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Effect of Hypoglycemia on Inflammatory Responses and the Response to Low-Dose Endotoxemia in Humans

CONTEXT: Hypoglycemia is emerging as a risk for cardiovascular events in diabetes. We hypothesized that hypoglycemia activates the innate immune system, which is known to increase cardiovascular risk. OBJECTIVE: To determine whether hypoglycemia modifies subsequent innate immune system responses. DE...

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Autores principales: Iqbal, Ahmed, Prince, Lynne R, Novodvorsky, Peter, Bernjak, Alan, Thomas, Mark R, Birch, Lewis, Lambert, Danielle, Kay, Linda J, Wright, Fiona J, Macdonald, Ian A, Jacques, Richard M, Storey, Robert F, McCrimmon, Rory J, Francis, Sheila, Heller, Simon R, Sabroe, Ian
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Endocrine Society 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6391720/
https://www.ncbi.nlm.nih.gov/pubmed/30252067
http://dx.doi.org/10.1210/jc.2018-01168
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author Iqbal, Ahmed
Prince, Lynne R
Novodvorsky, Peter
Bernjak, Alan
Thomas, Mark R
Birch, Lewis
Lambert, Danielle
Kay, Linda J
Wright, Fiona J
Macdonald, Ian A
Jacques, Richard M
Storey, Robert F
McCrimmon, Rory J
Francis, Sheila
Heller, Simon R
Sabroe, Ian
author_facet Iqbal, Ahmed
Prince, Lynne R
Novodvorsky, Peter
Bernjak, Alan
Thomas, Mark R
Birch, Lewis
Lambert, Danielle
Kay, Linda J
Wright, Fiona J
Macdonald, Ian A
Jacques, Richard M
Storey, Robert F
McCrimmon, Rory J
Francis, Sheila
Heller, Simon R
Sabroe, Ian
author_sort Iqbal, Ahmed
collection PubMed
description CONTEXT: Hypoglycemia is emerging as a risk for cardiovascular events in diabetes. We hypothesized that hypoglycemia activates the innate immune system, which is known to increase cardiovascular risk. OBJECTIVE: To determine whether hypoglycemia modifies subsequent innate immune system responses. DESIGN AND SETTING: Single-blinded, prospective study of three independent parallel groups. PARTICIPANTS AND INTERVENTIONS: Twenty-four healthy participants underwent either a hyperinsulinemic-hypoglycemic (2.5 mmol/L), euglycemic (6.0 mmol/L), or sham-saline clamp (n = 8 for each group). After 48 hours, all participants received low-dose (0.3 ng/kg) intravenous endotoxin. MAIN OUTCOME MEASURES: We studied in-vivo monocyte mobilization and monocyte-platelet interactions. RESULTS: Hypoglycemia increased total leukocytes (9.98 ± 1.14 × 10(9)/L vs euglycemia 4.38 ± 0.53 × 10(9)/L, P < 0.001; vs sham-saline 4.76 ± 0.36 × 10(9)/L, P < 0.001) (mean ± SEM), mobilized proinflammatory intermediate monocytes (42.20 ± 7.52/μL vs euglycemia 20.66 ± 3.43/μL, P < 0.01; vs sham-saline 26.20 ± 3.86/μL, P < 0.05), and nonclassic monocytes (36.16 ± 4.66/μL vs euglycemia 12.72 ± 2.42/μL, P < 0.001; vs sham-saline 19.05 ± 3.81/μL, P < 0.001). Following hypoglycemia vs euglycemia, platelet aggregation to agonist (area under the curve) increased (73.87 ± 7.30 vs 52.50 ± 4.04, P < 0.05) and formation of monocyte-platelet aggregates increased (96.05 ± 14.51/μL vs 49.32 ± 6.41/μL, P < 0.05). Within monocyte subsets, hypoglycemia increased aggregation of intermediate monocytes (10.51 ± 1.42/μL vs euglycemia 4.19 ± 1.08/μL, P < 0.05; vs sham-saline 3.81± 1.42/μL, P < 0.05) and nonclassic monocytes (9.53 ± 1.08/μL vs euglycemia 2.86 ± 0.72/μL, P < 0.01; vs sham-saline 3.08 ± 1.01/μL, P < 0.05), with platelets compared with controls. Hypoglycemia led to greater leukocyte mobilization in response to subsequent low-dose endotoxin challenge (10.96 ± 0.97 vs euglycemia 8.21 ± 0.85 × 10(9)/L, P < 0.05). CONCLUSIONS: Hypoglycemia mobilizes monocytes, increases platelet reactivity, promotes interaction between platelets and proinflammatory monocytes, and potentiates the subsequent immune response to endotoxin. These changes may contribute to increased cardiovascular risk observed in people with diabetes.
