Abstract
Purpose.:
To investigate the association between myopia progression and time spent outdoors and in various visual activities.
Methods.:
Subjects were 835 myopes (both principal meridians −0.75 diopters [D] or more myopia by cycloplegic autorefraction) in the Collaborative Longitudinal Evaluation of Ethnicity and Refractive Error (CLEERE) Study with both progression data and at least one measure of activity associated with a progression interval. Activity data were collected by parental survey. Average activity level (mean of the activity at the beginning and the end of a 1-year progression interval) was the primary predictor in a repeated-measures mixed model. The model controlled for age, sex, ethnicity, refractive error at the beginning of the progression interval, clinic site, and type of autorefractor used. Effects were scaled based on performing an additional 10 hours per week of an activity.
Results.:
In the multivariate model, the number of hours of reading for pleasure per week was not significantly associated with annual myopia progression at an a priori level of P ≤ 0.01, nor were the other near activities, the near-work composite variable diopter-hours, or outdoor/sports activity. The magnitude of effects was clinically small. For example, the largest multivariate effect was that each additional 10 hours of reading for pleasure per week at the end of a progression interval was associated with an increase in average annual progression by −0.08 D.
Conclusions.:
Despite protective associations previously reported for time outdoors reducing the risk of myopia onset, outdoor/sports activity was not associated with less myopia progression following onset. Near work also had little meaningful effect on the rate of myopia progression.
Subjects were myopic children (−0.75 D or more myopic in each principal meridian on cycloplegic autorefraction) who participated in the CLEERE Study between 1989 and 2009. The CLEERE Study is a multicenter, observational cohort study evaluating ocular component development and risk factors for juvenile-onset myopia in children of different ethnicities. The original Orinda Longitudinal Study of Myopia (Orinda, CA) became the CLEERE Study in 1997 with the addition of sites enrolling African-American (Eutaw, AL); Asian (Irvine, CA); and Hispanic (Houston, TX) children. In 2000, a site to enroll Native-American children (Tucson, AZ) was added. Each affiliated university's institutional review board approved the protocol and informed consent documents in accordance with the tenets of the Declaration of Helsinki. In addition to written parental consent, children provided assent. Only myopic children were included in this analysis of the CLEERE data; these children had at least two consecutive annual myopic study visits (so that an annual progression rate could be calculated) and at least one measure of near work or outdoor/sports activity with a temporally associated myopia progression rate.
Activity data were gathered annually at the same time each year using a questionnaire that asked the parent: “During the school year, how many hours per week (outside of regular school hours) would you estimate this child: 1) studies or reads for school assignments; 2) reads for fun (pleasure); 3) watches TV; 4) uses a computer/plays video games; and 5) engages in outdoor/sports activities?”
Reported hours per week across all five activities that exceeded 82 hours were deleted (
n = 19), because it was assumed that 82 hours per week outside of school were not reasonably available to a child. This maximum value was calculated as follows: 168 (24 hours × 7 days) possible hours per week, minus an assumed 30 hours per week spent in school (6 hours × 5 days), and 56 hours were spent sleeping (7 days × 8 hours), leaving 82 hours for other activities. The range of the excluded responses was 84 hours to 347 hours per week. Over half of the excluded responses were between 90 and 100 hours per week. Diopter-hours were calculated to include the estimated accommodative effort as a result of performing near work at varying distances. This was calculated as a comprehensive near-work exposure, defined as: 3 × hours of reading + 3 × hours of studying + 2 × video/computer hours + hours watching television.
6 Parents also provided information on their own myopia on the baseline medical history form consisting of both parents' year of birth, whether they wore spectacles or contact lenses, and, if so, the age when they were first prescribed spectacles and how they primarily used the spectacles at the time of the survey (distance, near, or both). A parent was considered myopic if he or she used the spectacles primarily for distance or for both distance and near with the spectacles first prescribed before age 17 years.
