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From The College of Optometry, Ohio State University, Columbus, Ohio.
| Abstract |
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METHODS. Wavelength-dependent interference was used to measure the tear film thinning rates in 20 normal contact lens wearers, and spectra were captured at a rate of 4.5 per second for 20 seconds. Four recordings of precorneal tear film (PCTF) thinning were made, followed by 1 hour of hydrogel lens wear and then four recordings of prelens tear film (PLTF) thinning. Subjects were asked to blink 1 second after the beginning of the recording and then hold their eyes open for an additional 19 seconds, followed by 2 minutes of rest between recordings.
RESULTS. The average thinning rate of the PLTF was greater than that of the PCTF and average initial tear film thickness of the PLTF was less than that of the PCTF. For both these reasons, the "tear thinning time" (time to reach 0 thickness) was typically shorter for the PLTF than for the PCTF. Histograms of PCTF and PLTF thinning rates showed a narrow peak corresponding to slow thinning of approximately 1 µm/min, but also many examples of rapid thinning of approximately 10 µm/min, with greater variability. Both the initial thickness and thinning rate of the PLTF correlated with corresponding values for the PCTF, although many more rapidly changing values were associated with the PLTF. Plots of rapid thinning of PCTF and PLTF were both linear and were not accompanied by any significant increase in thickness of corneal epithelium or contact lens, respectively.
CONCLUSIONS. Tear film thinning can be analyzed in terms of flow in three spatial directions: (1) outward (evaporation), (2) inward (into the epithelium or contact lens), and (3) parallel to the tear film surface. The results indicate that the second mechanism may be unimportant. Studies have shown a range of tear film evaporation rates from 0.24 to 1.45 µm/min, whereas, when the lipid layer is washed away from the tear film, the thinning rate, due to evaporation, would be approximately 7µm/min. Thus, slow thinning rates may be due to tear film evaporation, whereas rapid rates (which are often greater than 7 µm/min) presumably include other mechanisms such as dewetting, Marangoni flow (i.e., surface tension gradients), and pressuregradient flow.
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Evaporation (or outward flow of the tear fluid) is probably the most recognized mechanism of tear film thinning, and investigators have reported tear film evaporation rates ranging from 0.24 to 1.45 µm/min.7 8 9 10 11 However, if the PCTF thickness is approximately 3 µm and it thins at approximately 1 µm/min, it would take approximately 3 minutes for the PCTF to evaporate, causing a dry spot to form. This is approximately 5 to 15 times greater than estimates of noninvasive tear breakup time and dry spot formation reported in the literature.12 13 14 15 16 17 Thus, although evaporation seems to be an important factor in tear film breakup, it is too slow to offer a complete explanation of tear film thinning.
Benedetto et al.18 used fluorescence to study changes in tear film thickness between blinks. They found that, over the superior cornea, the tear film thickened for about 1 second after a blink, whereas a corresponding thinning of the tear film was found over inferior cornea. When equilibrium thickness (fluorescence) was reached, the superior tear film was thicker than the inferior. These thickness changes were ascribed to the upward drift of the lipid layer of the tear film that occurs over a similar period after a blink.1 19 It should be noted that in dry eye conditions, this upward drift can continue for many seconds, thus increasing the potential contribution of this drift to tear film breakup.20 A limitation of the method of Benedetto et al.18 is that it is insensitive to the first two mechanisms of thinning mentioned earlier. For example, evaporation of the tear film does not reduce the total amount of fluorescein in the tear film and so does not reduce fluorescence. Thus, there is a need for new noninvasive methods of studying tear thinning between blinks, particularly during the later interblink period after the initial upward drift of the tear film.
