4.5 Article

Glycemic control is not related to cerebral small vessel disease in neurologically asymptomatic individuals with type 1 diabetes

Journal

ACTA DIABETOLOGICA
Volume 59, Issue 4, Pages 481-490

Publisher

SPRINGER-VERLAG ITALIA SRL
DOI: 10.1007/s00592-021-01821-8

Keywords

Cerebral small vessel disease; Magnetic resonance imaging; Fructosamine; Glycated albumin; Long-term glycemic fluctuations

Funding

  1. Helsinki University Central Hospital
  2. Folkhalsan Research Foundation
  3. Academy of Finland [316664, UAK1021MRI]
  4. Wilhelm and Else Stockmann Foundation
  5. Liv och Halsa Society
  6. Novo Nordisk Foundation [NNF OC0013657]
  7. Sigrid Juselius Foundation
  8. Paivikki and Sakari Sohlberg Foundation
  9. Finnish Foundation for Cardiovascular Research
  10. Medical Society of Finland (Finska Lakaresallskapet)
  11. Karl Walter and Jarl Walter Perklen's Foundation
  12. University of Helsinki
  13. University of Gothenburg
  14. Sahlgrenska University Hospital
  15. European Union
  16. Wennerstrom Foundation

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There was no association between glycemic control and cSVD in neurologically asymptomatic individuals with type 1 diabetes, prompting further studies to search for underlying factors of cSVD, despite the presence of a large number of signs of cerebrovascular pathology in these individuals after two decades of chronic hyperglycemia.
Aims To determine if medium- and long-term blood glucose control as well as glycemic variability, which are known to be strong predictors of vascular complications, are associated with underlying cerebral small vessel disease (cSVD) in neurologically asymptomatic individuals with type 1 diabetes. Methods A total of 189 individuals (47.1% men; median age 40.0, IQR 33.0-45.2 years) with type 1 diabetes (median diabetes duration of 21.7, IQR 18.3-30.7 years) were enrolled in a cross-sectional retrospective study, as part of the Finnish Diabetic Nephropathy (FinnDiane) Study. Glycated hemoglobin (HbA(1c)) values were collected over the course of ten years before the visit including a clinical examination, biochemical sampling, and brain magnetic resonance imaging. Markers of glycemic control, measured during the visit, included HbA(1c), fructosamine, and glycated albumin. Results Signs of cSVD were present in 66 (34.9%) individuals. Medium- and long-term glucose control and glycemic variability did not differ in individuals with signs of cSVD compared to those without. Further, no difference in any of the blood glucose variables and cSVD stratified for cerebral microbleeds (CMBs) or white matter hyperintensities were detected. Neither were numbers of CMBs associated with the studied glucose variables. Additionally, after dividing the studied variables into quartiles, no association with cSVD was observed. Conclusions We observed no association between glycemic control and cSVD in neurologically asymptomatic individuals with type 1 diabetes. This finding was unexpected considering the large number of signs of cerebrovascular pathology in these people after two decades of chronic hyperglycemia and warrants further studies searching for underlying factors of cSVD.

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