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a International Centre for Circulatory Health, National Heart and Lung Institute, St Mary's Hospital and Imperial College London, United Kingdom
b Department of Epidemiology and Preventive Medicine, Monash University, Melbourne, Australia
c Department of Social Medicine, University of Bristol, United Kingdom
| ABSTRACT |
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OBJECTIVES. We hypothesized that small birth size may be associated with structural variations in the retinal vasculature in children.
METHODS. The Avon Longitudinal Study of Parents and Children followed a cohort of children born in 1991–1992 from birth. The current study included the first 263 children who were systematically screened in the year-12 follow-up. Complete data were available for 166 children with a gestation of
37 weeks. Retinal circulatory measures were evaluated, including retinal microvascular tortuosity and bifurcation optimality deviance, an indicator of abnormal endothelial function.
RESULTS. Optimality deviance and retinal tortuosity were higher among those with lower birth weight. Linear regression modeling was used to assess the association of retinal microvascular measures with birth weight. The standardized β coefficient between optimality deviance and birth weight was –.182 adjusted for gender and age in weeks; additional adjustment for systolic blood pressure and heart rate had little impact on the β coefficient. A similar association was observed for retinal tortuosity.
CONCLUSION. The findings of this study suggest that early life factors may have an important impact on retinal vascular structure, possibly through an adverse effect on endothelial function.
Key Words: ALSPAC retinal vascular geometry birth weight
Abbreviations: CVD—cardiovascular disease ALSPAC—Avon Longitudinal Study of Parents and Children BP—blood pressure
The role of the microcirculation in the pathogenesis of cardiovascular disease (CVD) is being increasingly recognized.1 Retinal microvascular abnormalities have been associated with an increased risk of stroke,2 ischemic heart disease,3,4 and diabetes,5 independent of other well-established risk factors in adults. These are important observations that could further our understanding of mechanisms linking the long-observed association among low birth weight and CVD,6 hypertension,7 and diabetes8 in adults. Determining whether these associations represent cause or effect has been difficult in adult populations where these conditions are common. A population of children where the frequency of hypertension and other metabolic disorders is low provides the ideal setting to determine whether retinal microvascular abnormalities are associated with early life factors. We hypothesized that small birth size may be associated with structural variations in the retinal vasculature in children.
| METHODS |
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37 weeks. There were no significant differences in the ages (P = .269) or genders (P = .628) of the youth with complete and incomplete data. The date of the last menstrual period as reported by the mother at enrollment and the date of delivery were used to estimate gestation. Term birth was defined as birth on or after 37 completed weeks of gestation. Infant gender and birth weight were recorded in the delivery room and abstracted from obstetric records and/or birth notifications. Measures of childhood weight, height, heart rate, and blood pressure (BP) used in the present study were taken at age 9 years. Height was measured with shoes and socks removed using a Harpenden stadiometer (Holtain Ltd, Crymych, Pembs, United Kingdom) to the nearest 0.1 cm, and weight was measured by using a Tanita TBF 305 body-fat analyzer and weighing scales (Tanita UK Ltd, Yewsley, Middlesex, United Kingdom). BMI was calculated as weight (kilograms)/height (meters squared). Systolic and diastolic BP were recorded on the right arm while the subject was seated using a Dinamap 9301 vital signs monitor (Critikon, Tampa, FL).
We took 45° digital retinal images of the macular center of each retina using a Topcon nonmydriatic retinal camera (Topcon TRC-NW6s, Topcon Technologies, Paramus, NJ) fitted with a Nikon D1X (Nikon, Tokyo, Japan). Images were graded by 2 observers who were blinded to subject data using a semiautomated system that captures a wide range of retinal geometric parameters, and reproducibility of this technique has been reported previously.4,10–14 Measured parameters included the (1) arteriolar diameters, (2) arteriolar bifurcation angles, (3) length/diameter ratios of arteriolar segments and arteriolar/venular diameter ratios (these parameters provide measures of arteriolar narrowing that are relatively unaffected by differences in optical refraction), (4) arteriolar tortuosity (estimated as the actual length of the vessel divided by the straight line distance between bifurcations minus 1), and (5) arteriolar optimality ratio and optimality deviance. Optimality ratio is the ratio of sum of "daughter" arteriolar diameters divided by the "parent" arteriolar diameter corrected for asymmetry.4 For a theoretically optimal bifurcation, the optimality ratio should be 0.79, and the optimality deviance was calculated as the absolute value of the optimality ratio minus 0.79.
Ethical approval of the study was obtained from the ALSPAC Law and Ethics Committee. Written informed consent for the study was obtained.
Statistical Methods
The data analysis was performed with SPSS 14.0 for Windows (SPSS Inc, Chicago, IL). Descriptive information for each of the variables was derived, and the distribution was assessed. Baseline data are presented as mean ± SE or percentages. Linear regression was used to assess the association of birth weight with measures of the retinal microcirculation. Standardized β coefficients were used, because they allow for direct comparison of the strength of associations between risk factors and disease.
| RESULTS |
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| DISCUSSION |
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The present study suggests that early life factors may have an important impact on microvascular structure and function in children. Optimality deviance is an indicator of endothelial dysfunction,16 and this may imply that a primary disorder of the endothelium in early life is the mechanistic link between birth weight and CVD. This is consistent with previous findings of impaired endothelial function in large conduit arteries in children and young adults of low birth weight17,18 and decreased capillary recruitment and reduced vasodilator responses to acetylcholine in the skin of children of low birth weight.19 Although this question has not been examined previously in the retinal microvasculature of children, Chapman et al12 observed that adult men of low birth weight had narrower bifurcation angles compared with normal birth weight control subjects, indicative of retinal arteriolar rarefaction. Similarly, in a study by Kistner et al20 of women born preterm, the researchers observed a higher length index for arterioles and a decreased number of vascular branching points compared with women born at term. Both of these studies concluded that the observed architectural changes in the retinal microvasculature might be related to impaired fetal growth. The present study was small and underpowered to detect some associations. Further investigation is warranted in a well-documented large prospective study of children at risk of future vascular disease.
| CONCLUSION |
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| ACKNOWLEDGMENTS |
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We are extremely grateful to all of the families who took part in this study, the midwives for their help in recruiting them, and the whole ALSPAC team, which includes interviewers, computer and laboratory technicians, clerical workers, research scientists, volunteers, managers, receptionists, and nurses.
| FOOTNOTES |
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Address correspondence to Robyn J. Tapp, PhD, International Centre for Circulatory Health, NHLI, Imperial College London, St Mary's Campus, London W2 1LA, United Kingdom. E-mail: rtapp{at}imperial.ac.uk
This publication is the responsibility of the authors; Dr Tapp serves as guarantor for the contents of this article.
The authors have indicated they have no financial relationships relevant to this article to disclose.
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S. W. Lim and N. Cheung Birth Weight and Retinal Vascular Changes Hypertension, June 1, 2008; 51(6): e56 - e56. [Full Text] [PDF] |
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