Glucometabolic changes influence hospitalization and outcome in patients with COVID-19: An observational cohort study
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Glucometabolic changes influence hospitalization and outcome in patients with COVID-19: An observational cohort study. / Clausen, Clara L.; Leo-Hansen, Christian; Faurholt-Jepsen, Daniel; Krogh-Madsen, Rikke; Ritz, Christian; Kirk, Ole; Jørgensen, Henrik L.; Benfield, Thomas; Almdal, Thomas P.; Snorgaard, Ole.
I: Diabetes Research and Clinical Practice, Bind 187, 109880, 2022.Publikation: Bidrag til tidsskrift › Tidsskriftartikel › Forskning › fagfællebedømt
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TY - JOUR
T1 - Glucometabolic changes influence hospitalization and outcome in patients with COVID-19: An observational cohort study
AU - Clausen, Clara L.
AU - Leo-Hansen, Christian
AU - Faurholt-Jepsen, Daniel
AU - Krogh-Madsen, Rikke
AU - Ritz, Christian
AU - Kirk, Ole
AU - Jørgensen, Henrik L.
AU - Benfield, Thomas
AU - Almdal, Thomas P.
AU - Snorgaard, Ole
N1 - Publisher Copyright: © 2022
PY - 2022
Y1 - 2022
N2 - Aims: The aim was to report the prevalence of diabetes status in patients hospitalized with COVID-19 and assess the association between the glucometabolic status at admission and 90-day mortality. Methods: Consecutive patients hospitalized with COVID-19 were included in the study. All participants included had an HbA1c measurement 60 days prior to or within 7 days after admission. We studied the association between diabetes status, the glycemic gap (difference between admission and habitual status), admission plasma-glucose, and mortality using Cox proportional hazards regression. Results: Of 674 patients included, 114 (17%) had normal glucose level, 287 (43%) had pre-diabetes, 74 (11%) had new-onset, and 199 (30%) had diagnosed diabetes. No association between diabetes status, plasma-glucose at admission, and mortality was found. Compared to the 2nd quartile (reference) of glycemic-gap, those with the highest glycemic gap had increased mortality (3rd (HR 2.38 [1.29–4.38], p = 0.005) and 4th quartile (HR 2.48 [1.37–4.52], p = 0.002). Conclusion: Abnormal glucose metabolism was highly prevalent among patients hospitalized with COVID-19. Diabetes status per se or admission plasma-glucose was not associated with a poorer outcome. However, a high glycemic gap was associated with increased risk of mortality, suggesting that, irrespective of diabetes status, glycemic stress serves as an important prognostic marker for mortality.
AB - Aims: The aim was to report the prevalence of diabetes status in patients hospitalized with COVID-19 and assess the association between the glucometabolic status at admission and 90-day mortality. Methods: Consecutive patients hospitalized with COVID-19 were included in the study. All participants included had an HbA1c measurement 60 days prior to or within 7 days after admission. We studied the association between diabetes status, the glycemic gap (difference between admission and habitual status), admission plasma-glucose, and mortality using Cox proportional hazards regression. Results: Of 674 patients included, 114 (17%) had normal glucose level, 287 (43%) had pre-diabetes, 74 (11%) had new-onset, and 199 (30%) had diagnosed diabetes. No association between diabetes status, plasma-glucose at admission, and mortality was found. Compared to the 2nd quartile (reference) of glycemic-gap, those with the highest glycemic gap had increased mortality (3rd (HR 2.38 [1.29–4.38], p = 0.005) and 4th quartile (HR 2.48 [1.37–4.52], p = 0.002). Conclusion: Abnormal glucose metabolism was highly prevalent among patients hospitalized with COVID-19. Diabetes status per se or admission plasma-glucose was not associated with a poorer outcome. However, a high glycemic gap was associated with increased risk of mortality, suggesting that, irrespective of diabetes status, glycemic stress serves as an important prognostic marker for mortality.
KW - COVID-19
KW - Glucometabolic changes
KW - Glycemic gap
KW - Hospitalization
KW - Mortality
U2 - 10.1016/j.diabres.2022.109880
DO - 10.1016/j.diabres.2022.109880
M3 - Journal article
C2 - 35483546
AN - SCOPUS:85129523626
VL - 187
JO - Diabetes Research and Clinical Practice
JF - Diabetes Research and Clinical Practice
SN - 0168-8227
M1 - 109880
ER -
ID: 307014077