Evidence map›Paper›PMID 26003174›Full record

ArticleCardiovascular diabetology2015

Increased plasma BMP-2 levels are associated with atherosclerosis burden and coronary calcification in type 2 diabetic patients.

Ming Zhang, Jaskanwal Deep Sara, Fei-long Wang, Li-Ping Liu, Li-Xiao Su, Jing Zhe, Xi Wu, Jing-hua Liu

Open access · goldAbstract read
In one paragraph

Article in Cardiovascular diabetology, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 41 papers.

0numbers the graph read from it
0cells of the map it votes in
41citing papers in PubMed
3.3field-weighted citation impact, top 8% 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

41 citing papers in PubMed, 73 citations in OpenAlex.

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  14. Metabolic Health and Disease: A Role of Osteokines?Calcified tissue international · 2023
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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

8 authors at 7 institutions in 2 countries.

Ming ZhangDepartment of Cardiology, Beijing Anzhen Hospital, Capital Medical University, Beijing, 100029, PR China. zhangming2279@hotmail.com.
Jaskanwal Deep SaraDivision of Cardiovascular Diseases, Mayo College of Medicine, Rochester, MN, USA. Sara.Jaskanwal@mayo.edu.
Fei-long WangDivision of Cardiovascular Diseases, Mayo College of Medicine, Rochester, MN, USA. Wang.Fei-long@mayo.edu.
Li-Ping LiuDepartment of Nephrology, First Hospital of Tsinghua University, Beijing, China. llp9076@icloud.com.
Li-Xiao SuDepartment of Biostatistics, Rutgers School of Public Health, The State University of New Jersey, Piscataway, NJ, USA. sulixiaousa@gmail.com.
Jing ZheDepartment of Biostatistics, University at Buffalo, the State University of New York, Buffalo, NY, 14214, USA. zhejing0@gmail.com.
Xi WuDepartment of Cardiology, Beijing Anzhen Hospital, Capital Medical University, Beijing, 100029, PR China. wuxi123@163.com.
Jing-hua LiuDepartment of Cardiology, Beijing Anzhen Hospital, Capital Medical University, Beijing, 100029, PR China. liujinghua@vip.sina.com.
Mayo Clinic · USBeijing Anzhen Hospital · CNBeijing Hua Xin Hospital · CNBeijing Institute of Water · CNCapital Medical University · CNRutgers, The State University of New Jersey · USUniversity at Buffalo, State University of New York · US

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundAlthough Bone morphogenetic protein-2 (BMP-2) is a known mediator of bone regeneration and vascular calcification, to date no study has investigated the relationship between BMP-2 and type 2 diabetes mellitus (T2DM) and its possible role in coronary artery disease (CAD). The purpose of this study is to evaluate the relationship of BMP-2 with atherosclerosis and calcification in patients with T2DM.

methods124 subjects were enrolled in this study: 29 patients with T2DM and CAD; 26 patients with T2DM and without CAD; 36 patients with CAD and without T2DMand 34 without T2DM or CAD (control group). Severity of coronary lesions was assessed using coronary angiography and intravascular ultrasound (IVUS). Plasma BMP-2 levels were quantified using a commercially available ELISA kit.

resultsCompared to the control group, the mean plasma BMP-2 level was significantly higher in T2DM patients with or without CAD (20.1 ± 1.7 or 19.3 ± 1.5 pg/ml, vs 17.2 ± 3.3 pg/ml, P < 0.001). In a multivariable linear regression analysis, both T2DM and CAD were significantly and positively associated with BMP-2 (Estimate, 0.249; standard error (SE), 0.063; p <0.0001; Estimate, 0.400; SE, 0.06; p < 0.0001). Plasma BMP-2 was also strongly correlated with glycosylated hemoglobin A1c (HbA1c) (Spearman ρ = -0.31; p = 0.0005). SYNTAX score was also significantly associated with BMP-2 (Spearman ρ = 0.46; p = 0.0002). Using the results from IVUS, plasma BMP-2 levels were shown to positively correlate with plaque burden (Spearman ρ = 0.38, P = 0.002) and plaque calcification (Spearman ρ =0.44, P = 0.0003) and to negatively correlate with lumen volume (Spearman ρ =0.31, P = 0.01).

conclusionsOur study demonstrates that patients with T2DM had higher circulating levels of BMP-2 than normal controls. Plasma BMP-2 levels correlated positively with plaque burden and calcification in patients with T2DM.

Indexed as

AgedAtherosclerosisBone Morphogenetic Protein 2Coronary AngiographyCoronary Artery DiseaseDiabetes Mellitus, Type 2FemaleHumansMaleMiddle AgedSeverity of Illness IndexUltrasonography, InterventionalVascular CalcificationBMP2 protein, humanBone Morphogenetic Protein 2

Identifiers

PMID26003174
PMCPMC4450848
OpenAlexW1607933713

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LicenceCC BY
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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.