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
Baseline
After 3 months
value
Baseline
After 3 months
value
A-1.5 cpd
Mean. SD
Range
4.0–9.0
5.0–9.0
0.0–9.0
5.0–9.0
Median
7.0
7.0
7.0
7.0
95% CI
[6.4; 7.4]
[6.3; 7.1]
[6.4; 7.0]
[6.6; 7.1]
B-3 cpd
Mean. SD
Range
3.0–9.0
3.0–9.0
0.0–9.0
3.0–9.0
Median
6.5
7.0
6.0
7.0
95% CI
[6.3; 7.3]
[6.2; 7.2]
[5.8; 6.4]
[6.2; 6.7]
C-6 cpd
Mean. SD
Range
1.0–9.0
2.0–8.0
0.0–8.0
0.0–8.0
Median
6.0
6.0
5.0
6.0
95% CI
[5.3; 6.4]
[5.5; 6.4]
[5.1; 5.8]
[5.2; 5.8]
D-12 cpd
Mean. SD
Range
0.0–9.0
0.0–9.0
0.0–8.0
0.0–8.0
Median
4.0
4.5
4.0
4.0
95% CI
[3.7; 5.1]
[3.8; 5.2]
[3.9; 4.7]
[3.8; 4.5]
E-18 cpd
Mean. SD
Range
0.0–9.0
0.0–8.0
0.0–9.0
0.0–7.0
Median
3.0
2.0
3.0
2.0
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.