Serum Fetuin-A Levels in Patients with Bilateral Basal Ganglia Calcification

Neurosci Lett. 2018 Feb 14:666:148-152. doi: 10.1016/j.neulet.2017.12.050. Epub 2017 Dec 27.

Abstract

Background and purpose: The idiopathic basal ganglia calcification (Fahr syndrome) may occur due to senility. Fetuin-A is a negative acute phase reactant which inhibits calcium-phosphorus precipitation and vascular calcification. In this study, we aimed to evaluate whether serum fetuin-A levels correlate with bilateral basal ganglia calcification.

Method: Forty-five patients who had bilateral basal ganglia calcification on brain CT were selected according to the inclusion and exclusion criteria, and 45 age and gender-matched subjects without basal ganglia calcification were included for the control group. Serum fetuin-A levels were measured from venous blood samples. All participants were divided into two groups; with and without basal ganglia calcification. These groups were divided into subgroups regarding age (18-32 and 33-45 years of age) and gender (male, female).

Results: We detected lower levels of serum fetuin-A in patients with basal ganglia calcification compared with the subjects without basal ganglia calcification. In all subgroups (female, male, 18-32 years and 33-45 years), mean fetuin-A levels were significantly lower in patients with basal ganglia calcification (p = 0.017, p = 0.014, p = 0.024, p = 0.026, p = 0.01 respectively). And statistically significantly lower levels of fetuin-A was found to be correlated with the increasing densities of calcification in the calcified basal ganglia group (p-value: <0.001).

Conclusion: Considering the role of fetuin-A in tissue calcification and inflammation, higher serum fetuin-A levels should be measured in patients with basal ganglia calcification. We believe that the measurement of serum fetuin-A may play a role in the prediction of basal ganglia calcification as a biomarker.

Keywords: Basal ganglia; Calcification; Fetuin-A.

MeSH terms

  • Adolescent
  • Adult
  • Basal Ganglia / metabolism*
  • Biomarkers / blood
  • C-Reactive Protein / metabolism
  • Female
  • Humans
  • Inflammation / blood*
  • Male
  • Middle Aged
  • Young Adult
  • alpha-2-HS-Glycoprotein / biosynthesis*

Substances

  • AHSG protein, human
  • Biomarkers
  • alpha-2-HS-Glycoprotein
  • C-Reactive Protein