Evidence map›Paper›PMID 38584258›Full record

ArticleCell & bioscience2024

Klotho exerts protection in chronic kidney disease associated with regulating inflammatory response and lipid metabolism.

Junhui Liu, Huaicheng Wang, Qinyu Liu, Shushu Long, Yanfang Wu, Nengying Wang, Wei Lin, Gang Chen, Miao Lin, Junping Wen

Erratum issuedOpen access · goldAbstract read
In one paragraph

Article in Cell & bioscience, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. An erratum has been issued. Cited by 25 papers.

0numbers the graph read from it
0cells of the map it votes in
25citing papers in PubMed
11.5field-weighted citation impact, top 1% 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

25 citing papers in PubMed, 34 citations in OpenAlex.

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  11. [Potential of early diagnosis and targeted therapy for Klotho protein in chronic kidney disease].Zhong nan da xue xue bao. Yi xue ban = Journal of Central South University. Medical sciences · 2025
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4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

10 authors at 2 institutions in 1 country.

Junhui Liu *Shengli Clinical Medical College of Fujian Medical University, Fujian Medical University, Fuzhou, China.
Huaicheng Wang *Shengli Clinical Medical College of Fujian Medical University, Fujian Medical University, Fuzhou, China.
Qinyu Liu *Shengli Clinical Medical College of Fujian Medical University, Fujian Medical University, Fuzhou, China.
Shushu LongShengli Clinical Medical College of Fujian Medical University, Fujian Medical University, Fuzhou, China.
Yanfang WuShengli Clinical Medical College of Fujian Medical University, Fujian Medical University, Fuzhou, China.
Nengying WangShengli Clinical Medical College of Fujian Medical University, Fujian Medical University, Fuzhou, China.
Wei LinShengli Clinical Medical College of Fujian Medical University, Fujian Medical University, Fuzhou, China.
Gang ChenShengli Clinical Medical College of Fujian Medical University, Fujian Medical University, Fuzhou, China. chengangfj@163.com.
Miao LinShengli Clinical Medical College of Fujian Medical University, Fujian Medical University, Fuzhou, China. 10151246@qq.com.
Junping WenShengli Clinical Medical College of Fujian Medical University, Fujian Medical University, Fuzhou, China. junpingwen@163.com.
Fujian Medical University · CNFujian Provincial Hospital · CN

Funding

National Key Research and Development Program of China 2018YFC2001100-5National Natural Science Foundation of China No. 82070878Natural Science Foundation of Fujian Province No. 2020J011081Natural Science Foundation of Fujian Province No. 2021J01381
6 · The paper itself

Abstract

backgroundThe anti-aging protein Klotho plays a protective role in kidney disease, but its potential as a biomarker for chronic kidney disease (CKD) is controversial. Additionally, the main pathways through which Klotho exerts its effects on CKD remain unclear. Therefore, we used bioinformatics and clinical data analysis to determine its role in CKD.

resultsWe analyzed the transcriptomic and clinical data from the Nephroseq v5 database and found that the Klotho gene was mainly expressed in the tubulointerstitium, and its expression was significantly positively correlated with estimated glomerular filtration rate (eGFR) and negatively correlated with blood urea nitrogen (BUN) in CKD. We further found that Klotho gene expression was mainly negatively associated with inflammatory response and positively associated with lipid metabolism in CKD tubulointerstitium by analyzing two large sample-size CKD tubulointerstitial transcriptome datasets. By analyzing 10-year clinical data from the National Health and Nutrition Examination Survey (NHANES) 2007-2016, we also found that Klotho negatively correlated with inflammatory biomarkers and triglyceride and positively correlated with eGFR in the CKD population. Mediation analysis showed that Klotho could improve renal function in the general population by modulating the inflammatory response and lipid metabolism, while in the CKD population, it primarily manifested by mediating the inflammatory response. Restricted cubic spline (RCS) analysis showed that the optimal concentration range for Klotho to exert its biological function was around 1000 pg/ml. Kaplan-Meier curves showed that lower cumulative hazards of all-cause mortality in participants with higher levels of Klotho. We also demonstrated that Klotho could reduce cellular inflammatory response and improve cellular lipid metabolism by establishing an in vitro model similar to CKD.

conclusionsOur results suggest that Klotho exerts protection in CKD, which may be mainly related to the regulation of inflammatory response and lipid metabolism, and it can serve as a potential biomarker for CKD.

Indexed as

BiomarkerChronic kidney diseaseInflammatory responseKlothoLipid metabolism

Identifiers

PMID38584258
PMCPMC11000353
OpenAlexW4394063753

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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.