Abstract
We aimed to investigate whether health-related quality of life (HRQoL) is associated with retinal vascular caliber, an indicator of subclinical cardiovascular disease risk. 1600 students aged between 11–19 years (821 girls and 779 boys) were examined during 2009–2011. Retinal vessel caliber was measured from digital retinal images. HRQoL was assessed by the Pediatric Quality of Life Inventory (PedsQL). In the overall cohort, each 1-unit increase in PedsQL total score and the psychosocial summary score was associated with ~0.05 μm narrowing in retinal arteriolar caliber (multivariable-adjusted p-value = 0.01). Participants in the lowest versus highest tertile of PedsQL total score, psychosocial summary, social and school item scores had significantly wider retinal arteriolar caliber: 161.7 μm versus 160.2 μm (p = 0.02); 161.6 μm versus 160.0 μm (p = 0.02); 161.6 μm versus 159.9 μm (p = 0.002); and 161.6 μm versus 159.9 μm (p = 0.01), respectively. Significant interactions (p < 0.05) were observed between gender and PedsQL total score with retinal arteriolar calibre. In boys, inverse associations were observed between PedsQL total score (p = 0.01), psychosocial summary (p = 0.01), and social scores (p = 0.01) and retinal arteriolar caliber. No significant associations were observed between PedsQL scores and retinal vessel caliber in girls. Diminished HRQoL in adolescents was independently associated with structural retinal microvascular changes.
Introduction
Health-related quality of life (HRQoL) refers to the subset of quality of life directly related to an individual’s health1, which as defined by the World Health Organization includes physical, mental, and social well-being2,3. Recent studies have shown a significant influence of HRQoL on long-term outcomes. For instance, poor HRQoL has been shown to be a marker of morbidity and mortality in patients with coronary heart disease, even after controlling for traditional vascular risk factors4–6. Moreover, HRQoL has also been reported to be associated with several cardiovascular risk factors, including obesity7,8, diabetes9 and smoking10.
Microvascular abnormality may underlie the association between subsets of HRQoL, particularly mental wellbeing, and vascular disease11–13. The retina offers a readily accessible site to non-invasively evaluate the microcirculation and is a recognized marker of early subclinical vascular disease14. Reliable methods of quantifying retinal microvascular changes from retinal photographs have been developed15, and subtle changes in the retinal vasculature may mirror pre-clinical structural changes in both the cerebral16 and coronary microcirculations17, and thus, could have prognostic information useful for predicting clinical cardiovascular events18. Further, structural retinal microvascular changes have shown to be associated with cardiovascular disease risk factors, including obesity and hypertension19,20.
While studies in adults and adolescents have shown that depression and anxiety symptoms are associated with measurable signs in the retinal microvasculature11–13; there have been no population-based studies that have examined the associations between overall HRQoL and retinal vessel caliber in either adults or children. Therefore, we aimed to assess the cross-sectional relationship between HRQoL (exposure) and retinal vessel caliber (study outcome) using a large cohort of adolescents. We hypothesize that lower HRQol scores is independently associated with modest structural retinal microvascular changes in adolescents. Hence, the epidemiological data from this study will help elucidate whether microvasculature structural alterations might be involved in the early mechanisms leading to cardiovascular disease and impaired HRQoL in later life.
Participants and Methods
Study Population
The Sydney Childhood Eye Study is a population-based survey of eye conditions in school children living within the Sydney Metropolitan Area, Australia. It was approved by the Human Research Ethics Committee, University of Sydney, the Department of Education and Training, and Catholic Education Office, New South Wales, Australia21. We obtained informed written consent from at least one parent of each child, as well as verbal assent from each child before the examinations. Study methods have been previously described21. All methods in this study were performed in accordance with the relevant guidelines and regulations. Briefly, Year 1 students from a stratified random cluster sample of 34 primary schools across Sydney (6–7 years of age) were eligible to participate. Data for the 6-year-old cohort (n = 1740) were collected during 2003–2004; and of these 1125 (64.7%) were followed up 5 years later i.e. aged 11–12 years. Also, students in Year 7 (12–13 years of age) in a stratified random cluster sample of 21 high schools across Sydney were eligible to participate. Data for this 12-year-old cohort (n = 2353) were collected during 2004–2005. Of the baseline participants 12 years of age, 1217 (51.7%) were resurveyed 5 years later (during 2009–2011), and includes children 16–19 years of age. Additional participants (n = 475) aged 17–18 years were recruited when we visited the same schools as in the baseline survey. Therefore, the total number of participants surveyed at the 5-year follow-up was 2817; comprising 1125 participants aged 11–12 and 1692 participants aged 16–19 years. Information on retinal vessel caliber was collected at baseline and follow-up surveys; however, health-related HRQoL was collected only at the 5-year examination. Therefore, the current study reports on cross-sectional data obtained from the 5-year survey only.
