-
Something wrong with this record ?
Severe COVID-19 associated hyperglycemia is caused by beta cell dysfunction: a prospective cohort study
J. Gojda, K. Koudelková, A. Ouřadová, A. Lang, M. Krbcová, A. Gvozdeva, V. Šebo, L. Slagmolen, J. Potočková, P. Tůma, L. Rossmeislová, M. Anděl, F. Karpe, S. Schlesinger
Language English Country England, Great Britain
Document type Journal Article, Research Support, Non-U.S. Gov't
NLK
Directory of Open Access Journals
from 2011
Free Medical Journals
from 2011
PubMed Central
from 2011
Europe PubMed Central
from 2011
Open Access Digital Library
from 2011-01-01
Open Access Digital Library
from 2011-01-01
ROAD: Directory of Open Access Scholarly Resources
from 2010
Springer Nature OA/Free Journals
from 2011-01-01
Springer Nature - nature.com Journals - Fully Open Access
from 2011-01-01
- MeSH
- COVID-19 * complications MeSH
- Hyperglycemia * MeSH
- Insulin MeSH
- Insulin Resistance * physiology MeSH
- Blood Glucose MeSH
- Middle Aged MeSH
- Humans MeSH
- Prospective Studies MeSH
- SARS-CoV-2 MeSH
- Check Tag
- Middle Aged MeSH
- Humans MeSH
- Male MeSH
- Female MeSH
- Publication type
- Journal Article MeSH
- Research Support, Non-U.S. Gov't MeSH
BACKGROUND: COVID-19, an infectious disease caused by SARS-CoV-2, was shown to be associated with an increased risk of new-onset diabetes. Mechanisms contributing to the development of hyperglycemia are still unclear. We aimed to study whether hyperglycemia is related to insulin resistance and/or beta cell dysfunction. MATERIALS AND METHODS: Survivors of severe COVID-19 but without a known history of diabetes were examined at baseline (T0) and after 3 (T3) and 6 (T6) months: corticosteroids use, indirect calorimetry, and OGTT. Insulin response and sensitivity (IS) were expressed as insulinogenic (IGI), disposition (DI), and Matsuda insulin sensitivity index (ISI). Resting energy expenditure (REE) and respiratory quotient (RQ) was calculated from the gas exchange and nitrogen losses. RESULTS: 26 patients (out of 37) with complete outcome data were included in the analysis (age ~59.0 years; BMI ~ 30.4, 35% women). Patients were hypermetabolic at T0 (30.3 ± 4.0 kcal/kg lean mass/day, ~120% predicted) but REE declined over 6 months (ΔT6-T0 mean dif. T6-T0 (95% CI): -5.4 (-6.8, -4.1) kcal/kg FFM/day, p < 0.0001). 17 patients at T0 and 13 patients at T6 had hyperglycemia. None of the patients had positive islet autoantibodies. Insulin sensitivity in T0 was similarly low in hyperglycemic (H) and normoglycemic patients (N) (T0 ISIH = 3.12 ± 1.23, ISIN = 3.47 ± 1.78, p = 0.44), whereas insulin response was lower in the H group (DIH = 3.05 ± 1.79 vs DIN = 8.40 ± 5.42, p = 0.003). Over 6 months ISI (ΔT6-T0 mean dif. T6-T0 for ISI (95% CI): 1.84 (0.45, 3.24), p = 0.01)) increased in the H group only. CONCLUSIONS: Patients with severe COVID-19 had increased REE and insulin resistance during the acute phase due to the infection and corticosteroid use, but these effects do not persist during the follow-up period. Only patients with insufficient insulin response developed hyperglycemia, indicating that beta cell dysfunction, rather than insulin resistance, was responsible for its occurrence.
