Evidence map›Paper›PMID 25588520›Full record

ArticleDigestive diseases and sciences2015

Circulating mitochondrial DNA content associated with the risk of liver cirrhosis: a nested case-control study.

Chun Wang, Hie-Won Hann, Richard S Hann, Shaogui Wan, Ronald E Myers, Zhong Ye, Jinliang Xing, Hushan Yang

Abstract read
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In one paragraph

Article in Digestive diseases and sciences, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 8 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
8citing papers in PubMed, 1 pooled it
1.1field-weighted citation impact, top 21% 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, 1 synthesis or guideline pooled it, 15 citations in OpenAlex.

  1. Pooled it
  2. Article
  3. [Research Progress on the Role of Mitochondrial DNA in the Pathogenesis of Chronic Liver Disease].Zhonghua gan zang bing za zhi = Zhonghua ganzangbing zazhi = Chinese journal of hepatology · 2022
    Article
  4. Review
  5. Article
  6. 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

8 authors at 3 institutions in 2 countries.

Chun WangDivision of Population Science, Department of Medical Oncology, Sidney Kimmel Cancer Center, Thomas Jefferson University, Philadelphia, PA, USA.
Hie-Won Hann
Richard S Hann
Shaogui Wan
Ronald E Myers
Zhong Ye
Jinliang Xing
Hushan Yang
Thomas Jefferson University · USAir Force Medical University · CNSidney Kimmel Cancer Center · US

Funding

Serum microRNA signature as prospective HCC biomarker in HBV patientsR21CA159047 · NCI · THOMAS JEFFERSON UNIVERSITY · PI YANG, HUSHAN · 2011 to 2012
$371k
Inflammation Variants and Risk of Hepatocellular Carcinoma in HBV PatientsR03CA153099 · NCI · THOMAS JEFFERSON UNIVERSITY · PI YANG, HUSHAN · 2010 to 2011
$153k
NCI NIH HHS CA153099NCI NIH HHS CA159047NCI NIH HHS R03 CA153099NCI NIH HHS R21 CA159047
6 · The paper itself

Abstract

BACKGROUND AND

aimsAccumulating evidence has indicated that variations of mitochondrial DNA (mtDNA) content may affect the susceptibility to hepatocellular carcinoma (HCC). However, no study has been conducted to evaluate the association of circulating mtDNA content and the risk of liver cirrhosis, a leading cause of HCC.

methodsWe conducted a nested case-control study including 136 cirrhotic hepatitis B virus (HBV) cases and 136 frequency-matched non-cirrhotic HBV controls. We determined mtDNA content in serum DNA using quantitative real-time PCR and analyzed its association with cirrhosis risk.

resultsWe found that cirrhotic HBV patients had significantly lower levels of mtDNA content than non-cirrhotic HBV controls (P = 0.0184). Compared to patients with high mtDNA content, those with low mtDNA content had a 2.25-fold increased risk of cirrhosis [odds ratio (OR) 2.25, 95 % confidence interval (CI) 1.26-4.02]. This association exhibited a significant dose relationship as evidenced in both tertile and quartile analyses (P for trend = 0.0018 and 0.0008, respectively). Stratified analyses showed that the association was prominent in younger patients (P = 0.0122), males (P = 0.0069), never smokers (P = 0.0063), never drinkers (P = 0.0078), patients with a family history of HBV infection (P = 0.0062), and patients with low values of aspartate aminotransferase to platelet ratio index (APRI), a commonly used noninvasive marker for cirrhosis (P = 0.0109). Moreover, a joint effect was observed between low mtDNA content and high APRI values on cirrhosis risk (OR 24.07, 95 % CI 6.72-86.24).

conclusionsLow circulating mtDNA content may confer an increased cirrhosis risk in HBV patients. Further prospective studies are warranted to validate these findings and explore the clinical significance.

Indexed as

BiopsyCase-Control StudiesDiagnostic ImagingDNA, MitochondrialFemaleHepatitis B, ChronicHumansLiver CirrhosisMaleMiddle AgedReal-Time Polymerase Chain ReactionRepublic of KoreaRisk FactorsDNA, Mitochondrial

Identifiers

PMID25588520
OpenAlexW2096684497

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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.