Assessment of HRQoL
The Pediatric Quality of Life Inventory (PedsQL) 4.0 was used to assess HRQoL in preadolescents and adolescents and was only administered at the 5-year follow-up. The PedsQL is a validated 23-item questionnaire for children aged 2 to 18 years22, which takes students approximately 5–7 minutes to complete. The self-reported version of PedsQL was used in this study. Students reported how much of a problem they are experiencing in each of the PedsQL items in the past one month and mean scores were calculated based on a 5-point response scale for each item: (i) 0 - if it is never a problem; (ii) 1 - if it is almost never a problem; (iii) 2 - if it is sometimes a problem; (iv) 3 – if it is often a problem; and (v) 4 – if it is almost always a problem. Mean scores are then transformed to a 0 to 100 scale with a higher score representing better HRQoL. The PedQL yields 3 summary scores: a total scale score, a physical health summary score and a psychosocial health summary score. There are 4 sub-scale scores: physical functioning, emotional functioning, social functioning and school functioning. The total score is comprised of the average of all items in the questionnaire. The psychosocial summary is an average of the items in the emotional, social and school functioning scales. The physical health summary score comprises the average of items in the physical functioning scale22.
Retinal Photography and Analysis
Children had dilated, digital photographs taken of the optic disk and macula of both eyes using a Canon 60UVID10 fundus camera (Canon Inc., Tokyo, Japan). For this study, retinal vascular caliber measurements for the right eye of each child were used. Left eye measurements were used when, occasionally, the photographs of the right eye were not gradable. One grader, masked to participant identity and characteristics, measured retinal vessel width using a computer-assisted program (Retinal Analysis, University of Wisconsin) with high reproducibility15,23. The six largest arteriolar and venular diameters measured for each eye, were then summarized as central retinal arteriolar equivalent (CRAE) or central retinal venular equivalent (CRVE), respectively, using a formula developed by Knudtson-Hubbard24.
Assessment of Covariates
Parents were asked to complete a comprehensive 193-item questionnaire (at baseline and follow-up), from which socio-demographic information including ethnicity, and highest level of parental education was collected. Data were collected during a pre-organized visit to each school. Anthropometric measures were obtained by a trained medical officer. Height was measured to the nearest 0.1 cm with shoes off using a freestanding SECA height rod (Model 220, Hamburg, Germany). Weight in kilograms was measured to the nearest 0.1 kg using a standard portable weighing machine, after removing any heavy clothing. BMI was calculated as weight divided by height squared (kg/m2). After 5 minutes resting, blood pressure (BP) was measured in a seated position using an automated sphygmomanometer (HEM 907; Omron Healthcare Inc) with appropriate cuff size. Three separate BP measurements were taken, and averaged for analysis. Mean arterial BP (MABP) was calculated as one-third of the systolic plus two thirds of the diastolic BP.
A Canon autorefractor (Model RK-F1, Canon Inc., New York, U.S.A.) was used to perform cycloplegic autorefraction and keratometry. Children also had a comprehensive eye examination, which included mydriatic digital retinal photography. Axial length was measured before cycloplegia with an optical biometer (IOLMaster; Carl Zeiss Meditec, Oberkochen, Germany), using dual-beam partial coherence interferometry25. The average of 5 measurements was used for analysis.
Statistical Analyses
Statistical analyses were performed using SAS (v9.2, SAS Institute, NC) including t-tests, χ2-tests and linear regression. Linear regression models were constructed to examine possible cross-sectional associations between HRQoL (independent variable) with retinal vascular caliber (dependent variable). PedsQL item scores were included in the analyses as continuous (each 1-unit increase) or as categorical variables (tertiles). Covariates that were previously found to be significantly associated with retinal vessel caliber26,27 were included in the final multivariable models i.e. age, sex, ethnicity, BMI, mean arterial BP, and axial length. Subsequently, analysis of covariance was used to calculate differences in mean retinal vascular caliber adjusted for age, sex, ethnicity, BMI, mean arterial BP, and axial length. After multivariable adjustment, linear regression analyses indicated interactions between sex and the associations of PedsQL total score (Pinteraction = 0.02); psychosocial summary (Pinteraction = 0.02); social item (Pintera ction = 0.001); and school item (Pinteraction = 0.02) with retinal arteriolar caliber. Therefore, analyses of PedsQL and retinal vascular caliber were also stratified by sex.
