Evidence map›Paper›PMID 26286205›Full record

ArticleEBioMedicine2015

Selective Impairment of Spatial Cognition Caused by Autoantibodies to the N-Methyl-D-Aspartate Receptor.

Eric H Chang, Bruce T Volpe, Meggan Mackay, Cynthia Aranow, Philip Watson, Czeslawa Kowal, Justin Storbeck, Paul Mattis, RoseAnn Berlin, Huiyi Chen and 4 more

Open access · goldAbstract read
In one paragraph

Article in EBioMedicine, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 43 papers.

0numbers the graph read from it
0cells of the map it votes in
43citing papers in PubMed
6.4field-weighted citation impact, top 3% 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

43 citing papers in PubMed, 84 citations in OpenAlex.

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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

14 authors at 5 institutions in 2 countries.

Eric H ChangLaboratory of Immune & Neural Networks, Feinstein Institute for Medical Research, North Shore LIJ Health System, Manhasset, NY 11030, USA.
Bruce T VolpeLaboratory of Functional Neuroanatomy, Feinstein Institute for Medical Research, North Shore LIJ Health System, Manhasset, NY 11030, USA ; Department of Molecular Medicine, Hofstra North Shore-LIJ School of Medicine, Manhasset, NY 11030, USA.
Meggan MackayAutoimmune & Musculoskeletal Disease Center, Feinstein Institute for Medical Research, North Shore LIJ Health System, Manhasset, NY 11030, USA.
Cynthia AranowAutoimmune & Musculoskeletal Disease Center, Feinstein Institute for Medical Research, North Shore LIJ Health System, Manhasset, NY 11030, USA.
Philip WatsonDepartment of Psychology, Queens College, Flushing, NY 11367, USA.
Czeslawa KowalAutoimmune & Musculoskeletal Disease Center, Feinstein Institute for Medical Research, North Shore LIJ Health System, Manhasset, NY 11030, USA.
Justin StorbeckDepartment of Psychology, Queens College, Flushing, NY 11367, USA.
Paul MattisSusan and Leonard Feinstein Center for Neurosciences, Feinstein Institute for Medical Research, North Shore LIJ Health System, Manhasset, NY 11030, USA.
RoseAnn BerlinLaboratory of Functional Neuroanatomy, Feinstein Institute for Medical Research, North Shore LIJ Health System, Manhasset, NY 11030, USA.
Huiyi ChenSchool of Biological Sciences, Lee Kong Chian School of Medicine, Nanyang Technological University, Singapore 637551, Singapore.
Simone MaderAutoimmune & Musculoskeletal Disease Center, Feinstein Institute for Medical Research, North Shore LIJ Health System, Manhasset, NY 11030, USA.
Tomás S HuertaLaboratory of Immune & Neural Networks, Feinstein Institute for Medical Research, North Shore LIJ Health System, Manhasset, NY 11030, USA.
Patricio T HuertaLaboratory of Immune & Neural Networks, Feinstein Institute for Medical Research, North Shore LIJ Health System, Manhasset, NY 11030, USA ; Autoimmune & Musculoskeletal Disease Center, Feinstein Institute for Medical Research, North Shore LIJ Health System, Manhasset, NY 11030, USA ; Department of Molecular Medicine, Hofstra North Shore-LIJ School of Medicine, Manhasset, NY 11030, USA.
Betty DiamondAutoimmune & Musculoskeletal Disease Center, Feinstein Institute for Medical Research, North Shore LIJ Health System, Manhasset, NY 11030, USA ; Department of Molecular Medicine, Hofstra North Shore-LIJ School of Medicine, Manhasset, NY 11030, USA.
Northwell Health · USFeinstein Institute for Medical Research · USQueens College, CUNY · USHofstra University · USNanyang Technological University · SG

Funding

The Monoclonal Antibody and Reagent CoreP01AI073693 · NIAID · FEINSTEIN INSTITUTE FOR MEDICAL RESEARCH · PI Czeslawa Helena Kowal · 2008 to 2026
$45.8M
Targeting cognitive and immune impairment in sepsis survivorsP01AI102852 · NIAID · FEINSTEIN INSTITUTE FOR MEDICAL RESEARCH · PI VOLPE, BRUCE THOMAS · 2014 to 2018
$11.5M
NIAID NIH HHS P01 AI073693NIAID NIH HHS P01-AI073693NIAID NIH HHS P01 AI102852NIAID NIH HHS P01-AI102852
6 · The paper itself

Abstract

Patients with systemic lupus erythematosus (SLE) experience cognitive abnormalities in multiple domains including processing speed, executive function, and memory. Here we show that SLE patients carrying antibodies that bind DNA and the GluN2A and GluN2B subunits of the N-methyl-d-aspartate receptor (NMDAR), termed DNRAbs, displayed a selective impairment in spatial recall. Neural recordings in a mouse model of SLE, in which circulating DNRAbs penetrate the hippocampus, revealed that CA1 place cells exhibited a significant expansion in place field size. Structural analysis showed that hippocampal pyramidal cells had substantial reductions in their dendritic processes and spines. Strikingly, these abnormalities became evident at a time when DNRAbs were no longer detectable in the hippocampus. These results suggest that antibody-mediated neurocognitive impairments may be highly specific, and that spatial cognition may be particularly vulnerable to DNRAb-mediated structural and functional injury to hippocampal cells that evolves after the triggering insult is no longer present.

Indexed as

CognitionSpace PerceptionAdultAnimalsAntibodies, AntinuclearAutoantibodiesCell MembraneDendritesFemaleHEK293 CellsHippocampusHumansLupus Erythematosus, SystemicMaleMice, Inbred BALB CMiddle AgedAntibodies, AntinuclearAutoantibodiesReceptors, N-Methyl-D-AspartateAP, alkaline phosphataseBBB, blood–brain barrierBDI, Beck depression indexC3, C4, complements 3 and 4, respectivelyCA1, cornus ammonis area 1 of the hippocampusCA1 place cellCNS, central nervous systemCSF, cerebrospinal fluidDMARD, disease-modifying drugsDNRAb, anti-DNA antibody reactive to the GluN2A and GluN2B subunits of the NMDARdsDNA, double stranded DNADWEYS, amino acid consensus sequence (D/E, W, D/E, Y, S/G) for DNRAb bindingFA, Freund's adjuvantHC, healthy controlHEK-293T, human embryonic kidney 293 T cellHippocampusIgG, immunoglobulin Gi.p, intraperitoneallyLPS, lipopolysaccharideLupusMAP, multi-antigenic polylysine backboneMouse lupus modelNeuropsychiatric lupusNMDAR, N-methyl-d-aspartate receptorNOR, novel object recognitionNPSLE, neuropsychiatric lupusOPM, object place memorySELENA, safety of estrogens in lupus erythematosus national assessmentSLEDAI, systemic lupus erythematosus disease activity indexSLE, systemic lupus erythematosusSLICCDI, systemic lupus international collaborating clinics damage index

Identifiers

PMID26286205
PMCPMC4534689
OpenAlexW2104101370

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC-ND
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.