Evidence map›Paper›PMID 27882137›Full record

ArticleExperimental and therapeutic medicine2016

Von Willebrand factor and coagulation factor VIII in Moyamoya disease associated with Graves' disease: A case report.

Shou-Chen Ren, Bao-Qin Gao, Wei-Li Yang, Wei-Xin Feng, Jian Xu, Shao-Wu Li, Yong-Jun Wang

Abstract read
In one paragraph

Article in Experimental and therapeutic medicine, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.

0numbers the graph read from it
0cells of the map it votes in
2citing 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

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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

2 citing papers in PubMed.

  1. Article
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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.

Shou-Chen RenDepartment of Pediatrics, Beijing Tian Tan Hospital, Capital Medical University, Beijing 100050, P.R. China.
Bao-Qin GaoDepartment of Pediatrics, Beijing Tian Tan Hospital, Capital Medical University, Beijing 100050, P.R. China.
Wei-Li YangDepartment of Pediatrics, Beijing Tian Tan Hospital, Capital Medical University, Beijing 100050, P.R. China.
Wei-Xin FengDepartment of Pediatrics, Beijing Tian Tan Hospital, Capital Medical University, Beijing 100050, P.R. China.
Jian XuDepartment of Endocrinology, Beijing Tian Tan Hospital, Capital Medical University, Beijing 100050, P.R. China.
Shao-Wu LiDepartment of Functional Neuroimaging, Beijing Neurosurgical Institute, Capital Medical University, Beijing 100050, P.R. China.
Yong-Jun WangDepartment of Neurology, Beijing Tian Tan Hospital, Capital Medical University, Beijing 100050, P.R. China.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

The present study reported the case of a Chinese boy who was diagnosed with Moyamoya disease (MMD) associated with Graves' disease (GD). An overactivation of von Willebrand factor (vWF) and coagulation factor VIII (FVIII) was identified in the plasma of the patient. Thiamazole and metoprolol treatment was thus administrated. After 2 months of treatment, the patient's thyroid function returned to normal and the neurological symptoms improved gradually. At the same time, the activities of vWF and FVIII were depressed. During the 20-month follow-up, information regarding the neurological symptoms, cerebrovascular imaging, thyroid function, thyroid autoantibodies and coagulation parameters was collected. High levels of thyroid autoantibodies persisted throughout the follow-up period, while other coagulation parameters remained in the normal range. In conclusion, considering the vital role of vWF and FVIII in vascular diseases, it is hypothesized that these two factors may serve an important role in the occurrence of GD associated with MMD.

Indexed as

coagulation factor VIIIGraves' diseaseMoyamoya diseasevon Willebrand factor

Identifiers

PMID27882137
PMCPMC5103767

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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.