Clinical and morphological characteristics of newly diagnosed diabetes mellitus in elderly patients with COVID-19

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Abstract

Background: This study examined the pathomorphological changes in the pancreatic islet tissue and their association with glucose metabolism disorders and clinical and laboratory markers of COVID-19 severity in elderly patients.

Materials and methods: In a pilot study, 11 elderly patients (mean age: 67.9 ± 4.2 years; 7 men, 4 women) with COVID-19 who had a fatal outcome between 2021 and 2022 were analyzed. Based on clinical diagnosis, the patients were categorized into three groups: group 1, three patients with newly diagnosed diabetes mellitus (DM) associated with COVID-19; group 2, three patients with preexisting type 2 DM and COVID-19; and group 3 (control group), five patients with COVID-19 and no glucose metabolism disorders. Group 1 manifested the smallest pancreatic islet volume.

Results: Across the cohort, islet size showed a significant negative correlation with blood glucose levels and a positive correlation with platelet count and total bilirubin (within physiological limits) and antiplatelet therapy use. Moreover, the patients in group 1 exhibited the highest systemic inflammatory activity, higher fasting blood glucose levels, the lowest platelet count, the most pronounced pancreatic lipomatosis and fibrosis, the highest Charlson Comorbidity Index, and the longest hospital stay. Furthermore, preexisting pancreatic morphological changes were found in these patients prior to COVID-19 infection. The patients in group 2 showed the most pronounced bone marrow suppression, which affected peripheral blood cell composition and was possibly associated with a worse prognosis and the shortest time to fatal outcome.

Conclusions: These indicate that pancreatic islet damage in COVID-19 is related to the development of DM and occurs in the presence of preexisting pancreatic abnormalities, including lipomatosis and fibrosis.

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About the authors

Vitaliy I. Odin

Kirov Military Medical Academy

Author for correspondence.
Email: vmeda-nio@mil.ru
ORCID iD: 0000-0003-1638-6510
SPIN-code: 2685-0746

MD, Dr. Sci. (Medicine), Professor

Russian Federation, Saint Petersburg

Vadim S. Chirsky

Kirov Military Medical Academy

Email: vmeda-nio@mil.ru
ORCID iD: 0000-0003-3215-3901
SPIN-code: 7295-3369

MD, Dr. Sci. (Medicine), Professor

Russian Federation, Saint Petersburg

Maxim Yu. Kabanov

Hospital for War Veterans

Email: vmeda-nio@mil.ru
ORCID iD: 0000-0002-9901-8520
SPIN-code: 3057-1995

MD, Dr. Sci. (Medicine), Professor

Russian Federation, Saint Petersburg

Elizaveta A. Evdoshchenko

Kirov Military Medical Academy

Email: vmeda-nio@mil.ru
ORCID iD: 0009-0005-4456-7820
SPIN-code: 1728-8914

clinical resident

Russian Federation, Saint Petersburg

Elena A. Andreeva

Kirov Military Medical Academy

Email: vmeda-nio@mil.ru
ORCID iD: 0000-0002-8418-952X
SPIN-code: 6004-3633

MD, Cand. Sci. (Medicine), Associate Professor

Russian Federation, Saint Petersburg

Gleb D. Trukhin

Kirov Military Medical Academy

Email: vmeda-nio@mil.ru
ORCID iD: 0000-0001-7946-9626
SPIN-code: 2023-3308

clinical resident

Russian Federation, Saint Petersburg

Tatiana А. Garan

Hospital for War Veterans

Email: vmeda-nio@mil.ru
ORCID iD: 0000-0003-3425-4140
SPIN-code: 8509-3257

pathologist

Russian Federation, Saint Petersburg

Yulia S. Ivchenko

Hospital for War Veterans

Email: vmeda-nio@mil.ru
ORCID iD: 0000-0003-1336-7277
SPIN-code: 6697-6543

endocrinologist

Russian Federation, Saint Petersburg

Tatyana E. Pogoda

Hospital for War Veterans

Email: vmeda-nio@mil.ru
ORCID iD: 0009-0006-9937-832X
SPIN-code: 9136-8199

MD, Cand. Sci. (Medicine)

Russian Federation, Saint Petersburg

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Supplementary files

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1. JATS XML
2. Fig. 1. Pancreatic lipomatosis in group 1 patients, hematoxylin and eosin staining, ×200

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3. Fig. 2. Interlobular proliferation of connective tissue and fibrosis (arrow) of the pancreas in group 1 patients, hematoxylin and eosin staining, ×100 (а), ×200 (b)

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4. Fig. 3. Pancreatic parenchyma autolysis without inflammatory response in group 1 patients, hematoxylin and eosin staining, ×200

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5. Fig. 4. Edema of the pancreatic islets of Langerhans, hematoxylin and eosin staining, ×100 (а), ×200 (b)

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