<HashMap><database>biostudies-literature</database><scores/><additional><submitter>Verhulst CEM</submitter><funding>Innovative Medicines Initiative</funding><funding>JDRF, International Diabetes Federation (IDF), The Leona M. and Harry B. Helmsley Charitable Trust</funding><funding>European Union</funding><funding>EFPIA</funding><pagination>2716-2727</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC9750956</full_dataset_link><repository>biostudies-literature</repository><omics_type>Unknown</omics_type><volume>71(12)</volume><pubmed_abstract>Iatrogenic hypoglycemia activates the immune system and is associated with an increased risk for atherosclerotic disease. We determined acute and long-term effects of insulin-induced hypoglycemia on inflammatory markers in humans with or without type 2 diabetes. A total of 15 adults with type 2 diabetes and 16 matched control subjects (17 men and 14 women, age 59.6 ± 7.1 years, BMI 28.5 ± 4.3 kg/m2) underwent a hyperinsulinemic-euglycemic (5.31 ± 0.32 mmol/L) hypoglycemic (2.80 ± 0.12 mmol/L) glucose clamp. Blood was drawn during euglycemia and hypoglycemia and 1, 3, and 7 days later to determine circulating immune cell composition, function, and inflammatory proteins. In response to hypoglycemia, absolute numbers of circulating lymphocytes and monocytes significantly increased and remained elevated for 1 week. The proportion of CD16+ monocytes increased, and the proportion of CD14+ monocytes decreased, which was sustained for 1 week in people without diabetes. During hypoglycemia, ex vivo stimulated monocytes released more tumor necrosis factor-α and interleukin 1β, and less interleukin 10, particularly in people with diabetes. hs-CRP and 25 circulating inflammatory proteins increased, remaining significantly elevated 1 week after hypoglycemia. While levels at euglycemia differed, responses to hypoglycemia were broadly similar in people with or without type 2 diabetes. We conclude that hypoglycemia induces a proinflammatory response at the cellular and protein level that is sustained for 1 week in people with type 2 diabetes and control subjects.</pubmed_abstract><journal>Diabetes</journal><pubmed_title>Sustained Proinflammatory Effects of Hypoglycemia in People With Type 2 Diabetes and in People Without Diabetes.</pubmed_title><pmcid>PMC9750956</pmcid><funding_grant_id>777460</funding_grant_id><pubmed_authors>van Heck JIP</pubmed_authors><pubmed_authors>de Galan BE</pubmed_authors><pubmed_authors>McCrimmon RJ</pubmed_authors><pubmed_authors>Tack CJ</pubmed_authors><pubmed_authors>Fabricius TW</pubmed_authors><pubmed_authors>Verhulst CEM</pubmed_authors><pubmed_authors>Stienstra R</pubmed_authors><pubmed_authors>Teerenstra S</pubmed_authors><pubmed_authors>Pedersen-Bjergaard U</pubmed_authors></additional><is_claimable>false</is_claimable><name>Sustained Proinflammatory Effects of Hypoglycemia in People With Type 2 Diabetes and in People Without Diabetes.</name><description>Iatrogenic hypoglycemia activates the immune system and is associated with an increased risk for atherosclerotic disease. We determined acute and long-term effects of insulin-induced hypoglycemia on inflammatory markers in humans with or without type 2 diabetes. A total of 15 adults with type 2 diabetes and 16 matched control subjects (17 men and 14 women, age 59.6 ± 7.1 years, BMI 28.5 ± 4.3 kg/m2) underwent a hyperinsulinemic-euglycemic (5.31 ± 0.32 mmol/L) hypoglycemic (2.80 ± 0.12 mmol/L) glucose clamp. Blood was drawn during euglycemia and hypoglycemia and 1, 3, and 7 days later to determine circulating immune cell composition, function, and inflammatory proteins. In response to hypoglycemia, absolute numbers of circulating lymphocytes and monocytes significantly increased and remained elevated for 1 week. The proportion of CD16+ monocytes increased, and the proportion of CD14+ monocytes decreased, which was sustained for 1 week in people without diabetes. During hypoglycemia, ex vivo stimulated monocytes released more tumor necrosis factor-α and interleukin 1β, and less interleukin 10, particularly in people with diabetes. hs-CRP and 25 circulating inflammatory proteins increased, remaining significantly elevated 1 week after hypoglycemia. While levels at euglycemia differed, responses to hypoglycemia were broadly similar in people with or without type 2 diabetes. We conclude that hypoglycemia induces a proinflammatory response at the cellular and protein level that is sustained for 1 week in people with type 2 diabetes and control subjects.</description><dates><release>2022-01-01T00:00:00Z</release><publication>2022 Dec</publication><modification>2025-04-04T09:50:05.692Z</modification><creation>2025-02-19T01:17:08.138Z</creation></dates><accession>S-EPMC9750956</accession><cross_references><pubmed>35848804</pubmed><doi>10.2337/db22-0246</doi></cross_references></HashMap>