Recent developments in methods of measuring tear film thickness should enable better measurements of tear film thinning between blinks. Methods of measuring the complete thickness of the PCTF and the PLTF have recently been reviewed.21 Because invasive methods may alter the thickness of the tear film, the preferred methods are noninvasive and are generally based on optical interference principles (e.g., thickness-, angle- and wavelength-dependent fringes, reviewed by King-Smith et al.22 ). The first interferometric measurements of the PLTF were made with thickness-dependent fringes.23 24 25 However, this method is difficult to apply to measuring the complete thickness of the PCTF, because the corresponding interference fringes are weak and masked by the higher-contrast image from the superficial lipid layer.26 Danjo et al.27 was the first to apply another interferometric method, wavelength-dependent fringes (WDFs) or spectral oscillations to measuring the PCTF thickness. This method has the advantages of high resolution (permitting direct measurement of thin layers such as the PCTF and PLTF) and good signal-to-noise ratio and has been used in our laboratory for measuring PCTF and PLTF thickness,28 29 30 as well as that of other layers, such as the epithelial and corneal layers,28 and postlens tear film and contact lens thickness.29 30 31 Recent measurements made with optical coherence tomography, although less precise and less direct than those made with WDFs, have been reasonably consistent with our reported measurements of PCTF and PLTF thickness of approximately 2 to 3 µm.32 Based on these considerations, the present study of PCTF and PLTF thinning was based on the WDF method. The purpose of this report is to describe the thinning of both the PCTF and PLTF and the relation between these measures.
| Methods |
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where n is the refractive index of tears and
is wavelength in a vacuum.28 Because the thickness of any layer is indicated by its frequency, the Fourier analysis of the reflectance spectrum shows corresponding peaks due to various layers. The reflectance spectrum (5621030 nm) is recorded on a charge-coupled device (CCD) camera that samples the spectral image from a spectrograph. For these measures, spectra were captured at a rate of 4.5 per second for a period of 20 seconds (providing 90 spectra in total). The measurement area was nominally 33 x 35 µm (in practice, probably larger due to aberrations, defocus, and eye movements). PCTF thickness measurements were considered valid if the nominal reflectance from the cornea exceeded 0.5% (thus avoiding blinks), the contrast of spectral oscillations (at 800 nm) exceeded 0.2%, and the thickness exceeded 1 µm. PLTF thickness measurements were considered valid if the nominal reflectance exceeded 0.5%, the contrast of spectral oscillations exceeded 1%, and the thickness exceeded 0.5 µm. Epithelial and contact lens thicknesses were determined by methods described in previous studies.28 30 The mean temperature and humidity were 26°C and 49%, respectively. Refractive indexes (at 589 nm) of the tears, epithelium, and contact lens were assumed to be 1.337, 1.401, and 1.405, respectively, and correction was made for dispersion.30 34 35
Clinical Study
All patients recruited for the study were required to review and sign informed consent documents, that had been approved by the Biomedical Institutional Review Board of The Ohio State University, according to the tenets of the Declaration of Helsinki. Twenty experienced contact-lenswearing subjects (mean age, 31.8 ± 8.6, four men) participated in the study. Each subject was free of ocular disease (including dry eye), and each was a current contact lens wearer. Subjects were asked not to wear contact lenses on the day of the experiment and to report for testing wearing their spectacles. Subjects first completed four PCTF thinning measures, wherein they were asked to blink 1 second into the experiment, while the thinning measure continued for an additional 19 seconds. Between each thinning measure, subjects rested for a period of 2 minutes. All measures of tear film thinning were taken on the right eye. After completion of the PCTF thinning measures, subjects were asked to apply etafilcon A contact lenses to both eyes (Acuvue 1-Day, Vistakon; Johnson and Johnson, Jacksonville, FL; power, 0.50 D; base curve, 8.5 mm), which were worn for 1 hour to allow for lens settling.29 Four measures to determine PLTF thinning were then taken in a manner identical to that described for the measures of PCTF thinning. After completion of this, the fit of the lenses was verified using standard clinical techniques, including the assessment of movement, centration, and coverage.
Outcomes assessed from the interferometric spectra when measures were taken without a contact lens included PCTF thickness over time (i.e., the PCTF thinning rate) and epithelial thickness over time (i.e., epithelial thickness during tear film thinning). Outcomes assessed from the interferometric spectra when measures were taken with a contact lens on the eye included PLTF thickness over time (i.e., the PLTF thinning rate), and contact lens thickness over time.