Results
Of the 2817 participants re-examined 5 years later, 1600 participants had complete information on retinal vessel caliber and PedsQL scores. Participants compared to non-participants were likely to be older and Caucasian, and to have higher BMI and systolic BP (Table 1). Table 2 shows the study characteristics of the 1600 participants stratified by gender. Significant differences were observed between boys and girls in regards to ethnic distribution, systolic and diastolic BP, axial length and in PedsQL total score, physical summary, emotional and social domain scores. For instance, boys compared to girls were more likely to be Caucasian, have higher systolic BP, axial length and PedsQL total scores (Table 2).
Table 1.
Characteristics | Non-participantsa (n = 1217) | Participants (n = 1600) | P-value |
---|---|---|---|
Age, years, mean (SD) | 14.3 (1.7) | 16.3 (1.8) | <0.0001 |
Male, n (%) | 625 (51.3) | 779 (48.7) | 0.17 |
Ethnicity, n (%) | |||
Caucasian | 583 (46.3) | 1020 (63.8) | <0.0001 |
East Asian | 388 (30.8) | 229 (14.3) | |
South Asian | 53 (4.2) | 77 (4.8) | |
Middle Eastern | 89 (7.1) | 116 (7.3) | |
Other | 146 (11.6) | 158 (9.9) | |
Body mass index, kg/m2, mean (SD) | 20.8 (4.2) | 22.2 (4.4) | <0.0001 |
Systolic blood pressure, mm Hg, mean (SD) | 117.1 (13.2) | 119.0 (13.3) | <0.0001 |
Diastolic blood pressure, mm Hg, mean (SD) | 67.8 (9.5) | 68.4 (9.6) | 0.14 |
Axial length, mm, mean (SD)1 | 23.6 (1.0) | 23.6 (0.9) | 0.02 |
PedsQL | |||
Total score | 79.7 (12.7) | 80.8 (12.3) | 0.15 |
Physical summary | 88.6 (14.4) | 89.9 (13.3) | 0.11 |
Psychosocial summary | 75.3 (14.6) | 76.2 (14.6) | 0.28 |
Emotional | 72.5 (19.1) | 74.6 (19.2) | 0.08 |
Social | 88.7 (15.5) | 88.9 (14.9) | 0.80 |
School | 65.7 (22.4) | 65.8 (22.1) | 0.93 |
Data presented are mean (SD) or proportions.
aNon-participants are those who were excluded from analysis because they had incomplete information on retinal vessel caliber and/or PedsQL scores.
Table 2.
Characteristics | Girls (n = 821) | Boys (n = 779) | P-value |
---|---|---|---|
Age, years, mean (SD) | 16.3 (1.7) | 16.2 (1.8) | 0.44 |
Ethnicity, n (%) | |||
Caucasian | 491 (59.8) | 530 (68.0) | 0.003 |
East Asian | 140 (17.1) | 89 (11.4) | |
South Asian | 43 (5.2) | 34 (4.4) | |
Middle Eastern | 57 (6.9) | 58 (7.5) | |
Other | 90 (11.0) | 68 (8.7) | |
Body mass index, kg/m2, mean (SD) | 22.2 (4.5) | 22.2 (4.2) | 0.88 |
Systolic blood pressure, mm Hg, mean (SD) | 114.1 (11.2) | 124.3 (13.4) | <0.0001 |
Diastolic blood pressure, mm Hg, mean (SD) | 69.4 (9.4) | 67.3 (9.8) | <0.0001 |
Axial length, mm, mean (SD)1 | 23.4 (0.9) | 23.9 (0.9) | <0.0001 |
PedsQL | |||
Total score | 79.7 (13.1) | 81.9 (11.4) | 0.0001 |
Physical summary | 87.5 (14.6) | 92.0 (12.0) | <0.0001 |
Psychosocial summary | 75.8 (15.1) | 76.7 (14.0) | 0.25 |
Emotional | 71.8 (20.4) | 77.4 (17.4) | <0.0001 |
Social | 90.1 (13.7) | 87.6 (15.9) | 0.001 |
School | 66.9 (22.4) | 64.8 (21.6) | 0.06 |
Data presented are mean (SD) or proportions.
