Evidence map›Paper›PMID 31574813›Full record

Observational studyMedicine2019

Increased perihematomal neuron autophagy and plasma thrombin-antithrombin levels in patients with intracerebral hemorrhage: An observational study.

Chenghan Wu, Xiaohua Yan, Yuansheng Liao, Lianming Liao, Shengyue Huang, Quanting Zuo, Linying Zhou, Lili Gao, Yinzhou Wang, Jushan Lin and 6 more

Open access · goldAbstract readObservational Study
In one paragraph

Observational study in Medicine, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 15 papers, 2 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
15citing papers in PubMed, 2 pooled it
1.7field-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, 2 syntheses or guidelines pooled it, 18 citations in OpenAlex.

  1. Pooled it
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  3. Review
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  7. Review
  8. Article
  9. Modes of Brain Cell Death Following Intracerebral Hemorrhage.Frontiers in cellular neuroscience · 2022
    Review
  10. Review
  11. 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

16 authors at 4 institutions in 2 countries.

Chenghan WuDepartment of Neurology, Second Affiliated Clinical College of Fujian University of Traditional Chinese Medicine.
Xiaohua YanDepartment of Neurosurgery and TCM, Fujian Provincial Hospital.
Yuansheng LiaoDepartment of Neurology, Second Affiliated Clinical College of Fujian University of Traditional Chinese Medicine.
Lianming LiaoCentral Laboratory, Union Hospital of Fujian Medical University.
Shengyue HuangDepartment of Neurosurgery and TCM, Fujian Provincial Hospital.
Quanting ZuoDepartment of Neurology, Second Affiliated Clinical College of Fujian University of Traditional Chinese Medicine.
Linying ZhouLaboratory of Electron Microscopy, Department of Pathology, School of Basic Medical Sciences, Fujian Medical University, Fuzhou, China.
Lili GaoDepartment of Neurology, Second Affiliated Clinical College of Fujian University of Traditional Chinese Medicine.
Yinzhou WangDepartment of Neurosurgery and TCM, Fujian Provincial Hospital.
Jushan LinDepartment of Neurology, Second Affiliated Clinical College of Fujian University of Traditional Chinese Medicine.
Shiju LiDepartment of Neurology, Second Affiliated Clinical College of Fujian University of Traditional Chinese Medicine.
Kaiyu WangDepartment of Neurosurgery and TCM, Fujian Provincial Hospital.
Xiuming GeDepartment of Neurology, Second Affiliated Clinical College of Fujian University of Traditional Chinese Medicine.
Hailong SongDepartment of Pathology and Anatomical Sciences, University of Missouri, Columbia, MO.
Ruiling YangDepartment of Neurology, Second Affiliated Clinical College of Fujian University of Traditional Chinese Medicine.
Feng LuFujian University of Traditional Chinese Medicine, Fuzhou, China.
Fujian University of Traditional Chinese Medicine · CNFujian Provincial Hospital · CNFujian Medical University · CNUniversity of Missouri · US

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Animal studies have demonstrated that autophagy was involved in neuronal damage after intracerebral hemorrhage (ICH). Several studies showed thrombin-antithrombin (TAT) plasma levels were elevated in patients with ICH. In this study, we aimed to evaluate if autophagy occurred in patients with ICH; and the relationship between the severity of brain injury and plasma TAT levels.A novel tissue harvesting device was used during hematoma removal surgery to collect loose fragments of tissue surrounding the affected brain area in 27 ICH patients with hematoma volumes of >30 mL in the basal ganglia. Control tissues were obtained from patients who underwent surgery for arteriovenous malformation (n = 25). Transmission electron microscopy (TEM) and immunohistochemistry for autophagy-related proteins were used to evaluate the ultrastructural and morphologic cellular characteristics; and the extent of autophagy in the recovered tissue specimens. Stroke severity was assessed by using the Glasgow Coma Scale (GCS) and the National Institutes of Health Stroke Scale (NIHSS). An enzyme-linked immunosorbent assay (ELISA) was used to measure plasma TAT levels.Transmission electron microscopy showed autophagosomes and autolysosomes exist in neurons surrounding the hematoma, but not in the control tissues. The number of cells containing autophagic vacuoles correlated with the severity of brain injury. Immunohistochemistry showed strong LC3, beclin 1, and cathepsin D staining in ICH tissue specimens. Plasma TAT levels correlated positively with autophagic cells and ICH severity (P < .01).Autophagy was induced in perihematomal neurons after ICH. Autophagy and plasma TAT levels correlated positively with severity of brain injury. These results suggest that autophagy and increased plasma TAT levels may contribute to the secondary damage in ICH patients.

Indexed as

AutophagyAdultAgedAntithrombin IIIBasal GangliaCerebral HemorrhageFemaleGlasgow Coma ScaleHematomaHumansMaleMiddle AgedNeuronsPeptide HydrolasesAntithrombin IIIantithrombin III-protease complexPeptide Hydrolases

Identifiers

PMID31574813
PMCPMC6775380
OpenAlexW2975722668

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC-ND
Read underepoch 390

Registered trials

None linked

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.