Role of Inflammatory Cytokines in the Conversion of Mild Cognitive Impairment to Dementia: A Prospective Study

Raúl Romero-Sevilla1, Fidel López-Espuela2, José Manuel Fuentes3,4,5

  • 1Department of Neurology, Hospital Universitario de Caceres, Cáceres, Spain.

Abstract

Insights

Alpha 1-antichymotrypsin (ACT) levels predict dementia conversion in mild cognitive impairment (MCI) patients. Interleukin-10 (IL-10) may offer protection against dementia progression.

Area of Science:

  • Neuroscience
  • Immunology
  • Geriatrics

Background:

  • The role of cytokines in the progression from mild cognitive impairment (MCI) to dementia is debated, with conflicting research findings.
  • Subclinical inflammation markers' impact on MCI to dementia conversion requires further clarification.

Purpose of the Study:

  • To investigate the influence of subclinical inflammation markers on the progression of MCI to dementia.
  • To identify specific inflammatory markers associated with MCI conversion to dementia.

Main Methods:

  • A prospective cohort study followed 105 patients aged 65+ diagnosed with MCI for 3 years.
  • Serum concentrations of inflammatory markers were measured, and dementia conversion rates were tracked.

Main Results:

  • 44.76% of patients progressed to dementia within the follow-up period.
  • Higher Alpha 1-antichymotrypsin (ACT) levels were significantly associated with dementia progression (p=0.012) and increased dementia risk (p=0.007).
  • Interleukin-10 (IL-10) levels were significantly higher in patients who remained stable (p=0.04), suggesting a protective role. Higher IL-4 levels were observed in those who developed mixed dementia compared to Alzheimer's disease (p=0.03).

Conclusions:

  • Alpha 1-antichymotrypsin (ACT) is a significant predictor of MCI to dementia conversion.
  • Interleukin-10 (IL-10) may act as a protective factor against dementia progression.
  • Further research with serial inflammatory marker measurements is needed to fully elucidate their impact on MCI progression.

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