Evidence map›Paper›PMID 35753602›Full record

ArticleInternational journal of infectious diseases : IJID : official publication of the International Society for Infectious Diseases2022

Host genetic loci LZTFL1 and CCL2 associated with SARS-CoV-2 infection and severity of COVID-19.

Jule Rüter, Srinivas Reddy Pallerla, Christian G Meyer, Nicolas Casadei, Michael Sonnabend, Silke Peter, Dennis Nurjadi, Le Thi Kieu Linh, Rolf Fendel, Siri Göpel and 3 more

Open access · goldAbstract read
In one paragraph

Article in International journal of infectious diseases : IJID : official publication of the International Society for Infectious Diseases, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 13 papers.

0numbers the graph read from it
0cells of the map it votes in
13citing papers in PubMed
2.1field-weighted citation impact, top 11% 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

13 citing papers in PubMed, 21 citations in OpenAlex.

  1. Article
  2. Article
  3. Article
  4. Article
  5. Review
  6. Article
  7. Article
  8. Single nucleotide variants in theFrontiers in cellular and infection microbiology · 2024
    Observational
  9. Article
  10. Host Genetic Factors, Comorbidities and the Risk of Severe COVID-19.Journal of epidemiology and global health · 2023
    Article
  11. Genetic susceptibility to severe COVID-19.Infection, genetics and evolution : journal of molecular epidemiology and evolutionary genetics in infectious diseases · 2023
    Review
  12. Human genetic basis of severe or critical illness in COVID-19.Frontiers in cellular and infection microbiology · 2022
    Review
  13. Development and evaluation of anFrontiers in nuclear medicine · 2022
    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

13 authors at 7 institutions in 3 countries.

Jule RüterInstitute of Tropical Medicine, University Hospital Tübingen, Tübingen, Germany.
Srinivas Reddy PallerlaInstitute of Tropical Medicine, University Hospital Tübingen, Tübingen, Germany; Vietnamese-German Center for Medical Research, VG-CARE, Hanoi, Vietnam.
Christian G MeyerInstitute of Tropical Medicine, University Hospital Tübingen, Tübingen, Germany; Vietnamese-German Center for Medical Research, VG-CARE, Hanoi, Vietnam; Duy Tan University, Da Nang, Vietnam.
Nicolas CasadeiInstitute for Medical Genetics and Applied Genomics, University of Tübingen, Tübingen, Germany; NGS Competence Center Tübingen (NCCT), Tübingen, Germany.
Michael SonnabendInstitute for Medical Microbiology and Hygiene, University Hospital Tübingen, Tübingen, Germany.
Silke PeterInstitute for Medical Microbiology and Hygiene, University Hospital Tübingen, Tübingen, Germany.
Dennis NurjadiDepartment of Infectious Diseases, Medical Microbiology and Hygiene, Heidelberg University Hospital, Germany.
Le Thi Kieu LinhInstitute of Tropical Medicine, University Hospital Tübingen, Tübingen, Germany; Vietnamese-German Center for Medical Research, VG-CARE, Hanoi, Vietnam.
Rolf FendelInstitute of Tropical Medicine, University Hospital Tübingen, Tübingen, Germany.
Siri GöpelDepartment of Internal Medicine I, Tübingen University Hospital, Tübingen, Germany.
Olaf RiessInstitute for Medical Genetics and Applied Genomics, University of Tübingen, Tübingen, Germany.
Peter G KremsnerInstitute of Tropical Medicine, University Hospital Tübingen, Tübingen, Germany; Centre de Recherches Médicales de Lambaréné (CERMEL), Gabon.
Thirumalaisamy P VelavanInstitute of Tropical Medicine, University Hospital Tübingen, Tübingen, Germany; Vietnamese-German Center for Medical Research, VG-CARE, Hanoi, Vietnam. Electronic address: velavan@medizin.uni-tuebingen.de.
University Children's Hospital Tübingen · DEInstitute of Medical Microbiology and Hygiene · DEBernstein Center for Computational Neuroscience Tübingen · DECentre de Recherche Médicales de Lambaréné · GADuy Tan University · VNHeidelberg University · DEUniversity of Tübingen · DE

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

objectivesHost genetic factors contribute to the variable severity of COVID-19. We examined genetic variants from genome-wide association studies and candidate gene association studies in a cohort of patients with COVID-19 and investigated the role of early SARS-CoV-2 strains in COVID-19 severity.

methodsThis case-control study included 123 COVID-19 cases (hospitalized or ambulatory) and healthy controls from the state of Baden-Wuerttemberg, Germany. We genotyped 30 single nucleotide polymorphisms, using a custom-designed panel. Cases were also compared with the 1000 genomes project. Polygenic risk scores were constructed. SARS-CoV-2 genomes from 26 patients with COVID-19 were sequenced and compared between ambulatory and hospitalized cases, and phylogeny was reconstructed.

resultsEight variants reached nominal significance and two were significantly associated with at least one of the phenotypes "susceptibility to infection", "hospitalization", or "severity": rs73064425 in LZTFL1 (hospitalization and severity, P <0.001) and rs1024611 near CCL2 (susceptibility, including 1000 genomes project, P = 0.001). The polygenic risk score could predict hospitalization. Most (23/26, 89%) of the SARS-CoV-2 genomes were classified as B.1 lineage. No associations of SARS-CoV-2 mutations or lineages with severity were observed.

conclusionThese host genetic markers provide insights into pathogenesis and enable risk classification. Variants which reached nominal significance should be included in larger studies.

Indexed as

Chemokine CCL2COVID-19Transcription FactorsCase-Control StudiesGenetic LociGenome-Wide Association StudyHumansSARS-CoV-2CCL2 protein, humanChemokine CCL2LZTFL1 protein, humanTranscription FactorsCOVID-19Cytokine stormGWASHost geneticsPolygenic risk scoreSARS-CoV-2

Identifiers

PMID35753602
PMCPMC9222649
OpenAlexW4283326618

What OpenQuestion holds

Textmetadata
Read underepoch 390

Registered trials

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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.