Evidence map›Paper›PMID 28289280›Full record

Trial reportMolecular psychiatry2018

Biochemical, physiological and clinical effects of l-methylfolate in schizophrenia: a randomized controlled trial.

J L Roffman, L J Petruzzi, A S Tanner, H E Brown, H Eryilmaz, N F Ho, M Giegold, N J Silverstein, T Bottiglieri, D S Manoach and 3 more

Registry-linked trialOpen access · greenAbstract readRandomized Controlled Trial
In one paragraph

Trial report in Molecular psychiatry, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. It is linked to trial NCT01091506 (A Placebo-Controlled Study of Physiologic Effects of L-methylfolate in Schizophrenia Patients), which is not on this map. Cited by 26 papers, 4 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
26citing papers in PubMed, 4 pooled it
5.3field-weighted citation impact, top 4% of its field
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

NCT01091506 nacompletednot on this map

A Placebo-Controlled Study of Physiologic Effects of L-methylfolate in Schizophrenia Patients

TypeinterventionalSponsorPamlab, Inc.Ran2010 to 2014Enrolled55ConditionsSchizophreniaArmsPlacebo, L-methylfolate
3 · Its place in the literature

Who cites it

26 citing papers in PubMed, 4 syntheses or guidelines pooled it, 67 citations in OpenAlex.

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  10. Epigenetic Control in Schizophrenia.Sub-cellular biochemistry · 2025
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4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

13 authors at 3 institutions in 1 country.

J L RoffmanDepartment of Psychiatry, Massachusetts General Hospital and Harvard Medical School, Boston, MA, USA.
L J PetruzziDepartment of Psychiatry, Massachusetts General Hospital and Harvard Medical School, Boston, MA, USA.
A S TannerDepartment of Psychiatry, Massachusetts General Hospital and Harvard Medical School, Boston, MA, USA.
H E BrownDepartment of Psychiatry, Massachusetts General Hospital and Harvard Medical School, Boston, MA, USA.
H EryilmazDepartment of Psychiatry, Massachusetts General Hospital and Harvard Medical School, Boston, MA, USA.
N F HoDepartment of Psychiatry, Massachusetts General Hospital and Harvard Medical School, Boston, MA, USA.
M GiegoldDepartment of Psychiatry, Massachusetts General Hospital and Harvard Medical School, Boston, MA, USA.
N J SilversteinDepartment of Psychiatry, Massachusetts General Hospital and Harvard Medical School, Boston, MA, USA.
T BottiglieriCenter of Metabolomics, Institute of Metabolic Disease, Baylor Research Institute, Dallas, TX, USA.
D S ManoachDepartment of Psychiatry, Massachusetts General Hospital and Harvard Medical School, Boston, MA, USA.
J W SmollerDepartment of Psychiatry, Massachusetts General Hospital and Harvard Medical School, Boston, MA, USA.
D C HendersonDepartment of Psychiatry, Massachusetts General Hospital and Harvard Medical School, Boston, MA, USA.
D C GoffDepartment of Psychiatry, New York University School of Medicine and Nathan Kline Institute, New York, NY, USA.
Massachusetts General Hospital · USHarvard University · USNew York University · US

Funding

MRI Studies of Folate-Related Genes, Diet, and Development: Promise for PsychosisR01MH101425 · NIMH · MASSACHUSETTS GENERAL HOSPITAL · PI ROFFMAN, JOSHUA LAWRENCE · 2013 to 2017
$2.8M
A Storage Area Network for Structural and Functional Image AnalysisS10RR023401 · NCRR · MASSACHUSETTS GENERAL HOSPITAL · PI FISCHL, BRUCE · 2009 to 2009
$2.0M
SILICON GRAPHICS PRISM EXTREME 128P/1TBS10RR023043 · NCRR · MASSACHUSETTS GENERAL HOSPITAL · PI SORENSEN, ALMA GREGORY · 2006 to 2006
$1.5M
Research and Mentoring on Integrating Psychiatric Genetics and NeuroscienceK24MH094614 · NIMH · MASSACHUSETTS GENERAL HOSPITAL · PI SMOLLER, JORDAN W · 2012 to 2016
$925k
NCRR NIH HHS S10 RR023043NCRR NIH HHS S10 RR023401NIMH NIH HHS K24 MH094614NIMH NIH HHS R01 MH101425
6 · The paper itself

Abstract

Folic acid supplementation confers modest benefit in schizophrenia, but its effectiveness is influenced by common genetic variants in the folate pathway that hinder conversion to its active form. We examined physiological and clinical effects of l-methylfolate, the fully reduced and bioactive form of folate, in schizophrenia. In this randomized, double-blind trial, outpatients with schizophrenia (n=55) received l-methylfolate 15 mg or placebo for 12 weeks. Patients were maintained on stable doses of antipsychotic medications. The pre-defined primary outcome was change in plasma methylfolate at 12 weeks. Secondary outcomes included change in symptoms (Positive and Negative Syndrome Scale (PANSS), Scale for Assessment of Negative Symptoms, Calgary Depression Scale for Schizophrenia), cognition (Measurement and Treatment Research to Improve Cognition in Schizophrenia composite) and three complementary magnetic resonance imaging measures (working memory-related activation, resting connectivity, cortical thickness). Primary, mixed model, intent-to-treat analyses covaried for six genetic variants in the folate pathway previously associated with symptom severity and/or response to folate supplementation. Analyses were repeated without covariates to evaluate dependence on genotype. Compared with placebo, l-methylfolate increased plasma methylfolate levels (d=1.00, P=0.0009) and improved PANSS Total (d=0.61, P=0.03) as well as PANSS Negative and General Psychopathology subscales. Although PANSS Total and General Psychopathology changes were influenced by genotype, significant PANSS Negative changes occurred regardless of genotype. No treatment differences were seen in other symptom rating scales or cognitive composite scores. Patients receiving l-methylfolate exhibited convergent changes in ventromedial prefrontal physiology, including increased task-induced deactivation, altered limbic connectivity and increased cortical thickness. In conclusion, l-methylfolate supplementation was associated with salutary physiological changes and selective symptomatic improvement in this study of schizophrenia patients, warranting larger clinical trials. ClinicalTrials.gov, NCT01091506.

Indexed as

AdultAntipsychotic AgentsCognitionDouble-Blind MethodFemaleFolic AcidHumansMaleMiddle AgedPsychiatric Status Rating ScalesSchizophreniaTetrahydrofolatesTreatment Outcome5-methyltetrahydrofolateAntipsychotic AgentsFolic AcidTetrahydrofolates

Identifiers

PMID28289280
PMCPMC5599314
OpenAlexW2600736754

What OpenQuestion holds

Textmetadata
LicenceTDM
Read underepoch 390

Registered trials

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.