Clinical Study

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

Table 3

Characteristics of contrast sensitivity examinations in T2DM patients with and without ALA supplementation at baseline and after 3 months.

Spatial frequencies T2DM patients without
ALA supplementation
CS × LC = 132 measurements
T2DM patients with
ALA supplementation
CS × LC = 200 measurements
BaselineAfter 3 months valueBaselineAfter 3 months value

A-1.5 cpd
 Mean. SD
 Range1.0–9.00.0–9.0   0.0–9.01.0–9.0
 Median6.05.06.06.0
 95% CI[5.4; 6.0][5.0; 5.5][5.6; 6.0][5.5; 5.9]

B-3 cpd
 Mean. SD
 Range0.0–8.00.0–9.0   0.0–8.00.0–9.0
 Median5.05.05.05.0
 95% CI[4.7; 5.4][4.3; 5.0][5.0; 5.5][5.0; 5.5]

C-6 cpd
 Mean. SD
 Range0.0–9.00.0–8.0   0.0–9.00.0–9.0
 Median4.04.05.04.5
 95% CI[3.5; 4.3][3.1; 3.9][3.9; 4.6][4.1; 4.7]

D-12 cpd
 Mean. SD
 Range0.0–7.00.0–7.0 0.0–8.00.0–9.0  
 Median1.02.03.03.0
 95% CI[1.7; 2.5][1.7; 2.5][2.3; 3.0][2.7; 3.3]

E-18 cpd
 Mean. SD
 Range0.0–7.00.0–7.0 0.0–9.00.0–8.0  
 Median0.00.00.00.0
 95% CI[0.9; 1.5][0.8; 1.4][1.0; 1.6][1.3; 1.9]

CS × LC: the number of contrast sensitivity measurements of each eye in 4 luminance conditions and under 5 spatial frequencies.
A-1.5, B-3, C-6, D-12, and E-18 cpd: spatial frequencies.
*Statistically significant differences between the baseline examination of T2DM patients with ALA supplementation versus after 3 months.
**Statistically significant differences between the baseline examination of T2DM patients without ALA supplementation versus after 3 months.