In the overall cohort, each 1-unit increase in PedsQL total score and the psychosocial summary score were significantly associated with ~0.05 μm narrowing in retinal arteriolar caliber (Table 3). After multivariable adjustment for age, sex, ethnicity, body mass index, mean arterial blood pressure, and axial length, a significant narrowing of retinal arteriolar caliber was also observed with each 1-unit increase in the PedsQL emotional (p = 0.04), social (p = 0.01) and school subscale scores (p = 0.04). Each 1-unit increase in the PedsQL social item score was significantly associated with ~0.07 μm widening of retinal venular caliber, no other significant associations were observed with retinal venules (Table 3). In boys, similar inverse associations were observed between PedsQL total score (p = 0.01), psychosocial summary (p = 0.01), and social scores (p = 0.01) and retinal arteriolar caliber after multivariable adjustment (Table 4). Also, each 1-unit increase in the PedsQL social item score was associated with ~0.09 μm widening of retinal venular caliber (multivariable-adjusted p-value = 0.01). No significant associations were observed between PedsQL item scores and retinal vascular caliber measures in girls (data not shown).
Table 3.
PedsQL scores (each 1-unit increase) | Retinal vascular caliber, mean (SE)a | |||
---|---|---|---|---|
Arteriolar caliber, μm | p-value | Venular caliber, μm | p-value | |
Total score | −0.05 (0.02) | 0.01 | 0.03 (0.03) | 0.40 |
Physical summary | −0.01 (0.02) | 0.54 | −0.008 (0.03) | 0.78 |
Psychosocial summary | −0.05 (0.02) | 0.004 | 0.03 (0.03) | 0.24 |
Emotional | −0.03 (0.01) | 0.04 | 0.001 (0.02) | 0.64 |
Social | −0.05 (0.02) | 0.01 | 0.07 (0.03) | 0.01 |
School | −0.02 (0.02) | 0.04 | 0.001 (0.02) | 0.96 |
aAdjusted for age, sex, ethnicity, body mass index, mean arterial blood pressure, axial length.
Table 4.
PedsQL scores (each 1-unit increase) | Retinal vascular caliber, mean (SE)a | |||
---|---|---|---|---|
Arteriolar caliber, μm | p-value | Venular caliber, μm | p-value | |
Total score | −0.07 (0.03) | 0.01 | 0.06 (0.04) | 0.24 |
Physical summary | −0.02 (0.03) | 0.54 | −0.02 (0.05) | 0.67 |
Psychosocial summary | −0.07 (0.03) | 0.01 | 0.06 (0.04) | 0.11 |
Emotional | −0.04 (0.02) | 0.06 | 0.02 (0.03) | 0.52 |
Social | −0.06 (0.02) | 0.01 | 0.09 (0.03) | 0.01 |
School | −0.03 (0.02) | 0.07 | 0.01 (0.03) | 0.56 |
aAdjusted for age, ethnicity, body mass index, mean arterial blood pressure, axial length.
Table 5 shows that in the overall cohort, those in the lowest tertile compared to those in the highest tertile of PedsQL total score, psychosocial summary, social and school item scores had significantly wider retinal arteriolar caliber: 161.7μm versus 160.2 μm (p = 0.02); 161.6 μm versus 160.0 μm (p = 0.02); 161.6 μm versus 159.9 μm (p = 0.002); and 161.6 μm versus 159.9 μm (p = 0.01), respectively. Similar significant associations were observed in boys after multivariable adjustment (Table 5). No significant associations were observed between tertiles of PedsQL item scores and retinal arteriolar caliber in girls (data not shown).
Table 5.
