Evidence map›Paper›PMID 30048584›Full record

ArticlePsychiatry investigation2018

Higher Serum C Reactive Protein Determined C Reactive Protein Single-Nucleotide Polymorphisms Are Involved in Inherited Depression.

Shiliang Wang, Hua Zhong, Meijuan Lu, Guohua Song, Xiaomei Zhang, Min Lin, Shengliang Yang, Mincai Qian

Open access · diamondAbstract read
In one paragraph

Article in Psychiatry investigation, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 7 papers, 2 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
7citing papers in PubMed, 2 pooled it
0.4field-weighted citation impact, top 45% 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

7 citing papers in PubMed, 2 syntheses or guidelines pooled it, 12 citations in OpenAlex.

  1. Pooled it
  2. Pooled it
  3. Article
  4. Article
  5. C-Reactive Protein as a Biomarker for Major Depressive Disorder?International journal of molecular sciences · 2022
    Review
  6. Article
  7. 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

8 authors at 1 institution in 1 country.

Shiliang WangHuzhou Third People's Hospital, Zhejiang, China.
Hua ZhongHuzhou Third People's Hospital, Zhejiang, China.
Meijuan LuHuzhou Third People's Hospital, Zhejiang, China.
Guohua SongHuzhou Third People's Hospital, Zhejiang, China.
Xiaomei ZhangHuzhou Third People's Hospital, Zhejiang, China.
Min LinHuzhou Third People's Hospital, Zhejiang, China.
Shengliang YangHuzhou Third People's Hospital, Zhejiang, China.
Mincai QianHuzhou Third People's Hospital, Zhejiang, China.
Third People's Hospital of Huzhou · CN

Funding

Huzhou science and technology 2015GYB21
6 · The paper itself

Abstract

objectiveThe pathogenesis of depression is not fully understood yet, but studies have suggested higher circulating C reactive protein (CRP) level might relate to depression occurrence. However, due to high variability of patients' individual condition, the results to date are inconsistent. Considering CRP single-nucleotide polymorphisms (SNPs) could also regulate plasma CRP levels, in the present study, we hypothesized that inherited CRP allelic variations may co-vary with depressive symptomatology.

methodsWe recruited 60 depression patients with family depression history and 60 healthy control volunteers into this project. We detected circulation CRP level as well as genome CRP SNPs from participants of this project.

resultsWe have found a significantly higher circulating CRP level in patients with a positive family history. Furthermore, we also identified some certain inherited CRP SNPs (A allele in rs1417938 and C allele in rs1205) could up regulate serum CRP level and distributed more in depression patients with family history.

conclusionOur finding may raise new evidence that genetically increased serum CRP level through SNPs variation is likely to induce family inherited depression.

Indexed as

CRPDepressionFamilial inheritanceSNPs

Identifiers

PMID30048584
PMCPMC6111223
OpenAlexW2883412654

What OpenQuestion holds

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Registered trials

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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.