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
Baseline
After 3 months
value
Baseline
After 3 months
value
A-1.5 cpd
Mean. SD
Range
1.0–9.0
0.0–9.0
0.0–9.0
1.0–9.0
Median
6.0
5.0
6.0
6.0
95% CI
[5.4; 6.0]
[5.0; 5.5]
[5.6; 6.0]
[5.5; 5.9]
B-3 cpd
Mean. SD
Range
0.0–8.0
0.0–9.0
0.0–8.0
0.0–9.0
Median
5.0
5.0
5.0
5.0
95% CI
[4.7; 5.4]
[4.3; 5.0]
[5.0; 5.5]
[5.0; 5.5]
C-6 cpd
Mean. SD
Range
0.0–9.0
0.0–8.0
0.0–9.0
0.0–9.0
Median
4.0
4.0
5.0
4.5
95% CI
[3.5; 4.3]
[3.1; 3.9]
[3.9; 4.6]
[4.1; 4.7]
D-12 cpd
Mean. SD
Range
0.0–7.0
0.0–7.0
0.0–8.0
0.0–9.0
Median
1.0
2.0
3.0
3.0
95% CI
[1.7; 2.5]
[1.7; 2.5]
[2.3; 3.0]
[2.7; 3.3]
E-18 cpd
Mean. SD
Range
0.0–7.0
0.0–7.0
0.0–9.0
0.0–8.0
Median
0.0
0.0
0.0
0.0
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.