PedsQL scores | Overall | Boys |
---|---|---|
Arteriolar caliber, μm | Arteriolar caliber, μm | |
Total score | ||
1st tertile (≤75.8) | 161.7 (160.6–162.9) | 161.2 (159.6–162.9) |
2nd tertile (76.7–86.7) | 160.1 (158.9–161.2) | 159.5 (158.1–160.9) |
3rd tertile (≥87.1) | 160.2 (159.1–161.4) | 159.1 (157.5–160.6) |
P for trend | 0.02 | 0.02 |
Physical summary | ||
1st tertile (≤85.0) | 160.8 (159.7–162.0) | 160.1 (158.4–161.8) |
2nd tertile (90.0–95.0) | 161.1 (159.8–162.4) | 160.4 (158.7–162.1) |
3rd tertile (≥100.0) | 160.3 (159.3–161.4) | 159.5 (158.1–160.8) |
P for trend | 0.51 | 0.39 |
Psychosocial summary | ||
1st tertile (≤67.5) | 161.6 (160.4–162.8) | 160.8 (159.2–162.5) |
2nd tertile (70.0–82.5) | 160.5 (159.4–161.6) | 159.9 (158.5–161.3) |
3rd tertile (≥83.8) | 160.0 (158.9–161.2) | 158.9 (157.3–160.4) |
P for trend | 0.02 | 0.03 |
Emotional | ||
1st tertile (≤62.5) | 161.1 (159.9–162.2) | 160.3(158.6–161.9) |
2nd tertile (68.8–81.3) | 160.7 (159.6–161.9) | 160.3 (158.8–161.8) |
3rd tertile (≥87.5) | 160.1 (159.0–161.2) | 159.1 (157.6–160.5) |
P for trend | 0.13 | 0.16 |
Social | ||
1st tertile (≤83.3) | 161.6 (160.5–162.8) | 160.8 (159.4–162.2) |
2nd tertile (87.5–91.7) | 161.4 (160.0–163.0) | 160.4 (158.4–162.5) |
3rd tertile (≥100) | 159.9 (158.8–160.9) | 158.9 (157.5–160.2) |
P for trend | 0.002 | 0.02 |
School | ||
1st tertile (≤50.0) | 161.6 (160.4–162.8) | 160.7 (159.2–162.2) |
2nd tertile (58.3–75.0) | 160.4 (159.4–161.5) | 159.7 (158.3–161.2) |
3rd tertile (≥83.3) | 159.9 (158.7–161.1) | 158.7 (157.1–160.4) |
P for trend | 0.01 | 0.04 |
Bolded values indicate significant (p < 0.05) estimates in comparison with the highest or 3rd tertile.
aAdjusted for age, sex, ethnicity, body mass index, mean arterial blood pressure, axial length.
Participants in the lowest tertile compared to the highest tertile of social scores had significantly narrower retinal venules: 235.1 versus 236.9 μm; multivariable-adjusted p = 0.03. Similarly, boys in the lowest tertile compared to the highest tertile of social scores had significantly narrower retinal venules: 234.7 versus 238.1 μm; multivariable-adjusted p = 0.04. No significant associations between PedsQL scores and retinal venular caliber were observed in girls (data not shown).
Discussion
This is the first epidemiological study to demonstrate an independent association between HRQoL and structural retinal microvascular changes in a young population. Specifically, we show a modest cross-sectional association between lower HRQoL scores with wider retinal arteriolar caliber and narrower retinal venular caliber in a cohort of adolescents. In particular, the psychosocial aspects of HRQoL in adolescents showed a significant association with retinal vessel caliber changes. Further, observed associations were more marked in boys compared to girls.
There are few other cohort studies with which to compare our findings with. The most relevant studies are those showing significant associations between depression and anxiety and wider retinal arteriolar caliber in adolescents11 and adults12,13. This is in agreement with our data which showed that lower PedsQL psychosocial health summary scores (i.e. average of the items in the emotional, social and school functioning scales) were associated with retinal arteriolar dilatation. The specific pathophysiological mechanisms underlying wider retinal arteriolar caliber are unclear, but one speculated pathway is endothelial dysfunction (impairment of nitric oxide-mediated vasodilation)11. Wider retinal arteriolar caliber is a sign of impaired autoregulation28 and is associated with reduced flicker-induced vasodilatation11,29. Reduced endothelial function was associated with worse HRQoL in a prior study involving adolescents and young adults30, and endothelial dysfunction has also been observed in individuals with depression and anxiety31,32. In the present study, however, we were not able to assess endothelial function; hence, we are not able to confirm whether endothelial dysfunction is a potential mechanism underlying the link between HRQoL and retinal arteriolar dilatation. Additional studies would be needed to answer this question.
Another potential underlying mechanism is inflammation. There is research evidence to suggest that inflammatory biomarkers are meaningful correlates of HRQoL and robust inverse associations have been demonstrated between C-reactive protein (an inflammatory marker) and HRQoL33. Moreover, several studies reported that psychosocial factors were predictors of chronic inflammation and poor health34. The influence of psychological well-being on C-reactive protein may be supported by studies that reported an association between psychological stress and the dysregulation of the hypothalamic-pituitary-adrenal axis involved in inflammation35. Given that changes to retinal vascular calibers are related to systemic inflammation36, this could be a possible pathway by which HRQoL is independently associated with retinal microvascular signs in adolescents. Future prospective studies with adequate study power are warranted to focus on mechanisms to help explain these structural changes in retinal vessels in relation to poorer HRQoL.
