Myopia has seen a rapid rise in its prevalence worldwide over the last generation, such that half of the world's population is expected to be myopic by 2050.1 Myopia carries a significant economic burden (approximately US $268 billion)2 and a sight-threatening ocular disease burden.3 Although genetic factors play a role in the development of myopia,4–8 they cannot explain the rapid increase in myopia prevalence.
Several environmental factors have been implicated in the development and progression of myopia, with significant research directed at the possible role of near work9 and, more recently, of reduced time outdoors (discussed hereinafter10) as risk factors. However, in both cases, no general agreement has been reached on key contributing factors, and the etiology of myopia will likely prove to be multifactorial in nature. For example, early epidemiological studies of myopia noted an apparent link between the advent of formalized classroom education and the development of myopia in Inuit populations.11,12 However, during this period of increasing Western influence, diets also underwent significant modification.13,14
Overall, there has been limited investigation into the role of nutritional factors in myopia. In one early observational report, diets of high glycemic load were described as a risk factor for myopia by Cordain et al.,13 who speculated that hyperinsulinemia might modify scleral growth factors, as a possible underlying mechanism. However, in apparent contradiction of this hypothesis, a cross-sectional study of Singaporean children (aged 7 to 9 years)15 found that children with shorter stature and increased body mass index had less myopic refractions, assuming body mass index reflects glycemic load. Nonetheless, studies using animal models of myopia have provided evidence linking insulin with enhanced eye growth16 and also for protective effects of both caffeine and one of its metabolites, 7-methylxanthine, against myopia development,17–19 with choroidal and scleral targets as possible sites of action in the latter case.17
Significant attention has been paid recently to the protection afforded by outdoor exposure against myopia development, with four randomized controlled trials involving Asian schoolchildren reporting generally positive benefit from increased outdoor recess time.20–23 Although there is ongoing debate regarding the role of outdoor high light intensities,24–27 it is also important to note that exposure to sunlight and serum vitamin D levels are highly positively correlated. Nonetheless, although two relevant large cohort studies found an association between serum vitamin D levels and refractive error,28,29 their authors reached diverging interpretations of their results with respect to the role of low serum vitamin D levels as a risk factor for myopia development, with one group noting the likely confounding effect of time outdoors on vitamin D serum levels,29 which is consistent with observations from a previous genome-wide association study.30
The availability of the large U.S. National Health and Nutrition Examination Survey data set allowed for further investigation of the relationship between various nutritional and body metric factors and the presence and magnitude of myopia, which describes the scope of the study reported here. The National Health and Nutrition Examination Survey comprises a series of ongoing studies, which was initiated in 1960 by the U.S. Centers for Disease Control and Prevention, and aims to investigate the health and nutritional status of children and adults across the United States through the collection of data concerning demographic, socioeconomic, and health-related variables (via physiological and laboratory measurements).
The study reported here was limited to participants during study years 2003 to 2008. Because refractive error data were available only for participants 12 years or older, the current analyses were also limited to participants aged 12 to 25 years, with the upper limit taking into account the possibility of late-onset myopia.31–33 Both univariate and multivariate analyses were applied to extracted data. Initially, participants with available refractive error data were extracted (n = 6855) if they met the inclusion criteria of not having either previous refractive surgery (n = 18) or the possibility of corneal disease, as indicated by keratometric readings of more than 50 D (n = 21). Given that corneal power is, on average, approximately 48 to 50 D in full-term human infants34,35 and only decreases with age,36,37 cornea with 50 D or more in the steeper meridian was used as a potential biomarker for corneal disorders and used as a basis for excluding participants.
