Evidence map›Paper›PMID 39406395›Full record

ArticleSchizophrenia bulletin2025

N-Methyl-d-Aspartate Receptor Antibody and Sensory Gating Deficits in Non-smoking, Minimal Antipsychotic Medication Exposure, and First-Episode Patients With Schizophrenia.

Jinghui Tong, Kebing Yang, Wei Li, Leilei Wang, Yi Yin, Yanfang Zhou, Junchao Huang, Ping Zhang, Yanli Zhao, Song Chen and 10 more

Abstract read
In one paragraph

Article in Schizophrenia bulletin, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

0numbers the graph read from it
0cells of the map it votes in
1citing 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.

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

1 citing paper in PubMed.

  1. 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

20 authors.

Jinghui TongPeking University HuiLongGuan Clinical Medical School, Beijing Huilongguan Hospital, Beijing 100096, China.
Kebing YangPeking University HuiLongGuan Clinical Medical School, Beijing Huilongguan Hospital, Beijing 100096, China.
Wei LiPeking University HuiLongGuan Clinical Medical School, Beijing Huilongguan Hospital, Beijing 100096, China.
Leilei WangPeking University HuiLongGuan Clinical Medical School, Beijing Huilongguan Hospital, Beijing 100096, China.
Yi YinPeking University HuiLongGuan Clinical Medical School, Beijing Huilongguan Hospital, Beijing 100096, China.
Yanfang ZhouPeking University HuiLongGuan Clinical Medical School, Beijing Huilongguan Hospital, Beijing 100096, China.
Junchao HuangPeking University HuiLongGuan Clinical Medical School, Beijing Huilongguan Hospital, Beijing 100096, China.
Ping ZhangPeking University HuiLongGuan Clinical Medical School, Beijing Huilongguan Hospital, Beijing 100096, China.
Yanli ZhaoPeking University HuiLongGuan Clinical Medical School, Beijing Huilongguan Hospital, Beijing 100096, China.
Song ChenPeking University HuiLongGuan Clinical Medical School, Beijing Huilongguan Hospital, Beijing 100096, China.
Hongzhen FanPeking University HuiLongGuan Clinical Medical School, Beijing Huilongguan Hospital, Beijing 100096, China.
Yimin CuiDepartment of Pharmacy, Peking University First Hospital, Beijing 100034, China.
Xingguang LuoDepartment of Psychiatry, Yale University School of Medicine, New Haven, CT 06510, United States.
Shuping TanPeking University HuiLongGuan Clinical Medical School, Beijing Huilongguan Hospital, Beijing 100096, China.
Zhiren WangPeking University HuiLongGuan Clinical Medical School, Beijing Huilongguan Hospital, Beijing 100096, China.
Wei FengPeking University HuiLongGuan Clinical Medical School, Beijing Huilongguan Hospital, Beijing 100096, China.
Baopeng TianPeking University HuiLongGuan Clinical Medical School, Beijing Huilongguan Hospital, Beijing 100096, China.
Chiang-Shan R LiDepartment of Psychiatry, Yale University School of Medicine, New Haven, CT 06510, United States.ORCID 0000-0002-9393-1212
L Elliot HongDepartment of Psychiatry and Behavioral Sciences, University of Texas Health Science Center, Houston, TX 77030, United States.
Yunlong TanPeking University HuiLongGuan Clinical Medical School, Beijing Huilongguan Hospital, Beijing 100096, China.ORCID 0000-0002-3522-3912

Funding

The Role of Stress-Immune-Connectome Disruption in Mechanisms of Chinese Early Schizophrenia SpectrumR01MH112180 · NIMH · UNIVERSITY OF MARYLAND BALTIMORE · PI HONG, L ELLIOT ELLIOT · 2017 to 2021
$1.0M
Capital Health Research and Development of Special 2022-1-2131High level public health talents-leading talents project 2024National Natural Science Foundation of China 82171507NIH HHS R01MH112180NIMH NIH HHS R01 MH112180
6 · The paper itself

Abstract

background and hypothesisSensory gating deficit is considered a pathophysiological feature of schizophrenia, which has been linked to N-methyl-d-aspartate receptor (NMDAR) hypofunction as one of the potential underlying mechanisms. Here, we hypothesize that higher levels of NMDAR antibody (Ab) may contribute to the sensory gating deficits in schizophrenia. STUDY

designWe enrolled 72 non-smoking inpatients with first-episode schizophrenia (FES), most of them with only a relatively short duration of exposure to antipsychotic medications, and 51 non-smoking healthy controls (HC). Sensory gating was measured by P50 evoked potentials ratio and the difference between the two stimuli in an auditory paired-stimuli paradigm and serum NMDAR Ab levels were quantified by enzyme-linked immunosorbent assay. STUDY

resultsThe FES group showed higher serum NMDAR Ab levels [(9.23 ± 4.15) ng/mL vs. (7.08 ± 2.83) ng/mL; P = .002], higher P50 ratio (P = .002), and less P50 difference (P = .001) than HC. In partial correlation analysis, serum NMDAR Ab levels were positively correlated with the P50 ratio (r = 0.36, P = .003) and negatively with the P50 difference (r = -0.39, P = .001) in the FES group. The NMDAR Ab levels mediated the diagnosis of schizophrenia and P50 sensory gating deficits (P50 ratio and P50 difference).

conclusionsAutoimmunity targeting NMDAR is a crucial intermediate mechanism in impaired sensory gating in patients with schizophrenia. The findings support early intervention targeting NMDAR for patients with schizophrenia.

Indexed as

Antipsychotic AgentsAutoantibodiesEvoked Potentials, AuditoryReceptors, N-Methyl-D-AspartateSchizophreniaSensory GatingAdolescentAdultFemaleHumansMaleYoung AdultAntipsychotic AgentsAutoantibodiesReceptors, N-Methyl-D-Aspartatefirst episode schizophreniamediation analysisNMDAR antibodysensory gating deficits

Identifiers

PMID39406395
PMCPMC12236339

What Socratic holds

Textmetadata
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 Socratic graph.