Evidence map›Paper›PMID 26912606›Full record

ArticleThe international journal of neuropsychopharmacology2016

Altered Serum Levels of Matrix Metalloproteinase-2, -9 in Response to Electroconvulsive Therapy for Mood Disorders.

Chiyo Shibasaki, Minoru Takebayashi, Kei Itagaki, Hiromi Abe, Naoto Kajitani, Mami Okada-Tsuchioka, Shigeto Yamawaki

Abstract read
In one paragraph

Article in The international journal of neuropsychopharmacology, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 21 papers.

0numbers the graph read from it
0cells of the map it votes in
21citing 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

21 citing papers in PubMed.

  1. Trial
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  14. Activation of proprotein convertase in the mouse habenula causes depressive-like behaviors through remodeling of extracellular matrix.Neuropsychopharmacology : official publication of the American College of Neuropsychopharmacology · 2021
    Article
  15. Article
  16. Article
  17. MMPs in learning and memory and neuropsychiatric disorders.Cellular and molecular life sciences : CMLS · 2019
    Review
  18. Reduced Serum and Cerebrospinal Fluid Levels of Autotaxin in Major Depressive Disorder.The international journal of neuropsychopharmacology · 2019
    Article
  19. Article
  20. 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

7 authors.

Chiyo ShibasakiDivision of Psychiatry and Neuroscience, Institute for Clinical Research (Drs Shibasaki, Takebayashi, Itagaki, Abe, Kajitani, and Okada-Tsuchioka), and Department of Psychiatry (Drs Takebayashi and Itagaki), National Hospital Organization, Kure Medical Center and Chugoku Cancer Center, Hiroshima, Japan; Department of Psychiatry and Neurosciences, Division of Frontier Medical Science, Programs for Biomedical Research, Graduate School of Biomedical Sciences, Hiroshima University, Hiroshima, Japan (Drs Shibasaki, Itagaki, and Yamawaki).
Minoru TakebayashiDivision of Psychiatry and Neuroscience, Institute for Clinical Research (Drs Shibasaki, Takebayashi, Itagaki, Abe, Kajitani, and Okada-Tsuchioka), and Department of Psychiatry (Drs Takebayashi and Itagaki), National Hospital Organization, Kure Medical Center and Chugoku Cancer Center, Hiroshima, Japan; Department of Psychiatry and Neurosciences, Division of Frontier Medical Science, Programs for Biomedical Research, Graduate School of Biomedical Sciences, Hiroshima University, Hiroshima, Japan (Drs Shibasaki, Itagaki, and Yamawaki). mtakebayashi@kure-nh.go.jp yamawaki@hiroshima-u.ac.jp.
Kei ItagakiDivision of Psychiatry and Neuroscience, Institute for Clinical Research (Drs Shibasaki, Takebayashi, Itagaki, Abe, Kajitani, and Okada-Tsuchioka), and Department of Psychiatry (Drs Takebayashi and Itagaki), National Hospital Organization, Kure Medical Center and Chugoku Cancer Center, Hiroshima, Japan; Department of Psychiatry and Neurosciences, Division of Frontier Medical Science, Programs for Biomedical Research, Graduate School of Biomedical Sciences, Hiroshima University, Hiroshima, Japan (Drs Shibasaki, Itagaki, and Yamawaki).
Hiromi AbeDivision of Psychiatry and Neuroscience, Institute for Clinical Research (Drs Shibasaki, Takebayashi, Itagaki, Abe, Kajitani, and Okada-Tsuchioka), and Department of Psychiatry (Drs Takebayashi and Itagaki), National Hospital Organization, Kure Medical Center and Chugoku Cancer Center, Hiroshima, Japan; Department of Psychiatry and Neurosciences, Division of Frontier Medical Science, Programs for Biomedical Research, Graduate School of Biomedical Sciences, Hiroshima University, Hiroshima, Japan (Drs Shibasaki, Itagaki, and Yamawaki).
Naoto KajitaniDivision of Psychiatry and Neuroscience, Institute for Clinical Research (Drs Shibasaki, Takebayashi, Itagaki, Abe, Kajitani, and Okada-Tsuchioka), and Department of Psychiatry (Drs Takebayashi and Itagaki), National Hospital Organization, Kure Medical Center and Chugoku Cancer Center, Hiroshima, Japan; Department of Psychiatry and Neurosciences, Division of Frontier Medical Science, Programs for Biomedical Research, Graduate School of Biomedical Sciences, Hiroshima University, Hiroshima, Japan (Drs Shibasaki, Itagaki, and Yamawaki).
Mami Okada-TsuchiokaDivision of Psychiatry and Neuroscience, Institute for Clinical Research (Drs Shibasaki, Takebayashi, Itagaki, Abe, Kajitani, and Okada-Tsuchioka), and Department of Psychiatry (Drs Takebayashi and Itagaki), National Hospital Organization, Kure Medical Center and Chugoku Cancer Center, Hiroshima, Japan; Department of Psychiatry and Neurosciences, Division of Frontier Medical Science, Programs for Biomedical Research, Graduate School of Biomedical Sciences, Hiroshima University, Hiroshima, Japan (Drs Shibasaki, Itagaki, and Yamawaki).
Shigeto YamawakiDivision of Psychiatry and Neuroscience, Institute for Clinical Research (Drs Shibasaki, Takebayashi, Itagaki, Abe, Kajitani, and Okada-Tsuchioka), and Department of Psychiatry (Drs Takebayashi and Itagaki), National Hospital Organization, Kure Medical Center and Chugoku Cancer Center, Hiroshima, Japan; Department of Psychiatry and Neurosciences, Division of Frontier Medical Science, Programs for Biomedical Research, Graduate School of Biomedical Sciences, Hiroshima University, Hiroshima, Japan (Drs Shibasaki, Itagaki, and Yamawaki). mtakebayashi@kure-nh.go.jp yamawaki@hiroshima-u.ac.jp.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundInflammatory processes could underlie mood disorders. Matrix metalloproteinases (MMPs) and tissue inhibitors of MMPs (TIMP) are inflammation-related molecules. The current study sought an association between mood disorders and systemic levels of MMPs and TIMPs.