Analyses and Statistical Procedures
Regression lines were fitted to thickness-versus-time data starting 2 seconds after the blink for each recording, to determine PCTF and PLTF thinning rates (thus avoiding transients sometimes observed immediately after the blinke.g., Fig. 3A ). Regression line fits were terminated either at the end of the 20-second recording, or when the thickness became too thin for valid measurements, or if and when a second blink occurred in the 20-second recording. Regression lines were considered valid if they could be fitted over a period of at least 1 second. For both PCTF and PLTF, probability density functions (PDFs) of rates of thickness change (see Fig. 9 ) were estimated by a maximum-likelihood method on computer (SigmaPlot; SPSS, Chicago, IL).
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| Results |
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11.5 seconds, the regression line has been extrapolated to indicate that 0 thickness would be reached at a time of approximately 15 seconds (i.e., 14 seconds after the blink). Estimates of rates of thickness change were obtained in 76 of 80 recordings of the PLTF, which are summarized in Table 1 . As shown in Table 1 , the mean (±SD) thinning rate of the PCTF was 3.79 ± 4.20 µm/min, whereas it was 6.79 ± 4.32 µm/min for the PLTF. Mixed modeling regression for thinning rate of the combined PCTF/PLTF data set showed a significant effect of layer (PCTF versus PLTF, F = 28.17, P < 0.0001) no significant effect of trial number (trials 14, F = 1.52, P = 0.22) and no significant interaction effect (layer x trial; F = 0.84, P = 0.48). Table 1 also shows the mean (±SD) initial thickness of the PCTF was 3.98 ± 1.06 µm/min, whereas it was 2.54 ± 1.16 µm/min for the PLTF. The corresponding analysis for initial thickness (2 seconds after a blink) again showed a significant effect of layer (F = 60.89, P < 0.0001), a significant effect of trial number (F = 3.64, P = 0.03), but no significant interaction effect (F = 2.23, P = 0.12). Post hoc comparisons (Tukey method) between trials found a significant difference (P = 0.01) only between trials 1 and 4 of the PLTF (corresponding thicknesses, 2.21 and 2.87 µm). It is thus possible that initial thickness may have increased somewhat with trial number, perhaps due to some reflex tearing.
The linearity of thinning is analyzed in Figure 4 . Figure 4A shows thickness averaged at each time point for 15 PCTF recordings (in 10 subjects), with a thinning rate of more than 3 µm/min with measurements over the full 20-second period (0 on the time scale corresponds to 2 seconds after any of the blinks). Figure 4B shows equivalent plots for an average of 10 PLTF recordings (in five subjects). In both cases, the linear regressions were good fits to the data. For both PCTF and PLTF, linear fits were slightly better than the fit based on an exponential decay. A second-order (quadratic) fit (not shown) was little better than a linear fit, deviating by only 0.03 µm at most over the measurement period of more than 16 seconds, for both PCTF and PLTF.
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2 µm/min) are more broadly distributed. This difference will be considered further later in the article (Fig. 9) . It may also be noted, from Figure 5A , that the thinning rate of the PCTF seemed more variable when the initial thickness was relatively large. This finding applies to both the individual data and subject averages. For example, in the 13 subjects with average initial thickness greater than 3.4 µm, the SD of the thinning rate was 4.64 µm/min, whereas in the 7 subjects with thickness less than 3.4 µm, the corresponding SD was 0.84 µm/min. This difference in SD between the two groups based on initial thickness is statistically significant (F = 30.6, P = 0.0002) and would still be significant after allowing for multiple possible comparisons (there are 19 distinct ways in which data for the 20 subjects could have been divided into "thick" and "thin" groups). However, this dependency of variance of thinning rate on initial thickness does not seem to apply to the PLTF (Fig. 5B) .