Department of Hygiene 3rd Faculty of Medicine Charles University Prague Czech Republic
Department of Pathophysiology 3rd Faculty of Medicine Charles University Prague Czech Republic
Faculty of Movement and Rehabilitation Sciences Katholieke Universiteit Leuven Leuven Belgium
German Center for Diabetes Research Partner Düsseldorf Düsseldorf Germany
Oxford Center for Diabetes Endocrinology and Metabolism University of Oxford Oxford UK
References provided by Crossref.org
- 000
- 00000naa a2200000 a 4500
- 001
- bmc23016871
- 003
- CZ-PrNML
- 005
- 20250924083556.0
- 007
- ta
- 008
- 231013s2023 enk f 000 0|eng||
- 009
- AR
- 024 7_
- $a 10.1038/s41387-023-00241-7 $2 doi
- 035 __
- $a (PubMed)37460458
- 040 __
- $a ABA008 $b cze $d ABA008 $e AACR2
- 041 0_
- $a eng
- 044 __
- $a enk
- 100 1_
- $a Gojda, Jan $u Department of Internal Medicine, Third Faculty of Medicine, Charles University, and Královské Vinohrady University Hospital, Prague, Czech Republic. jan.gojda@lf3.cuni.cz $1 https://orcid.org/0000000279955947
- 245 10
- $a Severe COVID-19 associated hyperglycemia is caused by beta cell dysfunction: a prospective cohort study / $c J. Gojda, K. Koudelková, A. Ouřadová, A. Lang, M. Krbcová, A. Gvozdeva, V. Šebo, L. Slagmolen, J. Potočková, P. Tůma, L. Rossmeislová, M. Anděl, F. Karpe, S. Schlesinger
- 520 9_
- $a BACKGROUND: COVID-19, an infectious disease caused by SARS-CoV-2, was shown to be associated with an increased risk of new-onset diabetes. Mechanisms contributing to the development of hyperglycemia are still unclear. We aimed to study whether hyperglycemia is related to insulin resistance and/or beta cell dysfunction. MATERIALS AND METHODS: Survivors of severe COVID-19 but without a known history of diabetes were examined at baseline (T0) and after 3 (T3) and 6 (T6) months: corticosteroids use, indirect calorimetry, and OGTT. Insulin response and sensitivity (IS) were expressed as insulinogenic (IGI), disposition (DI), and Matsuda insulin sensitivity index (ISI). Resting energy expenditure (REE) and respiratory quotient (RQ) was calculated from the gas exchange and nitrogen losses. RESULTS: 26 patients (out of 37) with complete outcome data were included in the analysis (age ~59.0 years; BMI ~ 30.4, 35% women). Patients were hypermetabolic at T0 (30.3 ± 4.0 kcal/kg lean mass/day, ~120% predicted) but REE declined over 6 months (ΔT6-T0 mean dif. T6-T0 (95% CI): -5.4 (-6.8, -4.1) kcal/kg FFM/day, p < 0.0001). 17 patients at T0 and 13 patients at T6 had hyperglycemia. None of the patients had positive islet autoantibodies. Insulin sensitivity in T0 was similarly low in hyperglycemic (H) and normoglycemic patients (N) (T0 ISIH = 3.12 ± 1.23, ISIN = 3.47 ± 1.78, p = 0.44), whereas insulin response was lower in the H group (DIH = 3.05 ± 1.79 vs DIN = 8.40 ± 5.42, p = 0.003). Over 6 months ISI (ΔT6-T0 mean dif. T6-T0 for ISI (95% CI): 1.84 (0.45, 3.24), p = 0.01)) increased in the H group only. CONCLUSIONS: Patients with severe COVID-19 had increased REE and insulin resistance during the acute phase due to the infection and corticosteroid use, but these effects do not persist during the follow-up period. Only patients with insufficient insulin response developed hyperglycemia, indicating that beta cell dysfunction, rather than insulin resistance, was responsible for its occurrence.