The demographic features (age, sex, ethnicity) of this final participant cohort (n = 6855) are summarized in Table 1. In the case of univariate analyses, participants with available refractive error data and factor(s) of interest were included, with the sample size varying accordingly, as indicated hereinafter. However, only participants with complete data sets (n = 1974 [29%]) were used in multivariate analyses. Importantly, a sensitivity analysis demonstrated that participants with complete versus incomplete data sets had similar ethnicity distributions (<3% difference in all ethnicity categories), range of refractive errors (+8.5 to −17.625 vs. +6.00 to −20.25 D), mean spherical equivalent refractive error (mean difference, 0.009 D), and proportion of participants with myopia (<0.3% difference). None of these differences were statistically significant (all comparisons, P > .05).
TABLE 1 -
Summary of participant demographic characteristics, expressed in terms of number and percentage of participant cohort, in those participants aged 12 to 25 years with available refractive error data
||Total (n = 6855)
| Non-Hispanic White
| Non-Hispanic Black
| Mexican American
| Other Hispanic
The mean (standard deviation) age of the participant cohort was 17.05 (3.63) years.
All study sampling methods pertaining to the National Health and Nutrition Examination Survey data set have been described elsewhere.38 All study methods followed the tenets of the Declaration of Helsinki and were approved by the National Center for Health Statistics Research Ethics Board, and informed consent was documented before participant participation. Note also that data collection is limited to National Health and Nutrition Examination Survey–trained health technicians, as a quality control measure. Pertinent to the analyses reported here, open-source data were extracted and used for analysis as described hereinafter.
The vision database includes noncycloplegic objective autorefractor (Nidek ARK-760; NIDEK Co., Ltd., Gamagori, Aichi, Japan) measurements. Recorded refractive errors (median of three repeated measures) were included in analyses only when a confidence rating of at least 5 (scale from 1 to 9) was achieved at the time of measurement. The mean (standard deviation) confidence rating of the refraction data used in our analyses was 8.86 (0.43). For use in analyses, spherical equivalent refractive errors (i.e., average of the refractions in two principal meridians) were calculated from the data for the right eyes of all included participants, and spherical equivalent refractive errors of −0.75 D or worse were classified as myopic. This more conservative definition of myopia was used to avoid misclassification of myopia, given that cyclopegic agents were not used in measuring refractive errors.
To monitor childhood growth and weight gain, the National Health and Nutrition Examination Survey collected a series of body metrics, including body mass index (in kilograms per meter squared) and standing height (in centimeters). From the National Health and Nutrition Examination Survey laboratory database, several nutritional factors were extracted for use in analyses. Total 25-hydroxyvitamin D levels (in nanomoles per liter) were measured in collected samples using a standardized liquid chromatography–tandem mass spectrometry method. Fasting (for at least 9 hours) plasma glucose (hexokinase method; in millimoles per liter) and serum insulin (enzyme-linked immunosorbent assay method; in picomoles per liter) were obtained for participants 12 years or older attending morning study visits as part of an ongoing effort by the National Health and Nutrition Examination Survey to estimate the prevalence of diabetes in the United States. Information about caffeine intake was extracted from dietary interviews performed as part of the “What We Eat in America” initiative. Using a validated U.S. Department of Agriculture survey method, participants were interviewed initially in person during a study visit and subsequently by telephone (3 to 10 days after the in-person interview, but not on the same day of the week). During both interviews, participants were encouraged to make use of a set of measuring guides (e.g., glasses/mugs, bowls, drink boxes and bottles, household spoons, and measuring cups and spoons) to more accurately estimate the amounts of foods and liquids consumed. For the purpose of the current study, estimates of daily caffeine intake (in milligrams) from each of the two interviews were averaged for each participant.
