Evidence map›Paper›PMID 32533832›Full record

ArticleClinical infectious diseases : an official publication of the Infectious Diseases Society of America2021

Impact of Intermediate Hyperglycemia and Diabetes on Immune Dysfunction in Tuberculosis.

Clare Eckold, Vinod Kumar, January Weiner, Bachti Alisjahbana, Anca-Lelia Riza, Katharina Ronacher, Jorge Coronel, Sarah Kerry-Barnard, Stephanus T Malherbe, Leanie Kleynhans and 11 more

Open access · greenAbstract read
In one paragraph

Article in Clinical infectious diseases : an official publication of the Infectious Diseases Society of America, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 47 papers, 3 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
47citing papers in PubMed, 3 pooled it
0.6field-weighted citation impact, top 18% 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

47 citing papers in PubMed, 3 syntheses or guidelines pooled it, 72 citations in OpenAlex.

  1. Pooled it
  2. Pooled it
  3. Cross-Study Meta-Analysis of Blood Transcriptomes in Type 2 Diabetes.International journal of molecular sciences · 2025
    Pooled it
  4. Trial
  5. Article
  6. Article
  7. Article
  8. Review
  9. Article
  10. Review
  11. Article
  12. Article
  13. Article
  14. Article
  15. Article
  16. Article
  17. Article
  18. Review
  19. Article
  20. 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

21 authors at 14 institutions in 8 countries.

Clare EckoldTuberculosis Centre and Department of Infection and Biology, London School of Hygiene and Tropical Medicine, London, United Kingdom.
Vinod KumarUniversity of Groningen, Department of Genetics, University Medical Center Groningen, Groningen, The Netherlands.
January WeinerMax Planck Institute for Infection Biology, Berlin, Germany.
Bachti AlisjahbanaTB-HIV Research Center, Faculty of Medicine, Universitas Padjadjaran, Bandung, Indonesia.
Anca-Lelia RizaDepartment of Internal Medicine and Radboud Center for Infectious Diseases, Radboud University Medical Center, Nijmegen, The Netherlands.
Katharina RonacherMater Research Institute-University of Queensland, Translational Research Institute, Brisbane, Australia.
Jorge CoronelLaboratorio de Investigación de Enfermedades Infecciosas, Universidad Peruana Cayetano Heredia, Lima, Peru.
Sarah Kerry-BarnardPopulation Health Research Institute, St George's, University of London, London, United Kingdom.
Stephanus T MalherbeSouth Africa Medical Research Council Centre for Tuberculosis Research, Department of Science and Technology/National Research Foundation Centre of Excellence for Biomedical Tuberculosis Research, Division of Molecular Biology and Human Genetics, Department of Biomedical Sciences, Faculty of Medicine and Health Sciences, Stellenbosch University, Cape Town, South Africa.
Leanie KleynhansSouth Africa Medical Research Council Centre for Tuberculosis Research, Department of Science and Technology/National Research Foundation Centre of Excellence for Biomedical Tuberculosis Research, Division of Molecular Biology and Human Genetics, Department of Biomedical Sciences, Faculty of Medicine and Health Sciences, Stellenbosch University, Cape Town, South Africa.
Kim StanleySouth Africa Medical Research Council Centre for Tuberculosis Research, Department of Science and Technology/National Research Foundation Centre of Excellence for Biomedical Tuberculosis Research, Division of Molecular Biology and Human Genetics, Department of Biomedical Sciences, Faculty of Medicine and Health Sciences, Stellenbosch University, Cape Town, South Africa.
Rovina RuslamiTB-HIV Research Center, Faculty of Medicine, Universitas Padjadjaran, Bandung, Indonesia.
Mihai IoanaHuman Genomics Laboratory, University of Medicine and Pharmacy, Craiova, Romania.
Cesar Ugarte-GilTuberculosis Centre and Department of Infection and Biology, London School of Hygiene and Tropical Medicine, London, United Kingdom.
Gerhard WalzlSouth Africa Medical Research Council Centre for Tuberculosis Research, Department of Science and Technology/National Research Foundation Centre of Excellence for Biomedical Tuberculosis Research, Division of Molecular Biology and Human Genetics, Department of Biomedical Sciences, Faculty of Medicine and Health Sciences, Stellenbosch University, Cape Town, South Africa.
Reinout van CrevelDepartment of Internal Medicine and Radboud Center for Infectious Diseases, Radboud University Medical Center, Nijmegen, The Netherlands.
Cisca WijmengaUniversity of Groningen, Department of Genetics, University Medical Center Groningen, Groningen, The Netherlands.
Julia A CritchleyPopulation Health Research Institute, St George's, University of London, London, United Kingdom.
Hazel M DockrellTuberculosis Centre and Department of Infection and Biology, London School of Hygiene and Tropical Medicine, London, United Kingdom.
Jacqueline M CliffTuberculosis Centre and Department of Infection and Biology, London School of Hygiene and Tropical Medicine, London, United Kingdom.
TANDEM consortium
London School of Hygiene & Tropical Medicine · GBUniversity of Groningen · NLUniversity Medical Center Groningen · NLSt George's, University of London · GBNational Research Foundation · ZAStellenbosch University · ZAPadjadjaran University · IDRadboud University Nijmegen · NLUniversidad Peruana Cayetano Heredia · PEUniversity of Medicine and Pharmacy of Craiova · RORadboud University Medical Center · NLMax Planck Institute for Infection Biology · DETranslational Research Institute · AUUniversity of Queensland · AU

Funding

Medical Research Council MC_PC_17218Medical Research Council MR/P017568/1Medical Research Council MR/R005850/1
6 · The paper itself

Abstract

backgroundPeople with diabetes have an increased risk of developing active tuberculosis (TB) and are more likely to have poor TB-treatment outcomes, which may impact on control of TB as the prevalence of diabetes is increasing worldwide. Blood transcriptomes are altered in patients with active TB relative to healthy individuals. The effects of diabetes and intermediate hyperglycemia (IH) on this transcriptomic signature were investigated to enhance understanding of immunological susceptibility in diabetes-TB comorbidity.

methodsWhole blood samples were collected from active TB patients with diabetes (glycated hemoglobin [HbA1c] ≥6.5%) or IH (HbA1c = 5.7% to <6.5%), TB-only patients, and healthy controls in 4 countries: South Africa, Romania, Indonesia, and Peru. Differential blood gene expression was determined by RNA-seq (n = 249).

resultsDiabetes increased the magnitude of gene expression change in the host transcriptome in TB, notably showing an increase in genes associated with innate inflammatory and decrease in adaptive immune responses. Strikingly, patients with IH and TB exhibited blood transcriptomes much more similar to patients with diabetes-TB than to patients with only TB. Both diabetes-TB and IH-TB patients had a decreased type I interferon response relative to TB-only patients.

conclusionsComorbidity in individuals with both TB and diabetes is associated with altered transcriptomes, with an expected enhanced inflammation in the presence of both conditions, but also reduced type I interferon responses in comorbid patients, suggesting an unexpected uncoupling of the TB transcriptome phenotype. These immunological dysfunctions are also present in individuals with IH, showing that altered immunity to TB may also be present in this group. The TB disease outcomes in individuals with IH diagnosed with TB should be investigated further.

Indexed as

Diabetes MellitusHyperglycemiaMycobacterium tuberculosisTuberculosisTuberculosis, PulmonaryHumansIndonesiaPeruSouth Africadiabeteshyperglycemiainflammationtuberculosis

Identifiers

PMID32533832
PMCPMC7823074
OpenAlexW3035593647

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC-ND
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.