The main finding of the study was that retinal capillary blood flow is higher in women with insulin-dependent diabetes than in nondiabetic women during pregnancy and after delivery. In the patients with diabetes, mean retinal capillary blood flow tended to increase from the first to the third trimester and decrease after delivery, but these changes did not reach statistical significance. In contrast, no tendency towards an increase in mean retinal capillary blood flow was seen in the nondiabetic women. In addition, no difference existed in blood flow between nonpregnant diabetic control subjects and nondiabetic pregnant control subjects, whereas pregnant diabetic women had higher flow values than did nonpregnant diabetic control subjects.
The results obtained with the retinal flowmeter system show a relatively large intersession variation that may reduce its power to detect time-dependent changes.
14 The magnitude of the increase caused by diabetic pregnancy compared with that caused by diabetes in general is somewhat unclear. Blood flows were higher in pregnant diabetic women during the third trimester than in a control group of nonpregnant diabetic women, but no significant difference was evident between nonpregnant diabetic women and nondiabetic pregnant women at any time point. These data suggest that the increase observed in retinal blood flow in diabetic women during pregnancy was at least in part connected with pregnancy, thus indicating an altered response of the retinal circulation to pregnancy in diabetes. Blood flows in diabetic women remained above the level in nondiabetic women at 3 months postpartum, and remained unchanged at 6 months postpartum, when the pregnancy-related cardiovascular circulatory changes should have been normalized. Our results are, however, somewhat inconclusive as to the timing of the normalization of retinal blood flow during the postpartum period.
Pregnancy provides a good model for the study of progression of retinopathy in diabetes, because retinal status often worsens during any defined period. To our knowledge, this is the first study to use direct objective measurement of capillary blood flow during pregnancy in diabetic and nondiabetic women. Previous studies involving total retinal blood flow, as measured from the main retinal vessels, have yielded conflicting results. Chen et al.,
7 measuring volumetric blood flow in the major retinal veins during pregnancy in diabetic women, found a connection between progression of retinopathy and increased volumetric total blood flow in a retinal quadrant. Although these results most likely imply changes in volumetric blood flow at the microcirculatory level, there was no direct measurement of blood flow velocity in retinal capillaries. Another study showed a decrease during pregnancy in volumetric retinal blood flow in diabetic women with no retinopathy (
n = 4) or with background retinopathy (
n = 3).
8 It is difficult to relate these observations directly to local measurements of retinal capillary blood flow, because the distribution of changes in blood flow and the proportion of perfused capillaries among different retinal regions may vary.
14 17 Data by Hellstedt et al.,
3 using the psychophysical blue-field entoptic simulation technique, suggest an increase in retinal capillary blood velocity during pregnancy in diabetic, but not in healthy, women.
Investigators in previous studies have also reported conflicting results concerning retinal blood flow in nonpregnant diabetic women. In a study using a retinal flowmeter, increased capillary blood flow was found in nonpregnant diabetic patients with background or preproliferative retinopathy,
18 which is in agreement with our findings in pregnant diabetic women. Another study found total retinal blood flow measured by laser Doppler velocimetry to be elevated by 23.4% in diabetic subjects with background retinopathy and poor glycemic control, compared with values in control subjects.
19 A mild increase in retinal volumetric blood flow was reported in diabetic patients with a duration of disease of less than 4 years and before the development of any clinically detectable retinopathy.
20 In contrast to the results in Grunwald et al.,
20 Arend et al. reported a significant reduction in retinal capillary blood velocity measured from digitized fluorescein angiograms in diabetic patients in comparison with healthy subjects.
21
We measured blood flow in the perimacular region below the fovea, because measurements temporal to the fovea would have been technically difficult. In diabetic retinopathy, the earliest changes are known to occur in the perimacular region, most often in the area temporal to the fovea.
22 23 Technically, it is easier to scan the peripapillary region of the retina than the macular area. Cuypers et al.
18 showed that valid retinal flowmeter measurements are more likely to be obtained from the papillomacular region than the foveal area. In another study of diabetic patients, microaneurysms and acellular capillaries were more than twice as common in the superior than in the inferior retina.
24 Chung et al.
25 reported that in healthy people, baseline blood flow in the inferior temporal quadrant is significantly greater than in the superior temporal quadrant, suggesting that the inferior temporal retina has slightly greater capillary perfusion. Young diabetic women were a suitable study group for the retinal flowmeter method. Few of them had media opacities limiting retinal scanning, and most of them were capable of maintaining stable fixation during the 1.6-second data-acquisition period.
We used both the conventional 10 × 10-pixel square (small-box) and point-wise analysis to estimate retinal capillary blood flow. The reproducibility of retinal flowmeter measurements has been shown to be improved if point-wise analysis is used,
14 because the pixels with DCs of less than 70 or more than 200 can easily be excluded to improve measurement reliability.
14 26 27 28 That blood flow measurements are known to be increased in underexposed images and decreased in overexposed images
27 could mean less accurate results with the conventional 10 × 10-pixel small-box method, in which one DC represents the whole area. The results obtained in our series with both of these methods were similar, however.
Most diabetic women in our study had reasonably good glycemic control and only minimal or moderate retinopathy. Retinal capillary blood flow in patients with more drastic progression of retinopathy may differ. Today, however, improved obstetric care, improved glycemic control before and during pregnancy, and improved insulin therapy with new insulin analogues have reduced the number of diabetic patients who are at risk for development of severe forms of retinopathy because of pregnancy.
In summary, the retinal capillary blood flow was higher in diabetic women during pregnancy and after delivery than in nondiabetic pregnant women. Hyperdynamic retinal capillary circulation may contribute to the progression of diabetic retinopathy, or alternatively, our findings may reflect only an altered vascular system in diabetic women and the fact that pregnancy facilitates the progression of retinopathy by an independent, but parallel, causative pathway.