Evidence map›Paper›PMID 41774528›Full record

ArticleDiabetes/metabolism research and reviews2026

Evaluation of Urine Exosome Lecithin Cholesterol Acyltransferase as a Biomarker for Diabetes Diagnosis and Dyslipidemia.

Tianci Liu, Na Liu, Qian Meng, Tao Li, Man Zhang

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Article in Diabetes/metabolism research and reviews, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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5 · Who and what money

Authors and funding

5 authors.

Tianci LiuClinical Laboratory Medicine, Beijing Shijitan Hospital, Capital Medical University, Beijing, China.
Na LiuClinical Laboratory Medicine, Beijing Shijitan Hospital, Capital Medical University, Beijing, China.
Qian MengClinical Laboratory Medicine, Beijing Shijitan Hospital, Capital Medical University, Beijing, China.
Tao LiClinical Laboratory Medicine, Beijing Shijitan Hospital, Capital Medical University, Beijing, China.
Man ZhangClinical Laboratory Medicine, Beijing Shijitan Hospital, Capital Medical University, Beijing, China.ORCID 0000-0001-5166-6804

Funding

Capital Medical University Scientific Research Development Fund PYZ24197The Beijing High-Level Innovation and Entrepreneurship Talent Support Program (Young Top Talent Projects) G202521124Validation and application development of a new urine diagnostic and monitoring marker test in type 2 diabetes-related diseases Z211100002921040
6 · The paper itself

Abstract

aimsGiven the necessity for diabetes monitoring, investigating the expression of lipid metabolism-related proteins may provide valuable insights for disease surveillance and mechanistic elucidation. MATERIALS AND

methodsLC-MS/MS was used to analyse the expression of lipid metabolism-related proteins in urine exosomes. Biomarkers were screened and their clinical significance was evaluated. Insulin-resistant hepatocytes and diabetic mouse models were established to validate and explore the underlying mechanisms.

resultsLogistic regression analysis revealed that elevated triglyceride (TG) and reduced high-density lipoprotein cholesterol (HDL-C) were independent risk factors for diabetes. In normal controls and those with prediabetes, females had higher total cholesterol (TC) and HDL-C but lower TG compared to males, whereas no gender differences were observed in the diabetic group. 29 lipid metabolism-related proteins were screened by proteomics, among which lecithin cholesterol acyltransferase (LCAT) was the target protein. Disordered lipid metabolism and upregulation of LCAT were observed in diabetic patients, insulin-resistant cells, and diabetic mice. The liver may be a key organ of early diabetic injury, as evidenced by disorganised hepatocyte arrangement and compensatory LCAT production during the prediabetic stage. As the disease progresses to diabetes, hepatic steatosis significantly worsens, accompanied by elevation of serum and urine LCAT. Urine exosome LCAT not only holds diagnostic value but also exhibits distinctive dynamic changes: an early rise in diabetes followed by a decline during periods of poor glycaemic control (HbA1c ≥ 8% or FBG > 7.8 mmol/L).

conclusionsLCAT, a critical regulator of lipid metabolism, could serve as a novel biomarker for detection and monitoring of diabetes.

Indexed as

BiomarkersDiabetes Mellitus, ExperimentalDiabetes Mellitus, Type 2DyslipidemiasExosomesPhosphatidylcholine-Sterol O-AcyltransferaseAnimalsCase-Control StudiesFemaleHumansInsulin ResistanceLipid MetabolismMaleMiceMice, Inbred C57BLMiddle AgedBiomarkersPhosphatidylcholine-Sterol O-Acyltransferaseanimal modelbiomarkerscell modeldiabetes mellitusLCATlipid metabolism

Identifiers

PMID41774528
PMCPMC12956041

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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.