Diabetes Status, c-Reactive Protein, and Insulin Resistance in Community-Acquired Pneumonia—A Prospective Cohort Study

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C-reactive protein (CRP) is commonly used to guide community-acquired pneumonia (CAP) treatment. A positive association between admission glucose and CRP levels has been observed in patients with CAP. The associations between prediabetes, unknown diabetes, acute-on-chronic hyperglycaemia, and CRP levels, and between admission CRP levels and insulin resistance (IR) in CAP, remain unexplored. This study investigated the associations firstly between chronic, acute, and acute-on-chronic hyperglycaemia and CRP levels, and secondly between admission CRP levels and IR in CAP. In a prospective cohort study of adults with CAP, the associations between chronic, acute, and acute-on-chronic hyperglycaemia (admission glucose minus HbA1c-derived average glucose) and CRP levels until admission day 3 were modelled with repeated-measures linear mixed models. IR was estimated with the homeostasis model assessment of IR (HOMA-IR). The association between admission CRP levels and HOMA-IR was modelled with linear regression. In 540 patients, no association between chronic, acute, or acute-on-chronic hyperglycaemia and CRP levels was found. In 266 patients, every 50 mg/L increase in admission CRP was associated with a 7% (95% CI 1–14%) higher HOMA-IR. In conclusion, our findings imply that hyperglycaemia does not influence CRP levels in patients with CAP, although admission CRP levels were positively associated with IR.
Keywords: community-acquired pneumonia; c-reactive protein; diabetes mellitus; chronic hyperglycaemia; acute hyperglycaemia; acute-on-chronic hyperglycaemia; insulin resistance
OriginalsprogEngelsk
Artikelnummer245
TidsskriftJournal of Clinical Medicine
Vol/bind13
Udgave nummer1
Antal sider17
ISSN2077-0383
DOI
StatusUdgivet - 2024

Bibliografisk note

Funding Information:
The Research Council at Copenhagen University Hospital, North Zealand (funding number: none), Grosserer L. F. Foghts Fond (funding number: none), Olga Bryde Nielsens Fond (funding number: none), Helen Rudes Fond (funding number: none), Kaptajnløjtnant Harald Jensens og Hustrus Fond (funding number: none), and Fonden til Lægevidenskabens Fremme (funding number: none) provided financial support. The foundations that provided financial support did not influence the study design, data collection, data analysis, interpretation of data, writing of the manuscript, or decision to submit the manuscript for publication.

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© 2023 by the authors.

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