Evidence map›Paper›PMID 41054696›Full record

ArticleCureus2025

Adropin as a Marker in Type 2 Diabetes: Insights Into Diabetic Kidney Disease and Chronic Heart Failure.

Satyendra K Sonkar, Madhusudan Agrawal, Gyanendra K Sonkar, Vivek Bhosale, Medhavi Gautam, Akshay Pradhan, Satish Kumar, Deepak Bhagchandani, Abhishek Singh

Abstract read
In one paragraph

Article in Cureus, 2025. 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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1 · What the graph read from it

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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

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No citing paper in PubMed yet.

4 · The record

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5 · Who and what money

Authors and funding

9 authors.

Satyendra K SonkarMedicine, King George's Medical University, Lucknow, IND.
Madhusudan AgrawalMedicine, King George's Medical University, Lucknow, IND.
Gyanendra K SonkarBiochemistry, King George's Medical University, Lucknow, IND.
Vivek BhosaleToxicology and Experimental Medicine, Central Drug Research Institute, Lucknow, IND.
Medhavi GautamNephrology, King George's Medical University, Lucknow, IND.
Akshay PradhanCardiology, King George's Medical University, Lucknow, IND.
Satish KumarMedicine, King George's Medical University, Lucknow, IND.
Deepak BhagchandaniMedicine, King George's Medical University, Lucknow, IND.
Abhishek SinghCommunity and Family Medicine, King George's Medical University, Lucknow, IND.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundType 2 diabetes mellitus (T2DM) is frequently associated with diabetic kidney disease (DKD) and chronic heart failure (CHF), conditions that share overlapping pathophysiological mechanisms. Adropin, a liver- and brain-derived peptide hormone, has emerged as a novel biomarker involved in metabolic regulation, endothelial function, and inflammation. However, its role in differentiating stages of T2DM-related complications remains underexplored.

objectivesThis study aimed to evaluate serum adropin levels in T2DM patients with and without DKD and to assess its association with coexisting CHF.

methodsThis was an observational case-control study which was conducted over a period of one year and included 111 participants divided into three groups: healthy controls, T2DM without nephropathy, and T2DM with nephropathy (with and without CHF). Serum adropin levels were measured using enzyme-linked immunosorbent assay (ELISA), and comprehensive clinical, biochemical, and echocardiographic assessments were done.

resultsSerum adropin levels were significantly reduced in T2DM patients (0.61 ± 0.13 ng/mL, p < 0.0001), with the lowest levels observed in those with both DKD and CHF (0.47 ± 0.12 ng/mL, p < 0.0001) compared to controls (0.76 ± 0.10 ng/mL, p < 0.0001). A progressive decline in adropin was noted with worsening glycemic control, renal dysfunction, chronic inflammation, and cardiac dysfunction. Significant inverse correlations were found between adropin and glycosylated hemoglobin (HbA1c) (

conclusionThe study demonstrated that serum adropin levels decline progressively with worsening cardiorenal-metabolic parameters. These findings reinforce the role of adropin as a sensitive marker of endothelial and metabolic dysfunction, especially in patients with coexisting T2DM, DKD, and CHF. Given its strong correlation with markers of glycemic control, renal impairment, and inflammation, adropin may serve as a noninvasive biomarker for early detection and risk stratification.

Indexed as

albuminuriacrpegfrhba1cpro-bnp

Identifiers

PMID41054696
PMCPMC12497421

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