We observed a sex-specific difference in the associations between PedsQL scores and retinal microvascular signs. These data align with the existing research evidence showing differences in the association of vascular disease risk factors with HRQoL between men and women e.g., for obesity7,8 and smoking37. Furthermore, Gijsberts et al.38 showed significant interactions of gender with diabetes and history of cardiovascular disease. Specifically, the association of these vascular risk factors with lower HRQoL was stronger in men than in women. The authors speculated that HRQoL in girls is not so much determined by CVD risk factors, a history of CVD or other general patient characteristics but more by other factors such as hormonal status and psychosocial factors that were not measured in their study38. We hypothesize that this is also likely to be applicable in our cohort study. Finally, our findings support data from a longitudinal study which found that the associations between mental stress with adverse changes to the vascular function and vascular response were more pronounced in boys rather than girls39. Together these epidemiological data, suggest that boys are likely to have changes in vascular health earlier than age-matched girls39.
Strengths of this study include its random cluster sample of a relatively large number of representative schoolchildren; satisfactory response rate; use of standardized retinal vessel caliber measurement protocols and a validated pediatric HRQoL instrument. Moreover, these young children were largely free of known systemic cardiovascular diseases, and thus, our findings are not likely to be subject to confounding effects CVD risk factors26. A study limitation is the cross-sectional design as PedsQL was not administered at the baseline survey, which does not permit causal inference from the observed associations. Second, we did not collect blood samples in our study; therefore, there is no data on biomarkers of chronic disease e.g. blood lipid and glucose levels, and measures of inflammatory markers. Third, given that participants versus non-participants differed significantly in e.g. age, ethnicity and BMI, we cannot disregard the potential for selection bias influencing observed associations. Finally, while we adjusted for a number of important confounders, we cannot discount the possibility that other unmeasured factors such as parental well-being and societal factors could have influenced HRQoL in adolescents.
In summary, our community-based study has made an original contribution by showing an independent association between poorer HRQoL scores and retinal microvascular abnormalities in adolescents. As these subtle structural retinal microvascular changes have shown to be markers of future vascular disease risk, the presence of this risk factor in schoolchildren could support the need for clinicians and researchers to incorporate assessments of HRQoL when evaluating the cardiovascular health of adolescents.
Acknowledgements
The Sydney Childhood Eye Study was supported by the Australian National Health and Medical Research Council (Grant No. 253732 and 512530); the Westmead Millennium Institute, University of Sydney; and the Vision Co-operative Research Centre, University of New South Wales, Sydney, Australia.
Author Contributions
Dr. Gopinath conceptualized and designed the study, analyzed and interpreted the data, drafted the initial manuscript, and reviewed and revised the manuscript. Prof Mitchell conceptualized and designed the study, collected data, analyzed and interpreted the data, and reviewed and revised the manuscript. Dr Liew, Mr Burlutsky and Prof Baur analyzed and interpreted the data, and reviewed and revised the manuscript. All authors approved the final manuscript as submitted and agree to be accountable for all aspects of the work.
Competing Interests
The authors declare no competing interests.
Footnotes
Publisher's note: Springer Nature remains neutral with regard to jurisdictional claims in published maps and institutional affiliations.
References
- 1.Sherman EM, et al. Validity of three measures of health-related quality of life in children with intractable epilepsy. Epilepsia. 2002;43:1230–1238. doi: 10.1046/j.1528-1157.2002.03602.x. [DOI] [PubMed] [Google Scholar]
- 2.Williams J, Wake M, Hesketh K, Maher E, Waters E. Health-related quality of life of overweight and obese children. JAMA. 2005;293:70–76. doi: 10.1001/jama.293.1.70. [DOI] [PubMed] [Google Scholar]
- 3.World Health Organization. Constitution of the World Health Organization. Forty-fifth edition, 1–18. World Health Organization. Basic Documents (2006).
