Evidence map›Paper›PMID 35177746›Full record

Trial reportScientific reports2022

An early prediction model for chronic kidney disease.

Jing Zhao, Yuan Zhang, Jiali Qiu, Xiaodan Zhang, Fengjiang Wei, Jiayi Feng, Chen Chen, Kai Zhang, Shuzhi Feng, Wei-Dong Li

Open access · goldAbstract readClinical Trial
In one paragraph

Trial report in Scientific reports, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 4 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
4citing papers in PubMed, 1 pooled it
3.0field-weighted citation impact, top 8% 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

4 citing papers in PubMed, 1 synthesis or guideline pooled it, 21 citations in OpenAlex.

  1. Pooled it
  2. Article
  3. Article
  4. 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

10 authors at 1 institution in 1 country.

Jing Zhao *Department of Genetics, College of Basic Medical Sciences, Tianjin Medical University, Tianjin, 300070, China.
Yuan Zhang *Department of Genetics, College of Basic Medical Sciences, Tianjin Medical University, Tianjin, 300070, China.
Jiali Qiu *Department of Genetics, College of Basic Medical Sciences, Tianjin Medical University, Tianjin, 300070, China.
Xiaodan Zhang *Department of Genetics, College of Basic Medical Sciences, Tianjin Medical University, Tianjin, 300070, China.
Fengjiang WeiDepartment of Genetics, College of Basic Medical Sciences, Tianjin Medical University, Tianjin, 300070, China.
Jiayi FengDepartment of Genetics, College of Basic Medical Sciences, Tianjin Medical University, Tianjin, 300070, China.
Chen ChenTianjin General Hospital, Tianjin Medical University, Tianjin, 300052, China.
Kai ZhangTianjin General Hospital, Tianjin Medical University, Tianjin, 300052, China.
Shuzhi FengTianjin General Hospital, Tianjin Medical University, Tianjin, 300052, China. shuzhifeng@hotmail.com.
Wei-Dong LiDepartment of Genetics, College of Basic Medical Sciences, Tianjin Medical University, Tianjin, 300070, China. liweidong98@tmu.edu.cn.
Tianjin Medical University · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Based on the high incidence of chronic kidney disease (CKD) in recent years, a better early prediction model for identifying high-risk individuals before end-stage renal failure (ESRD) occurs is needed. We conducted a nested case-control study in 348 subjects (116 cases and 232 controls) from the "Tianjin Medical University Chronic Diseases Cohort". All subjects did not have CKD at baseline, and they were followed up for 5 years until August 2018. Using multivariate Cox regression analysis, we found five nongenetic risk factors associated with CKD risks. Logistic regression was performed to select single nucleotide polymorphisms (SNPs) from which we obtained from GWAS analysis of the UK Biobank and other databases. We used a logistic regression model and natural logarithm OR value weighting to establish CKD genetic/nongenetic risk prediction models. In addition, the final comprehensive prediction model is the arithmetic sum of the two optimal models. The AUC of the prediction model reached 0.894, while the sensitivity was 0.827, and the specificity was 0.801. We found that age, diabetes, and normal high values of urea nitrogen, TGF-β, and ADMA were independent risk factors for CKD. A comprehensive prediction model was also established, which may help identify individuals who are most likely to develop CKD early.

Indexed as

Models, GeneticPolymorphism, Single NucleotideAgedFemaleGenome-Wide Association StudyHumansKidney Failure, ChronicMaleMiddle AgedPredictive Value of TestsRisk Factors

Identifiers

PMID35177746
PMCPMC8854510
OpenAlexW4213363652

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.