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Continuous Glucose Monitoring in Patients Following Simultaneous Pancreas–Kidney Transplantation: Time in Range and Glucose Variability

Simultaneous pancreas–kidney transplantation (SPKT) can improve long-term patient survival and restore endogenous insulin secretion in recipients with type 1 diabetes (T1D). There are currently few data on glucose fluctuations assessed by continuous glucose monitoring (CGM) after SPKT. Aim: to evalu...

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Autores principales: Dmitriev, Ilya V., Severina, Anastasia S., Zhuravel, Nikita S., Yevloyeva, Madina I., Salimkhanov, Rustam K., Shchelykalina, Svetlana P., Bezunov, Evgeniy A., Shamkhalova, Minara S., Semenova, Julia F., Klimontov, Vadim V., Shestakova, Marina V.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10177867/
https://www.ncbi.nlm.nih.gov/pubmed/37174997
http://dx.doi.org/10.3390/diagnostics13091606
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author Dmitriev, Ilya V.
Severina, Anastasia S.
Zhuravel, Nikita S.
Yevloyeva, Madina I.
Salimkhanov, Rustam K.
Shchelykalina, Svetlana P.
Bezunov, Evgeniy A.
Shamkhalova, Minara S.
Semenova, Julia F.
Klimontov, Vadim V.
Shestakova, Marina V.
author_facet Dmitriev, Ilya V.
Severina, Anastasia S.
Zhuravel, Nikita S.
Yevloyeva, Madina I.
Salimkhanov, Rustam K.
Shchelykalina, Svetlana P.
Bezunov, Evgeniy A.
Shamkhalova, Minara S.
Semenova, Julia F.
Klimontov, Vadim V.
Shestakova, Marina V.
author_sort Dmitriev, Ilya V.
collection PubMed
description Simultaneous pancreas–kidney transplantation (SPKT) can improve long-term patient survival and restore endogenous insulin secretion in recipients with type 1 diabetes (T1D). There are currently few data on glucose fluctuations assessed by continuous glucose monitoring (CGM) after SPKT. Aim: to evaluate CGM-derived time in range (TIR) and glucose variability (GV) in patients with T1D and functioning pancreatic grafts after SPKT. Fifty-four CGM recordings from 43 patients, 15 men and 28 women, aged 34 (31; 39) years were analyzed. Time since SKPT was up to 1 year (group 1, n = 13), from 1 to 5 years (group 2, n = 15), and from 5 to 12 years (group 3, n = 26). TIR (3.9–10 mmol/L), Time Above Range (TAR), Time Below Range (TBR), and GV parameters were estimated. There were no differences in mean glucose (5.5 [5.1; 6.2], 5.9 [5.4; 6.2], and 5.9 [5.6; 6.7] mmol/L), TIR (97.6 [92.8–99.1], 97.2 [93.2; 99.1], and 97.5 [93.4; 99]%); TAR (0, 1.8 [1.3; 3.7], and 2.5 [2; 5]%), TBR (5 [3.3; 12.7], 4.1 [2.2; 10.1], and 3.5 [1.3; 6.5]%) and GV parameters between three groups (all p > 0.05). Thus, recipients with functioning pancreatic grafts demonstrate remarkably high TIR and low GV after SPKT.
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spelling pubmed-101778672023-05-13 Continuous Glucose Monitoring in Patients Following Simultaneous Pancreas–Kidney Transplantation: Time in Range and Glucose Variability Dmitriev, Ilya V. Severina, Anastasia S. Zhuravel, Nikita S. Yevloyeva, Madina I. Salimkhanov, Rustam K. Shchelykalina, Svetlana P. Bezunov, Evgeniy A. Shamkhalova, Minara S. Semenova, Julia F. Klimontov, Vadim V. Shestakova, Marina V. Diagnostics (Basel) Article Simultaneous pancreas–kidney transplantation (SPKT) can improve long-term patient survival and restore endogenous insulin secretion in recipients with type 1 diabetes (T1D). There are currently few data on glucose fluctuations assessed by continuous glucose monitoring (CGM) after SPKT. Aim: to evaluate CGM-derived time in range (TIR) and glucose variability (GV) in patients with T1D and functioning pancreatic grafts after SPKT. Fifty-four CGM recordings from 43 patients, 15 men and 28 women, aged 34 (31; 39) years were analyzed. Time since SKPT was up to 1 year (group 1, n = 13), from 1 to 5 years (group 2, n = 15), and from 5 to 12 years (group 3, n = 26). TIR (3.9–10 mmol/L), Time Above Range (TAR), Time Below Range (TBR), and GV parameters were estimated. There were no differences in mean glucose (5.5 [5.1; 6.2], 5.9 [5.4; 6.2], and 5.9 [5.6; 6.7] mmol/L), TIR (97.6 [92.8–99.1], 97.2 [93.2; 99.1], and 97.5 [93.4; 99]%); TAR (0, 1.8 [1.3; 3.7], and 2.5 [2; 5]%), TBR (5 [3.3; 12.7], 4.1 [2.2; 10.1], and 3.5 [1.3; 6.5]%) and GV parameters between three groups (all p > 0.05). Thus, recipients with functioning pancreatic grafts demonstrate remarkably high TIR and low GV after SPKT. MDPI 2023-04-30 /pmc/articles/PMC10177867/ /pubmed/37174997 http://dx.doi.org/10.3390/diagnostics13091606 Text en © 2023 by the authors. https://creativecommons.org/licenses/by/4.0/Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (https://creativecommons.org/licenses/by/4.0/).
spellingShingle Article
Dmitriev, Ilya V.
Severina, Anastasia S.
Zhuravel, Nikita S.
Yevloyeva, Madina I.
Salimkhanov, Rustam K.
Shchelykalina, Svetlana P.
Bezunov, Evgeniy A.
Shamkhalova, Minara S.
Semenova, Julia F.
Klimontov, Vadim V.
Shestakova, Marina V.
Continuous Glucose Monitoring in Patients Following Simultaneous Pancreas–Kidney Transplantation: Time in Range and Glucose Variability
title Continuous Glucose Monitoring in Patients Following Simultaneous Pancreas–Kidney Transplantation: Time in Range and Glucose Variability
title_full Continuous Glucose Monitoring in Patients Following Simultaneous Pancreas–Kidney Transplantation: Time in Range and Glucose Variability
title_fullStr Continuous Glucose Monitoring in Patients Following Simultaneous Pancreas–Kidney Transplantation: Time in Range and Glucose Variability
title_full_unstemmed Continuous Glucose Monitoring in Patients Following Simultaneous Pancreas–Kidney Transplantation: Time in Range and Glucose Variability
title_short Continuous Glucose Monitoring in Patients Following Simultaneous Pancreas–Kidney Transplantation: Time in Range and Glucose Variability
title_sort continuous glucose monitoring in patients following simultaneous pancreas–kidney transplantation: time in range and glucose variability
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10177867/
https://www.ncbi.nlm.nih.gov/pubmed/37174997
http://dx.doi.org/10.3390/diagnostics13091606
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