21 Cycloplegic autorefraction was conducted by certified study personnel with an autorefractor (Canon R-1; Canon, Lake Success, NY; no longer manufactured) from 1989 to 2000 and with a different autorefractor model (Grand Seiko WR 5100-K; Grand Seiko Co., Hiroshima, Japan) from 2001 to 2009. For cycloplegic autorefraction, subjects fixated on a reduced Snellen target through a +4.00 D Badal lens in primary gaze. Immediately following measurement in primary gaze, the track holding the Snellen target was rotated 30° and placed before a front-surface mirror on the patient's right. Five autorefraction measurements were then taken in peripheral gaze. Relative peripheral refractive error was calculated as the spherical equivalent of the average refraction in primary gaze subtracted from the spherical equivalent of the average refractive error in 30° temporal gaze. For subjects with grade 1 or 2 iris color (in general, a blue or a gray iris, along with a green iris with a lesser amount of brown pigment),
22 testing was performed 30 minutes after one drop of proparacaine 0.5% and two drops of tropicamide 1.0%. When subjects had dark iris color greater than grade 2, testing was performed 30 minutes after one drop of proparacaine 0.5% and one drop each of tropicamide 1.0% and cyclopentolate 1.0%.
23 Ten autorefractor measurements were made according to a standard protocol.
24
These analyses measured refractive error progression by calculating the change in spherical equivalent over consecutive years. Myopia progression was considered to be any increase in the myopic spherical equivalent. For each progression interval (i.e., a year), two sources of activity data were potentially available. Baseline data were the “before” values of the very first progression interval. Data available at the beginning of the progression interval were identified as “before” data. The activity data from the end of the progression interval were identified as “after” data. This means that a given activity measurement could be defined as both “before” and “after” data for different intervals. For example, if we were to examine progression between year 2 and year 3, then activity data for year 2 would provide the “before” measurement and data from year 3 would be the “after” measurement. In investigating the progression from year 3 to year 4, year-3 data would now be the “before” activity data.
The choice of the most appropriate time point at which to select the activity data is somewhat arbitrary. In terms of potential causality, activity before the progression period would be the most logical choice, while activity at the end of the progression period may better represent more recent exposure or the effect rather than the cause of progression. We chose to use the average of the before and after data during the interval of progression as the primary variable in analyses of progression. If both observations were not available, the subject was not included in the average analysis but still appeared in the before or after analyses, as appropriate. A repeated-measures mixed model approach was the primary method used to analyze the progression data. The basic model included the following covariates: age, refractive error at the beginning of the progression interval, sex, site, an indicator for an autorefractor model change in the year 2001, and interaction terms for age × sex, age × ethnicity, and site × instrument. The predictor variables of average activity data were then added to this base model. Additional models included number of myopic parents and relative peripheral refraction evaluated along with interaction terms with the activity variables. Given that multiple comparisons were made, a P value of ≤ 0.01 was used as the criterion for statistical significance. To provide a reasonable estimate of the magnitude of an effect, the results have been rescaled to represent the increment in myopia progression with 10 hours of additional activity per week. All analyses were completed using statistical analysis software (SAS 9.2; SAS Institute, Cary, NC).
Clinical Centers. Franklin Primary Health Center, Inc. Sandral Hullett, MD, MPH (Principal Investigator, 1997–2007); Robert N. Kleinstein, OD, MPH, PhD (Co-Investigator, 1997–2007); Janene Sims, OD (Optometrist, 1997–2001 and 2004–2007); Raphael Weeks, OD (Optometrist, 1999–2007); Sandra Williams (Study Coordinator, 1999–2007); LeeAndra Calvin (Study Coordinator, 1997–1999), Melvin D. Shipp, OD, MPH, DrPH (Co-Investigator, 1997–2004). Drs. Kleinstein and Sims are affiliated with the University of Alabama at Birmingham School of Optometry.
University of California, Berkeley School of Optometry, Berkeley, CA. Nina E. Friedman, OD, MS (Principal Investigator, 1999–2001); Pamela Qualley, MA (Study Coordinator, 1997–2001); Donald O. Mutti, OD, PhD (Principal Investigator, 1996–1999); Karla Zadnik, OD, PhD (Optometrist, 1996–2001).
