Evidence map›Paper›PMID 29850574›Full record

ArticleBioMed research international2018

Bone Morphogenetic Proteins 2/4 Are Upregulated during the Early Development of Vascular Calcification in Chronic Kidney Disease.

Xiao Wei, Weihua Wu, Li Li, Jiaru Lin, Qi Liu, Linwang Gan, Santao Ou

Open access · hybridAbstract read
In one paragraph

Article in BioMed research international, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 15 papers.

0numbers the graph read from it
0cells of the map it votes in
15citing papers in PubMed
1.9field-weighted citation impact, top 16% 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

15 citing papers in PubMed, 26 citations in OpenAlex.

  1. Article
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  3. Article
  4. Review
  5. Article
  6. Article
  7. Review
  8. Review
  9. Review
  10. Article
  11. Article
  12. Vascular Calcification-New Insights Into Its Mechanism.International journal of molecular sciences · 2020
    Review
  13. Article
  14. Vascular calcification; Stony bridge between kidney and heart.Journal of cardiovascular and thoracic research · 2020
    Review
  15. Article
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

7 authors at 1 institution in 1 country.

Xiao WeiDepartment of Nephrology, The Affiliated Hospital of Southwest Medical University, Luzhou, Sichuan 646000, China.
Weihua WuDepartment of Nephrology, The Affiliated Hospital of Southwest Medical University, Luzhou, Sichuan 646000, China.
Li LiDepartment of Nephrology, The Affiliated Hospital of Southwest Medical University, Luzhou, Sichuan 646000, China.
Jiaru LinDepartment of Nephrology, The Affiliated Hospital of Southwest Medical University, Luzhou, Sichuan 646000, China.
Qi LiuDepartment of Nephrology, The Affiliated Hospital of Southwest Medical University, Luzhou, Sichuan 646000, China.
Linwang GanDepartment of Nephrology, The Affiliated Hospital of Southwest Medical University, Luzhou, Sichuan 646000, China.
Santao OuDepartment of Nephrology, The Affiliated Hospital of Southwest Medical University, Luzhou, Sichuan 646000, China.ORCID 0000-0003-4149-1996
Affiliated Hospital of Southwest Medical University · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Vascular calcification is a main cause of increased cardiovascular morbidity and mortality in chronic kidney disease (CKD) patients. This study aimed to investigate the role of the bone morphogenetic protein (BMP) signaling pathway in the early development of vascular calcification in CKD. A CKD vascular calcification rat model was established by providing rats with a 1.8% high-phosphorus diet and an intragastric administration of 2.5% adenine suspension. The kidney and aortic pathologies were analyzed. Blood biochemical indicators, serum BMP-2 and BMP-4 levels, and aortic calcium content were determined. The expression levels of BMP-2, BMP-4, bone morphogenetic protein receptor-IA (BMPR-IA), and matrix Gla protein (MGP) in aorta were examined by quantitative real-time polymerase chain reaction and immunohistochemistry. Compared with the normal control (Nor) rats, the CKD rats exhibited a significantly decreased body weight and an increased kidney weight as well as abnormal renal function and calcium-phosphorus metabolism. Aortic von Kossa and Alizarin red staining showed massive granular deposition and formation of calcified nodules in aorta at 8 weeks. The aortic calcium content was significantly increased, which was positively correlated with the serum BMP-2 (

Indexed as

AnimalsAortaBody WeightBone Morphogenetic Protein 2Bone Morphogenetic Protein 4Bone Morphogenetic Protein Receptors, Type ICalciumCalcium-Binding ProteinsEnzyme-Linked Immunosorbent AssayExtracellular Matrix ProteinsKidneyMaleMatrix Gla ProteinOrgan SizeProteinuriaRats, Sprague-DawleyBone Morphogenetic Protein 2Bone Morphogenetic Protein 4Bone Morphogenetic Protein Receptors, Type ICalciumCalcium-Binding ProteinsExtracellular Matrix ProteinsMatrix Gla Protein

Identifiers

PMID29850574
PMCPMC5925148
OpenAlexW2796486203

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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.