The National Health and Nutrition Examination Survey analytical guidelines for 1999 to 2010 are available at www.cdc.gov/nchs/data/series/sr_02/sr02_161.pdf. Analyses were performed using Stata 14.2 (StataCorp, College Station, TX). Statistical analyses (χ2 or Kruskal-Wallis) were performed to investigate the relationships between refractive errors and demographic and nutritional factors. Multivariable logistic and linear regression models were also created using myopia status (presence/absence) and magnitude of myopia (spherical equivalent refractive error) as outcome variables. The inclusion of covariates in the final models was hypothesis-driven, and collinearity was evaluated across all covariates. Ethnicity was included through the use of dummy variables, and interaction terms were included in the final models if their coefficients differed significantly from zero, as determined by the Wald test. An α value of 0.05 was used in all data analyses as an indicator of statistical significance. Summary statistics are reported as means, including standard deviations and/or 95% confidence intervals, unless indicated otherwise.
Demographic Factors and Myopia Status
Participant refractive error ranged from +8.5 D of hyperopia to −20.25 D of myopia, with a mean of low myopia (−0.86 ± 1.90 D). Approximately 35% (35.3%) of the cohort were myopic, with the mean spherical equivalent refractive error of this subgroup being −2.66 ± 2.05 D. The mean spherical equivalent refractive error of the remaining nonmyopic participants was 0.12 ± 0.74 D. Although there was a statistically significant increase in spherical equivalent refractive error with increasing participant age (P = .001), the difference across age groups was small, although extreme myopia outliers existed in all age groups (Fig. 1). Investigation into the possible influences of these outliers (DFBETA model diagnostics) found no meaningful effects for any age group. Both sex and ethnicity seemed to influence spherical equivalent refractive error (Fig. 2), although differences did not always reach statistical significance. Specifically, female participants were more likely to be myopic compared with male participants (37.8 vs. 32.8%, P < .0001), and they also had a significantly greater magnitude of myopia compared with male participants (−2.78 ± 2.04 vs. −2.54 ± 2.06 D, P = .0002). In relation to ethnicity, except for the multiethnic/other group, which was on average more myopic (−1.38 ± 2.31 D), the other ethnic groups had similar mean refractive errors (range, −0.75 to −0.89 D). Nonetheless, there were significant differences between these groups (based on ANOVA testing), both in terms of mean spherical equivalent refractive error (P = .0001) and in the proportion of myopic participants (P < .0001), with Blacks having the lowest (33.1%) and the other/multiethnic group having the highest (46.1%) values. Of those with myopia, mean spherical equivalent refractive errors also differed significantly with ethnicity (P = .001), with Mexican Americans having the least myopic spherical equivalent refractive error (−2.48 ± 1.86 D) and the other/multiethnic group having the highest (−3.15 ± 2.21 D).
Body Metrics and Nutritional Factors and Myopia Status
Summary statistics for all body metric and nutritional factors, partitioned by participant demographic characteristics, including age (stratified into 12- to 18- and 19- to 25-year age groups), are shown in Appendix Table A1, available at http://links.lww.com/OPX/A484, and described in more detail hereinafter. The relationships between each nutritional and body metric factor and age, stratified by ethnicity and myopia status, are illustrated in Fig. 3. Because the distributions for nutritional and body metric factors (except for standing height) proved to be quite skewed, significant outliers were identified for each factor via the interquartile range method (outlier identified as falling outside the lower and/or upper fences in a box-and-whisker plot) and removed from analyses. For any given factor, this method removed between 0.12% (vitamin D) and 2.67% (serum insulin) of the data. Nonetheless, no significant differences were identified in a sensitivity analysis performed to determine if the removal of outliers influenced the results of linear regression analyses for the respective nutritional/body metric factors.
