Evidence map›Paper›PMID 25542737›Full record

ArticleBrain, behavior, and immunity2015

Total and differential white blood cell counts, high-sensitivity C-reactive protein, and cardiovascular risk in non-affective psychoses.

Brian J Miller, Prianka Kandhal, Mark Hyman Rapaport, Andrew Mellor, Peter Buckley

Registry-linked trialAbstract read
In one paragraph

Article in Brain, behavior, and immunity, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. It is linked to trial NCT02796859 (A Randomized Controlled Trial of Adjunctive Siltuximab in Schizophrenia), which is not on this map. Cited by 11 papers.

0numbers the graph read from it
0cells of the map it votes in
11citing papers in PubMed
–field-weighted citation impact
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.

NCT02796859 phase1 / phase2unknown statusnot on this mapstarted 2016, after this paper: background citation

A Randomized Controlled Trial of Adjunctive Siltuximab in Schizophrenia

TypeinterventionalSponsorBrian MillerRan2016 to 2023Enrolled30ConditionsSchizophrenia, Psychotic DisordersArmsSiltuximab, normal saline
3 · Its place in the literature

Who cites it

11 citing papers in PubMed.

  1. Review
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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

5 authors.

Brian J MillerDepartment of Psychiatry and Health Behavior, Georgia Regents University, Augusta, GA, United States. Electronic address: brmiller@gru.edu.
Prianka KandhalMedical College of Georgia, Georgia Regents University, Augusta, GA, United States.
Mark Hyman RapaportDepartment of Psychiatry and Behavioral Sciences, Emory University, Atlanta, GA, United States.
Andrew MellorCancer Immunology, Inflammation and Tolerance Program, Georgia Regents University, Augusta, GA, United States.
Peter BuckleyMedical College of Georgia, Georgia Regents University, Augusta, GA, United States.

Funding

A Potential State and Relapse Predictive Marker in SchizophreniaK23MH098014 · NIMH · AUGUSTA UNIVERSITY · PI MILLER, BRIAN JAMES · 2012 to 2016
$921k
NIMH NIH HHS K23 MH098014NIMH NIH HHS K23MH098014
6 · The paper itself

Abstract

Schizophrenia is associated with increased cardiovascular disease morbidity and mortality. Schizophrenia is also associated with immune and inflammatory abnormalities, including aberrant blood levels of lymphocytes, cytokines and high-sensitivity C-reactive protein (hsCRP). The purpose of this study is to investigate the relationship between total and differential white blood cell (WBC) counts, hsCRP, and indices of cardiovascular disease risk in patients with schizophrenia and related non-affective psychoses. 108 inpatients and outpatients age 18-70 with non-affective psychoses and 44 controls participated in this cross-sectional study. Subjects had a fasting blood draw between 8 and 9am for glucose, lipids, total and differential WBC counts, and hsCRP. Vital signs and medical history were obtained. Patients with non-affective psychosis had significantly higher hsCRP levels than controls (p=0.04). In linear regression analyses, lymphocyte and monocyte counts were a significant predictor of the total-to-HDL cholesterol ratio in subjects with non-affective psychosis (p⩽0.02 for each). In binary logistic regression analyses, total WBC count was a significant predictor of an elevated 10-year estimated risk of myocardial infarction and cardiovascular disease in subjects with non-affective psychosis (p⩽0.03 for each). Associations between total and differential WBC counts and cardiovascular disease risk indices were stronger in males than females with non-affective psychosis. Our findings provide further evidence that measurement of total and differential WBC counts may be germane to the clinical care of patients with schizophrenia and related disorders, and support an association between inflammation and cardiovascular disease risk in these patients.

Indexed as

AdolescentAdultAgedBlood GlucoseCardiovascular DiseasesCase-Control StudiesCholesterolCholesterol, HDLC-Reactive ProteinCross-Sectional StudiesFemaleHumansInflammationLeukocyte CountLinear ModelsLogistic ModelsBlood GlucoseCholesterolCholesterol, HDLC-Reactive ProteinCardiovascular diseaseC-reactive proteinInflammationLeukocytesLymphocytesMonocytesNeutrophilsNon-affective psychosisRisk assessmentSchizophrenia

Identifiers

PMID25542737
PMCPMC4286154

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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.