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spelling pubmed-63917202019-03-04 Effect of Hypoglycemia on Inflammatory Responses and the Response to Low-Dose Endotoxemia in Humans Iqbal, Ahmed Prince, Lynne R Novodvorsky, Peter Bernjak, Alan Thomas, Mark R Birch, Lewis Lambert, Danielle Kay, Linda J Wright, Fiona J Macdonald, Ian A Jacques, Richard M Storey, Robert F McCrimmon, Rory J Francis, Sheila Heller, Simon R Sabroe, Ian J Clin Endocrinol Metab Clinical Research Articles CONTEXT: Hypoglycemia is emerging as a risk for cardiovascular events in diabetes. We hypothesized that hypoglycemia activates the innate immune system, which is known to increase cardiovascular risk. OBJECTIVE: To determine whether hypoglycemia modifies subsequent innate immune system responses. DESIGN AND SETTING: Single-blinded, prospective study of three independent parallel groups. PARTICIPANTS AND INTERVENTIONS: Twenty-four healthy participants underwent either a hyperinsulinemic-hypoglycemic (2.5 mmol/L), euglycemic (6.0 mmol/L), or sham-saline clamp (n = 8 for each group). After 48 hours, all participants received low-dose (0.3 ng/kg) intravenous endotoxin. MAIN OUTCOME MEASURES: We studied in-vivo monocyte mobilization and monocyte-platelet interactions. RESULTS: Hypoglycemia increased total leukocytes (9.98 ± 1.14 × 10(9)/L vs euglycemia 4.38 ± 0.53 × 10(9)/L, P < 0.001; vs sham-saline 4.76 ± 0.36 × 10(9)/L, P < 0.001) (mean ± SEM), mobilized proinflammatory intermediate monocytes (42.20 ± 7.52/μL vs euglycemia 20.66 ± 3.43/μL, P < 0.01; vs sham-saline 26.20 ± 3.86/μL, P < 0.05), and nonclassic monocytes (36.16 ± 4.66/μL vs euglycemia 12.72 ± 2.42/μL, P < 0.001; vs sham-saline 19.05 ± 3.81/μL, P < 0.001). Following hypoglycemia vs euglycemia, platelet aggregation to agonist (area under the curve) increased (73.87 ± 7.30 vs 52.50 ± 4.04, P < 0.05) and formation of monocyte-platelet aggregates increased (96.05 ± 14.51/μL vs 49.32 ± 6.41/μL, P < 0.05). Within monocyte subsets, hypoglycemia increased aggregation of intermediate monocytes (10.51 ± 1.42/μL vs euglycemia 4.19 ± 1.08/μL, P < 0.05; vs sham-saline 3.81± 1.42/μL, P < 0.05) and nonclassic monocytes (9.53 ± 1.08/μL vs euglycemia 2.86 ± 0.72/μL, P < 0.01; vs sham-saline 3.08 ± 1.01/μL, P < 0.05), with platelets compared with controls. Hypoglycemia led to greater leukocyte mobilization in response to subsequent low-dose endotoxin challenge (10.96 ± 0.97 vs euglycemia 8.21 ± 0.85 × 10(9)/L, P < 0.05). CONCLUSIONS: Hypoglycemia mobilizes monocytes, increases platelet reactivity, promotes interaction between platelets and proinflammatory monocytes, and potentiates the subsequent immune response to endotoxin. These changes may contribute to increased cardiovascular risk observed in people with diabetes. Endocrine Society 2018-09-24 /pmc/articles/PMC6391720/ /pubmed/30252067 http://dx.doi.org/10.1210/jc.2018-01168 Text en https://creativecommons.org/licenses/by/4.0/ This article has been published under the terms of the Creative Commons Attribution License (CC BY; https://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited. Copyright for this article is retained by the author(s).
spellingShingle Clinical Research Articles
Iqbal, Ahmed
Prince, Lynne R
Novodvorsky, Peter
Bernjak, Alan
Thomas, Mark R
Birch, Lewis
Lambert, Danielle
Kay, Linda J
Wright, Fiona J
Macdonald, Ian A
Jacques, Richard M
Storey, Robert F
McCrimmon, Rory J
Francis, Sheila
Heller, Simon R
Sabroe, Ian
Effect of Hypoglycemia on Inflammatory Responses and the Response to Low-Dose Endotoxemia in Humans
title Effect of Hypoglycemia on Inflammatory Responses and the Response to Low-Dose Endotoxemia in Humans
title_full Effect of Hypoglycemia on Inflammatory Responses and the Response to Low-Dose Endotoxemia in Humans
title_fullStr Effect of Hypoglycemia on Inflammatory Responses and the Response to Low-Dose Endotoxemia in Humans
title_full_unstemmed Effect of Hypoglycemia on Inflammatory Responses and the Response to Low-Dose Endotoxemia in Humans
title_short Effect of Hypoglycemia on Inflammatory Responses and the Response to Low-Dose Endotoxemia in Humans
title_sort effect of hypoglycemia on inflammatory responses and the response to low-dose endotoxemia in humans
topic Clinical Research Articles
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6391720/
https://www.ncbi.nlm.nih.gov/pubmed/30252067
http://dx.doi.org/10.1210/jc.2018-01168
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