The average height and body mass index of participants who had both refractive error and body metric data (n = 6764, 99%) were 166.18 ± 10.35 cm and 24.78 ± 6.53 kg/m2, respectively. Notably, the latter value is just outside the range for overweight, as defined by the U.S. Centers for Disease Control and Prevention (25.0 to <30 kg/m2; www.cdc.gov). Female participants had significantly higher body mass indexes compared with male participants (25.02 ± 6.34 vs. 24.19 ± 5.81 kg/m2, P = .0001) and were significantly shorter than male participants (160.95 ± 7.03 vs. 171.38 ± 10.52 cm, P < .0001). Ethnicity also significantly influenced height (P < .0001) and body mass index (P < .0001). In relation to height, Whites were the tallest (168.43 ± 10.29 cm) and Mexican Americans were the shortest (162.93 ± 9.52 cm). In relation to body mass index, Blacks had the highest values (25.40 ± 7.37 kg/m2) and the other/multiethnic group had the lowest values (23.32 ± 5.83 kg/m2). As expected, both body mass index and height significantly increased with age, regardless of ethnicity or myopia status, except for height in Mexican American myopes (Figs. 3A, B). However, neither height nor body mass index was significantly correlated with spherical equivalent refractive error (Figs. 4A, B, both R2 ≤ 0.0004 and P ≥ .12).
A total of 4838 participants (71%) had both serum vitamin D and refractive error data. The mean serum vitamin D level for these participants was 54.78 ± 22.11 nmol/L, with a large percentage (~48%) classifiable as deficient in vitamin D, as defined by the Vitamin D Council (<50 nmol/L; www.vitamindcouncil.org). On average, female participants had a small but significant decrease in serum vitamin D levels compared with male participants (54.08 ± 23.44 vs. 55.20 ± 19.89 nmol/L, P < .0001). There were also significant ethnicity-related differences (Fig. 3C; P < .0001), with Blacks having the lowest levels (41.45 ± 16.01 nmol/L) and Whites having the highest (71.28 ± 22.02 nmol/L). Myopic and nonmyopic groups had similar serum vitamin D levels (54.13 ± 21.58 vs. 54.92 ± 21.84 nmol/L, P = .23), as also reflected in the nonsignificant correlation between serum vitamin D levels and spherical equivalent refractive errors for this cohort overall (Fig. 5A; R2 = 0.0002, P = .32).
For participants who had both caffeine intake and refractive error data (n = 5864, 86%), the mean daily caffeine intake was 44.07 ± 53.60 mg and increased significantly with age, regardless of ethnicity or myopia status, as might be expected (Fig. 3D; all, P ≤ .04). Overall, male participants had significantly higher caffeine intake compared with female participants (47.14 ± 56.78 vs. 41.17 ± 50.25 mg, P = .006). There were also significant ethnicity-related differences in caffeine intake (P < .0001), with Blacks having the lowest intake (25.83 ± 38.32 mg) and Whites having the highest (64.30 ± 64.48 mg). However, there was no significant difference in the mean caffeine intake of myopic and nonmyopic participants (43.02 ± 52.64 vs. 44.64 ± 54.11 mg, respectively; P = .27) and no significant correlation between caffeine intake and spherical equivalent refractive error for this cohort overall (Fig. 5B, R2 = 0.0000, P = .93).
The mean serum glucose and insulin levels for those participants who also had refractive error data (n = 2895, 42%) were 5.10 ± 5.10 mmol/L and 70.20 ± 48.29 pmol/L, respectively. In general, there was no effect of age on insulin or glucose levels, regardless of ethnicity or myopia status, except for an observation in White participants as shown in Figs. 3E, F. Male participants had significantly higher glucose levels than did female participants (5.22 ± 0.45 vs. 4.97 ± 0.46 mmol/L, P < .00001), but lower insulin levels (64.89 ± 48.87 vs. 76.04 ± 49.17 pmol/L, P < .00001). Glucose levels varied significantly with ethnicity (P < .0001), with Blacks having the lowest levels (5.00 ± 0.45 mmol/L) compared with all other ethnic groups, who had similar glucose levels (5.11 [White] to 5.19 [other/multiethnic] mmol/L). Insulin levels also showed significant ethnicity-related differences (P < .0001), with the other/multiethnic group having the lowest levels (60.43 ± 39.89 pmol/L) and other Hispanics having the highest (77.27 ± 53.61 pmol/L). There was no statistically significant difference in glucose levels between myopic and nonmyopic participants (P = .81), although insulin levels were significantly higher in myopic participants (P = .01). However, neither glucose levels nor insulin levels proved to be significantly correlated with spherical equivalent refractive error (Figs. 5C, D; both R2 ≤ 0.004, P ≥ .30).
