Evidence map›Paper›PMID 25261882›Full record

Trial reportSchizophrenia research2014

A randomized placebo-controlled pilot study of pravastatin as an adjunctive therapy in schizophrenia patients: effect on inflammation, psychopathology, cognition and lipid metabolism.

Brenda Vincenzi, Shannon Stock, Christina P C Borba, Sarah M Cleary, Claire E Oppenheim, Liana J Petruzzi, Xiaoduo Fan, Paul M Copeland, Oliver Freudenreich, Corinne Cather and 1 more

Abstract readRandomized Controlled Trial
In one paragraph

Trial report in Schizophrenia research, 2014. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 34 papers, 6 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
34citing papers in PubMed, 6 pooled it
1.8field-weighted citation impact, top 17% 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.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

34 citing papers in PubMed, 6 syntheses or guidelines pooled it, 66 citations in OpenAlex.

  1. Pooled it
  2. Pooled it
  3. Pooled it
  4. Pravastatin for lowering lipids.The Cochrane database of systematic reviews · 2023 · on this map
    Pooled it
  5. Pooled it
  6. Pooled it
  7. Trial
  8. Trial
  9. Trial
  10. Trial
  11. Article
  12. Article
  13. Article
  14. Review
  15. Review
  16. Review
  17. Article
  18. Review
  19. Article
  20. Cytokine Imbalance as a Biomarker of Treatment-Resistant Schizophrenia.International journal of molecular sciences · 2022
    Review
4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

11 authors at 4 institutions in 1 country.

Brenda VincenziSchizophrenia Clinical and Research Program, Massachusetts General Hospital, 25 Staniford Street, Boston, MA 02114, United States. Electronic address: bvincenzi@partners.org.
Shannon StockDepartment of Mathematics and Computer Science, College of the Holy Cross, Worcester, MA, United States. Electronic address: sstock@holycross.edu.
Christina P C BorbaSchizophrenia Clinical and Research Program, Massachusetts General Hospital, Harvard Medical School, 25 Staniford Street, Boston, MA 02114, United States. Electronic address: cborba@partners.org.
Sarah M ClearySchizophrenia Clinical and Research Program, Massachusetts General Hospital, 25 Staniford Street, Boston, MA 02114, United States. Electronic address: sarah.m.cleary@gmail.com.
Claire E OppenheimSchizophrenia Clinical and Research Program, Massachusetts General Hospital, 25 Staniford Street, Boston, MA 02114, United States. Electronic address: coppenheim@partners.org.
Liana J PetruzziSchizophrenia Clinical and Research Program, Massachusetts General Hospital, 25 Staniford Street, Boston, MA 02114, United States. Electronic address: lpetruzzi@partners.org.
Xiaoduo FanUniversity of Massachusetts Medical School, UMass Memorial Medical Center, Worcester, MA, United States. Electronic address: xiaoduo.fan@umassmed.edu.
Paul M CopelandHarvard Medical School, Department of Medicine, Massachusetts General Hospital, Boston, MA, United States. Electronic address: pccopeland@partners.org.
Oliver FreudenreichSchizophrenia Clinical and Research Program, Massachusetts General Hospital, Harvard Medical School, 25 Staniford Street, Boston, MA 02114, United States. Electronic address: Freudenreich.Oliver@partners.org.
Corinne CatherSchizophrenia Clinical and Research Program, Massachusetts General Hospital, Harvard Medical School, 25 Staniford Street, Boston, MA 02114, United States. Electronic address: ccather@partners.org.
David C HendersonSchizophrenia Clinical and Research Program, Massachusetts General Hospital, Harvard Medical School, 25 Staniford Street, Boston, MA 02114, United States. Electronic address: dchenderson@partners.org.
Massachusetts General Hospital · USCollege of the Holy Cross · USHarvard University · USUniversity of Massachusetts Chan Medical School · US

Funding

Innovative Intervention Strategies for Metabolic Problems in SchizophreniaK23MH082098 · NIMH · UNIV OF MASSACHUSETTS MED SCH WORCESTER · PI FAN, XIAODUO · 2008 to 2012
$926k
Epidemiological and socio-cultural landscape of schizophrenia in rural EthiopiaK01MH100428 · NIMH · MASSACHUSETTS GENERAL HOSPITAL · PI BORBA, CHRISTINA PAULA CABRAL · 2014 to 2018
$903k
NIMH NIH HHS K01 MH100428NIMH NIH HHS K23 MH082098
6 · The paper itself

Abstract

objectiveThe aim of this study was to investigate the role of pravastatin, as an adjunctive therapy, on inflammatory markers, lipid and glucose metabolism, psychopathology, and cognition in subjects with schizophrenia and schizoaffective disorder.

methodsSchizophrenia or schizoaffective subjects (N=60) were randomized to receive either a 12-week supply of pravastatin 40 mg/day or placebo treatment. Anthropometric measures, lipids and glucose metabolism, inflammatory markers, psychopathology and cognitive performance were assessed at baseline, 6 weeks and 12 weeks.

resultsPravastatin use was associated with a significant decrease in total cholesterol, low density lipoprotein (LDL) cholesterol and LDL particle number levels, but was not associated with any significant changes in cognition or psychopathology in the participants, except a significant decrease in the Positive and Negative Syndrome Scale (PANSS) positive symptom score from baseline to week 6. However, this decrease failed to remain significant at 12 weeks. Interestingly, triglycerides, LDL-cholesterol, total cholesterol, LDL particle number, small LDL particle number, large very low density lipoprotein (VLDL) particle number and C-reactive protein (CRP) followed a similar pattern at 6 and 12 weeks as psychopathology.

conclusionsThese results suggest that a randomized trial with a larger sample size and a higher dosage of pravastatin would be helpful in further evaluating the anti-inflammatory properties of pravastatin, its association with improvements in cognitive symptoms, and its potential to reduce positive and negative symptoms associated with schizophrenia or schizoaffective disorders.

Indexed as

AdultAnticholesteremic AgentsCognition DisordersDrug SynergismFemaleHumansInflammationLipid MetabolismMaleMiddle AgedPilot ProjectsPravastatinPsychotic DisordersSchizophreniaTreatment OutcomeAnticholesteremic AgentsPravastatinCognitive functioningC-reactive proteinGlucose metabolismInflammationPsychosisStatins

Identifiers

PMID25261882
PMCPMC4311769
OpenAlexW2080339547

What OpenQuestion holds

Textmetadata
LicenceTDM
Read underepoch 390

Registered trials

None linked

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.