Evidence map›Paper›PMID 20417059›Full record

Trial reportSchizophrenia research2010

Niacin sensitivity and the arachidonic acid pathway in schizophrenia.

Erik Messamore, William F Hoffman, Jeffrey K Yao

Registry-linked trialAbstract readClinical Trial
In one paragraph

Trial report in Schizophrenia research, 2010. The graph could read no effect estimate from its abstract, so it casts no vote on the map. It is linked to trial NCT06382532 (Biological Diagnostic Techniques for the Diagnosis of Depressive Disorders Malinger Based on the Niacin Skin Response Test), which is not on this map. Cited by 19 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
19citing papers in PubMed, 1 pooled it
1.4field-weighted citation impact, top 21% 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.

NCT06382532 unknown statusnot on this mapstarted 2024, after this paper: background citation

Biological Diagnostic Techniques for the Diagnosis of Depressive Disorders Malinger Based on the Niacin Skin Response Test (NSRT)

Typeobservational_patient_registrySponsorAir Force Military Medical University, ChinaRan2024 to 2026Enrolled410ConditionsDepressive Disorder, MalingeringArmsNiacin skin reaction test
3 · Its place in the literature

Who cites it

19 citing papers in PubMed, 1 synthesis or guideline pooled it, 39 citations in OpenAlex.

  1. Pooled it
  2. Trial
  3. Article
  4. Review
  5. Observational
  6. Article
  7. Article
  8. Adrenic acid: A promising biomarker and therapeutic target (Review).International journal of molecular medicine · 2025
    Review
  9. Review
  10. Article
  11. Article
  12. Article
  13. Review
  14. Article
  15. Article
  16. Article
  17. Article
  18. Review
  19. Article
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

3 authors at 2 institutions in 1 country.

Erik MessamoreBehavorial Health and Clinical Neurosciences Division, Portland VA Medical Center, Portland, OR 97239, USA. Erik.Messamore@va.gov
William F Hoffman
Jeffrey K Yao
Portland VA Medical Center · USUniversity of Pittsburgh · US

Funding

MEMBRANE DEFICITS AND OUTCOME IN SCHIZOPHRENIAR01MH058141 · NIMH · UNIVERSITY OF PITTSBURGH AT PITTSBURGH · PI YAO, JEFFREY K · 1999 to 2003
$979k
Niacin Sensitivity and Fatty Acids in SchizophreniaR03MH070434 · NIMH · OREGON HEALTH AND SCIENCE UNIVERSITY · PI MESSAMORE, ERIK · 2004 to 2005
$126k
NIMH NIH HHS R01 MH058141NIMH NIH HHS R01 MH58141NIMH NIH HHS R03 MH070434
6 · The paper itself

Abstract

objectiveSchizophrenia is associated with a blunted flush response to niacin. Since niacin-induced skin flushing is mediated by vasodilators derived from arachidonic acid (AA), we tested whether the blunted flush response to niacin is a marker of AA deficiency.

methodsEight concentrations of methylnicotinate were applied to the forearms of 20 adults with schizophrenia and 20 controls. Laser Doppler measurement of blood flow responses was used to derive values for niacin sensitivity (defined as the concentration eliciting half-maximal response, i.e., EC(50) value) and efficacy (defined as the maximal evoked blood flow response). RBC membrane fatty acids were analyzed by gas chromatography.

resultsNiacin sensitivity and efficacy were reduced in schizophrenia. In the control group, there was significant correlation between AA levels and niacin sensitivity as well as a trend toward correlation between AA levels and niacin efficacy. In contrast, neither sensitivity nor efficacy of niacin correlated with AA levels in schizophrenia. An expected correlation between the levels of AA and its elongation product (adrenic acid) was absent in schizophrenia. Adrenic acid levels correlated with niacin efficacy in schizophrenia.

conclusionsThe schizophrenia-associated niacin response abnormality involves both diminished sensitivity and reduced efficacy. The lack of expected correlation between levels of AA and adrenic acid suggests homeostatic imbalance within the n-6 polyunsaturated fatty acid (PUFA) pathway in schizophrenia. Though AA levels were unrelated to measures of niacin response in schizophrenia, the correlation between adrenic acid and niacin efficacy in schizophrenia suggests relevance of the n-6 PUFA pathway to the blunted niacin response.

Indexed as

AdultAnti-Inflammatory AgentsArachidonic AcidDose-Response Relationship, DrugErucic AcidsFatty Acids, Omega-6Fatty Acids, UnsaturatedFemaleFlushingHumansMaleMiddle AgedModels, BiologicalNiacinNicotinic AcidsRegression Analysisadrenic acidAnti-Inflammatory AgentsArachidonic AcidErucic AcidsFatty Acids, Omega-6Fatty Acids, Unsaturatedmethyl nicotinateNiacinNicotinic Acids

Identifiers

PMID20417059
PMCPMC2947210
OpenAlexW1970242636

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.