Results for all multivariate models are summarized in Table 2. An initial linear regression multivariate model was created to identify the factors associated with participant refractive error (spherical equivalent refractive error). Given the collinearity of participant age and body mass index with height and the fact that height was not related to myopia status in univariate analysis, height was not included in our final models. In addition, age was standardized by centering the variable on the mean age of the cohort (17.05 years). Although no significant associations between either ethnicity or any of the nutritional factors and spherical equivalent refractive error were identified, the relationship between sex, age, and spherical equivalent refractive error proved to be statistically significant, with female participants having more myopic spherical equivalent refractive errors than male participants (by −0.20 D [−0.380 to −0.015], P = .03) and older participants having more myopic spherical equivalent refractive error (−0.04 D [−0.063 to −0.008] more myopia per 1-year increase in age; P = .01). Although not significant, participants in the multiethnic/other ethnicity group were also, on average, slightly more myopic compared with Whites (by −0.41 D [−0.862 to 0.051], P = .08). We also explored potential nonlinear effects of age by including age2 in our model; however, no increase in significance was found when all other model covariates were considered (combined age effect P = .16).
TABLE 2 -
Results generated from multivariate models, with adjustment for demographic, nutritional, and body metric factors in those participants with complete data sets (n = 1974)
||Mean refractive error (D)
||Presence of myopia
||Coefficient (95% CI)
||Odds ratio (95% CI)
||−0.20 (−0.380 to −0.015)
||1.27 (1.040 to 1.545)
|Age (per 1-y increase)
||−0.04 (−0.063 to −0.008)
||1.03 (1.002 to 1.064)
| Non-Hispanic White
| Non-Hispanic Black
||0.11 (−0.162 to 0.379)
||0.81 (0.605 to 1.088)
| Mexican American
||0.11 (−0.132 to 0.350)
||0.84 (0.650 to 1.095)
| Other Hispanic
||0.17 (−0.322 to 0.655)
||0.77 (0.452 to 1.324)
||−0.41 (−0.862 to 0.051)
||1.13 (0.700 to 1.837)
|Total vitamin D (per 1-nmol/L increase)
||0.002 (−0.002 to 0.007)
||1.00 (0.992 to 1.002)
|Daily caffeine intake (per 1-mg increase)
||−0.0008 (−0.0009 to 0.0026)
||1.00 (0.997 to 1.000)
|Fasting glucose (per 1-mmol/L increase)
||−0.07 (−0.272 to 0.138)
||1.05 (0.840 to 1.309)
|Insulin (per 1-pmol/L increase)
||−0.0005 (−0.0028 to 0.0019)
||1.003 (1.000 to 1.005)
|Body mass index (per 1-kg/cm2 increase)
||0.002 (−0.017 to 0.020)
||0.99 (0.971 to 1.010)
Statistically significant effects are shown in bold. Body height was removed from models because of collinearity with age and body mass index. CI = confidence interval.
For participant myopia status, sex showed a significant effect such that the odds of having myopia were significantly greater for female than male participants (odds ratio, 1.27 [1.040 to 1.545]; P = .02). Although ethnicity had no significant effect, older age was significantly associated with greater odds of having myopia (odds ratio, 1.03 [1.002 to 1.064]; P = .04). In relation to body metrics and nutritional factor, only increased insulin levels were associated with significantly increased odds of having myopia (odds ratio, 1.003 [1.0002 to 1.005]; P = .04).