If the initial tear film thickness is t (in micrometers), and the thinning rate is r (in micrometers/minute), then the tear film would theoretically thin to 0 thickness in t/r minutes; as the "initial thickness" is actually measured 2 seconds after the blink, 0 thickness would be reached in a tear thinning time of
![]() | (1) |
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![]() | (2) |
![]() | (3) |
1, r1,
2, and r2 were adjusted to maximize the likelihood. The second type of fit was a skewed PDF with a single peak (at r = r0) of the form
![]() | (4) |
, r0, a, and b were adjusted to maximize likelihood. The parameter k was adjusted so that, for any values of a and b
![]() | (5) |
The possibility that rapid thinning of the PCTF could be caused by passage of tear fluid into the epithelium was studied as follows. (It should be noted that only a fraction of the recordings gave satisfactory measurements of epithelial thicknessthat is, measurements at most time points with low variability.) First, four PCTF recordings (from three subjects) were selected because they had rapid PCTF thinning (>3 µm/min) with measurements over the full 20-second period, and good recordings of epithelial thickness. Solid curves in Figures 10A and 10B show averaged thickness data for PCTF and epithelium, respectively. Vertical magnification is the same in these two figures. Dotted curves are fitted regression lines over the period starting at least 2 seconds after any of the blinks. Rates of change in thickness in the PCTF and epithelium were 8.74 and 0.28 µm/min, respectively. These results indicate that rapid thinning of the PCTF is not caused by passage of tear fluid into the epithelium.
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| Discussion |
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The results also show several significant differences between the thinning of the PCTF and PLTF. Figure 8 and Table 1 show that, in these studies, the average PLTF initial thickness is significantly less, by approximately 1.4 µm, than that of the PCTF. Figure 7 and Table 1 show that the average PLTF thinning rate is significantly faster, by about a factor of 1.8, than that of the PCTF. Both the smaller initial thickness of the PLTF and its more rapid thinning rate contribute to a faster tear thinning timeequation 1 and Figure 6 . Substituting the mean data from Table 1 , typical tear thinning times for PCTF and PLTF are 65 seconds and 24 seconds, respectively.
The histogram of thinning rates for the PCTF in Figure 9A were fit better by a skewed PDF (equation 4) than by a bimodal PDF (equation 3) , whereas the reverse was true of the histogram for PLTF rates in Figure 9B . A bimodal PDF, such as that fitted for the PLTF (Fig. 9B) suggests that at least two different mechanisms of tear film thinning are involved, with perhaps one acting in cases of slow thinning, and another acting (perhaps in addition to the first) in cases of rapid thinning. A skewed PDF, such as that fitted to the PCTF (Fig. 9A) could be interpreted in terms of a single mechanism with a skewed distribution of thinning rates, but may also correspond to variable contributions from more than one mechanism. An additional observation is that slow thinning rates, corresponding to the narrow peaks of the two PDFs in Figure 9 , were greater for the PLTF (1.25 µm/min), than for the PCTF (0.79 µm/min). Figure 9 also shows that there are relatively more cases of rapid thinning (e.g., approximately 10 µm/min) of the PLTF than of the PCTF.
Slow thinning of the PCTF and PLTF may be caused by evaporation (Fig. 1 , arrow 1). Previous studies have reported a range of PCTF evaporation rates from 0.24 to 1.45 µm/min.7 8 9 10 11 The mean of 0.79 µm/min for the slow mode of PCTF thinning, derived from the PDF of Figure 9A , is reasonably consistent with these evaporation rates. The corresponding mean for PLTF thinning is 1.25 µm/min and so is somewhat greater than that of the PCTF. Hamano et al.7 and Thai et al.36 have suggested that the PLTF evaporates approximately 30% to 35% faster than the PCTF, and so their data are reasonably consistent with our proposal that slow thinning is due to evaporation, and the PLTF thus evaporates faster than the PCTF.
