Evidence map›Paper›PMID 35982301›Full record

ArticleExperimental & molecular medicine2022

Inhibiting peripheral and central MAO-B ameliorates joint inflammation and cognitive impairment in rheumatoid arthritis.

Woojin Won, Hyun-Ji Choi, Ji-Young Yoo, Daeun Kim, Tai Young Kim, YeonHa Ju, Ki Duk Park, Hyunbeom Lee, Sang Youn Jung, C Justin Lee

Open access · goldAbstract read
In one paragraph

Article in Experimental & molecular medicine, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 23 papers.

0numbers the graph read from it
0cells of the map it votes in
23citing papers in PubMed
1.8field-weighted citation impact, top 15% 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

23 citing papers in PubMed, 29 citations in OpenAlex.

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  10. Role of the STING→IRF3 Pathway in Ambient GABA Homeostasis and Cognitive Function.The Journal of neuroscience : the official journal of the Society for Neuroscience · 2024
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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

10 authors at 6 institutions in 1 country.

Woojin WonKU-KIST Graduate School of Converging Science and Technology, Korea University, 145 Anam-ro, Seongbuk-gu, Seoul, 02841, Republic of Korea.ORCID http://orcid.org/0000-0001-5262-039X
Hyun-Ji ChoiDepartment of Biotechnology, CHA University, Seongnam, 13488, Republic of Korea.
Ji-Young YooDepartment of Biotechnology, CHA University, Seongnam, 13488, Republic of Korea.
Daeun KimCenter for Cognition and Sociality, Institute for Basic Science (IBS), Daejeon, 34126, Republic of Korea.
Tai Young KimCenter for Cognition and Sociality, Institute for Basic Science (IBS), Daejeon, 34126, Republic of Korea.
YeonHa JuCenter for Cognition and Sociality, Institute for Basic Science (IBS), Daejeon, 34126, Republic of Korea.
Ki Duk ParkConvergence Research Center for Diagnosis, Treatment and Care System of Dementia, Korea Institute of Science and Technology (KIST), Seoul, 02792, Republic of Korea.
Hyunbeom LeeCenter for Advanced Biomolecular Recognition, Korea Institute of Science and Technology, Seoul, 02792, South Korea.
Sang Youn JungDivision of Rheumatology, Department of Internal Medicine, CHA Bundang Medical Center, CHA University, Seongnam, 13496, Republic of Korea. jungsy7597@cha.ac.kr.
C Justin LeeKU-KIST Graduate School of Converging Science and Technology, Korea University, 145 Anam-ro, Seongbuk-gu, Seoul, 02841, Republic of Korea. cjl@ibs.re.kr.ORCID http://orcid.org/0000-0002-3555-0980
Institute for Basic Science · KRCHA University · KRKorea University · KRCHA University Bundang Medical Center · KRKorea Institute of Science and Technology · KRKyung Hee University · KR

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Rheumatoid arthritis (RA) is an autoimmune disorder characterized by chronic inflammation and the destruction of joints and systemic organs. RA is commonly accompanied by neuropsychiatric complications, such as cognitive impairment and depression. However, the role of monoamine oxidase (MAO) and its inhibitors in controlling neurotransmitters associated with these complications in RA have not been clearly identified. Here, we report that peripheral and central MAO-B are highly associated with joint inflammation and cognitive impairment in RA, respectively. Ribonucleic acid (RNA) sequencing and protein expression quantification were used to show that MAO-B and related molecules, such as gamma aminobutyric acid (GABA), were elevated in the inflamed synovium of RA patients. In primary cultured fibroblast-like synoviocytes in the RA synovium, MAO-B expression was significantly increased by tumor necrosis factor (TNF)-α-induced autophagy, which produces putrescine, the polyamine substrate for GABA synthesis. We also observed that MAO-B-mediated aberrant astrocytic production of GABA was augmented by interleukin (IL)-1β and inhibited CA1-hippocampal pyramidal neurons, which are responsible for memory storage, in an animal model of RA. Moreover, a newly developed reversible inhibitor of MAO-B ameliorated joint inflammation by inhibiting cyclooxygenase (Cox)-2. Therefore, MAO-B can be an effective therapeutic target for joint inflammation and cognitive impairment in patients with RA.

Indexed as

Arthritis, RheumatoidCognitive DysfunctionAnimalsCells, CulturedFibroblastsgamma-Aminobutyric AcidInflammationMonoamine OxidaseTumor Necrosis Factor-alphagamma-Aminobutyric AcidMonoamine OxidaseTumor Necrosis Factor-alpha

Identifiers

PMID35982301
PMCPMC9440195
OpenAlexW4292491636

What Socratic holds

Textmetadata
LicenceCC BY
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.