Evidence map›Paper›PMID 30278546›Full record

SynthesisMedicine2018

Association between NR3C1 rs41423247 polymorphism and depression: A PRISMA-compliant meta-analysis.

Qiuju Peng, Huacheng Yan, Yuguan Wen, Chongfa Lai, Lei Shi

Open access · goldAbstract readMeta-Analysis
In one paragraph

Synthesis in Medicine, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 11 papers.

0numbers the graph read from it
0cells of the map it votes in
11citing papers in PubMed
0.6field-weighted citation impact, top 41% 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

11 citing papers in PubMed, 18 citations in OpenAlex.

  1. Review
  2. Review
  3. Article
  4. Review
  5. Article
  6. Article
  7. Familial Linkage and Association of theInternational journal of molecular sciences · 2022
    Article
  8. Frontiers in cell and developmental biology · 2022
    Article
  9. Review
  10. Review
  11. Association between genetic variants and depression in a Romanian cohort.Romanian journal of morphology and embryology = Revue roumaine de morphologie et embryologie
    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

5 authors at 4 institutions in 1 country.

Qiuju PengCollege of Pharmacy, Guangdong Pharmaceutical University.
Huacheng YanCenter for Disease Control and Prevention of Guangzhou Military Command.
Yuguan WenDepartment of Pharmacy, Guangzhou Brain Hospital, Guangzhou Medical University, Guangzhou, China.
Chongfa LaiDepartment of Pharmacy, Guangzhou General Hospital of Guangzhou Military Command.
Lei ShiCollege of Pharmacy, Guangdong Pharmaceutical University.
Guangdong Pharmaceutical University · CNGeneral Hospital of Guangzhou Military Command · CNGuangzhou Center for Disease Control and Prevention · CNGuangzhou Psychiatric Hospital · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundA dysfunction of the hypothalamic-pituitary-adrenal (HPA) axis is closely related to the occurrence of depression. The glucocorticoid receptor, also known as the nuclear receptor subfamily 3, group C, member 1 (NR3C1), provides negative feedback to the HPA axis by binding to glucocorticoids. Some studies have demonstrated an association between the NR3C1 rs41423247 polymorphism and depression, but results from other studies have been controversial.

methodIn this study, the association between the NR3C1 rs41423247 polymorphism and depression was evaluated by a meta-analysis using the RevMan 5.3 software, and the Stata 10.0 software was used for sensitivity analysis and publication bias test. According to the inclusion criteria, related studies in databases were retrieved and screened.

resultsIn total, 9 articles were selected, including 1630 depressed patients and 3362 controls. The meta-analysis showed that homozygous mutation of NR3C1 rs41423247 was associated with depression in the total population (OR = 0.77, 95% CI = 0.64-0.94, P = .01) and in Caucasians (OR = 0.78, 95% CI = 0.63-0.96, P = .02).

conclusionThis meta-analysis demonstrates that the NR3C1 rs41423247 homozygous mutation may be a risk factor for depression.

Indexed as

DepressionGenetic Predisposition to DiseaseHumansHypothalamo-Hypophyseal SystemPituitary-Adrenal SystemPolymorphism, Single NucleotideReceptors, GlucocorticoidNR3C1 protein, humanReceptors, Glucocorticoid

Identifiers

PMID30278546
PMCPMC6181539
OpenAlexW2895333119

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC
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.