Clinical Study

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

Table 2

Characteristics of contrast sensitivity examinations in T1DM patients with and without ALA supplementation at baseline and after 3 months.

Spatial frequencies T1DM patients without
ALA supplementation
CS × LC = 48 measurements
T1DM patients with
ALA supplementation
CS × LC = 40 measurements
BaselineAfter 3 months valueBaselineAfter 3 months value

A-1.5 cpd
 Mean. SD
 Range3.0–9.03.0–9.0   4.0–8.03.0–8.0
 Median7.06.05.05.0
 95% CI[6.1; 7.0][5.5; 6.4][5.3; 6.0][5.2; 5.9]

B-3 cpd
 Mean. SD
 Range2.0–8.01.0–9.0   2.0–8.01.0–9.0
 Median6.06.05.05.0
 95% CI[5.6; 6.5][5.1; 6.0][4.5; 5.6][4.5; 5.5]

C-6 cpd
 Mean. SD
 Range0.0–8.00.0–8.0   0.0–8.00.0–8.0
 Median6.05.04.04.0
 95% CI[4.6; 5.9][4.2; 5.3][3.5; 4.9][3.5; 4.9]

D-12 cpd
 Mean. SD
 Range0.0–8.00.0–8.0   0.0–7.00.0–7.0
 Median4.04.03.02.0
 95% CI[2.8; 4.4][2.4; 3.8][2.1; 3.6][2.0; 3.5]

E-18 cpd
 Mean. SD
 Range0.0–7.00.0–5.0 0.0–5.00.0–6.0
 Median1.01.50.50.0
 95% CI[1.4; 2.7][1.4; 2.5][1.1; 2.3][0.8; 2.1]

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 T1DM patients without ALA supplementation versus after 3 months.