- 650 _2
- $a lidé $7 D006801
- 650 _2
- $a ženské pohlaví $7 D005260
- 650 _2
- $a lidé středního věku $7 D008875
- 650 _2
- $a mužské pohlaví $7 D008297
- 650 12
- $a inzulinová rezistence $x fyziologie $7 D007333
- 650 _2
- $a prospektivní studie $7 D011446
- 650 _2
- $a krevní glukóza $7 D001786
- 650 12
- $a COVID-19 $x komplikace $7 D000086382
- 650 _2
- $a SARS-CoV-2 $7 D000086402
- 650 _2
- $a inzulin $7 D007328
- 650 12
- $a hyperglykemie $7 D006943
- 655 _2
- $a časopisecké články $7 D016428
- 655 _2
- $a práce podpořená grantem $7 D013485
- 700 1_
- $a Koudelková, Kateřina $u Department of Internal Medicine, Third Faculty of Medicine, Charles University, and Královské Vinohrady University Hospital, Prague, Czech Republic
- 700 1_
- $a Ouřadová, Anna $u Department of Internal Medicine, Third Faculty of Medicine, Charles University, and Královské Vinohrady University Hospital, Prague, Czech Republic
- 700 1_
- $a Lang, Alexander $u Institute for Biometrics and Epidemiology, German Diabetes Center (Deutsches Diabetes-Zentrum/DDZ), Leibniz Center for Diabetes Research at Heinrich Heine University Düsseldorf, Düsseldorf, Germany $u German Center for Diabetes Research (DZD), Partner Düsseldorf, Düsseldorf, Germany $1 https://orcid.org/0000000205843213
- 700 1_
- $a Krbcová, Magdaléna $u Department of Internal Medicine, Third Faculty of Medicine, Charles University, and Královské Vinohrady University Hospital, Prague, Czech Republic $1 https://orcid.org/000000017376611X
- 700 1_
- $a Gvozdeva, Alexandra $u Department of Internal Medicine, Third Faculty of Medicine, Charles University, and Královské Vinohrady University Hospital, Prague, Czech Republic
- 700 1_
- $a Šebo, Viktor $u Department of Pathophysiology, Third Faculty of Medicine, Charles University, Prague, Czech Republic $7 xx0335505
- 700 1_
- $a Slagmolen, Lotte $u Faculty of Movement and Rehabilitation Sciences, Katholieke Universiteit Leuven, Leuven, Belgium
- 700 1_
- $a Potočková, Jana $u Department of Internal Medicine, Third Faculty of Medicine, Charles University, and Královské Vinohrady University Hospital, Prague, Czech Republic
- 700 1_
- $a Tůma, Petr $u Department of Hygiene, Third Faculty of Medicine, Charles University, Prague, Czech Republic
- 700 1_
- $a Rossmeislová, Lenka $u Institute for Biometrics and Epidemiology, German Diabetes Center (Deutsches Diabetes-Zentrum/DDZ), Leibniz Center for Diabetes Research at Heinrich Heine University Düsseldorf, Düsseldorf, Germany
- 700 1_
- $a Anděl, Michal $u Department of Internal Medicine, Third Faculty of Medicine, Charles University, and Královské Vinohrady University Hospital, Prague, Czech Republic
- 700 1_
- $a Karpe, Fredrik $u Oxford Center for Diabetes, Endocrinology, and Metabolism, University of Oxford, Oxford, UK $1 https://orcid.org/0000000227511770
- 700 1_
- $a Schlesinger, Sabrina $u German Center for Diabetes Research (DZD), Partner Düsseldorf, Düsseldorf, Germany $u Department of Pathophysiology, Third Faculty of Medicine, Charles University, Prague, Czech Republic $1 https://orcid.org/0000000342440832
- 773 0_
- $w MED00181736 $t Nutrition & diabetes $x 2044-4052 $g Roč. 13, č. 1 (2023), s. 11
- 856 41
- $u https://pubmed.ncbi.nlm.nih.gov/37460458 $y Pubmed
- 910 __
- $a ABA008 $b sig $c sign $y - $z 0
- 990 __
- $a 20231013 $b ABA008
- 991 __
- $a 20250924083551 $b ABA008
- 999 __
- $a ok $b bmc $g 2000414 $s 1203233
- BAS __
- $a 3
- BAS __
- $a PreBMC-MEDLINE
- BMC __
- $a 2023 $b 13 $c 1 $d 11 $e 20230717 $i 2044-4052 $m Nutrition & diabetes $n Nutr Diabetes $x MED00181736
- LZP __
- $a Pubmed-20231013