methodsSerum was obtained from patients with mood disorders (n=21) and patients with schizophrenia (n=13) scheduled to undergo electroconvulsive therapy. Serum was also obtained from healthy controls (n=40). Clinical symptoms were assessed by the Hamilton Rating Score for Depression and the Brief Psychiatric Rating Scale. Serum levels of MMPs and TIMPs were quantified by ELISA.

resultsThe serum levels of MMP-2 in mood disorder patients, but not in schizophrenia patients, prior to the first electroconvulsive therapy session (baseline) was significantly lower than that of healthy controls. At baseline, levels of MMP-9 and TIMP-2, -1 were not different between patients with mood disorder and schizophrenia and healthy controls. After a course of electroconvulsive therapy, MMP-2 levels were significantly increased in mood disorder patients, but MMP-9 levels were significantly decreased in both mood disorder and schizophrenia patients. In mood disorder patients, there was a significant negative correlation between depressive symptoms and serum levels of MMP-2 and a positive correlation between depressive symptoms and MMP-9. In addition, alterations of serum levels of MMP-2 and MMP-9 were significantly correlated each other and were associated with certain depressive symptoms.

conclusionA change in inflammatory homeostasis, as indicated by MMP-2 and MMP-9, could be related to mood disorders, and these markers appear to be sensitive to electroconvulsive therapy.

Indexed as

Electroconvulsive TherapyBiomarkersCase-Control StudiesFemaleHumansMaleMatrix Metalloproteinase 2Matrix Metalloproteinase 9Middle AgedMood DisordersPsychiatric Status Rating ScalesSchizophreniaTissue Inhibitor of Metalloproteinase-1Tissue Inhibitor of Metalloproteinase-2BiomarkersMatrix Metalloproteinase 2Matrix Metalloproteinase 9Tissue Inhibitor of Metalloproteinase-1Tissue Inhibitor of Metalloproteinase-2electroconvulsive therapyMMP-2MMP-9mood disordersschizophrenia

Identifiers

PMID26912606
PMCPMC5043640

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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.