Evidence map›Paper›PMID 36769016›Full record

ArticleInternational journal of molecular sciences2023

Pyruvate Kinase M2: A New Biomarker for the Early Detection of Diabetes-Induced Nephropathy.

Yeon Su Park, Joo Hee Han, Jae Hyeon Park, Ji Soo Choi, Seung Hyeon Kim, Hyung Sik Kim

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Article in International journal of molecular sciences, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 10 papers.

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0cells of the map it votes in
10citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

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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

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3 · Its place in the literature

Who cites it

10 citing papers in PubMed.

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  7. Energy metabolism in health and diseases.Signal transduction and targeted therapy · 2025
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4 · The record

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5 · Who and what money

Authors and funding

6 authors.

Yeon Su ParkSchool of Pharmacy, Sungkyunkwan University, Suwon 16419, Republic of Korea.
Joo Hee HanSchool of Pharmacy, Sungkyunkwan University, Suwon 16419, Republic of Korea.ORCID 0000-0003-0797-3019
Jae Hyeon ParkSchool of Pharmacy, Sungkyunkwan University, Suwon 16419, Republic of Korea.
Ji Soo ChoiSchool of Pharmacy, Sungkyunkwan University, Suwon 16419, Republic of Korea.
Seung Hyeon KimSt. Mark's School, 25 Marlboro Rd, Southborough, MA 01772, USA.
Hyung Sik KimSchool of Pharmacy, Sungkyunkwan University, Suwon 16419, Republic of Korea.ORCID 0000-0001-7657-3970

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Diabetic nephropathy (DN) is a common complication of diabetes. DN progresses to end-stage renal disease, which has a high mortality rate. Current research is focused on identifying non-invasive potential biomarkers in the early stage of DN. We previously indicated that pyruvate kinase M2 (PKM2) is excreted in the urine of rats after cisplatin-induced acute kidney injury (AKI). However, it has not been reported whether PKM2 can be used as a biomarker to diagnose DN. Therefore, we try to compare whether the protein PKM2 can be detected in the urine samples from diabetic patients as shown in the results of DN models. In this study, high-fat diet (HFD)-induced Zucker diabetic fatty (ZDF) rats were used for DN phenotyping. After 19 weeks of receiving a HFD, the DN model's blood glucose, blood urea nitrogen, and serum creatinine levels were significantly increased; severe tubular and glomerular damages were also noted. The following protein-based biomarkers were increased in the urine of these models: kidney injury molecule-1 (KIM-1), neutrophil gelatinase-associated lipocalin (NGAL), and PKM2. PKM2 had the earliest detection rate. In the urine samples of patients, PKM2 protein was highly detected in the urine of diabetic patients but was not excreted in the urine of normal subjects. Therefore, PKM2 was selected as the new biomarker for the early diagnosis of DN. Our results reflect current knowledge on the role of PKM2 in DN.

Indexed as

Diabetes MellitusDiabetic NephropathiesAnimalsBiomarkersEarly DiagnosisLipocalin-2Pyruvate KinaseRatsRats, ZuckerBiomarkersLipocalin-2Pyruvate Kinasebiomarkerdiabetesnephropathypyruvate kinase M2urinary excretion

Identifiers

PMID36769016
PMCPMC9916947

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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.