Evidence map›Paper›PMID 35721789›Full record

ReviewCanadian respiratory journal2022

Genetic Variants Associated with Chronic Obstructive Pulmonary Disease Risk: Cumulative Epidemiological Evidence from Meta-Analyses and Genome-Wide Association Studies.

Caiyang Liu, Ran Ran, Xiaoliang Li, Gaohua Liu, Xiaoyang Xie, Ji Li

Open access · goldAbstract readReview
In one paragraph

Review in Canadian respiratory journal, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 7 papers.

0numbers the graph read from it
0cells of the map it votes in
7citing papers in PubMed
1.4field-weighted citation impact, top 18% 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, 9 citations in OpenAlex.

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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

6 authors at 2 institutions in 1 country.

Caiyang LiuDepartment of Cardiothoracic Surgery, The First People's Hospital of Neijiang, Neijiang 641000, Sichuan, China.ORCID 0000-0001-7812-7122
Ran RanBreast Surgery Center of Sichuan Cancer Hospital, Chengdu 610041, China.ORCID 0000-0002-8660-722X
Xiaoliang LiDepartment of Cardiothoracic Surgery, The First People's Hospital of Neijiang, Neijiang 641000, Sichuan, China.ORCID 0000-0002-8809-0893
Gaohua LiuDepartment of Cardiothoracic Surgery, The First People's Hospital of Neijiang, Neijiang 641000, Sichuan, China.ORCID 0000-0003-2458-7216
Xiaoyang XieDepartment of Cardiothoracic Surgery, The First People's Hospital of Neijiang, Neijiang 641000, Sichuan, China.ORCID 0000-0002-3854-8982
Ji LiDepartment of Cardiothoracic Surgery, The First People's Hospital of Neijiang, Neijiang 641000, Sichuan, China.ORCID 0000-0002-9891-223X
Neijiang Normal University · CNSichuan Cancer Hospital · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Background: Last two decades, many association studies on genetic variants and chronic obstructive pulmonary disease (COPD) risk have been published. But results from different studies are inconsistent. Therefore, we performed this article to systematically evaluate results from previous meta-analyses and genome-wide association studies (GWASs). Results: As a result, eighty-eight meta-analyses and 5 GWASs were deemed eligible for inclusion. Fifty variants in 26 genes obtained from meta-analyses were significantly associated with COPD risk. Cumulative epidemiological evidence of an association was graded as strong for 10 variants in 8 genes ( Conclusion: In summary, more than half (52.38%) of genetic variants reported in previous meta-analyses showed no association with COPD risk. However, 13 variants in 9 genes had moderate to strong evidence for an association. This article can serve as a useful reference for further studies.

Indexed as

Genome-Wide Association StudyPulmonary Disease, Chronic ObstructiveADAM ProteinsGenetic Predisposition to DiseaseHumansPolymorphism, Single NucleotideTumor Necrosis Factor-alphaADAM33 protein, humanADAM ProteinsTumor Necrosis Factor-alpha

Identifiers

PMID35721789
PMCPMC9203202
OpenAlexW4285744347

What OpenQuestion 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 OpenQuestion graph.