALITY; UTILITY; UPDATE;
D O I
10.1136/gpsych-2023-101050
中图分类号
R749 [精神病学];
学科分类号
100205 ;
摘要
Background Pharmacogenomics (PGx) is a promising tool to realise tailored drug therapy for depression. Aims To investigate the treatment efficacy of PGx for treatment-resistant depression (TRD) compared with treatment as usual.Methods A systematic search was conducted in PubMed, Embase, the Cochrane Library, Web of Science and PsycINFO to identify relevant studies published from inception to 15 April 2023. Two arm randomised controlled trials (RCTs) exploring the efficacy of PGx-guided versus unguided treatment for TRD were included. The risk of bias in the included studies was evaluated using the Cochrane risk of bias assessment tool. The overall quality of evidence was assessed using the Grading of Recommendations, Assessment, Development and Evaluation (GRADE) approach.Results Seven RCTs (n=3003) comparing PGx-guided (n=1492) and unguided (n=1511) groups were identified and analysed. PGx-guided treatment was superior to treatment as usual in response (relative risk (RR)=1.31; 95% confidence interval (95% CI): 1.15 to 1.49; p<0.001) and remission (RR=1.40; 95% CI: 1.09 to 1.80; p=0.009) improvements. Effect sizes for acceptability (RR=0.90; 95% CI: 0.80 to 1.02; p=0.100) and side effect burden (RR=0.58; 95% CI: 0.29 to 1.15; p=0.120) between the two groups were not statistically different. The overall quality of evidence was rated from 'very low' (25%) to 'low' (75%) based on the GRADE criteria.Conclusions PGx-guided treatment has shown a small overall effect in improving the response and remission rates for patients with TRD. However, these results should be interpreted cautiously because of the few included studies and the low quality of evidence. Further high quality clinical trials are warranted to confirm the findings.PROSPERO registration number CRD42022340182.
引用
收藏
页数:11
相关论文
共 63 条
  • [1] Asken MJ., 2007, Therapy, V45, P2317
  • [2] Atkins D, 2004, BMJ-BRIT MED J, V328, P1490
  • [3] Major Depression in the National Comorbidity Survey-Adolescent Supplement: Prevalence, Correlates, and Treatment
    Avenevoli, Shelli
    Swendsen, Joel
    He, Jian-Ping
    Burstein, Marcy
    Merikangas, Kathleen Ries
    [J]. JOURNAL OF THE AMERICAN ACADEMY OF CHILD AND ADOLESCENT PSYCHIATRY, 2015, 54 (01) : 37 - 44
  • [4] What's in a gold standard? In defence of randomised controlled trials
    Backmann, Marius
    [J]. MEDICINE HEALTH CARE AND PHILOSOPHY, 2017, 20 (04) : 513 - 523
  • [5] GRADE guidelines: 3. Rating the quality of evidence
    Balshem, Howard
    Helfand, Mark
    Schuenemann, Holger J.
    Oxman, Andrew D.
    Kunz, Regina
    Brozek, Jan
    Vist, Gunn E.
    Falck-Ytter, Yngve
    Meerpohl, Joerg
    Norris, Susan
    Guyatt, Gordon H.
    [J]. JOURNAL OF CLINICAL EPIDEMIOLOGY, 2011, 64 (04) : 401 - 406
  • [6] World Federation of Societies of Biological Psychiatry (WFSBP) Guidelines for Biological Treatment of Unipolar Depressive Disorders, Part 1: Update 2013 on the acute and continuation treatment of unipolar depressive disorders
    Bauer, Michael
    Pfennig, Andrea
    Severus, Emanuel
    Whybrow, Peter C.
    Angst, Jules
    Moeller, Hans-Juergen
    [J]. WORLD JOURNAL OF BIOLOGICAL PSYCHIATRY, 2013, 14 (05) : 334 - 385
  • [7] Examining the Use of Real-World Evidence in the Regulatory Process
    Beaulieu-Jones, Brett K.
    Finlayson, Samuel G.
    Yuan, William
    Altman, Russ B.
    Kohane, Isaac S.
    Prasad, Vinay
    Yu, Kun-Hsing
    [J]. CLINICAL PHARMACOLOGY & THERAPEUTICS, 2020, 107 (04) : 843 - 852
  • [8] Pharmacogenetic tests and depressive symptom remission: a meta-analysis of randomized controlled trials
    Bousman, Chad A.
    Arandjelovic, Katarina
    Mancuso, Serafino G.
    Eyre, Harris A.
    Dunlop, Boadie W.
    [J]. PHARMACOGENOMICS, 2019, 20 (01) : 37 - 47
  • [9] Improved efficacy with targeted pharmacogenetic-guided treatment of patients with depression and anxiety: A randomized clinical trial demonstrating clinical utility
    Bradley, Paul
    Shiekh, Michael
    Mehra, Vishaal
    Vrbicky, Keith
    Layle, Stacey
    Olson, Marilyn C.
    Maciel, Alejandra
    Cullors, Ali
    Garces, Jorge A.
    Lukowiak, Andrew A.
    [J]. JOURNAL OF PSYCHIATRIC RESEARCH, 2018, 96 : 100 - 107
  • [10] Switching to another SSRI or to venlafaxine with or without cognitive behavioral therapy for adolescents with SSRI-resistant depression - The TORDIA randomized controlled trial
    Brent, David
    Emslie, Graham
    Clarke, Greg
    Wagner, Karen Dineen
    Asarnow, Joan Rosenbaum
    Keller, Marty
    Vitiello, Benedetto
    Ritz, Louise
    Iyengar, Satish
    Abebe, Kaleab
    Birmaher, Boris
    Ryan, Neal
    Kennard, Betsy
    Hughes, Carroll
    DeBar, Lynn
    McCracken, James
    Strober, Michael
    Suddath, Robert
    Spirito, Anthony
    Leonard, Henrietta
    Melhem, Nadine
    Porta, Giovanna
    Onorato, Matthew
    Zelazny, Jamie
    [J]. JAMA-JOURNAL OF THE AMERICAN MEDICAL ASSOCIATION, 2008, 299 (08): : 901 - 913