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Folate augmentation of treatment - evaluation for depression (FolATED): protocol of a randomised controlled trial.

Roberts SH, Bedson E, Hughes D, Lloyd K, Menkes DB, Moat S, Pirmohamed M, Slegg G, Thome J, Tranter R, Whitaker R, Wilkinson C, Russell I - BMC Psychiatry (2007)

Bottom Line: The majority of sufferers are treated in primary care and only half respond well to active treatment.Some of the blood taken will be used to measure homocysteine levels and for genetic analysis (with additional consent).Patients with B12 deficiency or folate deficiency will be given appropriate treatment and will be monitored in the 'comprehensive cohort study'.

View Article: PubMed Central - HTML - PubMed

Affiliation: North Wales Section of Psychological Medicine, Institute of Medical and Social Care Research (IMSCaR), Bangor University, Academic Unit, Wrexham Technology Park, Wrexham, LL13 7YP, UK. seren.roberts@new-tr.wales.nhs.uk

ABSTRACT

Background: Clinical depression is common, debilitating and treatable; one in four people experience it during their lives. The majority of sufferers are treated in primary care and only half respond well to active treatment. Evidence suggests that folate may be a useful adjunct to antidepressant treatment: 1) patients with depression often have a functional folate deficiency; 2) the severity of such deficiency, indicated by elevated homocysteine, correlates with depression severity, 3) low folate is associated with poor antidepressant response, and 4) folate is required for the synthesis of neurotransmitters implicated in the pathogenesis and treatment of depression.

Methods/design: The primary objective of this trial is to estimate the effect of folate augmentation in new or continuing treatment of depressive disorder in primary and secondary care. Secondary objectives are to evaluate the cost-effectiveness of folate augmentation of antidepressant treatment, investigate how the response to antidepressant treatment depends on genetic polymorphisms relevant to folate metabolism and antidepressant response, and explore whether baseline folate status can predict response to antidepressant treatment. Seven hundred and thirty patients will be recruited from North East Wales, North West Wales and Swansea. Patients with moderate to severe depression will be referred to the trial by their GP or Psychiatrist. If patients consent they will be assessed for eligibility and baseline measures will be undertaken. Blood samples will be taken to exclude patients with folate and B12 deficiency. Some of the blood taken will be used to measure homocysteine levels and for genetic analysis (with additional consent). Eligible participants will be randomised to receive 5 mg of folic acid or placebo. Patients with B12 deficiency or folate deficiency will be given appropriate treatment and will be monitored in the 'comprehensive cohort study'. Assessments will be at screening, randomisation and 3 subsequent follow-ups.

Discussion: If folic acid is shown to improve the efficacy of antidepressants, then it will provide a safe, simple and cheap way of improving the treatment of depression in primary and secondary care.

Trial registration: Current controlled trials ISRCTN37558856.

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Related in: MedlinePlus

Flow diagram of trial.
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Figure 1: Flow diagram of trial.

Mentions: This is a multi-centred double blind, placebo-controlled, randomised trial of folic acid augmentation of pragmatic antidepressant treatment of moderate-to-severe depression. The trial investigates the effect of folic acid augmentation on new and continuing antidepressant treatment over 3 months. Assessments will be at week -2 (baseline 1 – antidepressant initiation if required), week -1 (telephone contact for tolerability of antidepressant), week 0 (baseline 2 – randomisation to folate or placebo), and weeks 4, 12 and month 6 (outcome measures). Figure 1 shows the flow diagram of the trial.


Folate augmentation of treatment - evaluation for depression (FolATED): protocol of a randomised controlled trial.

Roberts SH, Bedson E, Hughes D, Lloyd K, Menkes DB, Moat S, Pirmohamed M, Slegg G, Thome J, Tranter R, Whitaker R, Wilkinson C, Russell I - BMC Psychiatry (2007)

Flow diagram of trial.
© Copyright Policy - open-access
Related In: Results  -  Collection

License
Show All Figures
getmorefigures.php?uid=PMC2238748&req=5

Figure 1: Flow diagram of trial.
Mentions: This is a multi-centred double blind, placebo-controlled, randomised trial of folic acid augmentation of pragmatic antidepressant treatment of moderate-to-severe depression. The trial investigates the effect of folic acid augmentation on new and continuing antidepressant treatment over 3 months. Assessments will be at week -2 (baseline 1 – antidepressant initiation if required), week -1 (telephone contact for tolerability of antidepressant), week 0 (baseline 2 – randomisation to folate or placebo), and weeks 4, 12 and month 6 (outcome measures). Figure 1 shows the flow diagram of the trial.

Bottom Line: The majority of sufferers are treated in primary care and only half respond well to active treatment.Some of the blood taken will be used to measure homocysteine levels and for genetic analysis (with additional consent).Patients with B12 deficiency or folate deficiency will be given appropriate treatment and will be monitored in the 'comprehensive cohort study'.

View Article: PubMed Central - HTML - PubMed

Affiliation: North Wales Section of Psychological Medicine, Institute of Medical and Social Care Research (IMSCaR), Bangor University, Academic Unit, Wrexham Technology Park, Wrexham, LL13 7YP, UK. seren.roberts@new-tr.wales.nhs.uk

ABSTRACT

Background: Clinical depression is common, debilitating and treatable; one in four people experience it during their lives. The majority of sufferers are treated in primary care and only half respond well to active treatment. Evidence suggests that folate may be a useful adjunct to antidepressant treatment: 1) patients with depression often have a functional folate deficiency; 2) the severity of such deficiency, indicated by elevated homocysteine, correlates with depression severity, 3) low folate is associated with poor antidepressant response, and 4) folate is required for the synthesis of neurotransmitters implicated in the pathogenesis and treatment of depression.

Methods/design: The primary objective of this trial is to estimate the effect of folate augmentation in new or continuing treatment of depressive disorder in primary and secondary care. Secondary objectives are to evaluate the cost-effectiveness of folate augmentation of antidepressant treatment, investigate how the response to antidepressant treatment depends on genetic polymorphisms relevant to folate metabolism and antidepressant response, and explore whether baseline folate status can predict response to antidepressant treatment. Seven hundred and thirty patients will be recruited from North East Wales, North West Wales and Swansea. Patients with moderate to severe depression will be referred to the trial by their GP or Psychiatrist. If patients consent they will be assessed for eligibility and baseline measures will be undertaken. Blood samples will be taken to exclude patients with folate and B12 deficiency. Some of the blood taken will be used to measure homocysteine levels and for genetic analysis (with additional consent). Eligible participants will be randomised to receive 5 mg of folic acid or placebo. Patients with B12 deficiency or folate deficiency will be given appropriate treatment and will be monitored in the 'comprehensive cohort study'. Assessments will be at screening, randomisation and 3 subsequent follow-ups.

Discussion: If folic acid is shown to improve the efficacy of antidepressants, then it will provide a safe, simple and cheap way of improving the treatment of depression in primary and secondary care.

Trial registration: Current controlled trials ISRCTN37558856.

Show MeSH
Related in: MedlinePlus