Adjunctive simvastatin for treatment-resistant depression: study protocol of a 12-week randomised controlled trial

被引:16
|
作者
Husain, Muhammad I. [1 ]
Chaudhry, Imran B. [2 ,3 ]
Khoso, Ameer B. [4 ]
Husain, Mohammad Omair [5 ]
Rahman, Raza R. [6 ]
Hamirani, Munir M. [7 ]
Hodsoll, John [8 ]
Carvalho, Andre F. [1 ]
Husain, Nusrat [2 ]
Young, Allan H. [9 ]
机构
[1] Ctr Addict & Mental Hlth, 100 Stokes St, Toronto, ON, Canada
[2] Univ Manchester, Psychiat, Manchester, Lancs, England
[3] Ziauddin Univ Karachi, Karachi, Pakistan
[4] Pakistan Inst Living & Learning, Karachi, Pakistan
[5] Univ Manchester, Manchester, Lancs, England
[6] Dow Univ Hlth Sci, Psychiat, Karachi, Pakistan
[7] Abbasi Shaheed Hosp, Psychiat, Karachi, Pakistan
[8] Kings Coll London, Inst Psychiat Psychol & Neurosci, London, England
[9] Kings Coll London, Inst Psychiat Psychol & Neurosci, Mood Disorders, London, England
来源
BJPSYCH OPEN | 2019年 / 5卷 / 01期
关键词
Depressive disorders; low and middle income countries; novel CNS drugs; randomized controlled trial; neuroimmunology; ENHANCE PHAGOCYTOSIS; BRAIN CHOLESTEROL; DOUBLE-BLIND; IN-VITRO; STATINS; METAANALYSIS; PLACEBO; DISORDER; ATORVASTATIN; MACROPHAGES;
D O I
10.1192/bjo.2018.84
中图分类号
R749 [精神病学];
学科分类号
100205 ;
摘要
Background A third of patients diagnosed with major depressive disorder (MDD) experience treatment-resistant depression (TRD). Relatively few pharmacological agents have established efficacy for TRD. Therefore, the evaluation of novel treatments for TRD is a pressing priority. Statins are pleiotropic agents and preclinical studies as well as preliminary clinical trials have suggested that these drugs may have antidepressant properties. Aims To report on a protocol for a 12-week, randomised, double-blind, placebo-controlled trial of add-on treatment with simvastatin for patients meeting DSM-5 criteria for MDD who have failed to respond to at least two adequate trials with approved antidepressants. The trial has been registered with Clinicaltrials.gov in (ClinicalTrials.gov identifier: NCT03435744). Method After screening and randomisation to the two parallel arms of the trial, 75 patients will receive simvastatin and 75 patients will receive placebo as adjuncts to treatment as usual. The primary outcome is change in Montgomery-Asberg Depression Rating Scale scores from baseline to week 12 and secondary outcomes include changes in scores on the 24-item Hamilton Rating Scale for Depression, the Clinical Global Impression scale, the 7-item Generalized Anxiety Disorder scale and change in body mass index from baseline to week 12. Assessments will take place at screening, baseline, and weeks 2, 4, 8 and 12. Checklists for adverse effects will be undertaken at each visit. Simvastatin (20 mg) will be given once daily. Other secondary outcomes include C-reactive protein and plasma lipids measured at baseline and week 12. Results This trial will assess simvastatin's efficacy and tolerability as an add-on treatment option for patients with TRD and provide insights into its putative mechanisms of action. Conclusions As the first trial investigating the use of simvastatin as an augmentation strategy in patients with TRD, if the results indicate that adjuvant simvastatin is efficacious in reducing depressive symptoms, it will deliver immediate clinical benefit.
引用
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页数:7
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