The impact of prior exposure to hypoglycaemia on the inflammatory response to a subsequent hypoglycaemic episode

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  • Clementine E.M. Verhulst
  • Julia I.P. van Heck
  • Therese W. Fabricius
  • Rinke Stienstra
  • Steven Teerenstra
  • Rory J. McCrimmon
  • Cees J. Tack
  • Pedersen-Bjergaard, Ulrik
  • Bastiaan E. de Galan
Background
Hypoglycaemia has been shown to induce a systemic pro-inflammatory response, which may be driven, in part, by the adrenaline response. Prior exposure to hypoglycaemia attenuates counterregulatory hormone responses to subsequent hypoglycaemia, but whether this effect can be extrapolated to the pro-inflammatory response is unclear. Therefore, we investigated the effect of antecedent hypoglycaemia on inflammatory responses to subsequent hypoglycaemia in humans.

Methods
Healthy participants (n = 32) were recruited and randomised to two 2-h episodes of either hypoglycaemia or normoglycaemia on day 1, followed by a hyperinsulinaemic hypoglycaemic (2.8 ± 0.1 mmol/L) glucose clamp on day 2. During normoglycaemia and hypoglycaemia, and after 24 h, 72 h and 1 week, blood was drawn to determine circulating immune cell composition, phenotype and function, and 93 circulating inflammatory proteins including hs-CRP.

Results
In the group undergoing antecedent hypoglycaemia, the adrenaline response to next-day hypoglycaemia was lower compared to the control group (1.45 ± 1.24 vs 2.68 ± 1.41 nmol/l). In both groups, day 2 hypoglycaemia increased absolute numbers of circulating immune cells, of which lymphocytes and monocytes remained elevated for the whole week. Also, the proportion of pro-inflammatory CD16+-monocytes increased during hypoglycaemia. After ex vivo stimulation, monocytes released more TNF-α and IL-1β, and less IL-10 in response to hypoglycaemia, whereas levels of 19 circulating inflammatory proteins, including hs-CRP, increased for up to 1 week after the hypoglycaemic event. Most of the inflammatory responses were similar in the two groups, except the persistent pro-inflammatory protein changes were partly blunted in the group exposed to antecedent hypoglycaemia. We did not find a correlation between the adrenaline response and the inflammatory responses during hypoglycaemia.

Conclusion
Hypoglycaemia induces an acute and persistent pro-inflammatory response at multiple levels that occurs largely, but not completely, independent of prior exposure to hypoglycaemia.

Clinical Trial information Clinicaltrials.gov no. NCT03976271 (registered 5 June 2019).
OriginalsprogEngelsk
Artikelnummer55
TidsskriftCardiovascular Diabetology
Vol/bind23
Udgave nummer1
Antal sider13
ISSN1475-2840
DOI
StatusUdgivet - 2024

Bibliografisk note

Funding Information:
This study has received funding from the Innovative Medicines Initiative 2 Joint Undertaking (JU) under Grant Agreement No 777460. The JU receives support from the European Union’s Horizon 2020 research and innovation program and EFPIA and T1D Exchange, JDRF, International Diabetes Federation (IDF), The Leona M. and Harry B. Helmsley Charitable Trust.

Funding Information:
The authors thank all the volunteers for participating in this work. The authors also thank Evertine Abbink, Linda Drenthen, Karin Saini, Marjolein Eybergen, Emma Lenssen and Esther Eggenhuizen for assistance during the clamps, and Anneke Hijmans and Ajie Mandala for assistance in the lab in the Netherlands, and Stine Tving Kjøller, Charlotte Hansen, Pernille Banck-Petersen, Rikke Carstensen, for assisting as research nurses and Charlotte Pietraszek and Susanne Månsson for preparation of blood and other practicalities during the clamp, and Thore Hillig and Dorthe Kjeldgård Hansen for assistance in the lab in Denmark.

Publisher Copyright:
© The Author(s) 2024.

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