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
Baseline
After 3 months
value
Baseline
After 3 months
value
A-1.5 cpd
Mean. SD
Range
3.0–9.0
3.0–9.0
4.0–8.0
3.0–8.0
Median
7.0
6.0
5.0
5.0
95% CI
[6.1; 7.0]
[5.5; 6.4]
[5.3; 6.0]
[5.2; 5.9]
B-3 cpd
Mean. SD
Range
2.0–8.0
1.0–9.0
2.0–8.0
1.0–9.0
Median
6.0
6.0
5.0
5.0
95% CI
[5.6; 6.5]
[5.1; 6.0]
[4.5; 5.6]
[4.5; 5.5]
C-6 cpd
Mean. SD
Range
0.0–8.0
0.0–8.0
0.0–8.0
0.0–8.0
Median
6.0
5.0
4.0
4.0
95% CI
[4.6; 5.9]
[4.2; 5.3]
[3.5; 4.9]
[3.5; 4.9]
D-12 cpd
Mean. SD
Range
0.0–8.0
0.0–8.0
0.0–7.0
0.0–7.0
Median
4.0
4.0
3.0
2.0
95% CI
[2.8; 4.4]
[2.4; 3.8]
[2.1; 3.6]
[2.0; 3.5]
E-18 cpd
Mean. SD
Range
0.0–7.0
0.0–5.0
0.0–5.0
0.0–6.0
Median
1.0
1.5
0.5
0.0
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.