- 4.De Smedt D, et al. Health related quality of life in coronary patients and its association with their cardiovascular risk profile: results from the EUROASPIRE III survey. Int.J.Cardiol. 2013;168:898–903. doi: 10.1016/j.ijcard.2012.10.053. [DOI] [PubMed] [Google Scholar]
- 5.Spertus JA, Jones P, McDonell M, Fan V, Fihn SD. Health status predicts long-term outcome in outpatients with coronary disease. Circulation. 2002;106:43–49. doi: 10.1161/01.CIR.0000020688.24874.90. [DOI] [PubMed] [Google Scholar]
- 6.Grool AM, et al. Self-rated health status as a risk factor for future vascular events and mortality in patients with symptomatic and asymptomatic atherosclerotic disease: the SMART study. J.Intern.Med. 2012;272:277–286. doi: 10.1111/j.1365-2796.2012.02521.x. [DOI] [PubMed] [Google Scholar]
- 7.Gopinath, B., Baur, L. A., Burlutsky, G. & Mitchell, P. Adiposity Adversely Influences Quality of Life Among Adolescents. J.Adolesc.Health (2013). [DOI] [PubMed]
- 8.Muller-Nordhorn J, et al. Longitudinal association between body mass index and health-related quality of life. PLoS.ONE. 2014;9:e93071. doi: 10.1371/journal.pone.0093071. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 9.Hlatky MA, et al. The effect of obesity on quality of life in patients with diabetes and coronary artery disease. Am.Heart J. 2010;159:292–300. doi: 10.1016/j.ahj.2009.11.004. [DOI] [PubMed] [Google Scholar]
- 10.Stafford L, Berk M, Jackson HJ. Tobacco smoking predicts depression and poorer quality of life in heart disease. BMC.Cardiovasc.Disord. 2013;13:35. doi: 10.1186/1471-2261-13-35. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 11.Meier MH, et al. Associations between depression and anxiety symptoms and retinal vessel caliber in adolescents and young adults. Psychosom.Med. 2014;76:732–738. doi: 10.1097/PSY.0000000000000117. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 12.Nguyen TT, et al. Evidence of early retinal microvascular changes in patients with type 2 diabetes and depression. Psychosom.Med. 2010;72:535–538. doi: 10.1097/PSY.0b013e3181da90f4. [DOI] [PubMed] [Google Scholar]
- 13.Nguyen TT, et al. Is depression associated with microvascular disease in patients with type 2 diabetes? Depress.Anxiety. 2008;25:E158–E162. doi: 10.1002/da.20427. [DOI] [PubMed] [Google Scholar]
- 14.Patton N, et al. Retinal vascular image analysis as a potential screening tool for cerebrovascular disease: a rationale based on homology between cerebral and retinal microvasculatures. J Anat. 2005;206:319–348. doi: 10.1111/j.1469-7580.2005.00395.x. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 15.Hubbard LD, et al. Methods for evaluation of retinal microvascular abnormalities associated with hypertension/sclerosis in the Atherosclerosis Risk in Communities Study. Ophthalmology. 1999;106:2269–2280. doi: 10.1016/S0161-6420(99)90525-0. [DOI] [PubMed] [Google Scholar]
- 16.Kwa VI. Our eyes: windows to our souls or crystal balls? Lancet Neurol. 2006;5:108–110. doi: 10.1016/S1474-4422(06)70332-5. [DOI] [PubMed] [Google Scholar]
- 17.Tedeschi-Reiner E, Strozzi M, Skoric B, Reiner Z. Relation of atherosclerotic changes in retinal arteries to the extent of coronary artery disease. Am J Cardiol. 2005;96:1107–1109. doi: 10.1016/j.amjcard.2005.05.070. [DOI] [PubMed] [Google Scholar]
- 18.Gopinath B, et al. The associations between blood levels of homocysteine, folate, vitamin B12, and retinal vascular caliber. Am.J.Ophthalmol. 2009;148:902–909. doi: 10.1016/j.ajo.2009.07.018. [DOI] [PubMed] [Google Scholar]
- 19.Wang JJ, et al. Retinal vessel diameters and obesity: A population-based study in older persons. Obesity (Silver Spring) 2006;14:206–214. doi: 10.1038/oby.2006.27. [DOI] [PubMed] [Google Scholar]
- 20.Wang JJ, et al. Hypertensive retinal vessel wall signs in a general older population: the Blue Mountains Eye Study. Hypertension. 2003;42:534–541. doi: 10.1161/01.HYP.0000090122.38230.41. [DOI] [PubMed] [Google Scholar]
- 21.Ojaimi E, et al. Methods for a population-based study of myopia and other eye conditions in school children: the Sydney Myopia Study. Ophthalmic Epidemiology. 2005;12:59–69. doi: 10.1080/09286580490921296. [DOI] [PubMed] [Google Scholar]
