4.7 Article

Glycemic Dysregulations Are Associated With Worsening Cognitive Function in Older Participants at High Risk of Cardiovascular Disease: Two-Year Follow-up in the PREDIMED-Plus Study

Journal

FRONTIERS IN ENDOCRINOLOGY
Volume 12, Issue -, Pages -

Publisher

FRONTIERS MEDIA SA
DOI: 10.3389/fendo.2021.754347

Keywords

cognitive function; diabetes duration; glycated (glycosylated) hemoglobin; insulin resistance; type 2 diabetes; prediabetes

Funding

  1. CIBER Fisiopatologi'a de la Obesidad y Nutricio'n (CIBEROBN)
  2. Instituto de Salud Carlos III (ISCIII), through the Fondo de Investigacion para la Salud (FIS)
  3. European Regional Development Fund [PI13/00673, PI13/00492, PI13/00272, PI13/01123, PI13/00462, PI13/00233, PI13/02184, PI13/00728, PI13/01090, PI13/01056, PI14/01722, PI14/00636, PI14/00618, PI16/00366, PI16/01522, PI16/01120, PI17/00764, PI17/01183, PI17/00855]
  4. Especial Action Project [340918]
  5. Recercaixa [2013ACUP00194]
  6. Consejeri'a de Salud de la Junta de Andaluci'a [PI0458/2013, PS0358/2016, PI0137/2018]
  7. Generalitat Valenciana [PROMETEO/2017/017, APOSTD/2020/164]
  8. SEMERGEN
  9. Horizon 2020 PRIME study (Prevention and Remediation of Insulin Multimorbidity in Europe) [847879]
  10. Instituto de Salud Carlos III [CPII19/00015]
  11. European Social Fund Investing in your future
  12. 'FOLIUM' programme within the FUTURMed project from the Fundacio'n Instituto de Investigacio'n Sanitaria Illes Balears
  13. University of Rovira i Virgili [2020PMF-PIPF-37]
  14. Department of Health of the Generalitat de Catalunya [SLT006/17/00246]
  15. ICREA
  16. [PI17/01347]
  17. [PI17/00525]
  18. [PI17/01827]
  19. [PI17/00532]
  20. [PI17/00215]
  21. [PI17/01441]
  22. [PI17/00508]
  23. [PI17/01732]
  24. [PI17/00926]
  25. [PI19/00957]
  26. [PI19/00386]
  27. [PI19/00309]
  28. [PI19/01032]
  29. [PI19/00576]
  30. [PI19/00017]
  31. [PI19/01226]
  32. [PI19/00781]
  33. [PI19/01560]
  34. [PI19/01332]
  35. [PI20/01802]
  36. [PI20/00138]
  37. [PI20/01532]
  38. [PI20/00456]
  39. [PI20/00339]
  40. [PI20/00557]
  41. [PI20/00886]
  42. [PI20/01158]
  43. [PI14/00696]
  44. [PI14/01206]
  45. [PI14/01919]
  46. [PI14/00853]
  47. [PI14/01374]
  48. [PI14/00972]
  49. [PI14/00728]
  50. [PI14/01471]
  51. [PI16/00473]
  52. [PI16/00662]
  53. [PI16/01873]
  54. [PI16/01094]
  55. [PI16/00501]
  56. [PI16/00533]
  57. [PI16/00381]

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This study found that prediabetes was not associated with cognitive decline, but longer duration of diabetes, insulin resistance, HbA(1c) levels, poor diabetes control, and insulin treatment were related to worsened cognitive function changes in the short term in individuals at high cardiovascular risk.
Introduction Type 2 diabetes has been linked to greater cognitive decline, but other glycemic parameters such as prediabetes, diabetes control and treatment, and HOMA-IR and HbA(1c) diabetes-related biomarkers have shown inconsistent results. Furthermore, there is limited research assessing these relationships in short-term studies. Thus, we aimed to examine 2-year associations between baseline diabetes/glycemic status and changes in cognitive function in older participants at high risk of cardiovascular disease. Methods We conducted a 2-year prospective cohort study (n=6,874) within the framework of the PREDIMED-Plus study. The participants (with overweight/obesity and metabolic syndrome; mean age 64.9 years; 48.5% women) completed a battery of 8 cognitive tests, and a global cognitive function Z-score (GCF) was estimated. At baseline, participants were categorized by diabetes status (no-diabetes, prediabetes, and <5 or >= 5-year diabetes duration), and also by diabetes control. Furthermore, insulin resistance (HOMA-IR) and glycated hemoglobin (HbA(1c)) levels were measured, and antidiabetic medications were recorded. Linear and logistic regression models, adjusted by potential confounders, were fitted to assess associations between glycemic status and changes in cognitive function. Results Prediabetes status was unrelated to cognitive decline. However, compared to participants without diabetes, those with >= 5-year diabetes duration had greater reductions in GCF (beta=-0.11 (95%CI -0.16;-0.06)], as well as in processing speed and executive function measurements. Inverse associations were observed between baseline HOMA-IR and changes in GCF [beta=-0.0094 (95%CI -0.0164;-0.0023)], but also between HbA(1c) levels and changes in GCF [beta=-0.0085 (95%CI -0.0115, -0.0055)], the Mini-Mental State Examination, and other executive function tests. Poor diabetes control was inversely associated with phonologic fluency. The use of insulin treatment was inversely related to cognitive function as measured by the GCF [beta=-0.31 (95%CI -0.44, -0.18)], and other cognitive tests. Conclusions Insulin resistance, diabetes status, longer diabetes duration, poor glycemic control, and insulin treatment were associated with worsening cognitive function changes in the short term in a population at high cardiovascular risk.

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