Mishima and Maurice37 showed that when the lipid layer is washed away from the tear film, the thinning rate due to evaporation would be approximately 7 µm/min. Accordingly, it is likely that the observed rapid thinning rates are not entirely due to evaporation, as they are often greater than 7 µm/min; evaporation should, of course, make a contribution to this thinning, and it is possible that evaporation rate is greater for rapid thinning than for slow thinning. Cases of thickening of the PCTF (Figs. 2C 5 and 9) cannot, of course, be explained by evaporation. Mechanisms other than evaporation should therefore be considered in rapid tear film thinning measures especially as they relate to the other two components of tear film thinning: tear film flow into the cornea or contact lens (Fig. 1 , arrow 2) and flow of the tear fluid parallel to the tear film surface (Fig. 1 , arrows 3). As Figures 10 and 11 show, it seems unlikely that much fluid passes into or out of the corneal epithelium or a contact lens during the interblink period. Thus, mechanisms associated with the third component of tear film thinning (i.e., flow parallel to the tear film surface) should be considered.
For the PLTF, wettability is known to be important for tear film stability, so it seems probable that poor wettability may make an important contribution to rapid thinning.38 39 40 41 42 43 44 The finding that tear thinning rates of the PLTF are significantly greater than those of the PCTF (see Fig. 7 ; Table 1 ) may relate to the fact that contact lenses are less wettable than the corneal epithelium. A wettable surface is one that would maintain a stable, uniform liquid film, resisting the formation of dry spots. Typically, determinations of wettability are conducted by in vitro measures of contact angle, but these measures are limited in that they are not possible in the eye with a dynamic, natural tear film. Early observations with highly hydrophobic silicone-based lenses showed that indeed these surfaces are not wettable by aqueous-type tears due to the low surface energy of the material.38 Although the surface energy of a hydrophilic lens is much higher, these lenses still have a tendency to dewet when on the eye. This dewetting of hydrogels may be related to the chemical nature of the polymer, the deposition of substances such as lipids on the lens surface, and the tear film itself (as the tear film contains various surfactants). In any of these situations, a dry spot on the lens surface is the energetically favorable situation. Measures of tear film breakup time over a lens (whether invasive with fluorescein or noninvasive without fluorescein) provide somewhat crude, subjective estimates of tear film thinning (and potentially, wettability). Noninvasive optical studies, including the methods used in the present study, could provide quantitative in vivo measures of wettability of hydrogel lenses.
Although wettability may be important for rapid thinning of the PLTF, other factors should be considered, for both the PCTF and PLTF. Surface tension generates a pressure in the tear film that depends on the curvature of the outer surface of the tear film. Spatial variation of curvature can thus cause "pressuregradient" tear flow and tear thinning. For example, the concave tear meniscus near the lids or the edge of a contact lens, generates negative pressure, sucking fluid from the nearby tear film.45 For the PCTF, this typically generates a very thin region next to the meniscus (the "dark line") that prevents any further significant flow. The PCTF is therefore sometimes described as a "perched" tear film.46 Another example of pressuregradient flow is a bump (or ridge) on the epithelial surface that could generate a corresponding bump on the outer PCTF surface immediately after a blink. This convexity would generate an increased pressure in the tear film over the bump and hence a divergent flow away from the bump, causing thinning.21 Although this mechanism could be at least partly responsible for some cases of rapid thinning, it should be expected that, at other positions (e.g., near the edge of the bump), there would be relatively concave regions that would tend to cause thickening of the tear film, so that the average effect of this type of thinning would be small. Thus, it seems that pressuregradient flow cannot explain the relatively high average rate of thinning observed for rapid thinning at the center of the cornea. In addition, pressuregradient flow over a bump would be expected to occur relatively rapidly at first and then more slowly as the tear film thins and there is more viscous resistance to tear flow21 . The fact that tear thinning is rather linear (Fig. 4) is also evidence that pressuregradient flow is not the only mechanism involved in rapid thinning.