- 22.Varni JW, Seid M, Rode CA. The PedsQL: measurement model for the pediatric quality of life inventory. Med.Care. 1999;37:126–139. doi: 10.1097/00005650-199902000-00003. [DOI] [PubMed] [Google Scholar]
- 23.Wong TY, et al. Retinal arteriolar narrowing and risk of coronary heart disease in men and women. The Atherosclerosis Risk in Communities Study. JAMA. 2002;287:1153–1159. doi: 10.1001/jama.287.9.1153. [DOI] [PubMed] [Google Scholar]
- 24.Knudtson MD, et al. Revised formulas for summarizing retinal vessel diameters. Curr.Eye Res. 2003;27:143–149. doi: 10.1076/ceyr.27.3.143.16049. [DOI] [PubMed] [Google Scholar]
- 25.Hitzenberger CK. Optical measurement of the axial eye length by laser Doppler interferometry. Invest Ophthalmol Vis Sci. 1991;32:616–624. [PubMed] [Google Scholar]
- 26.Gopinath B, et al. Carbohydrate nutrition is associated with changes in the retinal vascular structure and branching pattern in children. Am.J.Clin.Nutr. 2012;95:1215–1222. doi: 10.3945/ajcn.111.031641. [DOI] [PubMed] [Google Scholar]
- 27.Gopinath B, et al. Effect of obesity on retinal vascular structure in pre-adolescent children. Int.J.Pediatr.Obes. 2011;6:e353–e359. doi: 10.3109/17477166.2010.500390. [DOI] [PubMed] [Google Scholar]
- 28.Gardiner TA, Archer DB, Curtis TM, Stitt AW. Arteriolar involvement in the microvascular lesions of diabetic retinopathy: implications for pathogenesis. Microcirculation. 2007;14:25–38. doi: 10.1080/10739680601072123. [DOI] [PubMed] [Google Scholar]
- 29.Nguyen TT, et al. Correlation of light-flicker-induced retinal vasodilation and retinal vascular caliber measurements in diabetes. Invest Ophthalmol.Vis.Sci. 2009;50:5609–5613. doi: 10.1167/iovs.09-3442. [DOI] [PubMed] [Google Scholar]
- 30.Goldstein, B. H. et al. Endothelial Function and Arterial Stiffness Relate to Functional Outcomes in Adolescent and Young Adult Fontan Survivors. J.Am.Heart Assoc. 5 (2016). [DOI] [PMC free article] [PubMed]
- 31.Osika W, et al. Anger, depression and anxiety associated with endothelial function in childhood and adolescence. Arch.Dis.Child. 2011;96:38–43. doi: 10.1136/adc.2008.152777. [DOI] [PubMed] [Google Scholar]
- 32.Cooper DC, et al. Depressed mood and flow-mediated dilation: a systematic review and meta-analysis. Psychosom.Med. 2011;73:360–369. doi: 10.1097/PSY.0b013e31821db79a. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 33.Nowakowski AC. Chronic inflammation and quality of life in older adults: a cross-sectional study using biomarkers to predict emotional and relational outcomes. Health Qual.Life Outcomes. 2014;12:141. doi: 10.1186/s12955-014-0141-0. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 34.Morozink JA, Friedman EM, Coe CL, Ryff CD. Socioeconomic and psychosocial predictors of interleukin-6 in the MIDUS national sample. Health Psychol. 2010;29:626–635. doi: 10.1037/a0021360. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 35.Faugere M, et al. Quality of life is associated with chronic inflammation in schizophrenia: a cross-sectional study. Sci.Rep. 2015;5:10793. doi: 10.1038/srep10793. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 36.Daien V, et al. Retinal Vascular Caliber Is Associated with Cardiovascular Biomarkers of Oxidative Stress and Inflammation: The POLA Study. PLoS.ONE. 2013;8:e71089. doi: 10.1371/journal.pone.0071089. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 37.Coste J, Quinquis L, D’Almeida S, Audureau E. Smoking and health-related quality of life in the general population. Independent relationships and large differences according to patterns and quantity of smoking and to gender. PLoS.ONE. 2014;9:e91562. doi: 10.1371/journal.pone.0091562. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 38.Gijsberts CM, et al. Gender differences in health-related quality of life in patients undergoing coronary angiography. Open.Heart. 2015;2:e000231. doi: 10.1136/openhrt-2014-000231. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 39.Chen Y, et al. Age- and sex-related differences in vascular function and vascular response to mental stress. Longitudinal and cross-sectional studies in a cohort of healthy children and adolescents. Atherosclerosis. 2012;220:269–274. doi: 10.1016/j.atherosclerosis.2011.10.030. [DOI] [PubMed] [Google Scholar]