Evidence map›Paper›PMID 36352372›Full record

ArticleBMC gastroenterology2022

Natural history of decompensated cirrhosis with serum hepatitis B DNA < 2000 IU/mL: a retrospective study.

Xu Huang, Meimei Yan, Zerun Deng, Lei Yao, Dan Han, Lihua Sun

Open access · goldAbstract read
In one paragraph

Article in BMC gastroenterology, 2022. 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
0.3field-weighted citation impact, top 40% 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

2 citing papers in PubMed, 2 citations in OpenAlex.

  1. Article
  2. Review
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

6 authors at 3 institutions in 1 country.

Xu HuangDepartment of Epidemiology, The First Affiliated Hospital of Shandong First Medical University & Shandong Provincial Qianfoshan Hospital, No. 16766, Jingshi Road, Ji'nan City, Shandong Province, 250000, People's Republic of China.
Meimei YanInfectious Diseases Center, The First Affiliated Hospital of Xinjiang Medical University, No.137, Liyushan South Road830000, Urumqi City, Xinjiang Province, People's Republic of China.
Zerun DengInfectious Diseases Center, The First Affiliated Hospital of Xinjiang Medical University, No.137, Liyushan South Road830000, Urumqi City, Xinjiang Province, People's Republic of China.
Lei YaoInfectious Diseases Center, The First Affiliated Hospital of Xinjiang Medical University, No.137, Liyushan South Road830000, Urumqi City, Xinjiang Province, People's Republic of China.
Dan HanInfectious Diseases Center, The First Affiliated Hospital of Xinjiang Medical University, No.137, Liyushan South Road830000, Urumqi City, Xinjiang Province, People's Republic of China.
Lihua SunInfectious Diseases Center, The First Affiliated Hospital of Xinjiang Medical University, No.137, Liyushan South Road830000, Urumqi City, Xinjiang Province, People's Republic of China. lihuasun126@126.com.
Xinjiang Medical University · CNFirst Affiliated Hospital of Xinjiang Medical University · CNShandong Provincial QianFoShan Hospital · CN

Funding

National Natural Science Foundation of China 82060121
6 · The paper itself

Abstract

BACKGROUND AND

aimsPatients with low HBV DNA levels (< 2000 IU/mL), HBV DNA negative, and HBsAg-negative hepatitis B virus(HBV)infection can still progress to decompensated cirrhosis; however, clinical research data in such patients, especially treatment-naïve patients, are currently insufficient. This study assessed the natural history of aforementioned patients.

methodsWe retrospectively reviewed the data of 250 patients with HBV-associated decompensated cirrhosis(HBV DNA < 2000 IU/mL) who had not been treated with antiviral medication.

resultsThe mean age of the 250 patients was 53.90 ± 11.73 years and 183 patients (73.2%) were male. HBV DNA, HBsAg, and HBeAg positivity was detected in 77 (30.8%), 200 (80%), and 137 (54.8%) patients, respectively. HBsAg (odds ratio [OR], 3.303; 95% confidence interval [CI], 1.338-8.152; P = 0.010) and HBeAg (OR, 0.200; 95% CI, 0.107-0.376; P < 0.001) positivity were independent factors for low HBV DNA levels. The incidence of hepatocellular carcinoma (HCC) (P < 0.001) and portal vein thrombosis (P = 0.001) was higher in the low HBV DNA levels group. Multivariate analysis showed that HBV DNA positivity (OR, 3.548; 95% CI, 1.463-8.604; P = 0.005), HBeAg positivity (OR, 0.080; 95% CI, 0.022-0.289; P < 0.001), and glutamyltransferase (GGT) (OR, 1.003; 95% CI, 1.000-1.006; P = 0.040) were independent factors for HCC. Age was not related to the occurrence of cirrhosis complications.

conclusionPatients with decompensated cirrhosis with HBV DNA < 2000 IU/mL still had severe liver damage and could develop severe cirrhosis complications. HCC risk was higher in low HBV DNA levels patients. HBsAg positivity and HBeAg negativity may be associated to the occurrence of low HBV DNA levels.

Indexed as

Carcinoma, HepatocellularHepatitis BHepatitis B, ChronicLiver NeoplasmsAdultAgedDNA, ViralFemaleHepatitis B e AntigensHepatitis B Surface AntigensHepatitis B virusHumansLiver CirrhosisMaleMiddle AgedRetrospective StudiesDNA, ViralHepatitis B e AntigensHepatitis B Surface AntigensDecompensated cirrhosisHepatitis B virusLow HBV DNA levelsRetrospective study

Identifiers

PMID36352372
PMCPMC9647958
OpenAlexW4308624849

What OpenQuestion holds

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LicenceCC BY
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.