Evidence map›Paper›PMID 7876386›Full record

ArticleJournal of clinical pathology1994

Hepatic expression of tumour necrosis factor-alpha in chronic hepatitis B virus infection.

M J Hussain, J Y Lau, R Williams, D Vergani

Open access · bronzeAbstract read
In one paragraph

Article in Journal of clinical pathology, 1994. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 8 papers.

0numbers the graph read from it
0cells of the map it votes in
8citing papers in PubMed
1.2field-weighted citation impact, top 22% 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

8 citing papers in PubMed, 28 citations in OpenAlex.

  1. Article
  2. Article
  3. Hepatitis mouse models: from acute-to-chronic autoimmune hepatitis.International journal of experimental pathology · 2014
    Review
  4. Article
  5. Review
  6. Endocrine manifestations of hepatitis C virus infection.Nature clinical practice. Endocrinology & metabolism · 2009
    Review
  7. Review
  8. 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

4 authors at 1 institution in 1 country.

M J HussainDepartment of Immunology, King's College School of Medicine and Dentistry, London.
J Y Lau
R Williams
D Vergani
King's College School · GB

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

aimTo determine the hepatic expression of tumour necrosis factor-alpha (TNF alpha) in patients with chronic hepatitis B virus (HBV) infection.

methodsFrozen liver biopsy sections from 19 patients with chronic HBV infection were studied, 12 of whom were HBeAg positive and 10 serum HBV DNA positive. Hepatic expression of TNF alpha was determined using immunohistochemistry.

resultsOnly infiltrating mononuclear cells showed immunoreactive staining for TNF alpha (median 2, range 0-3; n = 19) which appeared as diffuse positive staining material in the cytoplasm. Patients with active liver disease, assessed histologically and biochemically, had a higher level of expression, both in the number of TNF alpha positive cells and the proportion of TNF alpha positive infiltrating mononuclear cells. There was no correlation between the expression of TNF alpha and serological parameters of viral infection (HBeAg and HBV DNA status and HBV DNA concentrations).

conclusionHepatic expression of TNF alpha is increased in chronic HBV infection and is related to the activity of liver disease and not to the level of HBV replication.

Indexed as

AdultChronic DiseaseDNA, ViralFemaleHepatitis BHepatitis B e AntigensHepatitis B virusHumansImmunohistochemistryLiverMaleMiddle AgedTumor Necrosis Factor-alphaDNA, ViralHepatitis B e AntigensTumor Necrosis Factor-alpha

Identifiers

PMID7876386
PMCPMC502205
OpenAlexW2033458709

What OpenQuestion holds

Textmetadata
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.