Additional linear regression modeling was undertaken using the data from those participants who were both myopic and had data for all other variables (n = 703), with specific interest in associations between the magnitude of myopia and demographic, body metrics, and nutritional factors (data not shown). Although female participants had more myopic spherical equivalent refractive errors than did male participants on average (by −0.19 D), this difference was not statistically significant (P = .26). Older myopic participants also tended to be more myopic than younger participants, although this effect of age was also neither statistically nor clinically significant (−0.03 D more per 1-year increase in age; P = .24). In relation to ethnicity, the largest difference was between myopes in the other/mixed compared with White groups (by −0.66 D), although this was not statistically significant (P = .10). None of the body metric and nutritional factors proved to have predictive value as determinants of the magnitude of myopia (all, P > .20).
To our knowledge, the current study represents one of only three studies to exploit the National Health and Nutrition Examination Survey database as a resource for investigating environmental contributions to the development of myopia,39–41 with one of the other studies also investigating nutritional but not body metric factors.40,41 The analyses used in our study revealed more female participants to be affected by myopia than male participants overall (12- to 25-year cohort: 38 vs. 33%). Female participants were also found to have more myopic refractive errors and a greater odds of having myopia, as were older participants. Although univariate analyses identified ethnicity-related differences in mean spherical equivalent refractive errors and participant myopia, there was no significant association with either the presence of myopia or its magnitude, after controlling for other participant factors. In general, none of the nutritional factors examined (serum vitamin D, plasma glucose, and caffeine intake) proved to be significantly related to the presence of myopia in this participant cohort, although participants with increased insulin levels had a significantly increased odds of being myopic.
In relation to the influence of body metrics and consistent with the results of the current analysis, a number of population-based studies across the globe have reported relationships between increased eye length and/or myopia in taller individuals.15,42–48 Although these studies have generally involved older cohorts (≥40 years of age) with likely stable refractive errors, two Asian studies involving children (aged 7 to 9 years) provide exceptions.15,48 In one study involving Taiwanese children48 and another population-based study involving Chinese adults,49 height was found to be positively associated with longer eyes but not with myopia, with the likely explanation for this apparent discrepancy lying in the other structural differences found in the eyes of taller individuals, namely, deeper anterior chambers, thinner lenses, and flatter corneas. The latter findings are also generally consistent with sex differences identified in a systematic review of ocular biometry data, which found male participants to have longer eyes (by ∼0.50 mm), flatter corneas (by ∼0.50 D), and deeper anterior chamber depths (by ∼0.16 mm) compared with female participants, except for those male participants of Asian ethnicity who had steeper corneas than did female participants.50 Further challenging the relevance of body metrics to myopia is a large Israeli cohort study (N = 106,926) of conscripted male participants aged 17 to 19 years in which no relationship between myopia and either body height or mass index was found.51
As noted earlier and consistent with our results, Cordain et al.13 proposed a link between hyperinsulinemia with myopia development. Other studies have also reported links between diabetics and myopia.52,53 However, that lenticular changes offer an explanation for the increased prevalence in myopia in diabetic individuals is supported by results from a later, small study by some of the same researchers.54 Nonetheless, that the glycemic profiles of populations worldwide might explain observed increases in myopia prevalence figures was suggested by the authors of a recent review of related epidemiological literature, which included speculation on possible mechanisms by which insulin could promote ocular growth.55 However, evidence for the latter from studies involving animal models is equivocal; although insulin was found to promote myopia development in a few studies involving chicks, the pattern of axial elongation was atypical in that anterior segment changes contributed most to the overall increases in eye length.16,56
