Clinical Study

Effect of the Administration of Alpha-Lipoic Acid on Contrast Sensitivity in Patients with Type 1 and Type 2 Diabetes

Table 4

Characteristics of contrast sensitivity examinations in the control group with and without ALA supplementation at baseline and after 3 months.

Spatial frequencies Control group without
ALA supplementation
CS × LC = 44 measurements
Control group with
ALA supplementation
CS × LC = 108 measurements
BaselineAfter 3 months valueBaselineAfter 3 months value

A-1.5 cpd
 Mean. SD
 Range4.0–9.05.0–9.0 0.0–9.05.0–9.0
 Median7.07.07.07.0
 95% CI[6.4; 7.4][6.3; 7.1][6.4; 7.0][6.6; 7.1]

B-3 cpd
 Mean. SD
 Range3.0–9.03.0–9.0 0.0–9.03.0–9.0  
 Median6.57.06.07.0
 95% CI[6.3; 7.3][6.2; 7.2][5.8; 6.4][6.2; 6.7]

C-6 cpd
 Mean. SD
 Range1.0–9.02.0–8.0 0.0–8.00.0–8.0
 Median6.06.05.06.0
 95% CI[5.3; 6.4][5.5; 6.4][5.1; 5.8][5.2; 5.8]

D-12 cpd
 Mean. SD
 Range0.0–9.00.0–9.0 0.0–8.00.0–8.0
 Median4.04.54.04.0
 95% CI[3.7; 5.1][3.8; 5.2][3.9; 4.7][3.8; 4.5]

E-18 cpd
 Mean. SD
 Range0.0–9.00.0–8.0 0.0–9.00.0–7.0
 Median3.02.03.02.0
 95% CI[2.1; 3.7][1.8; 3.3][2.5; 3.3][2.3; 3.0]

CS × LC: the number of contrast sensitivity measurements of each eye in 4 luminance conditions and under 5 spatial frequencies.
Spatial frequencies: A-1.5, B-3, C-6, D-12, and E-18 cpd.
*Statistically significant differences between the baseline examination of control group with ALA supplementation versus after 3 months.