Abstract
The objective was to investigate any possible relationship between functional and structural vascular changes in women with low gestational age and/or low birth weight by analyzing the retinal vascular pattern in women with thoroughly documented blood pressure. Retinal vessel morphology was evaluated by digital image analysis of ocular fundus photographs in 47 subjects, aged 23–30 y. The women were allocated into three groups: 1) those born preterm and appropriate for gestational age (AGA), with a median gestational age at birth of 30 wk and a median birth weight of 1250 g (n = 14); 2) those born small for gestational age (SGA) but full term (median 40 wk), with a median birth weight of 2130 g (n = 17), and 3) those born full term, AGA, and with a median birth weight of 3640 g (n = 16). Women born preterm had significantly higher length index for arterioles compared with the other two groups (median 1.11 and 1.08, respectively, p = 0.005). In addition, the preterm-born women had significantly fewer number of vascular branching points compared with the controls (median 27 and 30, respectively, p = 0.03). The abnormal retinal vascularization observed in ex-preterm women together with an increased casual blood pressure observed in these subjects suggests that being born preterm does have effects on the vascular system that persist into adult life. In addition, it demonstrates that preterm birth seems to affect the vascular system both functionally and structurally, which, in adulthood, could result in a lower threshold for the development of vascular disease.
Similar content being viewed by others
Log in or create a free account to read this content
Gain free access to this article, as well as selected content from this journal and more on nature.com
or
Abbreviations
- ROP:
-
retinopathy of prematurity
- SGA:
-
small for gestational age
- AGA:
-
appropriate for gestational age
- GA:
-
gestational age
References
Hagberg B, Hagberg G, Beckung E, Uvebrant P 2001 Changing panorama of cerebral palsy in Sweden. VIII. Prevalence origin in the birth year period 1991–94. Acta Paediatr 90: 271–277
Gorman WA, Fallon M, Kelly M, Clarke T, Griffin E, Matthews T, Murphy J, O'Brien N, Sheridan M 1996 The Dublin outcome for low birth-weight infants. Ir Med J 89: 186–187
Kocur I, Kuchynka P, Rodny S, Barakova D, Schwartz EC 2001 Causes of severe visual impairment blindness in children attending schools for the visually handicapped in the Czech Republic. Br J Ophthalmol 85: 1149–1152
Rowlands E, Ionides AC, Chinn S, Mackinnon H, Davey CC 2001 Reduced incidence of retinopathy of prematurity. Br J Ophthalmol 85: 933–935
Jacobson L, Lundin S, Flodmark O, Ellström K 1998 Periventricular leukomalacia causes visual impairment in preterm children. Acta Opthalmol Scand 76: 593–598
Barker DJP, Osmond C, Golding J, Kuh D, Wadsworth MEJ 1989 Growth in utero, blood pressure in childhood adult life, mortality from cardiovascular disease. BMJ 298: 564–567
Barker DJP, Osmond C, Winter PD, Margetts B 1989 Weight in infancy death from ischaemic heart disease. Lancet 9: 577–580
Phipps K, Barker DJP, Hales CN, Fall CHD, Osmond C, Clark PMS 1993 Fetal growth impaired glucose tolerance in men women. Diabetologia 36: 225–228
Barker DJP, Gluckman PD, Godfrey KM, Harding JE, Owens JA, Robinson JS 1993 Fetal nutrition cardiovascular disease in adult life. Lancet 341: 938–941
Barker DJP, Bull AR, Osmond C, Simmonds SJ 1990 Fetal placental size risk of hypertension in adult life. BMJ 301: 259–262
Law CM, Barker DJP, Bull AR, Osmond C 1991 Maternal fetal influences on blood pressure. Arch Dis Child 61: 1291–1295
Law CM, de Swiet M, Osmond C, Fayers PM, Barker DJ, Cruddas AM, Fall CH 1993 Initiation of hypertension in utero amplification throughout life. BMJ 306: 24–27
Barker DJP, Osmond C, Simmonds SJ, Wield GA 1993 The relation of small head circumference thinness at birth to death from cardiovascular disease in adult life. BMJ 306: 422–426
Martyn CN, Barker DJP, Osmond C 1996 Mothers' pelvic size, fetal growth, death from stroke coronary heart disease in men in the UK. Lancet 348: 1264–1268
Kistner A, Celsi G, Vanpee M, Jacobson SH 2000 Increased blood pressure but normal renal function in adult women born preterm. Pediatr Nephrol 15: 215–220
De Reuck J, Chatta A, Richardson E 1972 Pathogenesis evolution of periventricular leukomalacia in infancy. Arch Neurol 27: 229–236
1984 An international classification of retinopathy of prematurity. The Committee for the Classification of Retinopathy of Prematurity. Arch Ophthalmol 102: 1130–1134
Amir J, Metzker A, Krikler R, Reisner SH 1986 Strawberry hemangioma in preterm infants. Pediatr Dermatol 3: 131–132
Niklasson A, Ericson A, Fryer JG, Karlberg J, Lawrence C, Karlberg P 1991 An update of the Swedish reference standards for weight, length head circumference at birth for given gestational age (1977–1981). Acta Paediatr Scand 80: 756–762.