Another possible cause of tear film thinning is Marangoni flow due to surface tension gradients.1 For example, in Figure 1 , imagine that there is a surface tension gradient at the top of the figure that is greater than that at the bottom. The difference would cause more outflow of tear fluid at the top than inflow at the bottom (as indicated in Fig. 1 ), and hence thinning of the tear film. Marangoni flow should be distinguished from pressuregradient flow. Although they both involve surface tension, Marangoni flow can occur when the outer surface of the tears is perfectly spherical, so that pressuregradients are very small (for a spherical tear surface, the ratio of pressuregradient flow to Marangoni flow is of the order of the ratio of tear film thickness to corneal radius). Marangoni flow is thought to be responsible for the upward drift of the PCTF for approximately 1 second after a blink1 19 . At least in dry eye conditions, this drift can go on for considerably more than 1 second,20 and so Marangoni flow could be responsible for the rapid thinning observed in this study. Doane has noted that the PLTF seems to be dragged toward the lids, as the lids cover the edge of the contact lens.44 Marangoni flow may help to explain this observation, with a higher surface tension near the lids than at the center of the lens. These surface tension gradients might be explained by the deposition of lipids on the surface of contact lenses and a resultant alteration in the lipid layer of the tear film. The possible contribution of Marangoni flow to breakup of the PCTF has been discussed recently.47
Figure 5A showed that the variance of thinning rates of the PCTF increases with the tear films initial thickness. This may be expected for both pressuregradient and Marangoni flow. For pressuregradient flow, the total flux (tear thickness x mean velocity) of tear flow, for a given pressure gradient, is proportional to h3, where h is tear film thickness. For Marangoni flow, flux, for a given surface tension gradient, is proportional to h2.21 Thus, if pressuregradient flow and/or Marangoni flow contribute to PCTF thinning, one might expect that variance of thinning rate would increase with PCTF thickness and that is what we observed. One might also expect the PCTF thinning rate would increase with PCTF thickness. The regression line in Figure 5A shows such a trend, even though the slope is not significant. It seems more difficult to explain these observations in terms of evaporation. For the PLTF (Fig. 5B) , there is no obvious relation between either thinning rate or variance of thinning rate and PLTF thickness. This difference from the findings for the PCTF may be related to the contribution of dewetting to PLTF thinning. In this regard, it should be remembered, despite the evidence of differences in thinning mechanisms between the PCTF and PLTF, that the correlation between thinning rates shown in Figure 7 indicates that there are also some common factors in PCTF and PLTF thinning.
The possible relation of the current studies to tear film breakup in front of the cornea or contact lens is illustrated in Figure 6 . In some cases, the tear thinning time can be less than 15 seconds for the PCTF and less than 10 seconds of the PLTF. These values are comparable to noninvasive breakup times.12 13 14 15 16 17 It should be noted that tear film breakup can occur anywhere on the cornea, whereas the tear thinning times in Figure 6 correspond to a single point at the center of the cornea. Thus, tear breakup times, which correspond to the earliest breakup observed at any position, would presumably tend to match the smallest tear thinning times in Figure 6 . It thus seems probable that the current tear thinning studies are relevant to predictions of tear film breakup times.
The thinning of the tear film is a complex process that involves mechanisms such as evaporation, dewetting, pressuregradient flow, and Marangoni flow. The interferometric method discussed in this article has the advantage that quantitative estimates of tear film thinning can be obtained. However, interferometric imaging systems, such as those based on thickness-dependent fringes could provide additional information about the spatial distribution of tear film thinning.26 36 44 Such studies should help to elucidate the role of different mechanisms in tear film thinning and breakup, especially as these ideas relate to dry eye disease.
| Footnotes |
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Submitted for publication January 25, 2005; revised March 10, 2005; accepted March 24, 2005.
Disclosure: J.J. Nichols, None;, G.L. Mitchell, None; P.E. King-Smith, None
The publication costs of this article were defrayed in part by page charge payment. This article must therefore be marked "advertisement" in accordance with 18 U.S.C.
1734 solely to indicate this fact.
Corresponding author: Jason J. Nichols, The Ohio State University, 320 West 10th Avenue, PO Box 182342, Columbus, OH 43218-2342; nichols.142{at}osu.edu.
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