Evidence map›Paper›PMID 32606706›Full record

ArticleNeuropsychiatric disease and treatment2020

Impact of Expression and Genetic Variation of microRNA-34b/c on Cognitive Dysfunction in Patients with Major Depressive Disorder.

Ning Sun, Chunxia Yang, Xiaoting He, Zhifen Liu, Sha Liu, Xinrong Li, Yanfang Wang, Ruihua Jin, Kerang Zhang

Open access · goldAbstract read
In one paragraph

Article in Neuropsychiatric disease and treatment, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 20 papers.

0numbers the graph read from it
0cells of the map it votes in
20citing papers in PubMed
1.2field-weighted citation impact, top 24% of its field
1 · What the graph read from it

What it found

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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

20 citing papers in PubMed, 25 citations in OpenAlex.

  1. Article
  2. Review
  3. Review
  4. Review
  5. Article
  6. Article
  7. Role of miRNA Gene Variants (miR-22 and miR-155) as the Factors Affecting Susceptibility to Panic Disorder.Clinical psychopharmacology and neuroscience : the official scientific journal of the Korean College of Neuropsychopharmacology · 2024
    Article
  8. Article
  9. Review
  10. Article
  11. Article
  12. The role of microRNAs in depression.Frontiers in pharmacology · 2023
    Review
  13. Article
  14. Review
  15. Review
  16. The miRNome of Depression.International journal of molecular sciences · 2021
    Review
  17. Article
  18. Review
  19. Review
  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

9 authors at 1 institution in 1 country.

Ning SunDepartment of Psychiatry, First Hospital of Shanxi Medical University, Taiyuan, People's Republic of China.
Chunxia YangDepartment of Psychiatry, First Hospital of Shanxi Medical University, Taiyuan, People's Republic of China.
Xiaoting HeDepartment of Psychiatry, First Hospital of Shanxi Medical University, Taiyuan, People's Republic of China.
Zhifen LiuDepartment of Psychiatry, First Hospital of Shanxi Medical University, Taiyuan, People's Republic of China.
Sha LiuDepartment of Psychiatry, First Hospital of Shanxi Medical University, Taiyuan, People's Republic of China.
Xinrong LiDepartment of Psychiatry, First Hospital of Shanxi Medical University, Taiyuan, People's Republic of China.
Yanfang WangDepartment of Psychiatry, First Hospital of Shanxi Medical University, Taiyuan, People's Republic of China.
Ruihua JinNursing College of Shanxi Medical University, Taiyuan, People's Republic of China.
Kerang ZhangDepartment of Psychiatry, First Hospital of Shanxi Medical University, Taiyuan, People's Republic of China.ORCID 0000-0002-7397-2738
Shanxi Medical University · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundPatients suffering from major depressive disorder (MDD) commonly demonstrate lower performance across multiple cognitive domains. Cognitive impairment is an intrinsic characteristic of MDD status and is often influenced by genetic factors. microRNAs (miRNAs or miRs) have been shown to have important implications in the etiology of MDD. Therefore, we aimed to identify and analyze the impact of expression and genetic variation of miR-34b/c on cognitive dysfunction in MDD.

methodsFirst, we analyzed miR-34c-5p expression in 48 cases of MDD and 54 healthy controls in a Chinese population using qRT-PCR. We assessed the relationship between the level of miR-34c-5p expression and cognitive performance by Repeatable Battery for the Assessment of Neuropsychological Status (RBANS) and the Trail Making Test (TMT). Second, in order to characterize allelic effects of miR-34b/c on cognitive performance in MDD patients, we performed genetic association analysis of single-nucleotide polymorphism (SNP) loci of the MIR34B/C genes with cognitive function in a second group consisting of 531 MDD patients and 267 healthy controls.

resultsWe found a significant negative correlation between the level of miR-34c-5p expression and both the language and delayed memory index scores in patients with MDD. We also found a significant positive correlation between the level of miR-34c-5p expression and the time required to complete tests A and B of the TMT. The interaction between the rs2187473 genotype and the disease was significant for both immediate memory and delayed memory. In the patient group, the rs2187473 CC genotype was significantly associated with higher performance on immediate memory (

conclusionOur findings suggest that changes in miR-34c expression level have important impacts on cognitive function in patients with MDD. In particular, the polymorphism rs2187473 is a potential genetic risk factor for cognitive function in MDD, which may be of clinical use.

Indexed as

cognitive functionmajor depressive disorderMDDmicroRNA-34csingle-nucleotide polymorphism

Identifiers

PMID32606706
PMCPMC7311205
OpenAlexW3036231100

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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.