Hellström A, Svensson E 1998 Optic disc size retinal vessel characteristics in healthy children. Acta Ophthalmol 76: 260–267
Mushin AS 1974 Retinopathy of prematurity—a disease of increasing incidence. Transactions of the Ophthalmological Society of the United Kingdom 94: 251–257
Fielder AR, Shaw DE, Robinson J, Ng YK 1992 Natural history of retinopathy of prematurity: a prospective study. Eye 6: 233–242
Hellström A, Hård A-L, Chen Y, Niklasson A, Albertsson-Wikland K 1997 Influence of gestational age, birth size, perinatal morbidity, postnatal growth. Invest Ophthalmol Vis Sci 38: 184–192
Fryczkowski AW, Peiffer RL, Merritt JC, Kraybill EN, Eifrig DE 1985 Scanning electron microscopy of the ocular vasculature in retinopathy of prematurity. Arch Ophthalmol 103: 224–228
Baum JD, Bulpitt CJ 1970 Retinal vasoconstriction in premature infants with increased arterial oxygen tensions. Arch Dis Child 45: 350–353
Adair TH, Guyton AC, Montani JP, Lindsay HL, Stanek KA 1987 Whole body structural adaption to prolonged hypoxia in chick embryos. Am J Physiol 252: 1228–1234
Adair TH, Montani JP, Guyton AC 1988 Effects of intermittent hypoxia on structural vascular adaptation in chick embryos. Am J Physiol 254: 1194–1199
Sharett AR, Hubbard LD, Cooper LS, Sorlie PD, Brothers RJ, Nieto FJ, Pinsky JL, Klein R 1999 Retinal arteriolar diameters elevated blood pressure. The atherosclerosis risk in communities study. Am J Epidemiol 150: 263–270
Pierce EA, Avery RL, Foley ED, Aiello LP, Smith LE 1995 Vascular endothelial growth factor/vascular permeability factor expression in a mouse model of retinal neovascularization. Proc Natl Acad Sci U S A 92: 905–909
Bracher D 1982 Changes in peripapillary tortuosity of the central retinal arteries in newborns. A phenomenon whose underlying mechanisms need clarification. Graefes Arch Clin Exp Ophthalmol 218: 211–217
Frankell S, Elwood P, Sweetnam P, Yarnell J, Smith DG 1996 Birthweight, adult risk factors incident coronary heart disease: the Caerphilly study. Public Health 110: 139–143
Stein CE, Fall CH, Kumaran K, Osmond C, Cox V, Barker DJP 1996 Fetal growth coronary heart disease in South India. Lancet 348: 1269–1273
Phillips DIW, Barker DJP, Hales CN, Hirst S, Osmond C 1994 Thinness at birth insulin resistance in adult life. Diabetologia 37: 150–154
Hellström A, Hård AL, Niklasson A, Svensson E, Jacobsson B 1998 Abnormal retinal vascularisation in preterm children as a general vascular phenomenon. Lancet 352: 1827
Stanton AV, Mullaney P, Mee F, O'Brian ET, O'Malley K 1995 A method of quantifying retinal microvascular alterations associated with blood pressure age. J Hypertens 13: 41–48
Ibrahim Y, Bots M, Mulder P, Grobbee D, Hofman A, de Jong P 1998 Number of perifoveal vessels in aging, hypertension, atherosclerosis: The Rotterdam Study. Invest Ophthalmol Vis Sci 39: 1049–1053
Chapman N, Mohamudully A, Cerutti A, Stanton A, Sayer AA, Cooper C, Barker D, Rauf A, Evans J, Wormald R, Sever P, Hughes A, Thom S 1997 Retinal vascular network architecture in low-birth-weight men. J Hypertens 15: 1449–1453
Acknowledgements
The authors thank Björn Folkow, Professor Emeritus, Department of Physiology, Sahlgrenska University Hospital, and Göran Berglund, Professor, Department of Medicine, University Hospital Malmö, for their most valuable discussions. We also thank Mireille Vanpée, M.D., Ph.D., Institute of Women and Child Health, Karolinska Institute, for help with collecting and distinguishing the preterm material; Bengt Persson, M.D., Ph.D., for providing part of the SGA material; and Petra Otterblad at the National Medical Birth Register, for valuable assistance.
Author information
Authors and Affiliations
Corresponding author
Additional information
Supported by grants from the Göteborg Medical Society, the Frimurare-Barnhusdirektionen, the Swedish Society for Medical Research, and the Swedish Medical Research Council (#10863 and #13515).
Rights and permissions
About this article
Cite this article
Kistner, A., Jacobson, L., Jacobson, S. et al. Low Gestational Age Associated with Abnormal Retinal Vascularization and Increased Blood Pressure in Adult Women. Pediatr Res 51, 675–680 (2002). https://doi.org/10.1203/00006450-200206000-00003
Received:
Accepted:
Issue date:
DOI: https://doi.org/10.1203/00006450-200206000-00003
This article is cited by
-
Oxygen therapy in premature low birth weight infants is associated with capillary loss and increases in blood pressure: a pilot study
Journal of Human Hypertension (2020)
-
Low birth weight trends: possible impacts on the prevalences of hypertension and chronic kidney disease
Hypertension Research (2020)
-
Repeated high blood pressure at 6 and 11 years at the Pelotas 2004 birth cohort study
BMC Public Health (2019)
-
A twin study of cilioretinal arteries, tilted discs and situs inversus
Graefe's Archive for Clinical and Experimental Ophthalmology (2018)
-
Association among prematurity (<30 weeks’ gestational age), blood pressure, urinary albumin, calcium, and phosphate in early childhood
Pediatric Nephrology (2017)