Evidence map›Paper›PMID 40211171›Full record

ArticleBMC nephrology2025

Serum midkine level and its association with subclinical coronary artery calcification and carotid atherosclerosis in chronic kidney disease.

Osama Nady Mohamed, Marwa Ibrahim Mohamed, Shaimaa F Kamel, Ahmed M Dardeer, Sayed Shehata, Hassan Mh Mohammed, Asmaa Khalf Kamel, Doaa Elzaeem Ismail, Nehal I Abbas, Mohamed Ahmed Abdelsamie and 5 more

Abstract read
In one paragraph

Article in BMC nephrology, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 3 papers.

0numbers the graph read from it
0cells of the map it votes in
3citing papers in PubMed
–field-weighted citation impact
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

3 citing papers in PubMed.

  1. The role of IL-6 in atherosclerosis: a narrative review.Frontiers in cardiovascular medicine · 2026
    Review
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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

15 authors.

Osama Nady MohamedDepartment of Internal Medicine, Faculty of Medicine, Minia University, Taha Hussein street, Minia, Egypt. osama.nady@mu.edu.eg.ORCID 0009-0009-7627-0617
Marwa Ibrahim MohamedDepartment of Internal Medicine, Faculty of Medicine, Minia University, Taha Hussein street, Minia, Egypt.
Shaimaa F KamelDepartment of Internal Medicine, Faculty of Medicine, Minia University, Taha Hussein street, Minia, Egypt.
Ahmed M DardeerDepartment of Cardiology, Faculty of Medicine, Minia University, Minia, Egypt.
Sayed ShehataDepartment of Cardiology, Faculty of Medicine, Minia University, Minia, Egypt.
Hassan Mh MohammedDepartment of Cardiology, Faculty of Medicine, Minia University, Minia, Egypt.
Asmaa Khalf KamelDepartment of Clinical Pathology, Faculty of Medicine, Minia University, Minia, Egypt.
Doaa Elzaeem IsmailDepartment of Clinical Pathology, Faculty of Medicine, Minia University, Minia, Egypt.
Nehal I AbbasDepartment of Clinical Pathology, Faculty of Medicine, Minia University, Minia, Egypt.
Mohamed Ahmed AbdelsamieDepartment of Radiology, Faculty of Medicine, Minia University, Minia, Egypt.
Ahmed Fathy Kamel ZiadyDepartment of Radiology, Faculty of Medicine, Minia University, Minia, Egypt.
Manar M SayedDepartment of Radiology, Faculty of Medicine, Minia University, Minia, Egypt.
Nermeen Dahi Mohammed ToniDepartment of Public and Preventive Medicine, Faculty of Medicine, Minia University, Minia, Egypt.
Shaimaa Moustafa HafezDepartment of Public and Preventive Medicine, Faculty of Medicine, Minia University, Minia, Egypt.
Shereen Mohammed Mohammed ElsaghirDepartment of Internal Medicine, Faculty of Medicine, Minia University, Taha Hussein street, Minia, Egypt.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundThere are no studies investigating the role of midkine (MK) in vascular calcification (VC) or vascular disease associated with chronic kidney disease (CKD). This study assessed serum MK level and investigated its relationship with carotid atherosclerosis and coronary artery calcification (CAC) in non-dialysis CKD.

methodsThe study comprised 80 controls and 185 adult patients with CKD at stages 3-5 who were free of cardiovascular diseases. Acute renal failure, chronic hemodialysis, severe liver disease, inflammatory states, anticoagulation therapy and cancer were excluded. The patients were classified based on presence of CAC score into severe and mild to moderate CAC groups. They were also divided into atherosclerotic and non-atherosclerotic groups based on carotid atherosclerosis. CBC, kidney function tests, lipid profile, intact parathyroid hormone (iPTH), and phosphorus were assessed. Serum levels of MK, tumor necrosis factor- α (TNF- α), interleukin-6 (IL-6), and high-sensitivity C-reactive protein (hs-CRP) were quantitatively tested using ELISA. Cardiac CT scan was done to calculate CAC score. Carotid ultrasonography was used to evaluate carotid intima media thickness (CIMT) and identify plaques.

resultsAll CKD categories, including CKD-3, CKD-4, and CKD-5, showed higher rates of carotid plaques (p = 0.007, p < 0.001, and p < 0.001, respectively), higher levels of MK (p < 0.001 for each), and higher CAC scores (p < 0.001 for each) as CKD worsened. Compared to mild to moderate CAC patients, severe CAC patients showed increased CIMT (p < 0.001) and raised serum levels of MK (p < 0.001), TNF-α (p = 0.001), IL-6 (p = 0.002), hs-CRP (p = 0.003), iPTH (p = 0.02), phosphorus (p < 0.001), total cholesterol (TC), and low density lipoprotein-cholesterol (LDL-C). Multivariate linear regression revealed that CAC was reliably predicted by MK (p = 0.008) and serum creatinine (p = 0.001). Carotid atherosclerotic patients had higher serum levels of MK, TNF-α, IL-6, hs-CRP, iPTH, phosphorus, TC, total triglycerides and LDL-C (p < 0.001 for each). Multivariate logistic regression showed that serum MK (p = 0.001), serum creatinine (p = 0.005), age (p < 0.001), iPTH (p = 0.007), and IL-6 (p = 0.024) were significant predictors of carotid atherosclerosis.

conclusionsAs CKD worsened, MK levels, carotid atherosclerosis and CAC increased. Serum MK was a reliable biomarker for asymptomatic carotid atherosclerosis and CAC in non-dialysis CKD, allowing prompt early diagnosis to avert cardiovascular morbidity and death in the future.

trial registrationThe trial number was 1138 and its registration was approved by the hospital's Research Ethics Committee in 4/2024.

Indexed as

Carotid Artery DiseasesCoronary Artery DiseaseMidkineRenal Insufficiency, ChronicVascular CalcificationAgedBiomarkersCarotid Intima-Media ThicknessCase-Control StudiesC-Reactive ProteinFemaleHumansMaleMiddle AgedBiomarkersC-Reactive ProteinMidkineAtherosclerosisChronic kidney diseaseMidkineVascular calcification

Identifiers

PMID40211171
PMCPMC11987434

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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.