Evidence map›Paper›PMID 39044261›Full record

ArticleMicrobiome2024

The plasma viral communities associate with clinical profiles in a large-scale haematological patients cohort.

Shuai Ma, Yuyao Yin, Yifan Guo, Chaoqun Yao, Siqi Xu, Qingqing Luo, Guankun Yin, Shuyi Wang, Qi Wang, Hongbin Chen and 4 more

Abstract read
In one paragraph

Article in Microbiome, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 3 papers.

0numbers the graph read from it
0cells of the map it votes in
3citing papers in PubMed
–field-weighted citation impact
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

3 citing papers in PubMed.

  1. Article
  2. Article
  3. 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

14 authors.

Shuai Ma *Department of Clinical Laboratory, Peking University People's Hospital, Beijing, 100044, China.
Yuyao Yin *Department of Clinical Laboratory, Peking University People's Hospital, Beijing, 100044, China.
Yifan Guo *Department of Clinical Laboratory, Peking University People's Hospital, Beijing, 100044, China.
Chaoqun YaoDepartment of Clinical Laboratory, Peking University People's Hospital, Beijing, 100044, China.
Siqi XuCenter for Infectious Disease Research, School of Medicine, Tsinghua University, Beijing, China.
Qingqing LuoCenter for Infectious Disease Research, School of Medicine, Tsinghua University, Beijing, China.
Guankun YinDepartment of Clinical Laboratory, Peking University People's Hospital, Beijing, 100044, China.
Shuyi WangDepartment of Clinical Laboratory, Peking University People's Hospital, Beijing, 100044, China.
Qi WangDepartment of Clinical Laboratory, Peking University People's Hospital, Beijing, 100044, China.
Hongbin ChenDepartment of Clinical Laboratory, Peking University People's Hospital, Beijing, 100044, China.
Ruobing WangDepartment of Clinical Laboratory, Peking University People's Hospital, Beijing, 100044, China.
Longyang JinDepartment of Clinical Laboratory, Peking University People's Hospital, Beijing, 100044, China.
Guanxiang LiangCenter for Infectious Disease Research, School of Medicine, Tsinghua University, Beijing, China.
Hui WangDepartment of Clinical Laboratory, Peking University People's Hospital, Beijing, 100044, China. whuibj@163.com.ORCID 0000-0001-9220-0357

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundHaematological patients exhibit immune system abnormalities that make them susceptible to viral infections. Understanding the relationship between the virome in the blood plasma of haematological patients and their clinical characteristic is crucial for disease management. We aimed to explore the presence of viral pathogens and identify close associations between viral infections and various clinical features.

resultsA total of 21 DNA viruses and 6 RNA viruses from 12 virus families were identified from 1383 patients. Patients with haematological diseases exhibited significantly higher diversity, prevalence, and co-detection rates of viral pathogens. During fever episodes, pathogen detection was notably higher, with Epstein-Barr virus (EBV) and Mucorales infections being the most probable culprits for fever symptoms in non-haematological patients. The detection rate of torque teno virus (TTV) significantly increases in haematological patients after transplantation and during primary lung infections. Additionally, TTV-positive patients demonstrate significantly higher absolute neutrophil counts, while C-reactive protein and procalcitonin levels are notably lower. Furthermore, TTV, cytomegalovirus, and parvovirus B19 (B19V) were found to be more prevalent in non-neutropenic patients, while non-viral pathogenic infections, such as Gram-negative bacteria and Mucorales, were more common in neutropenic patients. Pegivirus C (HPgV-C) infection often occurred post-transplantation, regardless of neutropenia. Additionally, some viruses such as TTV, B19V, EBV, and HPgV-C showed preferences for age and seasonal infections.

conclusionsAnalysis of the plasma virome revealed the susceptibility of haematological patients to plasma viral infections at specific disease stages, along with the occurrence of mixed infections with non-viral pathogens. Close associations were observed between the plasma virome and various clinical characteristics, as well as clinical detection parameters. Understanding plasma virome aids in auxiliary clinical diagnosis and treatment, enabling early prevention to reduce infection rates in patients and improve their quality of life. Video Abstract.

Indexed as

DNA VirusesHematologic DiseasesRNA VirusesVirus DiseasesAdultAgedCohort StudiesFemaleHerpesvirus 4, HumanHumansMaleMiddle AgedTorque teno virusViromeYoung AdultHaematologic disordersMetagenomic sequencingPlasma ViromeTTV

Identifiers

PMID39044261
PMCPMC11265361

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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.