Evidence map›Paper›PMID 35531331›Full record

ArticleFrontiers in cellular and infection microbiology2022

The Role of Autophagy in the Mother-to-Child Transmission of Pregnant Women With a High Level of HBV DNA.

Hong Gao, Ling Xu, Zihao Fan, Xiangying Zhang, Zhongping Duan, Feng Ren

Open access · goldAbstract read
In one paragraph

Article in Frontiers in cellular and infection microbiology, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

0numbers the graph read from it
0cells of the map it votes in
1citing papers in PubMed
0.3field-weighted citation impact, top 43% 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

1 citing paper in PubMed, 2 citations in OpenAlex.

  1. 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

6 authors at 3 institutions in 1 country.

Hong GaoBeijing Youan Hospital/Beijing Institute of Hepatology, Capital Medical University, Beijing, China.
Ling XuBeijing Youan Hospital/Beijing Institute of Hepatology, Capital Medical University, Beijing, China.
Zihao FanBeijing Youan Hospital/Beijing Institute of Hepatology, Capital Medical University, Beijing, China.
Xiangying ZhangBeijing Youan Hospital/Beijing Institute of Hepatology, Capital Medical University, Beijing, China.
Zhongping DuanBeijing Youan Hospital/Beijing Institute of Hepatology, Capital Medical University, Beijing, China.
Feng RenBeijing Youan Hospital/Beijing Institute of Hepatology, Capital Medical University, Beijing, China.
Capital Medical University · CNBeijing YouAn Hospital · CNSecond Hospital of Shanxi Medical University · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Background: Mother-to-child transmission (MTCT) is the most common propagation mode of hepatitis B virus (HBV) transmission. Exploring the mechanisms of HBV MTCT is the key to protect infant from infection. In this study, we aim to clarify the important role of autophagy complicated in HBV MTCT. Methods: A total of 169 placental samples were collected in this study, includes 144 HBV positive pregnant women and 25 normal pregnant women. Results: According to the number of autophagosomes and the expression level of autophagic genes mRNA and protein, autophagy was increased in HBV maternal placenta. Among the control, low viral load, medium viral load and high viral load groups, autophagy was significantly up-regulated with the increase of HBV viral loads. Also, autophagy was increased in the HBeAg positive pregnant women compared with their HBeAg negative counterparts. Also, autophagy in infant-infected group was up-regulated compared with infant-uninfected group. Conclusion: Our study determines the high levels of viremia could be the cause of both increase autophagy activities and MTCT. Autophagy was significantly up-regulated in pregnant women with high viral load or HBeAg positive, which plays an important part in the HBV MTCT.

Indexed as

Hepatitis BPregnancy Complications, InfectiousAutophagyCell Line, TumorDNA, ViralFemaleHepatitis B e AntigensHepatitis B Surface AntigensHepatitis B virusHumansInfantInfectious Disease Transmission, VerticalPlacentaPregnancyPregnant PeopleRNA, MessengerDNA, ViralHepatitis B e AntigensHepatitis B Surface AntigensRNA, Messengerautophagyhepatitis Bmother-to-child transmissionplacentavertical transmission of HBV

Identifiers

PMID35531331
PMCPMC9072787
OpenAlexW4224214726

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.