University of Houston College of Optometry. Ruth E. Manny, OD, PhD (Principal Investigator, 1997–2007); Suzanne M. Wickum, OD (Optometrist, 1999–2007); Ailene Kim, OD (Optometrist, 2003–2007); Bronwen Mathis, OD (Optometrist, 2002–2007); Mamie Batres (Study Coordinator, 2004–2007). Sally Henry (Study Coordinator, 1997–1998); Janice M. Wensveen, OD, PhD (Optometrist, 1997–2001); Connie J. Crossnoe, OD (Optometrist, 1997–2003); Stephanie L. Tom, OD (Optometrist, 1999–2002); Jennifer A. McLeod (Study Coordinator, 1998–2004); Julio C. Quiralte (Study Coordinator, 1998–2005); Gaby Solis (Study Coordinator, 2005–2007).
Southern California College of Optometry, Fullerton, CA. Susan A. Cotter, OD, MS (Principal Investigator, 2004–2007, Optometrist, 1997–2004); Julie A. Yu, OD (Principal Investigator, 1997–2004; Optometrist 2005–2007); Raymond J. Chu, OD (Optometrist, 2001–2007); Carmen N. Barnhardt, OD, MS (Optometrist 2004–2007); Jessica Chang, OD (Optometrist, 2005–2007); Kristine Huang, OD (Optometrist, 2005–2007); Rebecca Bridgeford (Study Coordinator, 2005–2006); Connie Chu, OD (Optometrist, 2004–2005), Soonsi Kwon, OD (Optometrist, 1998–2004); Gen Lee (Study Coordinator, 1999–2003); John Lee, OD (Optometrist, 2000–2003); Robert J. Lee, OD (Optometrist, 1997–2001); Raymond Maeda, OD (Optometrist, 1999–2003); Rachael Emerson (Study Coordinator, 1997–1999); Tracy Leonhardt (Study Coordinator, 2003–2004).
University of Arizona, Department of Ophthalmology and Vision Science, Tucson, AZ. J. Daniel Twelker, OD, PhD (Principal Investigator, 2000–present); Dawn Messer, OD, MDH (Optometrist, 2000–present); Denise Flores (Study Coordinator, 2000–2007); Rita Bhakta, OD (Optometrist, 2000–2004); Katie Garvey, OD (Optometrist, 2006–present); Mabel Crescioni, DrPH (2009–present).
Chairman's Office, The Ohio State University College of Optometry, Columbus, OH. Karla Zadnik, OD, PhD (Chairman, 1997-present); Jodi M. Malone, RN (Study Coordinator, 1997–present).
Videophakometry Reading Center, The Ohio State University College of Optometry, Columbus, OH. Donald O. Mutti, OD, PhD (Director, 1997–present); Vidya Subramanian, MS (Reader, 2006–2009); Huan Sheng, MD MS (Reader, 2000–2006); Holly Omlor (Reader, 2003–2006); Meliha Rahmani (Reader, 2004–2006); Jaclyn Brickman (Reader, 2002–2003); Amy Wang (Reader, 2002–2003); Philip Arner (Reader, 2002–2004); Samuel Taylor (Reader, 2002–2003); Myhanh T. Nguyen (Reader, 1998–2001); Terry W. Walker (Reader, 1997–2001).
Optometry Coordinating Center, The Ohio State University College of Optometry, Columbus, OH. Lisa A. Jones-Jordan, PhD (Director, 1997–present); Linda Barrett (Data Entry Operator, 1997–2008); John Hayes, PhD (Biostatistician, 2001–2007); G. Lynn Mitchell, MAS Biostatistician, 1998–present); Melvin L. Moeschberger, PhD (Consultant, 1997–present); Loraine Sinnott, PhD (Biostatistician, 2005–present); Pamela Wessel (Program Coordinator, 2000–present); Julie N. Swartzendruber, MA (Program Coordinator, 1998–2000); Austen Tanner (Data Entry 2008–2010).
Project Office, National Eye Institute, Rockville, MD. Donald F. Everett, MA.
Executive Committee. Karla Zadnik, OD, PhD (Chairman); Lisa A. Jones-Jordan, PhD; Robert N. Kleinstein, OD, MPH, PhD; Ruth E. Manny, OD, PhD; Donald O. Mutti, OD, PhD; J. Daniel Twelker, OD, PhD; Susan A. Cotter, OD, MS.