Evidence map›Paper›PMID 37452175›Full record

SynthesisCommunications biology2023

Mendelian randomization uncovers a protective effect of interleukin-1 receptor antagonist on kidney function.

Jeong Min Cho, Jung Hun Koh, Seong Geun Kim, Soojin Lee, Yaerim Kim, Semin Cho, Kwangsoo Kim, Yong Chul Kim, Seung Seok Han, Hajeong Lee and 6 more

Open access · goldAbstract readMeta-Analysis
In one paragraph

Synthesis in Communications biology, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 8 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
8citing papers in PubMed, 1 pooled it
1.5field-weighted citation impact, top 17% 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

8 citing papers in PubMed, 1 synthesis or guideline pooled it, 9 citations in OpenAlex.

  1. Pooled it
  2. Article
  3. Article
  4. Article
  5. Review
  6. Article
  7. Review
  8. 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

16 authors at 4 institutions in 1 country.

Jeong Min ChoDepartment of Internal Medicine, Seoul National University Hospital, Seoul, Korea.
Jung Hun KohDepartment of Internal Medicine, Seoul National University Hospital, Seoul, Korea.
Seong Geun KimDepartment of Internal Medicine, Inje University Sanggye Paik Hospital, Seoul, Korea.
Soojin LeeDepartment of Internal Medicine, Uijeongbu Eulji University Medical Center, Seoul, Korea.
Yaerim KimDepartment of Internal Medicine, Keimyung University School of Medicine, Daegu, Korea.
Semin ChoDepartment of Internal Medicine, Chung-Ang University Gwangmyeong Hospital, Gyeonggi-do, Korea.
Kwangsoo KimTransdisciplinary Department of Medicine & Advanced Technology, Seoul National University Hospital, Seoul, Korea.
Yong Chul KimDepartment of Internal Medicine, Seoul National University Hospital, Seoul, Korea.
Seung Seok HanDepartment of Internal Medicine, Seoul National University Hospital, Seoul, Korea.
Hajeong LeeDepartment of Internal Medicine, Seoul National University Hospital, Seoul, Korea.
Jung Pyo LeeDepartment of Internal Medicine, Seoul National University College of Medicine, Seoul, Korea.
Kwon Wook JooDepartment of Internal Medicine, Seoul National University Hospital, Seoul, Korea.
Chun Soo LimDepartment of Internal Medicine, Seoul National University College of Medicine, Seoul, Korea.
Yon Su KimDepartment of Internal Medicine, Seoul National University Hospital, Seoul, Korea.
Dong Ki KimDepartment of Internal Medicine, Seoul National University Hospital, Seoul, Korea.ORCID 0000-0002-5195-7852
Sehoon ParkDepartment of Internal Medicine, Seoul National University Hospital, Seoul, Korea. mailofsehoon@gmail.com.ORCID 0000-0002-4221-2453
Seoul National University · KRSeoul National University Hospital · KRChung-Ang University Hospital · KRInje University Sanggye Paik Hospital · KR

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Interleukins (ILs), key cytokine family of inflammatory response, are closely associated with kidney function. However, the causal effect of various ILs on kidney function needs further investigation. Here we show two-sample summary-level Mendelian randomization (MR) analysis that examined the causality between serum IL levels and kidney function. Genetic variants with strong association with serum IL levels were obtained from a previous genome-wide association study meta-analysis. Summary-level data for estimated glomerular filtration rate (eGFR) were obtained from CKDGen database. As a main MR analysis, multiplicative random-effects inverse-variance weighted method was performed. Pleiotropy-robust MR analysis, including MR-Egger with bootstrapped error and weighted median methods, were also implemented. We tested the causal estimates from nine ILs on eGFR traits. Among the results, higher genetically predicted serum IL-1 receptor antagonist level was significantly associated with higher eGFR values in the meta-analysis of CKDGen and the UK Biobank data. In addition, the result was consistent towards eGFR decline phenotype of the outcome database. Otherwise, nonsignificant association was identified between other genetically predicted ILs and eGFR outcome. These findings support the clinical importance of IL-1 receptor antagonist-associated pathway in relation to kidney function in the general individuals, particularly highlighting the importance of IL-1 receptor antagonist.

Indexed as

Genome-Wide Association StudyMendelian Randomization AnalysisGlomerular Filtration RateKidneyReceptors, Interleukin-1Receptors, Interleukin-1

Identifiers

PMID37452175
PMCPMC10349143
OpenAlexW4384340125

What Socratic 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 Socratic graph.