Evidence map›Paper›PMID 37680629›Full record

ReviewFrontiers in immunology2023

Neutrophil extracellular traps mediate deep vein thrombosis: from mechanism to therapy.

Mengting Yao, Jiacheng Ma, Dongwen Wu, Chucun Fang, Zilong Wang, Tianting Guo, Jianwen Mo

Abstract readReview
In one paragraph

Review in Frontiers in immunology, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 55 papers.

0numbers the graph read from it
0cells of the map it votes in
55citing 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

55 citing papers in PubMed.

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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

7 authors.

Mengting YaoThe First Clinical College, Gannan Medical University, Ganzhou, Jiangxi, China.
Jiacheng MaThe First Clinical College, Gannan Medical University, Ganzhou, Jiangxi, China.
Dongwen WuThe First Clinical College, Gannan Medical University, Ganzhou, Jiangxi, China.
Chucun FangThe First Clinical College, Gannan Medical University, Ganzhou, Jiangxi, China.
Zilong WangThe First Clinical College, Gannan Medical University, Ganzhou, Jiangxi, China.
Tianting GuoDepartment of Orthopedics, Guangdong Provincial People's Hospital Ganzhou Hospital, Ganzhou Municipal Hospital, Ganzhou, Jiangxi, China.
Jianwen MoDepartment of Orthopedic Surgery, The First Affiliated Hospital of Gannan Medical University, Ganzhou, Jiangxi, China.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Deep venous thrombosis (DVT) is a part of venous thromboembolism (VTE) that clinically manifests as swelling and pain in the lower limbs. The most serious clinical complication of DVT is pulmonary embolism (PE), which has a high mortality rate. To date, its underlying mechanisms are not fully understood, and patients usually present with clinical symptoms only after the formation of the thrombus. Thus, it is essential to understand the underlying mechanisms of deep vein thrombosis for an early diagnosis and treatment of DVT. In recent years, many studies have concluded that Neutrophil Extracellular Traps (NETs) are closely associated with DVT. These are released by neutrophils and, in addition to trapping pathogens, can mediate the formation of deep vein thrombi, thereby blocking blood vessels and leading to the development of disease. Therefore, this paper describes the occurrence and development of NETs and discusses the mechanism of action of NETs on deep vein thrombosis. It aims to provide a direction for improved diagnosis and treatment of deep vein thrombosis in the near future.

Indexed as

Extracellular TrapsVenous ThrombosisHumansLower ExtremityNeutrophilsPaindeep venous thrombosisdeoxyribonucleaseneutrophilneutrophil extracellular trapsplatelet

Identifiers

PMID37680629
PMCPMC10482110

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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.