Evidence map›Paper›PMID 32087699›Full record

ArticleBMC infectious diseases2020

MicroRNA expression profiling of peripheral blood mononuclear cells associated with syphilis.

Tao Huang, Jun Zhang, Wujian Ke, Xiaohui Zhang, Wentao Chen, Jieyi Yang, Yiwen Liao, Fangwen Liang, Shuqing Mei, Mingjiu Li and 4 more

Open access · goldAbstract read
In one paragraph

Article in BMC infectious diseases, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 9 papers.

0numbers the graph read from it
0cells of the map it votes in
9citing papers in PubMed
1.3field-weighted citation impact, top 20% 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

9 citing papers in PubMed, 21 citations in OpenAlex.

  1. Review
  2. Observational
  3. Article
  4. Review
  5. Article
  6. Review
  7. Oral SpirocheteInternational journal of molecular sciences · 2023
    Article
  8. Article
  9. 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

14 authors at 3 institutions in 1 country.

Tao HuangDermatology Hospital, Southern Medical University, Guangzhou, China.
Jun ZhangDermatology Hospital, Southern Medical University, Guangzhou, China.
Wujian KeDermatology Hospital, Southern Medical University, Guangzhou, China.
Xiaohui ZhangDermatology Hospital, Southern Medical University, Guangzhou, China.
Wentao ChenDermatology Hospital, Southern Medical University, Guangzhou, China.
Jieyi YangDermatology Hospital, Southern Medical University, Guangzhou, China.
Yiwen LiaoDermatology Hospital, Southern Medical University, Guangzhou, China.
Fangwen LiangYingde Center for Chronic Disease Control, Yingde, China.
Shuqing MeiZhuhai Center Chronic Disease Control, Zhuhai, China.
Mingjiu LiPanyu Institute of Chronic Disease, Guangzhou, China.
Zhenzhou LuoShenzhen Nanshan Center for Chronic Disease Control, Shenzhen, China.
Qiwei ZhangDermatology Hospital, Southern Medical University, Guangzhou, China.
Bin YangDermatology Hospital, Southern Medical University, Guangzhou, China.
Heping ZhengDermatology Hospital, Southern Medical University, Guangzhou, China. zhhpf@hotmail.com.ORCID http://orcid.org/0000-0002-9846-975X
Southern Medical University · CNPanyu Hospital of Chinese Medicine · CNShenzhen Nanshan Center for Chronic Disease Control · CN

Funding

Guangdong Science and Technology Department 2017A020212008Medical Science and Technology Foundation of Guangdong Province A2016269Medical Science and Technology Foundation of Guangdong Province C2017043The National Natural Science Foundation of China 81772240
6 · The paper itself

Abstract

backgroundTreponema pallidum (T. pallidum) infection evokes significant immune responses, resulting in tissue damage. The immune mechanism underlying T. pallidum infection is still unclear, although microRNAs (miRNAs) have been shown to influence immune cell function and, consequently, the generation of antibody responses during other microbe infections. However, these mechanisms are unknown for T. pallidum.

methodsIn this study, we performed a comprehensive analysis of differentially expressed miRNAs in healthy individuals, untreated patients with syphilis, patients in the serofast state, and serologically cured patients. miRNAs were profiled from the peripheral blood of patients obtained at the time of serological diagnosis. Then, both the target sequence analysis of these different miRNAs and pathway analysis were performed to identify important immune and cell signaling pathways. Quantitative reverse transcription-polymerase chain reaction (RT-PCR) was performed for microRNA analysis.

resultsA total of 74 differentially regulated miRNAs were identified. Following RT-qPCR confirmation, three miRNAs (hsa-miR-195-5p, hsa-miR-223-3p, hsa-miR-589-3p) showed significant differences in the serofast and serologically cured states (P < 0.05). One miRNA (hsa-miR-195-5p) showed significant differences between untreated patients and healthy individuals.

conclusionsThis is the first study of miRNA expression differences in peripheral blood mononuclear cells (PBMCs) in different stages of T. pallium infection. Our study suggests that the combination of three miRNAs has great potential to serve as a non-invasive biomarker of T. pallium infections, which will facilitate better diagnosis and treatment of T. pallium infections.

Indexed as

BiomarkersGene Expression ProfilingHumansLeukocytes, MononuclearMicroRNAsPrognosisReal-Time Polymerase Chain ReactionSerologic TestsSyphilisTranscriptomeTreponema pallidumBiomarkersMicroRNAsmicroRNA profilingPeripheral blood mononuclear cellsSexually transmitted infectionsSyphilisTreponema pallidum

Identifiers

PMID32087699
PMCPMC7036247
OpenAlexW3011715368

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.