Evidence map›Paper›PMID 38222994›Full record

ArticleCureus2024

Neutrophil-Lymphocyte Ratio in Patients With Acute Schizophrenia.

Shutaro Sugita, Hiroi Tomioka, Kensuke Mera, Taro Tazaki, Hana Nishiyama, Hiroki Yamada, Kenji Sanada, Atsuko Inamoto, Akira Iwanami

Abstract read
In one paragraph

Article in Cureus, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 6 papers.

0numbers the graph read from it
0cells of the map it votes in
6citing 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

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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

6 citing papers in PubMed.

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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

9 authors.

Shutaro SugitaDepartment of Psychiatry, Showa University School of Medicine, Tokyo, JPN.
Hiroi TomiokaMental Care Center, Showa University Northern Yokohama Hospital, Kanagawa, JPN.
Kensuke MeraDepartment of Psychiatry, Showa University School of Medicine, Tokyo, JPN.
Taro TazakiDepartment of Psychiatry, Showa University School of Medicine, Tokyo, JPN.
Hana NishiyamaDepartment of Psychiatry, Showa University School of Medicine, Tokyo, JPN.
Hiroki YamadaMental Care Center, Showa University Northern Yokohama Hospital, Kanagawa, JPN.
Kenji SanadaDepartment of Psychiatry, Showa University School of Medicine, Tokyo, JPN.
Atsuko InamotoMental Care Center, Showa University Northern Yokohama Hospital, Kanagawa, JPN.
Akira IwanamiDepartment of Psychiatry, Showa University School of Medicine, Tokyo, JPN.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Introduction Schizophrenia symptom severity is linked to neuroinflammation. Certain blood cell indexes such as neutrophil-lymphocyte ratio (NLR) and neutrophil-albumin ratio (NAR) have been used as biomarkers in various diseases, including schizophrenia. In acute clinical practice, it is challenging to decide whether to provide intravenous antipsychotic treatment in some cases due to the lack of objective biomarkers of psychiatric symptoms. The NLR of individuals with schizophrenia is thought to be associated with disease severity, and changes in NLR may reflect a patient's response to antipsychotic treatment. We investigated the application of NLR as a biomarker for identifying acute severity and determining acute treatment response in patients with schizophrenia. Methods We retrospectively examined 251 inpatients diagnosed with schizophrenia and classified them according to treatment (intravenous haloperidol vs. oral antipsychotic medication during the acute phase) and investigated their NLR and NAR while receiving inpatient care. Results A total of 48 inpatients were given intravenous haloperidol to manage their acute symptoms; 208 were given oral antipsychotics. The intravenous haloperidol group experienced more severe symptoms, such as agitation and disorganized thinking, during the acute phase. Further, those who received intravenous haloperidol had significantly higher Clinical Global Impression-Severity (CGI-S) scores than the oral antipsychotic group. NLR and NAR were also significantly higher in the haloperidol intravenous group. Conclusion Elevated NLR and NAR could be easily measured in patients with psychomotor agitation who should be treated at any facility. Further, they are useful biomarkers for determining disease severity and the effects of treatment on psychomotor excitement in patients who require intravenous haloperidol.

Indexed as

inflammationneutrophil-albumin rationeutrophil-lymphocyte ratiopsychomotor excitementschizophrenia

Identifiers

PMID38222994
PMCPMC10788114

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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.