Because increased time spent outdoors is recognized to be protective against myopia21,23,57,58 and also tightly tied linked to serum levels of vitamin D, there has been interest in whether vitamin D alone might be protective. A number of related hypotheses concerning how low serum vitamin D levels could increase the risk of myopia have been proposed, including upregulation of scleral extracellular remodeling and synergistic interaction with retinoic acid, a recognized ocular growth regulator.59 However, consistent with results of the current study, four large cohort studies, including one National Health and Nutrition Examination Survey cohort analysis, failed to establish a link between low level of vitamin D and myopia.28,29,40,60 Furthermore, in the current study, Blacks had the lowest serum levels of vitamin D, as has been reported in previous studies,61 yet Blacks also had the lowest proportion of myopes (35%; 1% below the average), with similar findings contained in other reports.62–64 A recent study that used Mendelian randomization to investigate the role of low serum vitamin D levels in myopia development, without the confounding effect of outdoor activity, also found no evidence of a causal relationship.30 Interestingly, a study in tree shrews involving experimentally induced myopia also failed to demonstrate a positive benefit from vitamin D3 supplementation, although control animals were not deficient (Siegwart JT, Jr., et al. IOVS 2011;52:E-Abstract 6298).65
A number of recent animal model studies have yielded strong supporting data for the potential therapeutic benefits of caffeine and one of its metabolites, 7-methylxanthine, a nonselective adenosine receptor antagonist.17–19 These results are also consistent with a relative reduction in axial elongation and myopia progression observed with oral 7-methylxanthine in an earlier pediatric clinical trial in Denmark.66 Longer-term clinical trials are ongoing in Denmark, the only country to have approved oral 7-methylxanthine tablets for myopia control to date. Unfortunately, analyses reported here were necessarily limited to the National Health and Nutrition Examination Survey–based data covering caffeine intake, as data covering caffeine metabolites in urine are only available from 2009, when refractive error measurements were discontinued. Related to other nutritional factors, to our knowledge, there have only been two other systematic analyses of this open-access National Health and Nutrition Examination Survey data set with respect to myopia development and/or progression and nutritional factors to date.40,41 One of these studies examined the association of total zinc intake and myopia in National Health and Nutrition Examination Survey participants aged 12 to 19 years and found no association.41
The large ethnically diverse National Health and Nutrition Examination Survey participant cohort combined with the analyses used in the current study represents its major strengths, with the availability of objective refractive error data representing an additional strength, given that axial length data were not available. In addition, that all measurements were performed in a standardized way by trained technicians, according to well-defined protocols, across all National Health and Nutrition Examination Survey sites, adds further value to this data set. Nonetheless, there are several limitations to consider, the most significant of which relates to the ethnic categories used during the study years analyzed. Given the high prevalence of myopia in Asian populations, both in Asian countries and in the United States, the lack of an “Asian” category represents a major limitation. Nonetheless, the fact that the other/mixed ethnic category, albeit small, had the highest proportion of myopes (46%; 11% more than the cohort average) and who were also relatively more myopic (−3.15 D; 0.67 D more than the myopic cohort average) likely reflects the fact that Asian participants were included in this ethnic category. In addition, it is important to note that the refractive error data were limited to children 12 years or older, after the typical age at onset of childhood myopia and as reflected in the presence of myopia in many of the participants in our study cohort. This may in part explain why age, which has been shown to influence refractive error in many other studies,62,66–68 proved to be of only borderline statistical significance in our multivariate modeling. In addition, the nutritional data captured from adolescents are likely to be different from those representing younger children. Finally, although it is important to disentangle the likely confounding effects of outdoor activity when considering the relationship between serum vitamin D levels and myopia, neither comprehensive measures of outdoor activity nor season of data collection is available in this data set, and only minimal data concerning sunlight exposure are available.
CONCLUSIONS AND CLINICAL RELEVANCE
The key risk factors related to myopia development and/or progression remain to be identified and are very likely multifactorial. However, clinicians are frequently called on to make recommendations about behavioral modifications that might reduce myopia development and progression. Although sex and age seem to be most closely tied to the presence and magnitude of myopia, the results presented here suggest that insulin levels may also be an important factor. No other nutritional or body metric factors seem to be closely tied to the presence or magnitude of myopia. These largely negative findings suggest that other environmental factors, such as those related to the visual environment, may contribute more to the development and/or progression of myopia and would argue for continued research in these areas in support of more evidence-based myopia clinical management.
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