Evidence map›Paper›PMID 36242604›Full record

ArticleAging2022

Development and assessment of diabetic nephropathy prediction model using hub genes identified by weighted correlation network analysis.

Xuelian Zhang, Yao Wang, Zhaojun Yang, Xiaoping Chen, Jinping Zhang, Xin Wang, Xian Jin, Lili Wu, Xiaoyan Xing, Wenying Yang and 1 more

Open access · hybridAbstract read
In one paragraph

Article in Aging, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
1citing papers in PubMed, 1 pooled it
0.3field-weighted citation impact, top 43% 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

1 citing paper in PubMed, 1 synthesis or guideline pooled it, 2 citations in OpenAlex.

  1. Pooled it
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

11 authors at 1 institution in 1 country.

Xuelian ZhangDepartment of Endocrinology, China-Japan Friendship Hospital, Beijing 100029, People's Republic of China.
Yao WangDepartment of Endocrinology, China-Japan Friendship Hospital, Beijing 100029, People's Republic of China.
Zhaojun YangDepartment of Endocrinology, China-Japan Friendship Hospital, Beijing 100029, People's Republic of China.
Xiaoping ChenDepartment of Endocrinology, China-Japan Friendship Hospital, Beijing 100029, People's Republic of China.
Jinping ZhangDepartment of Endocrinology, China-Japan Friendship Hospital, Beijing 100029, People's Republic of China.
Xin WangDepartment of Endocrinology, China-Japan Friendship Hospital, Beijing 100029, People's Republic of China.
Xian JinDepartment of Endocrinology, China-Japan Friendship Hospital, Beijing 100029, People's Republic of China.
Lili WuDepartment of Endocrinology, China-Japan Friendship Hospital, Beijing 100029, People's Republic of China.
Xiaoyan XingDepartment of Endocrinology, China-Japan Friendship Hospital, Beijing 100029, People's Republic of China.
Wenying YangDepartment of Endocrinology, China-Japan Friendship Hospital, Beijing 100029, People's Republic of China.
Bo ZhangDepartment of Endocrinology, China-Japan Friendship Hospital, Beijing 100029, People's Republic of China.
China-Japan Friendship Hospital · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Diabetic nephropathy (DN) is one microvascular complication of diabetes. About 30% of diabetic patients can develop DN, which is closely related to the high incidence and mortality of heart diseases, and then develop end-stage renal diseases. Therefore, early detection and screening of high-risk patients with DN is important. Herein, we explored the differences of serum transcriptomics between DN and non-DN in type II diabetes mellitus (T2DM) patients. We obtained 110 target genes using weighted correlation network analysis. Gene Ontology enrichment analysis indicates these target genes are mainly related to membrane adhesion, alpha-amino acid biosynthesis, metabolism, and binding, terminus, inhibitory synapse, clathrinid-sculpted vesicle, kinase activity, hormone binding, receptor activity, and transporter activity. Kyoto Encyclopedia of Genes and Genomes analysis indicates the process of DN in diabetic patients can involve synaptic vesicle cycle, cysteine and methionine metabolism, N-Glycan biosynthesis, osteoclast differentiation, and cAMP signaling pathway. Next, we detected the expression levels of hub genes in a retrospective cohort. Then, we developed a risk score tool included in the prediction model for early DN in T2DM patients. The prediction model was well applied into clinical practice, as confirmed by internal validation and several other methods. A novel DN risk model with relatively high prediction accuracy was established based on clinical characteristics and hub genes of serum detection. The estimated risk score can help clinicians develop individualized intervention programs for DN in T2DM. External validation data are required before individualized intervention measures.

Indexed as

Diabetes Mellitus, Type 2Diabetic NephropathiesCysteineHormonesHumansMethioninePolysaccharidesRetrospective StudiesCysteineHormonesMethioninePolysaccharidesdiabetic nephropathyprediction modelrisk factorsweighted correlation network analysis

Identifiers

PMID36242604
PMCPMC9596198
OpenAlexW4306249753

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.